Patterns of and Factors Associated with Postpartum Diabetes...

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i Patterns of and Factors Associated with Postpartum Diabetes Screening in Women Diagnosed with Gestational Diabetes Mellitus in Malappuram District Dr. Sakeena K Dissertation submitted in partial fulfillment of the Requirement for the award of Master of Public Health ACHUTHA MENON CENTRE FOR HEALTH SCIENCE STUDIES SREE CHITRA TIRUNAL INSTITUTE FOR MEDICAL SCIENCES AND TECHNOLOGY, TRIVANDRUM Thiruvananthapuram, Kerala. India 695011 OCTOBER 2016

Transcript of Patterns of and Factors Associated with Postpartum Diabetes...

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Patterns of and Factors Associated with Postpartum Diabetes Screening

in Women Diagnosed with Gestational Diabetes Mellitus in

Malappuram District

Dr. Sakeena K

Dissertation submitted in partial fulfillment of the

Requirement for the award of

Master of Public Health

ACHUTHA MENON CENTRE FOR HEALTH SCIENCE STUDIES

SREE CHITRA TIRUNAL INSTITUTE FOR MEDICAL SCIENCES

AND TECHNOLOGY, TRIVANDRUM

Thiruvananthapuram, Kerala. India – 695011

OCTOBER 2016

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Dedicated to my family members and to all those who have

supported me in the completion of the study.

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ACKNOWLEDGEMENTS

First and foremost I would like to thank my guide Dr. T. K. Sundari Ravindran for being

such a constant source of inspiration and directing me in the right path from the inception

of the idea regarding my topic to the completion of my dissertation. I would not have

been able to attain any concrete results without her incredible guidance and support

throughout the process.

I would like to thank my teachers Dr. P S Sankara Sarma for helping me in the sampling

process and methodology; Dr. V Raman Kutty, Dr. Manju Nair, Dr. Mala Ramanathan,

and Dr. Ravi Prasad Varma for guiding me whenever I had any doubts regarding my

thesis or otherwise. I would also like to thank Dr. K R Thankappan, Dr. Biju Soman, Dr.

Kannan Srinivasan and Ms. Jissa V T for teaching me the various areas of public health. I

express my heartfelt gratitude to my seniors Uma Santhosh, Dr. Malu Mohan, Dr. GK

Mini, Dr.Neethu Suresh for always lending a hand and helping me through my

presentations and thesis work.

I would like to acknowledge the love and support given by my family, especially my

husband Dr. Jafar M Backer over the years. This journey would not have been easy had

they not stood by me always. Lastly, I would like to thank all my batch mates for a

successful completion of these two years.

The study was funded by a research grant of Health Systems Research India Initiative

Trust (HSRII). I would like to express my sincere gratitude towards Mr.Ranjith R Menon

and Mr.Arun B Nair of HSRII Trust for their support.

With regards,

Dr. Sakeena K

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DECLARATION

I hereby declare that this dissertation titled ―Patterns of and Factors Associated with

Postpartum Diabetes Screening in Women Diagnosed with Gestational Diabetes Mellitus

in Malappuram District‖ is the bonafide record of my original research. It has not been

submitted to any other university or institution for the award of any degree or diploma.

Information derived from the published or unpublished work of others has been duly

acknowledged in the text.

Dr. Sakeena K

Achutha Menon Centre for Health Science Studies

Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum

Thiruvananthapuram, Kerala. India - 695011

October, 2016

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CERTIFICATE

Certified that the dissertation titled ―Patterns of and Factors Associated with Postpartum

Diabetes Screening in Women Diagnosed with Gestational Diabetes Mellitus in

Malappuram District‖ is a record of the research work undertaken by Dr. Sakeena K, in

partial fulfillment of the requirements for the award of the degree of ―Masters of Public

Health‖ under my guidance and supervision.

Guide:

Dr. TK Sundari Ravindran

Professor

Achutha Menon Centre for Health Science Studies

Sree Chitra Tirunal Institute for Medical Sciences and Technology,

TrivandrumThiruvananthapuram, Kerala. India - 695011

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Table of contents

Chapters Topic Page no.

List of tables and figures

Glossary of abbreviations

Abstract

Sections Sub sections Topic Page No

1 Chapter1- Introduction and review of literature 1

1 Background 1

1.1 Gestational Diabetes Mellitus (GDM) 1

1.2 Diagnostic Criteria 2

1.2.1 During pregnancy 2

1.2.1 During the postpartum period 3

1.3 Management of GDM 4

2 Prevalence of GDM 4

2.1 Prevalence in different parts of the world 4

2.2 Prevalence in India 6

3 Risk Factors 7

3.1 India 10

4 Prognosis 12

4.1 Poor pregnancy outcome and morbidities 12

4.2 Risk of developing Type2 Diabetes

mellitus(T2DM) in future

14

5 Universal postpartum screening of

women with GDM in pregnancy

15

5.1 Screening rates 15

5.2 Reasons for low postpartum screening rates

among women diagnosed with GDM

17

6 Rationale for the Study

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2 Chapter 2-Methodology 22

2.1 Objectives of the study 22

2.2 Study type/design 22

2.3 Study setting 22

2.4 Study population 23

2.5 Sample size estimation 23

2.6 Sample selection procedures 24

2.7 Inclusion Criteria- for GDM affected

women

26

2.8 Exclusion Criteria -for GDM affected

women

26

2.9 Inclusion Criteria –For the providers 26

2.10 Operational definitions 26

2.11 Data collection techniques 27

2.12 Analysis 28

2.13 Data storage 28

2.14 Ethical considerations 28

2.15 Dissemination of results 29

3 Chapter 3-Results and Explanations 30

Section1 30

3.1 Characteristics of the respondents 30

3.1.1 Socio-demographic characteristics of the

respondents

30

3.2 Reproductive profile of women affected

with GDM

32

3.3 Diagnostic profile of the respondents 34

3.4 Postpartum screening of the respondents 35

3.5 Morbidity profile of GDM affected women

with in their most recent pregnancy and

43

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delivery

3.6 Child characteristics 45

3.7 Morbidity profile among newborn babies 47

Section II

3.8 Timely postpartum screening and

associated factors

47

3.9 Results of age adjusted multiple logistic

regression of factors associated with timely

postpartum screening (≥6weeks)

51

Section III 53

Doctors’ perspectives on management and

postpartum screening and advice

53

3.10 Management of GDM during pregnancy 54

3.11 Management of GDM during labour 55

3.12 Postpartum advice and management 56

3.13 Postpartum screening 57

3.14 Perceived barriers to women using

postpartum screening

57

3.15 Recommendations and suggestions to

improve the rate of timely postpartum

screening

58

Chapter 4-Discussion and conclusions

59

4.1 Patterns of postpartum screening for diabetes 60

4.2 Factors associated with timely postpartum

screening for diabetes of women with GDM

62

4.3 Barriers to postpartum diabetes screening and

adequate post-screening follow-up

65

4.3.1 Barriers as reported by the women 65

4.3.2 Barriers related to doctors and the health system 66

4.4 Postpartum diabetes screening of GDM 67

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pregnancies-a case of repeated missed

opportunities to prevent T2DM

4.5 Strength and Limitations of the study 67

4.6 Conclusions and recommendations 67

References

Annexures

Annexure I Interview schedule for the survey (English)

Annexure II Interview schedule for the survey (Malayalam)

Annexure III Research information sheet (English)

Annexure IV Research information sheet (Malayalam)

Annexure V Informed consent form GDM affected women (English)

Annexure VI Informed consent form GDM affected women (Malayalam)

Annexure VII Research information sheet provider (English)

Annexure VIII Informed consent form provider (English)

Annexure IX In-depth interview guide provider

Annexure X Permission letter from District Medical Officer Malappuram

Annexure XI Permission letter from Almas hospital

Annexure XII Permission letter from MKHO hospital

Annexure XIII Permission letter from Laila‘s hospital

Annexure XIV Institute Ethics Committee clearance certificate

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List of tables and figures

Table

no:

Title Page

number

1.1 Risk factors of gestational diabetes mellitus 8

1.2 Maternal and fetal morbidity associated with gestational diabetes

mellitus

13

2.1 Details of deliveries of the four selected hospitals for the year 2015 23

3.1 Socio-demographic profile of the respondents in the study sample 31

3.2 Reproductive profile of women affected with GDM in the study

sample

32

3.3 Diagnostic profile of the respondents in the study sample 34

3.4 Postpartum diabetes screening profile of the respondents in the study

sample.

36

3.5 Reasons for not undergoing blood sugar examination after delivery. 37

3.6 Status of consultation after testing their blood in the postpartum

period.

38

3.7 Reasons for not consulting a doctor. 39

3.8 Instructions to respondents who consulted a doctor after testing their

blood sugar.

40

3.9 Status of adherence to doctors‘ instructions by the respondents. 41

3.10 Reasons for non-adherence for the respondents 43

3.11 Patterns of morbidity of women affected with GDM in their most

recent pregnancy, delivery and postpartum period

43

3.12 Child characteristics in the most recent delivery 46

3.13 Patterns of morbidity among new born babies of women affected

with GDM.

47

3.14 Timely postpartum screening and associated factors 48

3.15 Results of age adjusted multiple logistic regression of factors

associated with timely postpartum screening (≥6weeks)

52

3.16 Profile of the doctors included in the in-depth interviews 53

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Figure

no:

Title Page

number

1 Missed windows of opportunity to prevent or delay progression

from GDM to T2DM

69

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Glossary of abbreviations

WHO World Health Organization

DIP Diabetes In Pregnancy

GDM Gestational Diabetes Mellitus

ADA American Diabetes Association

IADPSG International Association of Diabetes and Pregnancy Study Groups

OGTT Oral Glucose Tolerance Test

DIPSI Diabetes in Pregnancy Study Group India

FPG Fasting Plasma Glucose

PPPG Post Prandial Plasma Glucose

HAPO Hyperglycemia and Adverse Pregnancy Outcome

T2DM Type 2 Diabetes Mellitus

IDF International Diabetes Federation

ASHA Accredited Social Health Activist

AWW Anganwadi worker

NICU Newborn Intensive Care Unit

Ob/Gyn Obstetrician/ Gynaecologist

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ABSTRACT

Background: The aim of this study is to examine rate and patterns of postpartum

diabetes screening for gestational diabetes mellitus (GDM) patients and factors associated

with the same. Other objectives are to document postpartum morbidity and provider

perspectives on appropriate postpartum follow up of this group.

Methodology: A cross sectional study was done among 200 women with GDM, who had

delivered in selected hospitals in Malappuram district between 9weeks and 6 months prior

to the survey using interviewer administered interview schedule in Malayalam. In depth

interviews were done of doctors who had managed the maximum number of GDM cases

from each of the four selected hospitals.

Results: Prevalence of timely postpartum diabetes screening among the respondents is

29%. Doctors‘ advice significantly influenced uptake of timely postpartum screening.

Only about 6% of the women with a GDM pregnancy received appropriate and adequate

postpartum follow-up. About a fifth of the respondents had a health problem during

pregnancy or in the postpartum period. A tenth of the infants experienced neonatal

morbidity. Doctors varied in the level of accurate knowledge and had diverse approaches

not consistent with standard guidelines in managing GDM cases postpartum. All doctors

reported difficulty in getting patients to come for screening beyond one month

postpartum.

Conclusion: There is urgent need to enforce adherence to national guidelines for

postpartum GDM screening. Increasing provider knowledge regarding high future risk of

Type 2 DM following a GDM pregnancy even among women who have normal blood

sugar levels postpartum is of utmost importance. Appropriate postpartum management of

GDM patients can be an important contribution to diabetes prevention and control in

Kerala.

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Chapter 1

Introduction and review of literature

1.1 Background

1.1.1. Gestational Diabetes Mellitus

Hyperglycemia (an excess of glucose in the blood stream) in pregnancy is one of the most

common medical conditions associated with pregnancy. Depending on the level of

hyperglycemia and the time of detection, WHO has classified hyperglycemia in

pregnancy as either diabetes mellitus in pregnancy (DIP) or as gestational diabetes

mellitus (GDM) (World Health Organisation, 2013).

Diabetes mellitus is defined as a condition where a person‘s blood glucose level is

increased, either due to the lack of production of enough insulin, or because the body

does not respond properly to it. Diabetes mellitus in pregnancy (DIP) is defined as

pregnancy in previously known diabetes or hyperglycemia diagnosed for the first time

during pregnancy that meets WHO criterion for diabetes mellitus in the non- pregnant

state. DIP may occur at any time during pregnancy including in the first trimester.

On the other hand, gestational diabetes mellitus (GDM) is defined as hyperglycemia

diagnosed for the first time in pregnancy that is not diabetes. This may occur at any time

during pregnancy but is most likely after 24 weeks. So hyperglycemia detected during

routine investigations in pregnancy which does not meet the criteria of diabetes mellitus

in pregnancy (DIP) is called gestational diabetes mellitus (GDM). This is a new and

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improved definition. Previously GDM was defined as ―any degree of glucose intolerance

with onset or first recognition during pregnancy‖ (Association, 2013).

1.2. Diagnostic Criteria

1.2.1 During pregnancy

The diagnostic criteria of GDM vary from country to country. As per the

recommendations of International Association of Diabetes and Pregnancy Study Groups

(IADPSG) (2010) and WHO (2013), the diagnosis of GDM is made using a single step

75-g oral glucose tolerance test (OGTT) when one of the following test results are

recorded during routine testing specifically between 24 and 28 weeks of pregnancy or at

any other time during the course of pregnancy:

(1) Fasting plasma glucose 5.1−6.9 m mol/L (92−125 mg/dl),

(2) 1-hour post 75-g oral glucose load ≥10 m mol/L (180 mg/dl),

(3) 2-hour post 75-g oral glucose load 8.5–11.0 m mol/L (153−199 mg/dl).

To standardize the diagnosis of GDM, the World Health Organization (WHO)

recommends using a 75 g oral glucose load which can be given in either a non-fasting or

fasting state or one blood sample to be drawn 2 hours after the glucose load. The

diagnostic cut-off point for GDM is with140 mg/dL, irrespective of whether the GTT is

done in the fasting or no fasting state(Mohan et al., 2015,Alberti and Zimmet, 1998). The

Diabetes in Pregnancy Study Group of India (DIPSI) guidelines also recommends the

same diagnostic criteria.

The usual recommendations are for screening pregnant women for GDM between 24 and

28 weeks of gestation, but there is a possibility of missing the chance for detection of

unrecognized type2 DM (pre-GDM) (Ben-Haroush et al., 2004,Bartha et al., 2000).

Universal screening of all pregnant women is recommended to identify mothers at high

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risk of GDM and follow them up appropriately. Life style modification and/or

pharmacological intervention with high risk women can delay or prevent progression to

type 2 DM of women diagnosed with GDM during pregnancy (Tandon et al, 2015,Ratner

et al, 2008). Regular postpartum screening of all women diagnosed with GDM is also

recommended (Buchanan and Page, 2011).

1.2.2 During the postpartum period

The 75-g oral glucose tolerance test (OGTT) is considered as the most sensitive test

for postpartum screening of GDM. It helps in detecting maximum number of cases of pre

diabetes /diabetes as compared to fasting plasma glucose (FPG) and glycated hemoglobin

(HbA1c) (ADA, 2014). FPG alone may miss 30–40% of cases of type 2 diabetes and will

not detect isolated impaired glucose tolerance (Tandon et al., 2015).

The National Diabetes Education Program and the American College of Obstetricians and

Gynecologists (the College) jointly recommend postpartum screening of women with a

history of GDM at 6-12 weeks postpartum. If the test is normal, retest every 3 years and

at the first prenatal visit in subsequent pregnancy is recommended. If pre-diabetes is

diagnosed, then annual testing must be done. The role of family support in healthy diet

and development of physical activity behavior is crucial, because of increased risk of

children of GDM mothers to obesity and T2DM (Gabbe et al., 2012) .

As per National Guidelines for Diagnosis and Management of Gestational Diabetes

Mellitus for India, a FPG and a 2hr postprandial plasma glucose(PPPG) is performed on

the third day of delivery at the place of delivery and hence GDM cases are discharged

only after 48 hours following delivery. Subsequently there are instructions to the

Auxiliary Nurse Midwife (ANM) who is the front-line health worker, to perform 75 g

OGTT at 6 weeks postpartum to evaluate glycemic status of women. Cut off values for

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normal blood glucose values are fasting plasma ≥ 126 mg/dl, 75g OGTT 2 hr plasma

glucose normal value <140mg/dl, impaired glucose tolerance 140-199mg/dl and

diabetes ≥ 200 mg/dl. The guidelines are silent on further screening of women detected to

be normal during postpartum screening.

1.3. Management of GDM

A comprehensive approach to managing GDM and preventing GDM from progressing to

type 2 diabetes includes life style interventions, breast feeding support, appropriate

pharmacological treatment, and continuous follow-up for the mother and child for their

future health (Ratner., 2007).

According to the ―The International Federation of Gynaecology and Obstetrics (FIGO)

Initiative on gestational diabetes mellitus: A pragmatic guide for diagnosis, management,

and care-2015‖, GDM should be managed as per the available infrastructure and

resources available in a specific setting. The management primarily starts from the

empowerment of women to choose the right quantity and quality of food and level of

physical activity, and nutritional counseling and physical activity should be the primary

tool. Repeated advice and reinforcement is needed. When the lifestyle modification alone

fails to achieve blood sugar control, metformin, glyburide, or insulin should be

considered as safe and effective treatment options for GDM (Hod, Kapur, et al., 2015)

2. Prevalence of GDM

2.1. Prevalence in different parts of the world

According to the 2015 estimates of the International Diabetic Federation (IDF), globally

16.2 % of women with live births had some form of hyperglycemia in pregnancy. Out of

this, GDM accounted for 85.1 %, other types of diabetes first detected in pregnancy was

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7.4% and diabetes detected prior to pregnancy was 7.5%. This shows the alarming nature

of the situation which needs urgent global action (IDF.,2015).

A survey on prevalence and country practices administered to diabetologists, obstetricians

and others working on gestational diabetes mellitus in 173 countries reported that there

was a variation in GDM prevalence, ranging from <1% to 28% ,which included data

derived from single or multisite studies, national data, and /or estimates from expert

assessments (Jiwani et al., 2012).

The prevalence of GDM in Europe is 6-10% of pregnancies (Buckley et al., 2012). In the

United States of America, the figures were 4.6 % as per birth certificate and 9.2% as per

both birth certificate and Pregnancy Risk Assessment Monitoring Questionnaire

(PRAMS) using 2007-2010 data from PRAMS (De Sisto et al., 2014) and in Africa the

prevalence was 3.2% (2.1%-6.7%) as per International Diabetic Federation diabetic atlas

of 2015.

This variability may be due to ethnicity and ethnic heterogeneity among different

populations, as well as differences in screening and diagnostic criteria used (Hod et al.,

2015). Variations in prevalence of GDM by ethnicity is also reported by a comparison

study in Melbourne in Australia among 1928 GDM diagnosed parturient women out of

35,253 (5.5%) pregnant women, during 1979 to 1988. There were more severe grades of

GDM in women born in the Indian subcontinent , Mediterranean region, Asia, Egypt and

Arab countries, and the incidence of GDM was rising in all racial groups from 3.3%

during 1979-1983 to 7.5% during 1984-1988 (Beischer et al., 1991) .

Women entering pregnancy are at an increased risk of hyperglycemia due to a decline in

the age at onset of diabetes and pre-diabetes, and the increase in some countries in the age

at child bearing. This along with the rise in prevalence of overweight and obesity

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globally are deemed to contribute to an increase in GDM in many parts of the globe

(Mendez et al., 2005).

2.2. Prevalence in India

Compared to other populations of Southeast Asia, the prevalence of GDM is high in the

Indian population (Seshiah et al., 2004). Women of Asian origin and especially ethnic

Indians are at a higher risk of developing GDM and subsequent type 2 diabetes. It is

possible that undiagnosed GDM in the past has resulted in the high prevalence of type 2

diabetes (T2DM) in India (Seshiah, Balaji et al., 2008).

The prevalence of GDM in India varies in different parts of the country, depending upon

the geographical locations and diagnostic methods used. A study by Rajesh Rajput and

others in 2011, estimated a prevalence of 7.1% in Haryana (Rajput et al., 2013). Studies

from southern states done in recent years have reported a much higher prevalence of

GDM. For example the prevalence in a prospective observational study in a tertiary care

hospital in north Kerala in 2014 was 15.9% (Mohan and Chandrakumar, 2015). A study

on prevalence and risk factors associated with gestational diabetes in a medical college in

south India during December 2013 to January 2014 found that the prevalence was 17%

(Sreekanthan et al., 2014). A high prevalence of 27% was reported by a study in

Pondicherry during August 2011 to June 2012 using the International Association of

Diabetes and Pregnancy Study Group‘s (IADPSG) diagnostic criteria (Nayak et al.,

2013). Another multi-centric study observed that the highest prevalence of GDM was in

southern region (Ernakulum, Kerala) and lowest prevalence in North Eastern region

(Manipur) (Baruah et al., 2014).

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GDM has been found to be more prevalent in urban areas than in rural areas (Zargar et

al., 2004, Seshiah et al., 2009, Seshiah et al., 2008 , Nayak et al., 2013) . In Tamil Nadu,

urban (Chennai), semi-urban (Saidapet), and rural (Thiruvallur) area prevalence were

17.8%, 13.8% and 9.9%, respectively in 2009 (Seshiah et al., 2009) .

The variations in the prevalence of GDM in India in different geographical locations may

be ascribed to variations in caste, religion, socioeconomic status, life style and food habits

and access to health care services (Baruah et al., 2014).

There are indications of a dramatic increase in the prevalence of GDM in India. A 2004

study in Kashmiri women reported GDM prevalence to be 3.8% but in 2014 (Zargar et

al., 2004), a study to determine the prevalence of GDM in urban block of Kashmir valley

found that the prevalence was 7.8% (Raja et al., 2014). In a multi centric study among

3674 pregnant women from different parts of India in 2004 the prevalence of GDM was

16.6%, with an increase in prevalence from 1% in 1998 to 16.6 % in 2004 in the country

(Seshiah et al., 2004). The increasing prevalence of GDM in general is attributed to the

urbanization and the epidemic of obesity and physical inactivity.

3. Risk factors

Knowledge regarding the nature and type of risk factors plays a significant role in

planning and implementing prevention strategies to control the epidemic of gestational

diabetes mellitus (GDM). Evidence from the literature shows that risk factors are more or

less same at the global, national and local levels except in certain factors like the

geographical peculiarity, ethnicity, life style and food habits.

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Table.1.1 Risk Factors of Gestational Diabetes Mellitus

Maternal Factors Past Obstetric

History

Pregnancy Factors Family

History

Diabetes

Protec

tive

Factor

s

Ethnicity(women of

Asian Origin,

especially Indians)

Increased

age*(women who are

older than 25 have a

greater risk )

Parity

Pre-pregnancy weight

Weight gain during

pregnancy

BMI >27

Polycystic ovarian

syndrome

Low birth weight

Abortions,

Fetal loss

Past history of GDM

Previous abnormal

GTT

Hydramnios*

( a condition with

excess amniotic

fluid accumulation

in pregnancy)

Bleeding*

Large weight

babies(macrosomia)

*

Previous fetal

malformations

Pregnancy induced

hypertension

Degree of hyperglycemiain

pregnancy and immediate

postpartum period1

Multiple pregnancy

Sex of the fetus (4% more

relative risk for male than

female)

Prematurity2

Polyhydramnios2(Excess of

amniotic fluid in the

amniotic sac)

Macrosomia2

Preterm labor2

GDM in

women‘s

mother*

Young

age

Physic

al

activity

1

Health

y diet2

Breast

feeding

3

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Maternal Factors Past Obstetric

History

Pregnancy Factors Family

History

Diabetes

Protec

tive

Factor

s

Educational level*

Socioeconomic

status*

Acanthosis nigricans*

Lack of exercise and

diet control

Dietary fat

Smoking

Certain drugs

(influence insulin

resistance)

Urban habitat*

low adult height*

Premature rupture of

membranes*2

Hyperbilirubinemia*

*Indian studies; 1, 2, 3- potentially prevent progression to type 2 diabetes

1-risk factor for subsequent pregnancies, 2-complications during previous pregnancy is a

major risk factor (Sreekanthan et al., 2014)

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Other than the above factors, ethnicity (women of Asian origin, especially ethnic Indians)

and maternal factors such as polycystic ovarian syndrome (PCOS), a past history of poor

pregnancy outcome (abortion, foetal loss) are also contributing to Gestational diabetes

mellitus incidence(Cheung et al., 2001).

Factors such as persistent obesity, weight gain in future and subsequent pregnancies can

be modified (modifiable risk factors), but factors like ethnicity, pre pregnancy weight,

age, parity, family history of diabetes, and degree of hyperglycemiain pregnancy and

immediate postpartum period unmodifiable risk factors. Another unmodifiable risk factor

is sex of the baby. In a systematic review and meta-analysis by Jaskolka D et al 2015,

pregnant women carrying a boy had a 4% higher relative risk of GDM than those

carrying a girl, thus the fetus had an unsuspected effect on the glucose metabolism of the

mother in pregnancy (Jaskolka et al., 2015).

Physical activity, dietary fat, and avoidance of certain life style factors that adversely

influence insulin resistance, such as smoking and certain drugs are additional modifiable

risk factors, and diabetic prevention strategies should address the potentially modifiable

risk factors using the unmodifiable risk factors to identify women at risk (Dornhorst and

Rossi., 1998).

3.1 India

In a case control study in a tertiary care hospital in south India carried out during August

2007 to June 2008, the results showed association of several modifiable and unmodifiable

risk factors to GDM. Those based on personal and family history were body mass index

(BMI), those who had treatment for infertility, family history of diabetes among first

degree relatives especially in the mother. Related to the past history were history of

previous pregnancy losses, past GDM, prematurity , pre eclampsia , urinary tract

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infections, moniliasis (yeast or fungal infection of vulva and vagina), polyhydramnios

(excess of amniotic fluid in the amniotic sac), macrosomia (a new born who‘s

significantly larger than average) and pre-term labor (Bhat et al., 2010).

In a study carried out during June 2009 to January 2011 in an antenatal care clinic at a

tertiary care hospital in Haryana, the risk factors identified were age, educational level,

socioeconomic status, pre - pregnancy weight and BMI, weight gain, acanthosisnigricans

(a brown to black, poorly defined, velvety hyper-pigmentation of the skin, usually found

in body folds), family history of diabetes or hypertension and past history of GDM. But

on multivariate analysis, only upper middle class and presence of acanthosisnigricans

were found to be significantly associated with GDM (Rajput et al., 2013).

A medical college- based study in Kollam district of Kerala during December 2013 to

January 2014 found that the risk factors were higher age of pregnant women, over weight

and obesity, GDM in first degree relatives, previous abnormal GTT, lack of exercise and

diet control. The study also identified that women with previous large weight babies

(macrosomia), previous loss of pregnancy, GDM in previous pregnancy, complications in

previous pregnancy like hydramnios, bleeding etc. had increased chances of getting GDM

(Sreekanthan et al., 2014).

A mixed methodology study in Kerala (2013) identified many environmental and

personal factors leading to unhealthy life styles along with inadequate accessibility and

availability of health care services, cultural bias, norms, other misconceptions to risks and

low expectations on life style modification and risk reduction. The prevalence of risk

factors were found to be very high and increasing in Kerala (Daivadanam et al., 2013).

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4. Prognosis

GDM is associated with poor pregnancy outcome and a range of maternal and neonatal

morbidities, and women with GDM are also at high risk of developing Type 2 Diabetes

Mellitus.

4.1. Poor pregnancy outcomes and morbidities

GDM affects both mother and offspring adversely. A study in Kerala in 2014, showed

that 80% of abortions had a history of previous GDM in pregnancy (Sreekanthan et al.,

2014, Metzger, 2007). According to the Hyperglycemia and Adverse Pregnancy Outcome

Study (HAPO study) which enrolled between July 2000 and April 2006 more than 25,000

non-diabetic pregnant women from 15 field centers located in 9 different countries, there

was a positive association of maternal blood glucose levels below those diagnostic of

diabetes with adverse perinatal outcomes (Coustan et al., 2010, The HAPO Study

Cooperative Research Group, 2008).

A retrospective study with a cohort of 180 from a rural area of Thiruvananthapuram

district, Kerala, taken from the database of INDADE (Indo Danish Collaboration on

Diabetes Epidemiology) from 2007 to2011 (the report is based on 2010 analysis)

observed that the major neonatal outcomes were increased birth weight and increased

IBN(in-born nursery ) admissions (Sreelakshmi et al., 2015). The risk for development of

obesity and abnormal glucose metabolism during child hood, adolescence, and adulthood

were more in offspring of mothers with GDM(Metzger., 2007). The perinatal and

neonatal morbidities include macrosomia, shoulder dystocia and other birth injuries,

respiratory distress, hypoglycemia (low blood glucose level), polycythaemia (abnormally

increased concentration of haemoglobin in the blood), and hyperbilirubinemia (elevated

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level of bilirubin in the blood). The long term sequelae of uterine exposure to maternal

hyperglycemia include higher risks of obesity, impaired glucose metabolism, and diabetes

later in life (Hod et al., 2015).

Common maternal outcomes in women with GDM were: delivering the child through

surgical intervention, progression to type 2 diabetes mellitus, and higher incidence of

maternal morbidity including birth trauma, hypertensive disorders of pregnancy

(including preeclampsia), and subsequent development of T2DM (Sreelakshmi et al.,

2015).

In a prospective cohort study in Pondicherry during August 2011 to July 2012, there was

significant association of family history and low gestational age with more antenatal

complications in GDM mothers, when compared to non GDM group (25% vs 12%)

(Maiti et al., 2012,Sreelakshmi et al., 2015). Table 2 below summarizes the major

maternal, neonatal, and infant and child morbidities associated with GDM.

Table 1.2: Maternal and fetal morbidity associated with gestational diabetes

mellitus.

Maternal morbidity Foetal/neonatal/child morbidity

Early pregnancy

Spontaneous abortions Neonatal death

Pregnancy Non-chromosomal congenital

malformations

Pre eclampsia Shoulder dystocia

Gestational hypertension Respiratory distress syndrome

Excessive foetal growth

(macrosomia, large for gestational age)

Cardiomyopathy

Urinary tract infections Neonatal polycythaemia

Delivery Neonatal hyperbilirubinemia

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Maternal morbidity Foetal/neonatal/child morbidity

Pre-term labour Neonatal hypocalcaemia

Traumatic labour NICU admissions*

Instrumental delivery

(as a consequence birth injury

Erb‘s palsy

Caesarian delivery Programming and imprinting:-

Foetal origins of disease: diabetes Obesity, hypertension, metabolic syndrome

Postoperative/postpartum infections

Postoperative/postpartum haemorrhage

Thromboembolism

Maternal morbidity and mortality

Haemorrhage

Pueparium

Failure to initiate and/or maintaining

breastfeeding

Infections

Long-term postpartum

Weight retention

GDM in subsequent pregnancies

Future overt diabetes

Future cardiovascular disease

Adapted from the International Journal of Gynaecology &obstetrics,volume 131,

supplement3(2015), *added from Sreelakshmi et al.

4.2. Risk of developing Type 2 Diabetes mellitus (T2DM) in future

Women with a history of GDM are more prone to develop type 2 diabetes mellitus in

future (Metzger., 2007,Bellamy et al., 2009a, Jiwani et al., 2012).

In a systematic review of 28 epidemiological studies published between January 1961

and August 2001, with follow up times ranging from 6 weeks to 28 years, the cumulative

incidence of diabetes ranged from 2.6% to 70% after the index pregnancy, and maximum

was in the first five years after delivery and appeared to plateau after 10 years (Kim et

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al., 2002). In a four year follow up study in 2000 in Hungary of previous GDM women

who received their care during pregnancy between 1996 and 1998 the prevalence of

diabetes was 21% (Madarász et al., 2009).

South Asians are found to have high rates of development of diabetes after GDM, and

they develop the condition earlier than people of other ethnicities (Girgis et al., 2012). A

five year follow up study during 1997-1998 in Mysore, India found the conversion rate to

T2DM to be 34% in 35 GDM women as compared to 2% among controls (Krishnaveni et

al., 2007).

The most important predictor of the development of type 2 diabetes following a GDM

pregnancy was found to be an elevated blood glucose value at GDM diagnosis or at an

early postpartum examination. In a study conducted in 1999-2002 among Danish women,

the incidence of diabetes with previous diet –treated GDM was very high and they had an

elevated blood sugar value in the postpartum period (Lauenborg et al., 2004).

Hence to modify natural history and reduce risk of future diabetes, uniform postpartum

screening of women with GDM is necessary (Tandon et al., 2015).

5. Universal postpartum screening of women with GDM in pregnancy

5.1. Screening rates

Across the world without any difference between advanced economic and low and middle

income countries the screening rates for postpartum diabetes are very low. Globally, the

postpartum screening rates are reported to be 50% or lower (Keely, 2012).

In a cross sectional study of women aged 18-44 years who gave birth at one medical

centre at Boston, USA between 2003 and 2009, only 23.4% of GDM affected women had

any kind of glucose test by 6 months postpartum. Half of them completed screening by

10 weeks and out of this only 29% had undergone the recommended oral glucose

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tolerance test (OGTT). This emphasizes the need for awareness among providers, family

as well as the need for system support to the women because unlike other diseases, here

the system as well as the provider misses the opportunity of providing primary care

(McCloskey et al., 2014).

Even though the testing rates have increased over fourteen years in a population based

cohort study in Ontario, Canada among women who had delivered between 1994 and

2008, the number of women who received the recommended oral glucose tolerance test

(OGTT) was low, showing lack of standard protocol and awareness among the concerned

health care providers (Shah et al., 2011).

Participation in follow up screening was low in North Denmark region, in a study among

2171 women who were selected from Danish National Registers covering the years 1994-

2011. Women with high income had comparatively low testing status than women in the

low income group, in a Danish national based registry (2014) (Olesen et al., 2014).

The International Diabetes Federation (IDF) is an umbrella organization of over 230

national diabetes associations over 173 countries and territories and functioning with its

mission, to promote diabetes care, prevention and a cure worldwide. The Abstract of IDF

World Diabetes Congress, 2013 indicates that Indian women with GDM should have

frequent post-partum screening if we aim to modify natural history and reduce the risk of

diabetes (IDF, 2015).

A longitudinal study in Delhi (2015) on the prevalence of glucose intolerance at 6 weeks

postpartum, according to American Diabetes Association (ADA) Criteria reported that

17.3 % did not return for the follow up screening. Out of those who were tested , 33%

had an abnormal oral glucose tolerance with 6.4 % of women having overt type 2

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diabetes, while 19.3% had borderline risk and 8% were at high risk of conversion to

T2DM (Jindal et al., 2015).

5.2 Reasons for low postpartum screening rates among women diagnosed with GDM

Low risk perception

Women with GDM may not believe that they are at risk of diabetes (Jones et al., 2009) .

In a cross sectional study among 217 women with a history of gestational diabetes within

the past 5 years, in US, 90% of women recognized a risk of future diabetes but only 16%

had a high perceived risk of future diabetes. The perceived risk increased to 39% when

they were asked to estimate their risk if they followed the same lifestyles (Kim et al.,

2002).

Low motivation for screening in the postpartum period

In a qualitative study using semi-structured interviews in 2013 in the UK, even though

women were aware of their future risk of diabetes, they did not follow the instructions

.While they were pregnant, the pregnancy itself motivated the behavioral change but after

delivery, the behavioral changes were not maintained. Further, factors like tiredness,

childcare demands, and maternal attachments were the prominent barriers in the early

postpartum period and after that work, family and child development become the barriers

(Lie et al., 2013). Personal factors such as low educational level, socio-economic status

and high parity, and the requirement for fasting before testing also contributed to

difficulties in getting screened (Yarrington, Zera, et al.,2015).

Provider and health-system factors

A number of studies point to provider factors such as lack of awareness and failure to

give proactive advice, as well as large health system factors such as poor access and

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availability and low level of coordination as contributing to low uptake of postpartum

screening for blood sugar levels in women experiencing GDM during pregnancy.

Lack of access to care (prenatal, postnatal) or barriers such as the unsuitable timing of

testing services, lack of availability of insulin for treatment during pregnancy were all

identified by studies as important factors (Coustan et al., 2010, Kwong et al., 2009). In a

Danish study, those who tested their blood from a biochemical unit rather than consulting

a health care provider, were at a high risk of treatment non-initiation (Olesen et al., 2014).

Hence access to providers is an important factor.

In a survey among health care professionals in September 2014, in East London and West

Midlands in England, it was found that 81% of midwives and 52% of obstetricians

underestimated or were unsure of future risk of diabetes in women experiencing GDM.

There was a lack of consensus among them regarding the responsibility for screening in

the immediate postpartum period (Rayanagoudar et al., 2015) .

A mixed method study in the greater Boston area during December 2011 and May 2012,

which recruited subjects with a history of GDM in their most recent completed pregnancy

6 months to 4 years before enrollment, examined reasons given by women who did not

present themselves for postpartum screening. Untested women stated their reason for not

testing as the providers‘ reassurance that diabetes would resolve after delivery. They

believed that the providers did not send reminders to reschedule missed appointments to

complete testing because the providers did not perceive the women‘s risks to be serious

(Paez et al., 2014) .

A qualitative study in North Denmark (2015) to understand the influence of women‘s

experiences with treatment and care during pregnancy on participation in follow-up

screening, found that there was lack of continuity in care between hospital departments

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and health sector, lack of coordination, ineffective communication and lack of

coordination of responsibility regarding follow-up screening among health care providers

and lack of focus on their individual needs and preferences (lack of patient-centeredness)

(Nielsen et al., 2015).

According to a cross-sectional study in Ohio in 2010 to identify factors associated with

high rates of postpartum screening by a randomly sampled licensed obstetricians and

gynaecologists, those who were frequent screeners followed a clinical protocol for

postpartum testing (67.2% vs 26.7%),an electronic reminder system for providers(10.8%

vs 2.2%) and sent reminders to patients (16.4% v/s 4.4%) (Ko et al., 2013).

Reminders on postpartum screening, written materials on GDM and use of standard

checklist showed an increase in screening rate ( Yarrington, Zera, et al., 2015, Nielsen et

al., 2015).

To address the increasing prevalence, the National Diabetes Education Program (USA)

brings to the notice of providers to take action to improve postpartum screening in order

to identify high- risk groups, provide early treatment and prevention, counsel the mother

to test for diabetes prior to subsequent pregnancy and also counsel regarding the risk of

offspring to future diabetes and their prevention strategies. The Program also alerts

obstetrician-gynaecologists and other primary care providers to keep a system in place to

test glucose intolerance as recommended, support breastfeeding, refer to a registered

dietitian or community program for weight management, consider pharmacological

agents for pre-diabetes, treatment of existing hypertension and counselling regarding

regular testing, contraceptive options to ensure planned pregnancy, healthy food, regular

physical activity, quit smoking and inform their treating pediatrician regarding the history

of GDM status of mother.

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6. Rationale for the Study

A large proportion of women with GDM in India progress to Type-2 diabetes mellitus

(T2DM). There is an urgent need to develop standardized protocols for GDM care in

India that can improve the maternal and fetal outcomes and help prevent future diabetes

in women with GDM (Metzger, 2007).

Kerala represents 1.8% of the total land area of India and 3.4% of the total Indian

population. During the past two decades, there is a significant improvement in the

economic status of the state, especially from income generated by family members

working abroad. This has resulted in improvement in living standards with subsequent

changes in diet and lifestyle of the population. These changes have resulted in a marked

increase in the prevalence of non-communicable diseases (lifestyle-related) especially

diabetes, hypertension and coronary artery disease among the population similar to the

demographic features of the western population.

From the evidence of prevalence studies conducted in India ,Kerala has the maximum

diabetes burden in India(Mohan et al., 2012, Reddy et al., 2006). Amrita Diabetes and

Endocrine Population Survey (2002-2005),a study from central Kerala, reported a T2DM

prevalence of 20% and a pre-diabetes prevalence of 11% (Menon et al., 2006) .

A study from southern Kerala (2000) shows wide variations in age-standardized

prevalence (30-64) of diabetes among urban, rural, midland and coastal regions

emphasizing the role of lifestyle factors. The prevalence was 16.9% in the urban, 10.1%

in the midland, 6.8% in the highland and 3.6% in the coastal area, respectively. Women

showed a higher prevalence in the highland and coastal area and men in the urban and

midland area. There were 23.5% undetected cases in the community (Kutty et al., 2000) .

A study by Thankappan et al (2010) on a total of 7449 individuals (51% women) reported

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a high burden of non-communicable disease risk factors in the community in Kerala,

which was comparable to that in the United States (Thankappan et al., 2010).

In a medical college based study in Kollam during December 2013 to January 2014

among pregnant women, there was a significant association of GDM with obesity and

older age. Due to lack of physical activity and diet control, obesity is becoming an

epidemic in Kerala.

A significant proportion of women in Kerala in the reproductive age group are

overweight and obese (NFHS 3). A proven risk factor in developing GDM is high BMI

(WHO 2015,WHO, 2010, Matyka, 2008). The current huge burden of diabetes in the

state of Kerala will increase with the increasing prevalence of GDM. The high prevalence

of type 2 diabetes in the state increases the probability that a woman has a family history

of T2DM or GDM, which also adds to the risk of gestational diabetes mellitus. In this

situation, preventing or delaying the development of type 2 diabetes is crucial. But no

standard GDM management is being followed in Kerala at the present time. Regular

postpartum screening of all GDM affected women will help to prevent progression to

T2DM.

In Kerala, the rate of postpartum screening is very low. According to gynaecologists in

Kerala compulsory postpartum screening is not a routine practice, and even if

postpartum screening is carried out, the standard test, viz., OGTT is followed very rarely.

Further, there are no published studies on postpartum screening rates and barriers to it in

the Kerala context. This study aims to bridge this gap in evidence.

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Chapter 2

Methodology

2.1 Objectives of the Study

I. Primary objectives of the Study

1. To assess the timely postpartum diabetes screening rate of GDM affected women

who had delivered at selected hospitals in Malappuram district.

2. To examine the patterns of and factors associated with postpartum diabetes

screening by women who had GDM during their most recent pregnancy.

II. Secondary Objective

1. To document postpartum morbidity patterns among women with GDM and morbidity

among their infants.

2. To understand provider perspectives on appropriate postpartum follow up of GDM

patients.

2.2 Study type/design

This is a mixed methodology study. In-depth interviews were carried out with doctors

and a cross sectional study was done with interviews of recently delivered women

diagnosed with GDM, using a structured interview schedule administered by the principal

investigator (PI). The study period was two months starting from July 2016-August 2016.

2.3 Study setting

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One public and three private hospitals were selected from Malappuram district. As per

data collected from government birth registries, the proportion of public hospital

deliveries is only 11 % of total deliveries in the district (HMIS 105-16 –public hospital

deliveries 19.6%& HMIS 2016 April –September 11.8%)

2.4 Study Population

Women residents of Malappuram district who experienced GDM during their most recent

pregnancy and had delivered in the selected hospitals in Malappuram district no less than

9 weeks and no more than 6 months before the survey.

2.5 Sample size estimation

a) In-depth interviews: A total of eight doctors were interviewed till saturation was

reached.

b) Cross-sectional study: For the four hospitals (one public and three private hospitals)

in the sample, the total number of deliveries for the year 2015 was collected from

government birth registration centers.

Table 2.1 Details of deliveries of the four selected hospitals for the year 2015.

Name of Hospital Total deliveries in 2015 Deliveries in 6 months

Private Hospital A 3820 1910

Private Hospital B 3044 1522

Private Hospital C 3600 1800

Public hospital D 999 500

Total study population 11,463 5732

The sample frame had a population of 5732women delivered with six months before the

study. Sample size was calculated based on the prevalence of GDM during pregnancy

(15.9 percent) reported from an earlier study in the same district in 2014 (Mohan and

Chandrakumar, 2015). The sample size was calculated with 95% confidence interval and

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1% precision using Open Epi version 3.03. This gives a sample size of 154. Adding 25%

to adjust for non-response, we arrived at a total of 193, which was rounded off to a total

sample size of 200.

Since the American Diabetes Association‘s (ADA) recommended time period for

postpartum screening is 6-12 weeks of delivery (National guidelines for diagnosis and

management of GDM recommends postpartum screening at 6weeks), and allowing

enough time for the women to undergo the test, we have selected a period of between 9

weeks and 6 months because in that period it would be possible to get an adequate sample

and recall bias can be minimized. We approached the respondent after getting consent for

the interview over telephone.

2.6: Sample selection procedures

Four hospitals (one public and three private) were selected purposively as they were

managing and keeping records of gestational diabetes mellitus (GDM) patients and were

willing to cooperate with the study. Anticipating complications to both mother and child,

the delivery of a woman diagnosed with GDM is always conducted in a facility where at

least physician, pediatrician and anesthesiologist are available along with facilities for

managing new born babies who need special care.

In our pilot study we came to notice that many hospitals including both public and

private, were not recording and documenting gestational diabetes mellitus unlike

pregnancy induced hypertension (PIH).Hence we could not select hospitals randomly.

Those who kept some records and were willing to participate in the study, and had a

sufficient number of deliveries were selected, because there were a few hospitals with

good records but where due number of deliveries per month were very few.

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A list of study subjects who fulfilled the inclusion criteria was prepared from the hospital

registers. A total of 200 respondents were randomly selected from the four hospitals. The

number of respondents selected from each hospital was proportionate to the total number

of deliveries in each hospital. The randomly selected study subjects were interviewed at

their houses using interviewer administered interview-schedule in local language. The

interview schedule had nine sections. First section was designed to capture socio-

demographic details of the respondents, second section for past history (excluding the

most recent pregnancy), third section had questions regarding most recent pregnancy and

delivery. The fourth section had details of child characteristics while the fifth had

questions on management of GDM in most recent pregnancy. This had two parts,

management during pregnancy and after delivery. The sixth section asked about personal

barriers for postpartum screening and seventh section regarding spacing/family planning

.The eighth and ninth sections were about risk perceptions and postpartum health

respectively.

The principal investigator alone did the data collection at their homes after getting prior

consent through their providers. Among the selected study subjects three were not able to

participate as one went abroad, one shifted to Tamil Nadu to her husband‘s residence

three days prior to my visit as she had to prepone her shifting, and the third had to move

to her parents‘ house at neighborhood district as her father had some illness. They were

replaced by subjects from the corresponding hospital registers randomly.

For the in-depth interviews, doctors who managed the highest numbers of GDM patients

were identified from the out-patient departments of the hospitals in which they worked.

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2.7 Inclusion Criteria- for GDM affected women

Women who had delivered in the selected health facilities within a period of not less than 9

weeks and not more than 6 months from the date of survey and were residing continuously in

the district for the past 6 months.

2.8 Exclusion Criteria -for GDM affected women

1. Not residing in the district at the time of interview. They delivered in the selected

hospital, but belonged to the neighboring districts.

2. Those who were seriously ill at the time of interview.

2.9 Inclusion Criteria –For the providers

Physicians specifically involved in the management of GDM-affected-women practicing

in the selected facilities in Malappuram district (Specialized in Obstetrics and

Gynecology or General Medicine) and managing the maximum number of GDM patients

in the selected facilities.

2.10 Operational definitions

Gestational diabetes mellitus (GDM): is defined as hyperglycemia diagnosed for the first

time in pregnancy that does not meet the criteria of diabetes mellitus in pregnancy (DIP).

This may occur at any time during pregnancy but is most likely after 24 weeks

Test for postpartum screening as per guidelines: 2 hr 75 –g oral glucose tolerance test

(OGTT) either in the fasting or non-fasting state.

Timely postpartum screening: Screening at ≥6 weeks postpartum and < 6 months using

any test for blood glucose level.

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2.11Data collection techniques

Two techniques are used for data collection.

a) Interview schedule

b) In-depth interview of the provider using in-depth interview guidelines

From those who were selected randomly, their consent to participate in the study was

obtained by the health providers known to the women. Once they agree to participate, the

principal investigator (PI) fixed a day and time suitable to the respondent and visited them

in their homes and conducted the interview using the interview schedule.

Data of GDM affected women was done using interview schedule in local language

(Malayalam). The interview schedule and consent forms were translated to local language

and back translated to English to maintain consistency.

Height in kilogram and weight in meters, of the respondents were measured using

standardized calibrated equipment along with the interviews to calculate the body mass

index (BMI).

For the in-depth interview: Doctors who were managing the largest numbers of GDM

cases were identified from the outpatient department register and interviews were

conducted till saturation was reached (n=8). In-depth interview guide in English was used

for conducting the in-depth interviews, which were done at their hospitals as all of them

suggested their hospitals as a convenient place for the interview. The interviews were

conducted by the Principal Investigator, and audio recording of the interviews was done

after getting the consent of the doctors. Each interview lasted for about 20-25 minutes.

The busy schedule of the doctors was one of the main challenges. All of them had a heavy

work load and had to manage both inpatients in labor room and outpatients (OPD) at the

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same time. I think that only because I was working as a senior government officer and

had worked in the field of public health, they cooperated for the interview.

2.12 Analysis

Data analysis was done using SPSS version 21(IBM). Data were first analyzed

descriptively which gave various patterns of postpartum screening. The factors associated

were explored using bivariate and multivariate analysis. The testimonies in the in-depth

interview were transcribed, read and re-read to identify codes. The identified codes were

collapsed into broader themes and linkages between the codes were identified and finally

the conceptual frame work was identified.

2.13 Data storage

The data collected are kept safely with the Principal Investigator, who is responsible for

safe keeping of data and respect of confidentiality. The data collected will be stored in the

computer with password encryption of the file. The hard copy of the filled interview

schedule, questionnaire and consent forms will be strictly confined to personal locker of

the principal investigator in sealed covers and will not be shared under any circumstances.

After one year, the entire hard copies will be destroyed. Only the final report will be

shared with the concerned persons, authorities, scientific or governmental bodies.

2.14 Ethical considerations

Confidentiality: Utmost priority was given to protect the privacy of the participant and

confidentiality of the participant‘s personal information by giving a unique identification

number. Any information given by the respondent was not disclosed to anyone.

Consent: Written informed consent was obtained from the participants before

administering the interview schedule and from the doctors before starting the in-depth

interview. Participants were free to refuse at the outset or during any stage even after they

had consented if they felt uncomfortable at any point. The data collected will be used for

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research purpose only. A clearance was obtained from the Institutional Ethics Committee

of SCTIMST before the commencement of the study (Reference number:

SCT/IEC/913/May 2016)

2.15 Dissemination of results

The final thesis report will be submitted to the Institute for evaluation. The conclusions

emerging from the study will be presented to experts in the field for comments and to

initiate further research. The findings will be shared with health department for

implementing new actions and policy changes and will be presented in scientific

conferences. Attempts will be made to publish the results in appropriate scientific

journals.

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Chapter 3

Results and Explanations

Section I

The findings of the study are presented in this chapter in three sections. In the first

section, the socio-demographic characteristics of the respondents, details of their past

obstetric history, details of recent pregnancy including postpartum screening, barriers to

screening, adherence to follow-up and morbidities during pregnancy and after delivery

are discussed. It also includes a brief description of the infants of the respondents

regarding their weight, general health status, postpartum care, immunization and

morbidities. The second section of the chapter describes the various factors associated

with timely postpartum diabetes screening in their most recent pregnancy. The third

section describes the providers‘ perceptions.

3.1 Characteristics of the respondents

3.1.1 Socio-demographic characteristics of the respondents

Table.3.1 shows the socio- demographic profile of the respondents. Out of 200

respondents, 68 were of age group 25-30years (34%) and the majority belonged to the age

group of 25-35years (65%).

More than half of the women had completed schooling between VIII and X standard

(59%) and the majority of the respondents (97%) were home makers. The remaining six

women, who were employed previously, left the jobs temporarily to take care of their

infants.

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Table 3.1 Socio-demographic profile of the respondents in the study

Variables Response N=200(100%)

Age group

<20 5(2.5)

20-25 28(14)

25-30 68(34)

30-35 62(31)

35-40 35(17.5)

>40 2(1)

Educational Status

1-7th std 23(11.5)

8-10th std 118(59)

Higher secondary 36(18)

Post higher secondary 8(4)

Graduate and above 14(7)

Others1

1(0.5)

Occupational status

Home maker 194(97)

Salaried employment 1(0.5)

Self-employment 1(0.5)

Other2 4(2)

Gravidity

One 33(16.5)

Two 38(19)

Three 49(24.5)

Four 47(23.5)

Five 19(9.5)

Six 11(5.5)

Seven 2(1)

Eight 1(0.5)

Parity One child 34(17)

Two children 52(26)

Three children 53(26.5)

Four children 49(24.5)

Five children 8(4)

Six children 3(1.5)

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Variables Response N=200(100%)

Eight children 1(0.5)

Caesarian section 66(33)

BMI

Underweight (<18.5) 5(2.5)

Normal weight (18.5-24.9) 79(39.5)

Overweight (24.91-30) 80(40)

Obese (>30) 36(18)

1- Others include ‗B tech‘ (n=1), 2- Others (specify) include ‗dental surgeon‘ (n=1),

engineer (n=1), tailor (n=1) and ‗teacher on leave‘ (n=1) to look after the baby.

The parity ranged from primipara (17%) to grand multipara (2%) and 57% had three or

more children. It appeared that those who had more than four children had experienced

child losses or only female children. About 40% of the women were overweight and 18%

were obese.

3.2Reproductive profile of women diagnosed with GDM

Table 3.2 Reproductive profile of women affected with GDM in the study sample 2016

Variables Response N=200(%)

History of most recent pregnancy

Pregnancy term completion Preterm(less than 37 weeks) 11(5.5)

Term (37-41 weeks) 189(94.5)

Type of delivery Normal 134(67)

C-section 66(33)

Pregnancy outcomes Still births 5(2.5)

Live births 195(97.5)

Previous pregnancy history (Total past pregnancies=611)

Pregnancy wastage Miscarriage 67(10.96)

Still births 17(2.78)

Neonatal death 4(0.65)

Infant deaths 2(0.32)

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Variables Response N=200(%)

Delivery complications including Caesarian sections in the past pregnancies (Total

past pregnancies=611)

Type of complications

Preterm delivery 6(0.98)

Retained placenta 2(0.32)

Hand prolapse 2(0.32)

Premature rupture of

membranes(PROM )and

cord prolapse

5(0.81)

Postpartum

Haemorrhage(PPH)

1(0.16)

Antepartum

haemorrhage(APH)

2(0.32)

High blood pressure 19(3.10)

Foetal distress 5(0.81)

C-section 17(2.78)

Past treatment advice for women diagnosed GDM before this pregnancy

GDM in past pregnancies in the study

sample

38(19)

Advice received for further follow up 4(10.81)

Those able to follow the advice 2(50)

In their most recent pregnancy, majority of the respondents had term deliveries (94.5%)

while 5.5% had preterm deliveries. One third of the respondents underwent C-sections

and 97.5% had live births. Of the 611 past pregnancies among the 200 respondents, 11%

had ended in miscarriages, about 3% were stillbirths and about 1% had ended in neonatal

or infant deaths.

Delivery complications in past pregnancies included preterm delivery in about 1%,

retained placenta (0.32%), hand prolapsed (0.32%), premature rupture of

membranes(PROM) and cord prolapsed(0.81%), high blood pressure(3.1%%), ante-

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partum(0.32%) and postpartum hemorrhage(0.16%), fetal distress(0.81%%) and C-

section in about 3%.

3.3 Diagnostic profile of the respondents:

Table 3.3 shows the diagnostic profile of the respondents.

Table 3.3 Diagnostic profile of the respondents in the study sample.

Variables

Response N=200(100%)

GDM diagnosed in previous

pregnancies

Yes 38 (19)

No 162 (81)

GDM diagnosed in all

pregnancies

Yes 7(18.42)

No 31(81.58)

Advice received for further

follow-up

Yes 4 (10.8)

No 34 (89.2)

Advice adhered to Yes 2(50)

No 2 (50)

GDM diagnosed in most

recent pregnancy

First trimester 59(29.5)

Second trimester 73(36.5)

Third trimester 68(34)

Reason for diagnosis

As part of routine investigations 169(84.5)

Family history of diabetes mellitus 1 (0.5)

Symptoms of diabetes mellitus* 20 (10)

Previous GDM 4 (2)

Big baby 2 (1)

Hypertension 3 (1.5)

Previous still births 1 (0.5)

*severe fatigue, thirst, non-healing ulcers, tiredness, giddiness, dryness of mouth etc

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Among the study respondents, 19% (n=38) had gestational diabetes (GDM) in their past

pregnancies. Among them, seven had GDM in all the previous pregnancies. However,

only 10.8% had received a medical advice for further follow up and screening and only

half of those who received advice were able to adhere.

Of those who were diagnosed with GDM during the most recent pregnancy, about 30%

were diagnosed in the first trimester and roughly equal proportions (36.5% and 34%)

were diagnosed in their second and third trimesters, respectively. Routine blood

examinations during antenatal visits were the most common mode of diagnosis (84.5%)

of the condition, while, symptoms of hyperglycemia led to diagnosis among 10% of the

respondents. Previous history of GDM was found to be the cause of diagnosis among 2%

of the women, although more than 18% had past histories of GDM.

3.4 Postpartum screening of the respondents

According to the existing guidelines, the blood sugar should be tested at six weeks or later

postpartum; based on the level of blood sugar further blood investigations are decided.

For the purpose of this study, those who had tested before 6 weeks or not tested were

taken as ―not tested‖ and those who had tested at or more than 6 weeks period were taken

as ―timely tested‖. Timely postpartum screening rate was found to be very low. Only

29% of respondents reported having undergone testing at or after six weeks postpartum

(Table 3.4).

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Table 3.4 Postpartum diabetes screening profile of the respondents in the study

sample

Variables Response N=200(100%)

Blood test after delivery Yes 115(57.5)

No 85(42.5)

Timing of blood test

Not tested& tested less than 6

weeks

142(71)

≥ 6 weeks after delivery 58(29)

Place where blood test was

conducted N=115(100%)

Public hospital 13(11.30)

Private hospital 58(50.43)

Laboratory (self-referred) 39(33.91)

Self (at home) 5(4.34)

Status of blood sugar level Hyperglycaemia Normal Total N=115(100%)

Tested from public hospital 0 13 13 (100)

Tested from private hospital 7(12.06) 51(85.93) 58 (100)

Self - tested at home 4(80) 1 (20) 5(100)

Tested at laboratory 15(38.46) 24 (61.54) 39(100)

Among the respondents who had tested their blood (57.5%), 11.3% had utilized public

hospitals, 50.4% had utilized private hospitals and 33.9 % had made use of laboratory for

testing. In addition to this 4.3% of respondents had self-tested at home using diagnostic

kits bought in pharmacies. Out of this, all respondents who had tested from public

hospitals, 85.9% of respondents who tested from private hospitals, 61.5% of respondents

tested from laboratory and 20% of those who had self –tested at home were

normoglycemics. Majority of those who had tested self at home (80%) had

hyperglycaemia. It may be noted that those who self-initiated the test were highly likely

to be hyperglycemic.

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Table 3.5 Reasons for not undergoing blood sugar examination after delivery.

Variable Responses N=85(100)

Reasons for not testing

blood after delivery

Doctor‘s reassurance that ―nothing

to worry, it will subside after

delivery‖

6(7.1)

Low blood sugar level before

delivery

4(4.7)

Difficulty in going out with a small

baby

10(11.8)

Nobody informed me 50(58.8)

Fear to know that I am diabetic 4(4.7)

I have no symptoms 5(5.8)

It will subside after delivery 6(7.1)

Total Not undergone blood testing after

delivery

85

When the reasons for not testing blood after delivery were explored (Table 3.5), 58.8% of

respondents stated that they were not aware of postpartum follow up and they complained

that nobody informed them about blood testing after delivery. Difficulty in going out with

a small baby was the reason cited by 11.8% of respondents. The other reasons reported by

women were doctor‘s reassurance of ‗nothing to worry, it will subside after delivery‘

(7.1%), general belief in society that GDM will subside after delivery (7.1) ,absence of

symptoms (5.9%), fear to know the diabetic status (4.7%) and a normal blood sugar result

before delivery (4.7) .

All the respondents who had undergone postpartum screening tests from either private or

public hospitals consulted their doctors after testing their blood glucose level. However,

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60% of those who tested at home and 38.5 % of respondents who tested at a laboratory on

their own initiative did not consult a doctor after obtaining their test results (Table 3.6).

Table 3.6 Status of consultation after testing their blood in the postpartum period by

glycemic status

Consulted a doctor after testing blood sugar

Categories Yes N (%) No N (%) Total N (%)

Tested from public hospital 13(100) 0 13 (100)

Tested from private hospital 58(100) 0 58(100)

Self at home 2 (40) 3 (60) 5(100)

Laboratory 24 (61.54) 15(38.46) 39(100)

Total 97(84.35) 18(15.65) 115(100)

Status of consultation among hyperglycemics

Tested from

Hyperglycemic

N (%)

Consulted a

doctor N (%)

Not consulted

N (%)

Public hospital 0 n. a n. a

Private hospital 7(100) 7(100) 0

Self -tested at home 4(100) 2(50) 2(50)

Laboratory 15(100) 9(60) 6(40)

Total 26(100) 18(69.23) 8(30.76)

Status of consultation among normoglycemics

Tested from

Normal blood sugar

N (%)

Consulted a

doctor N (%)

Not consulted

N (%)

Public hospitals 13(100) 13(100) 0

Private hospitals 51(100) 51(100) 0

Self at home 1(100) 0 1(100)

Laboratory 24(100) 15(62.5) 9(37.5)

Total 89(100) 79 (88.76) 10 (11.23)

Among those with hyperglycemia, 8(30.76%) had not consulted a doctor after getting the

blood examination results. Of these, two (25%) had self -tested at home and six (75 %)

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had tested from a laboratory through self-referral. Among those who were

normoglycemic, ten women (11.23 %) had not consulted a doctor, among whom one (10

%) had self-tested at home and 9(90 %) had tested from laboratory.

Table.3.7 Reasons for not consulting a doctor after obtaining test results

Reasons for not consulting a doctor after

obtaining test results

Response

N=18(100%)

Result was normal 10(55.6)

Doctor‘s reassurance 2 (11.1))

Fear to know the status 1 (5.5)

Waiting for symptoms 1 (5.5)

Difficult to go out with a small baby 3(16.8)

Self-medication 1 (5.5)

All normoglycemic women said that they did not consult a doctor after obtaining test

results because the results were normal. Reassurance from providers that GDM will

subside after delivery played a major role in not seeking consultation. Among the eight

women who had tested positive, difficulty in going out with the infant (3 women),

doctors‘ reassurance that ―everything will become normal after delivery (2 women) were

most frequently stated as reasons. Absence of symptoms, fear to know the diabetic status

and self-treatment (1 woman each) were the other reasons cited for not consulting a

doctor.

Of those who consulted a doctor following postpartum screening, many were not given

specific instructions to repeat the tests at regular intervals and especially in the first

antenatal visit of the next pregnancy. For example, among the 79 normoglycemic

respondents who consulted a doctor, the majority (78.48%) were reassured that there was

―nothing to worry‖ and were not given any instructions. Seventeen normoglycemic

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respondents (21.51%) were given some instructions along with ―Nothing to worry‖ on

consulting a doctor. One subject (1.26) reported that she was not given any instruction or

reassurance (Table 3.8).

Table 3.8 Instructions to respondents who consulted a doctor after testing their

blood sugar.

Management of normoglycemics

respondents

N (%)

Nothing to worry 62(78.48)

Nothing to worry, but control diet 5(6.32)

Nothing to worry, but test blood glucose

occasionally

7(8.8)

It will subside after delivery 3(3.79)

Test after six months, if the values are normal

do not report back

1(1.26)

No instructions 1 (1.26)

Total 79(100)

Management of hyperglycemic respondents*N

To start medicine 13

Diet control 3

To start medicine &diet control 3

To test blood occasionally 1

Continue injection insulin 2

Diet control &exercise 1

Psychiatry consultation for mood disorder 1

Total 24

*Same person may get more than one advice

Among the respondents who were hyperglycemic, 13 were advised to start medication

and 3 were advised a combination of both medication and diet control and an equal

proportion was advised diet control alone. Two were advised to continue insulin. One was

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advised diet control and exercise and another one who had mood disorder was advised

psychiatric consultation.

Table 3.9 shows the status of adherence among the respondents to various instructions. A

total of 17(21.51%) normoglycemic respondents and 18 hyperglycemic respondents who

consulted a doctor after blood test were given instructions of some kind. Only nineteen of

the thirty five respondents who were given instructions adhered to the instructions. Some

respondents have received more than one instruction. Both drug adherence (61.53%) and

injection insulin (100%) were found to be better than following diet control (37.5%) and

testing blood occasionally (25%). A combination of diet control and exercise and also

medicine and diet control were the major areas of non- adherence.

Table.3.9 Status of adherence to doctors’ instructions by the respondents.

Responses Normoglycemics who

had received advice for

life style changes or

future screening (N=17)

Hyperglycemics

N=18

Total

Advised

N(%)

Adhered to

advice

Advised Adhered

to

advice

Advise

d

Adhered to

advice

Diet control 5(6.32) 1(20) 3(16.66) 2 8 3(37.5%)

Test blood

occasionally

7(8.86) 1(14.28) 1 (5.55) 1 8 2(25%)

It will subside after

delivery

3(3.79) Not

applicable

3 No

instruction

s

Test after

6months,if normal

no need to come

1(1.26) NA** 1

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Responses Normoglycemics who

had received advice for

life style changes or

future screening (N=17)

Hyperglycemics

N=18

Total

Advised

N(%)

Adhered to

advice

Advised Adhered

to

advice

Advise

d

Adhered to

advice

No advice 1(1.26)

To start medicine 13(72.22) 8 13 8(61.53%)

To start medicine

&diet control

3(16.66) 0 3 0

Continue

injection Insulin

2 2 2 2(100)

Diet control

&exercise

1 0 1 0

Psychiatry

consultation for

mood disorder

1 1 1 1

Able to follow all

instructions

3 3

Total 17(21.51) 2 24* 17 40 19(47.5%)

*Total won‘t add up because same person may get more than one advice, ** the survey period

was within 6 months of delivery.

While exploring the reasons for non-adherence (Table 3.10), apprehension regarding

reduced quantity of breast milk caused 22.7 % of respondents to avoid diet control.

Difficulty in going out with the infant (13.6 %) especially when the husbands were out of

station were the other commonly reported reasons for non -adherence by the respondents.

About 22.7 % of respondents cited childcare demands as their reason for non-adherence

and an equal proportion expressed ignorance about the importance of adherence, and they

had not taken seriously. Household work was cited as the reason for non-adherence by

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13.6% of respondents. About 7.7 % reported that they did not receive any information

from any source to maintain a strict follow up.

Table. 3.10 Reasons for non-adherence for the respondents

Reasons for non-adherence N=22(%) Responses

Child care demands 5(22.7)

Diet restriction reduces breast milk 5(22.7)

Household work 3(13.6)

Difficult to go out with small baby 3(13.6)

No instructions from anywhere 1(7.7)

Not taken it seriously 5(22.7)

Total 22(100)*

*Included no instruction also

3.5 Morbidity profile of GDM affected women in their most recent pregnancy and

after delivery

Table 3.11 Patterns of morbidity of women affected with GDM in their most recent

pregnancy, delivery and postpartum period.

Variables Response N (%)

Health problems during

pregnancy (N=200)

Yes 97(48.5)

No 103(51.5)

Nature of Morbidities(N=97)

Symptoms of

hyperglycaemia

57(28.5)

Genitourinary infections1 7(3.5)

High Blood Pressure 19(9.5)

Ante-partum hemorrhage 8(4)

Gastrointestinal discomfort 4(2)

Mood disorder 1(0.5)

Hydramnios 1(0.5)

Delivery Yes 25 (12.5)

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complications(N=200) No 175(87.5)

Details of delivery

complication

Hypertension 6(3)

Foetal distress 4(2)

Postpartum haemorrhage 7(3.5)

Cord prolapse 1(0.5)

PROM2 6(3)

Retained placenta 1(0.5)

Total 25(12.5)

Details of complications after

delivery

Fatigue 8(4)

Stress due to low milk

secretion

1(0.5)

Delayed wound healing 2(1)

Recurrent UTI 1(0.5)

Recurrent vulvovaginal

candidiasis

3(1.5)

Peripheral neuritis 3(1.5)

Low back ache myalgia 8(4)

Others3 6(3)

Total 32(16)

Genitourinary infections include vulvo-vaginal candidiasis, urinary tract infections, low

back ache, 2- PROM is premature rupture of membrane,

3- Others include umbilical

hernia (1), skin diseases(1), abdominal discomforts(3), treatment for mood disorder (1)

and knee joint pain(1)

Out of the 200 respondents, 97 (48.5%) had health problems during pregnancy, of them,

majority being symptoms of hyperglycemia (28.5%) and high blood pressure (9.5%).

Antepartum bleeding requiring bed rest was seen in eight (4%) respondents.

Complications during delivery were found in 12.5% of women. Among this 3% were

hypertensive, 2% had foetal distress, 3.5%% had postpartum haemorrhage, 3% had

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premature rupture of membranes (PROM) and 0.5% had retained placenta and an equal

proportion had cord prolapse.

After delivery, 4% of respondents reported fatigue and another 4% reported low back

ache and myalgia. The other common conditions seen were vulvo-vaginal candidiasis

(1.5%) and symptoms of peripheral neuritis (1.5%).Delayed wound healing and recurrent

urinary tract infections were the other health problems. The rest was shared by umbilical

hernia (0.5%), skin disease (0.5%), abdominal discomforts (1.5%), treatment for mood

disorder (0.5%) and knee joint pain (0.5%).

3.6 Child Characteristics

Among the outcomes of most recent pregnancy, 2.5% was stillbirth and all others live

births, 2.5% of the babies were overweight and 11.5% were low birth weighted babies.

The proportion of female babies was 52% and 72% had initiated breastfeeding within half

an hour of delivery.

Maternal causes for delay in initiating breastfeeding were inadequate breast milk (4.10%)

and retracted nipple (1.02%). Low birth weight (1.02%), convulsions (1.02%), foetal

distress (2.05%) and baby kept in ICU (2.56%) were the infant-related reasons for delay

in initiating breast feeding. Routine blood examination (newborn screening) after delivery

was carried out in 69% of newborns. Among the infants, 37.5% had jaundice within one

week of delivery. The rate of ICU admission was 37%. Twelve percent of the babies were

unimmunized for age at the time of the survey.

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Table 3.12 Child characteristics in the most recent delivery

Variables Response N (%)

Birth weight

Low birth weight

23(11.5)

Normal weight 172(86)

Over weight

5(2.5)

Sex of the child

Male 96(48)

Female 104(52)

Breast feeding initiated Less than one hour 144(72)

Less than 24 hours 34(17)

More than 24 hours 15(7.5)

Others* 7(3.5)

Difficulty in initiating breast

feeding

Baby kept in ICU 7(2.56)

Inadequate breast milk 8((4.10)

Low birth weight (unable to

suck)

2(1)

Retracted nipple 2(1)

Convulsions 2(1)

Foetal distress 4(2.05)

Status of blood examination

after delivery

Yes 138(69)

No 21(10.5)

Don‘t know 36(18)

Still birth 5(2.5)

Unimmunized for age 24(12)

Jaundice within one week of

birth

75(37.5)

ICU admissions 74(37)

*5 still births,2 low birth weight babies kept in ICU for more than 3days ,<2.5kg-

underweight, 2.5-4kg-normal weight and >4kg-overweight .

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3.7 Morbidity profile among newborn babies

Table 3.13 Patterns of morbidity among new born babies of women affected with

GDM.

Variables Response N=200(100)

Health problems Recurrent respiratory

infections

8(4.10)

Hypoglycemia 3(1.53)

Convulsions 2(1.02)

Low birth weight 2(1.02)

Recurrent ADD 1(0.5)

Jaundice 1(0.5)1

Others* 3(1.53)

Jaundice within one week of

birth

75(38.5)

Still births 5(2.5)

Total live births 195(97.5)

Total infants who had

health problems

95(48.71)

*others include dermatitis (1) chickenpox (1) &delayed milestones (1) 1-jaundice after

one week.

Despite the protection offered by maternal antibodies (as the infants were aged six

months or less) 48.7 % of infants had health problems. Seventy five (38.5%) of the

newborn babies in the most recent delivery had jaundice within one week of delivery.

Excluding morbidity due to jaundice, which can be physiological, the proportion of

infants with morbidity was 10.26%. Other major problems included recurrent respiratory

infections (4.1%), hypoglycemia (1.5%) and convulsions (1%). Low birth weight was

seen in another 1 % of newborns.

Section II

3.8 Timely postpartum screening and associated factors

In this section we explore factors associated with the odds of postpartum screening (Table

3.14).Out of 200 respondents, 57.5% tested their blood after delivery for diabetes

screening. There was a statistically significant association between timely postpartum

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testing and age with high odds of timely screening. It was maximum in the age group 31-

35.

Proportion of women with timely screening was highest among graduates followed by

women with eight to ten years of education. The association between education and

timely screening was not statistically significant.

Parity had an association with timely postpartum screening (39.30%) and was highest in

respondents having four children or more. The association is significant at 10% level.

Past history of GDM had an association with timely postpartum screening and is

statistically significant.

Table 3.14 Timely postpartum screening and associated factors

Respondent

characteristics

Postpartum Screening Status P value

Response Not tested (not

tested+tested

>6weeks) N (%)

Timely

screening (≥6

weeks) N (%)

Total

N (%)

Age group 15-20 5(100.00) 0 5(100) 0.032

21-25 24(85.70) 4(14.30) 28(100)

26-30 51(75.00) 17(25.00) 68(100)

31-35 36(58.10) 26(41.90) 62(100)

36-42 26(70.30) 11(29.70) 37(100)

Total 142(71.00) 58(29.00) 200(100)

Education 1-7th standard 18(78.30) 5 ( 21.7) 23(100) 0.452

8-10th

standard

81(68.60) 37(31.40) 118(100)

Higher

secondary and

post higher

secondary

34 (77.30) 10 (22.70) 44(100)

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Respondent

characteristics

Postpartum Screening Status P value

Response Not tested (not

tested+tested

>6weeks) N (%)

Timely

screening (≥6

weeks) N (%)

Total

N (%)

Graduate and

above

9(60.00) 6 (40.00) 15(100)

Total 142 (71.00) 58 (29.00) 200(100)

Parity one to two

children

64(74.40) 22(25.60) 86(100) 0.095

Three children 41(77.40) 12(22.60) 53(100)

Four children

and above

37(60.70) 24(39.30) 61(100)

Total 142(71.00) 58(29.00) 200(100) .018

Past history of

GDM

Yes 21(55.30) 17(44.70) 38(100)

No 121(74.70) 41(25.30) 162(100)

Total 142(71.00) 58(29.00) 200(100)

Health

problems

during

pregnancy

Yes 65 (67.00) 32(33.00) 97(100) .228

No 77(74.80) 26(25.20) 103(100)

Total 142(71.00) 58(29) 200(100)

Blood glucose

testing

necessary after

delivery(Awar

eness)

Yes 77(60.20) 51(39.80) 128(100) <.0001

No 65(90.30) 7(9.70) 72(100)

Total 142(71.00) 58(29.00) 200(100)

Doctor‘s

advice

Doctor 29(47.50) 32(52.50) 61(100) .003

Others 51(72.90) 19(27.10) 70(100)

Total 80(61.10) 51(38.90) 131(100)

Higher chance

of getting

diabetes

mellitus(Risk

Yes 26(55.30) 21(44.70) 47(100) .010

No 116(75.80) 37(24.20) 153(100)

Total 142(71) 58(2) 200(100)

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Respondent

characteristics

Postpartum Screening Status P value

Response Not tested (not

tested+tested

>6weeks) N (%)

Timely

screening (≥6

weeks) N (%)

Total

N (%)

perception)

Feeling

―down‖

Yes 17(47.20) 19(52.80) 36(100) 0.001

No 125(76.20) 39(23.80) 164(100)

Total 142(71.00) 58(29.0) 200(100)

Ever had a

feeling of little

interest

Yes 16(45.70%) 19( 54.30% 35(100%

)

<.0001

No 126(76.40% 39(23.60%) 165(100

%)

Total 142(71.00%) 58(29.00%) 200(100)

About 33% of respondents who had health problems during pregnancy had undergone

timely postpartum screening but it is not statistically significant.

There was no significant association between health problems during pregnancy and

timely screening. However, women who had moods of feeling down‖ (52.8%) or felt

―little interest‖ in anything (54.30%) in their postpartum period were significantly more

likely to undergo timely postpartum screening.

The proportions undergoing timely screening were significantly higher among women

who were aware about the need for such screening, and among women who perceived

that they were at risk of developing diabetes in future. We examined whether family

history of diabetes was associated with risk perception and found no statistically

significant association. Neither was there a significant association between awareness and

risk perception (tables not included).

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The likelihood of timely screening was significantly higher among women who had been

directly advised by doctors to go for postpartum screening, as compared to those who had

received advice from others such as health workers, ASHA/AWW, media, community or

those who made self -decision.

There was significant association between psychological wellbeing and timely screening.

The proportion of respondents who were doing timely screening were 52.8% (―feeling

down‖) and 54.3% (those who were feeling little interest) and the association was highly

significant at the 1% level.

3.9 Results of age adjusted multiple logistic regression of factors associated with

timely postpartum screening (≥6weeks)

Independent variables having significance in the bivariate analysis and variables which

we had reason to believe to influence postpartum screening were selected as independent

variables for the multiple logistic regression analysis with timely postpartum screening as

dependent variable. We found that those who were advised by a doctor had a three times

higher chance of timely postpartum screening compared to those who had been advised

by other health workers or others.

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Table 3.15 Results of multiple logistic regression analysis of factors associated with

timely postpartum screening (≥6weeks)

*Others includes health worker, ASHA (Accredited social health

activist)/AWW(Anganwadi worker), media, community & self -decision, OR: Odds

Ratio, CI: confidence interval. The independent variables are past history of GDM,

advised by whom, risk perception, feeling down and age group

Respondent's

characteristics

N (%) Unadjusted

O.R(95% C.I)

Adjusted

O.R(95% C.I)

P value

Past history

of GDM

Yes

No

17(44.7)

41(25.3)

2.38(1.15-

0.96)

1.74(0.67-

4.53)

0.285

Reference

Advise by Doctor

Others*

32(52.5)

19(27.1)

2.96 (1.43-

6.13)

3.2(1.4-6.9)

0.004

Reference

Risk

perception

Yes

No

21(44.7)

2.53(1.27-

5.01)

1.81(0.78-4.2)

0.161

Reference

Feeling

down

Yes

No

19(52.8)

39(23.8)

3.58(1.69-

7.55)

2.17(0.87-

5.36)

0.081

Reference

Age group 35-42

26-35

≤25

37(18.5) 1.17(0.53-

2.59)

2.06(0.47-

8.99)

0.135

130(65) 0.33(0.09-

1.15)

2.59(0.74-

9.09)

0.338

33(16.5) Reference

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Section III

Doctors’ Perspectives on Management and Postpartum Screening and Advice

This section describes the perspectives of doctors who regularly manage a large number

of GDM patients in the four sample health facilities regarding postpartum screening and

management of GDM patients. We also gathered information about how they managed

GDM during pregnancy and delivery.

There were eight participants from the four selected hospitals and their selection criterion

was based on their GDM case load.

Table.3.16 Profile of the doctors included in the in-depth interviews

Characteristics of the Respondents

Serial

number

Sex Age Qualifications Years of

Experience

Studied

at

Medical

college

Working in

Public/private

sector

1 50 Male MBBS,MD

General

Medicine

22 Public Private sector

2 46 Female MBBS,DGO 19 Public Public sector

3 47 Female MBBS,MS

OBG &

Gynaecology

9 Public Private sector

4 44 Male MBBS,MD

O&G

10 Private Private sector

5 37 Female MBBS,MD

O&G

10 Public Public sector

6 39 Female MBBS,DGO 14 Public Public sector

7 41 Female MBBS,DGO 8 Private Private sector

8 35 Female MBBS,DGO 6 Private Private sector

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3.10 Management of GDM during pregnancy

All doctors reported seeing GDM patients very often. The perceived frequency of seeing

GDM patients ranged from about 25% to as high as four in a week or even one or two per

day. Advice and management varied widely and often was not as per the national

guidelines. Each doctor had his or her own protocol to manage GDM patients. For

example, while all of them reported giving routine advice on strict diet control, only one

had emphasized the importance of exercise and used medical nutrition therapy (MNT) for

management. As per the National Guidelines for Diagnosis and Management of

Gestational Diabetes Mellitus India, the principle behind MNT is healthy eating during

pregnancy. For this individualized nutritional assessment is done. It is a carbohydrate

controlled balanced diet which promotes optimal nutrition for maternal and gestational

weight gain along with maintenance and achievement of normoglycemia.1

Initiation of treatment also varied from referring to a physician, to a stepwise

management of GDM. Three of the providers had started with diet control and waited for

two weeks to control the blood sugar value. If the blood sugar value was not controlled by

diet alone, Metformin was prescribed along with diet control. After this step, if the sugar

value was still not controlled, insulin would be started. One of the provider started the

GDM patient on insulin if there was a family history of T2DM. The remaining four

providers were managing according to whether the patient was on diet control, metformin

or insulin (For patients on diet control and metformin, they were not much strict about

1 This assessment includes defining the Body Mass Index (BMI) or percentage of

desirable pre-pregnancy body weight and optimal pattern of weight gain during

pregnancy. The energy requirement is calculated using the formula

Energy requirement (K.cal/d) = BMR ×PAL

*BMR= Basal metabolic rate

*PAL= Physical activity level

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instructions). Except one, all the providers said they advised about frequent antenatal

visits of once in two weeks. One provider advised two-weekly antenatal visits only for

GDM patients with uncontrolled sugar values.

Almost all doctors reported to not have discussed with the women concerned about the

implications of GDM on health, pregnancy, fetal complication or on the outcome of

pregnancy. Four of the providers said that for women whose blood sugar levels were very

high in the very beginning, they would discuss the risk of congenital anomalies. Only one

respondent said that she discussed with her patients about their future risk for progression

to T2DM soon after GDM diagnosis. Future risk was often communicated very gently:

―in some patients there is a chance of continuation of this condition in future and hence

proper glycemic control is necessary‖.

3.11 Management during Labour:

Routine admission of GDM patients two weeks prior to the expected date of delivery

(EDD) seemed to be a routine practice for some (four of eight doctors), while others

decided on this on a case-by-case basis. All of them believed that management of GDM

patients during labour called for team work with a team having physician, paediatrician,

obstetrician; and facility to resuscitate the baby, Newborn Intensive Care Unit (NICU)

and facility to perform emergency cesarean sections and blood transfusion were very

important to have.

Only some (four of the eight) doctors reported withdrawing insulin prior to delivery as the

women are highly prone to hypoglycemia, which is recommended practice. Other

practices reported included using insulin along with a 5% dextrose drip, and skipping one

dose of insulin prior to delivery and giving one or two doses of insulin after delivery, and

testing blood glucose after 6 hours to decide further treatment. All of them reported that

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cesarean sections are not routinely performed on women with GDM, and that the usual

indications for cesarean sections applied also to GDM patients.

Two of the doctors reported hourly blood sugar level monitoring after delivery, while two

others said they monitored blood sugar every two hours. The fifth doctor was monitoring

4th

hourly blood sugar value, while one monitored the blood glucose level six hours

following delivery after giving immediate postpartum insulin doses. Referring patients

having uncontrolled DM to physicians was also mentioned by some doctors.

3.12 Postpartum advice and management

As with advice and management during pregnancy and labour, advice and management in

the postpartum period also varied even within this small group of doctors. Four of the

eight doctors reported advising diet control after delivery with one of them instructing

avoidance of primary sugars too. Advice regarding regular exercise postpartum (two of

eight) and frequent breastfeeding to prevent hypoglycemia (three of eight) was far less

common. None of them routinely prescribed drugs for glycemic control in the postpartum

period, and prescription of insulin or oral drugs depended on the status of hyperglycemia

of the patient. All except one said that they advised GDM patients at the time of

discharge after delivery on the use of contraceptive methods. The only doctor who did not

do so said, ―even if we say something about it, they will nod their head and go, the body

language itself will be self-explanatory that they are not going to use this”. According to

the doctors, Cu T is the best postpartum contraceptive method for women with GDM in a

previous pregnancy, if their blood sugar values were normal. Otherwise to prevent

infections, they would advise them to control blood sugar before inserting CuT. One

doctor felt that the advice regarding family planning can be given to the woman herself

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and not to her family members. From his experience, most husbands were working

abroad and mothers in law would not usually consider contraception to be important.

3.13 Postpartum screening: All doctors reported very low level of postpartum screening

ranging from 2% to 25%. While some (four of eight) doctors were advising postpartum

screening at or after 6 weeks routinely, they also reported that none of the women

returned for any reason after one month postpartum. Two of them were advising to test

blood at 10th

day and then on 15th

or 20th

days and then after one month. One doctor

referred all postpartum cases to a physician, but she was not sure if the patients were

following the physician‘s advice. One doctor was not concerned about this issue as

according to the doctor none of the patients obeyed their instructions. All reported good

follow up initially, that is within four weeks of delivery and after four weeks, losing

patients to follow-up. Some (three of eight) reported that they counseled both the patient

and the bystander at the time of diagnosis that ―it is a temporary condition and will

subside after delivery”.

3.14 Perceived barriers to women using postpartum screening

There was a perception among a couple of doctors that women did not take the problem

of hyperglycemia seriously and hence ignored the advice of doctors for postpartum

screening. One of the doctors summarized their patients‘ attitude as follows: ―We are too

young to control diet and sugar. It will come (sugar) after getting old. Why do we waste

our good time under stress thinking about all these things?‖ The difficulty in going out

with a small baby and the absence of a screening facility in the nearby locality were cited

by others as potential barriers. Another doctor expressed his view in terms of

prioritization as most of the mothers had a lot of family responsibility as their husbands

were working abroad.

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3.15 Recommendations and suggestions to improve the rate of timely postpartum

screening All providers suggested a reminder system to improve postpartum screening

status. Majority (seven) suggested a message as well as reminder call from hospital.

However some doctors were unsure about the authenticity of the phone number given at

the time of admission as the phone number given was usually of a relative accompanying

the patient at the time of hospitalization. One suggested giving a booklet/pamphlet or

some information to the patient at the time of discharge by the doctor and then a phone

call from hospital at the time of screening.

Health system initiatives to improve postpartum screening status were suggested by

almost all the doctors. These included:

Registering and documenting GDM cases at the health sub centre level and

keeping line list of cases in the PHCs

Counseling, advice and follow up of women with GDM both during pregnancy

and postpartum, including arrangement of facilities to screen them at local level

Seeking the help of ASHA to track defaulters and bring them for screening.

Mass IEC or community training programs to increase personal and public

awareness about GDM and its appropriate management to prevent or delay

progression to T2DM.

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Chapter 4

Discussion and conclusions

The prevalence of risk factors of diabetes are relatively high in Kerala as compared to

other states (Mohan et al., 2012, Reddy et al., 2006). Also, the prevalence of T2DM is

20% in Kerala (Baruah et al 2014). Women of reproductive age in Kerala have a higher

than average prevalence of obesity and a relatively high probability of a family history of

T2DM, which increases their risk of developing gestational diabetes mellitus (GDM).

Although the present study did not aim to assess the prevalence of GDM, the doctors who

were interviewed in-depth as part of this study reported seeing GDM patients were seen

very often in their practice, and perceived that GDM prevalence had increased in recent

times.

Previous GDM is associated with a significant life-time risk of T2DM (Kim et al., 2002).

The blood glucose level comes to normal in most of the women after delivery in GDM.

But they have up to seven times more chance of getting type 2 DM in future (Bellamy et

al., 2009b). According to a retrospective cohort study conducted in rural Kerala, the study

participants were followed up for a period of four years (Sreelakshmi et al 2015),

progression to T2DM was 10%. Life style modification and pharmacological intervention

can delay or prevent progression to T2DM in women with a history of GDM (Ratner et

al., 2008). For this, postpartum follow-up and timely and appropriate screening are of

utmost importance. Postpartum diabetes screening and appropriate follow-up have a

major role in reduction or delaying progression to T2DM in mothers and in reducing

future risk of obesity and diabetes in future among infants.

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4.1. Patterns of postpartum screening for diabetes

The aim of the present study was to assess the rate of ―timely‖ postpartum diabetes

screening in women affected with GDM in their most recent pregnancy and examining

the various patterns of and factors associated with the same. About 58% of the women in

our study had undergone postpartum screening at some time before 6 months following

delivery. These figures are lower than that reported by a recent longitudinal study in 2015

in Delhi, according to which more than 80% of the women diagnosed with GDM had

returned for follow-up screening at 6 weeks postpartum or later (Jindal et al., 2015).

However, low rates of postpartum screening for diabetes in women with GDM in the

immediately preceding pregnancy are reported from many sites across the globe including

in high income countries, usually below 50% (Blatt et al., 2011, Keely 2012, Clark, Keely

et al ., 2012).

The timing of postpartum diabetes screening of GDM mothers appears to be important,

and most of the available guidelines recommend screening after at least 6 weeks

postpartum. For example, the American Diabetes Association (ADA) recommends

screening between 6-12 weeks postpartum, the National Institute for Health and Care

Excellence (NICE), UK guidelines mention 6-13 weeks postpartum, while India‘s

National guidelines for Diagnosis and Management of Gestational Diabetes Mellitus

recommends screening at or after 6weeks postpartum.

In the present study we have defined ―timely testing‖ as diabetes testing in GDM mothers

done at or after 6 weeks but before 6 months postpartum. The rate of timely postpartum

diabetes screening in our study is 29%, while an equal proportion (28.5%) have tested

their blood after delivery but before 6 weeks. The rates of timely screening obtained in

our study are lower than that in a retrospective study carried out in USA between 7 weeks

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and 6 months among GDM affected women, in which 46% were tested during the 6-12

weeks postpartum and 12.3% during 12 weeks to 6 months (Lawrence et al., 2010).

Screening immediately after delivery may underestimate the proportion with

hyperglycemia especially if the patient was under drugs for glycaemic control during

pregnancy. A study comparing results from postpartum diabetes testing between 24-72

hours following delivery with those obtained from the same cohort at 6 weeks or later

found that the early test underestimated the prevalence of diabetes (3.7% versus 8.5% )

and over-estimated the prevalence of pre-diabetes (32.9% versus 20.7%) (Nabuco et al.,

2016). Accurate diagnosis and appropriate management requires that all GDM mothers be

tested at or after 6 weeks postpartum. Those who tested before 6 weeks postpartum and

were told that their status was ―normal‖ could well be cases of T2DM within the next few

weeks.

Postpartum screening for diabetes done too early by GDM affected women may be a

consequence of inaccurate advice given by their obstetrician/gynecologists at the time of

discharge after delivery. In a study by Mahalakshmi et al among diabetologists /

endocrinologists and obstetrician/gynecologists in India, more than 40% of both sets of

specialists had advised postpartum screening within 6 weeks of delivery (Mahalakshmi et

al., 2016).

Not only the timing of postpartum screening but also the type of screening test used for

postpartum diabetes screening of GDM mothers is very important in obtaining an

accurate diagnosis. The most widely recommended test in many high income countries

and in India is 75-g -2h OGTT, because HbA1c would miss many women with lower

levels of hyperglycemia and would be sensitive only to women with the highest glucose

levels. However, in places where it is not feasible to administer 75g-OGTT, HbA1C test

would at least detect those in need of urgent attention (Kitzmiller et al., 2007) .

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In our study we were not able to obtain accurate information on the type of screening test

performed. However, based on women‘s description of what was done when they

presented for screening, we deduce that practically none of the women had undergone the

recommended test. Thirty four percent of women who had undergone testing in our study

had self-referred themselves to a laboratory and 4% had carried out a test at home using a

kit. Both these groups of women did not undergo the appropriate test for diabetes

screening and those who were reported to be ―normal‖ from these tests could be at risk of

diabetes. Although facilities for OGTT were present in the public as well as private

hospitals where women tested, women did not report waiting for two hours to be tested

after a glucose load, which implies that some other test for diabetes was performed. From

the doctors interviewed in this study, we learnt that although they were aware of the

importance of the 75g-2hr- OGTT test postpartum, they did not insist on performing the

same for the women under their treatment, but used a suitable test convenient to the

women.

4.2. Factors associated with ‘timely’ postpartum screening for diabetes of women

with GDM

In the present study, doctors‘ advice on postpartum screening emerges as the single-most

significant factor associated with timely postpartum diabetes screening, both in the

bivariate and in the multivariate analysis. Age adjusted multiple logistic regression

analysis found that those who were advised by a doctor to undergo postpartum diabetes

screening had a three times higher chance of undergoing timely postpartum screening

compared to those who had been advised to do so by any other health care provider or lay

persons. While studies that have examined the role of physicians‘ advice on the rate of

postpartum screening are limited, a review of 58 studies from high, middle and low-

income countries (Nielesen et al., 2013) reported ―receiving postnatal information‖ as an

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important predictor of postpartum screening following a GDM pregnancy. Another study

(Kim 2007) similarly reported that women who recalled receiving advice about

postpartum diabetes screening and receiving a laboratory slip were more likely to undergo

screening. Direct advice regarding postpartum screening in the form of written or two-

way communication by treating doctors was found in an Australian study to increase the

odds of postpartum diabetes screening (Morrison et al., 2009). Unlike our study, none of

these studies specify any differences in the odds of screening by type of health provider.

There is another reason for the lack of direct advice from the physician to the woman with

GDM, which evolved from our study. This was that the doctor conducting delivery often

considered revealing any information to the mother regarding her health status and future

risk of diabetes as a sensitive issue which may affect the mother adversely by increasing

her anxiety. This attitude prevented him/her from disclosing routine advice directly to the

women and he/she tended to provide information only to the bystanders, usually other

members of the family. But after discharge from hospital there is not much

communication between the bystander and the patient, and the information does not reach

the woman concerned.

Studies have found a number of patient characteristics to be associated with postpartum

screening. These include among others, age, parity, past history of GDM, awareness

regarding the importance of postpartum screening and risk perception. In our study, we

found that older women (31-35yrs) and women of parity 4 or higher were more likely to

have undergone timely postpartum screening. While Tovar et al., similarly reported older

age to be a predictor of postpartum screening, their study found nulliparity and not

multiparity to be a predictor (Tovar et al., 2011). In the Indian setting, as age increases the

parity also increases. The rise in timely screening status among women of relatively older

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age and parity may be due to a greater autonomy enjoyed by them after many years of

marriage and several children.

We also found that a greater proportion of women with awareness on the importance of

postpartum diabetes screening had undergone timely screening. The association was

significant at the 5% level in the bivariate analysis alone. Based on an extensive review of

literature on postpartum diabetes screening after GDM, Case et al (2006) recommend that

improving awareness on timely postpartum screening, and mass IEC on future risk of

T2DM and scope for prevention of T2DM are possible areas of interventions (Case et al.,

2006). We need to concentrate not only on public awareness but also on training of health

workers and doctors regarding the implications of GDM and the importance of timely

screening (Mithal et al., 2015).

In our study, a higher proportion of those who had perceived risk of getting T2DM in

future had done timely screening as compared to others and the association was

statistically significant in the bivariate analysis. Other studies have also reported on the

role of risk perception, but its association with timely screening was not examined. For

example in a study to examine the risk perception (on progress to T2DM) in women with

a history of GDM, 90% believed that GDM was a risk factor for future diabetes in

general, but only 16% perceived that they specifically were at increased risk of getting

T2DM. Those who perceived moderate/high risk planned to modify their lifestyle

behaviors (Kim et al., 2007).

It may be of interest to note than in our study, timely screening was higher among those

who self-referred themselves to a laboratory or had undergone screening in a private

hospital (66.7% and 62.1% respectively), and three of five women who tested themselves

at home also had timely screening. Eighty percent of those who had tested their blood at

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home and around 40% of those who self- tested at laboratory were hyperglycemic. Thus,

awareness of the need for postpartum screening and probably ‗risk perception‘ motivated

their self-referral for timely testing.

GDM is known to increase risk of postpartum blues and even postpartum depression

(Mom et al., 1998), and we found almost a third of the respondents (36%) in our study

reported feeling thus. GDM mothers who reported that they felt ‖little interest in

anything‖ and were ―feeling down‖ were significantly more likely to have timely

postpartum diabetes screening as compared to other GDM mothers (in the bivariate

analysis). We did not find any other study reporting such an association. One possible

explanation for the association is that their inability to perform routine day- to-day work

may have compelled them to test to find out whether this condition was due to diabetes.

4.3. Barriers to postpartum diabetes screening and adequate post-screening follow-

up

4.3.1 Barriers as reported by the women

One of the most common barriers to postpartum diabetes screening was lack of

information, cited by almost 60% of women in our study who did not undergo screening.

Other reasons included doctors‘ reassurance that the condition would resolve after

delivery (14%), difficulty in going out with a small baby (12%), being asymptomatic, and

fear of learning about the diagnosis. Among those who tested at any time postpartum

(n=115) about 16% did not consult a doctor after testing their blood. A normal blood

glucose result (55.6%), difficulty in going out with a small baby (16.8%) and doctor‘s

reassurance (11.1%) were the major reasons for not consulting a doctor.

In a qualitative study conducted by Bennet et al among women affected with GDM in a

high risk obstetric clinic, a number of themes emerged as barriers to postpartum follow-

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up care including screening. These included recent delivery experiences and baby‘s health

issues; burden of child care, emotional stress, lack of time and feeling overwhelmed;

feeling healthy and not in need for care; fear of receiving bad news; and dissatisfaction

with the logistics of accessing care (Bennett et al., 2011) . Another qualitative study in the

US reported that the barriers cited by women were not finding time for testing amidst

demands of childcare and domestic chores, and interpreting physicians‘ reassurance of

resolution of GDM after delivery as indicating low importance for screening (Paez et al.,

2014).

4.3.2 Barriers related to doctors and the health system

According to doctors interviewed in this study, major barriers to postpartum screening

and follow-up included women‘s inability to find time to come for follow-up care

because of their workload; lack of decision-making power especially among younger

women and lack of appreciation of the importance of follow-up care by women‘s

bystanders, usually mothers-in-law.

Nielsen et al (2014) similarly report from their review of studies that barriers to

postpartum screening from the perspective of health care providers included loss of

patients to follow-up, patient‘s lack of information or lack of understanding of the need

for the test. Other barriers mentioned were the lack of uniform protocols for postpartum

screening and management.

From our in-depth interviews with doctors, our observation is that the National

Guidelines for Diagnosis and Management of Gestational Diabetes Mellitus, India were

not known to any of them. Each of them was following a different set of procedures for

diagnosing as well as management during pregnancy and postpartum. It may be that as

obstetricians / gynaecologists, they are mainly concerned about managing safely the

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GDM patient‘s pregnancy and doing their best to ensure a positive pregnancy outcome.

The subsequent management of the postpartum woman is not usually their concern.

Many doctors told this researcher that gestational diabetes is relieved after delivery and

only overt diabetes will continue after delivery, and did not seem to appreciate the

elevated risk of progression to T2DM. We wonder if this belief is gradually disseminated

into the society through their advice to the patient and bystanders during pregnancy. This

could prevent the majority from undergoing postpartum blood glucose testing and from a

consultation following the test.

About 80% of women in this study who had a normal blood sugar level in postpartum

screening and consulted their doctors were advised that there was nothing to worry. No

one was advised to repeat the test periodically, or to report their GDM history at the time

of their antenatal registration in their next pregnancy. The American Diabetes Association

(ADA) recommends three-yearly repeat screening for women testing normal in

postpartum screening. For Indian women, Tandon et al (2015) recommend screening

after one year in women with normal blood glucose results and 3-6 months in women

with abnormal blood glucose results instead of three yearly intervals as per ADA criteria

(Tandon et al., 2015).

4.4 Postpartum diabetes screening of GDM pregnancies – a case of repeated missed

opportunities to prevent T2DM.

Postpartum screening rate of GDM is very low. GDM affected women are not followed-

up or managed appropriately and those presenting with GDM in first pregnancy end up

with overt diabetes in succeeding pregnancies or present as overt diabetes adding to the

existing pool of diabetes mellitus in the community. There is also a high risk of morbidity

for the mother and the infant, causing avoidable suffering on a large scale.

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This study brings out the alarming failure of the health system to use the window of

opportunity provided during pregnancy and postpartum period in preventing mothers with

GDM from progressing to full-blown T2DM at an early age, and living for many years

with a progressively debilitating condition that can affect multiple organs and needs

continuous management with drugs for several decades. Figure 1 illustrates the tragedy of

how of 200 women who actually came to the health services and were managed well

during pregnancy and delivery, barely 6%, or 11 women received appropriate postpartum

advice and management that could help prevent future T2DM. The other 94% represent

missed opportunities that could be easily avoided through appropriate policies and

interventions.

4.5. Strengths and limitations of the study:

All the interviews were conducted by a single investigator who is a physician. The

respondents were interviewed in their residence, so detailed response could be captured.

Since the sample frame is taken from hospitals, it won‘t be a representative sample of the

population. Facilities were identified around 6 months prior to the study and hence, it

might have influenced the practices of providers and hence the postpartum screening rate

4.6. Conclusions and recommendations

Timely postpartum screening and follow up of women following a GDM pregnancy can

help significantly in preventing adverse health consequences to the mother and her baby.

While planning effective postpartum diabetes screening programs at the grass root level,

various barriers at the level of the client, the health care provider and the health system

have to be kept in consideration. Hence understanding of factors associated with timely

postpartum screening can help to plan proper interventions according to the local

scenario. The health system can play a central and key role in ensuring appropriate

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management of GDM during pregnancy and postpartum and through the rest of the

woman‘s lives.

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The following are some recommendations for the public health system in India and

Kerala:

Uniform protocol: A standard protocol for advice, management, and timelines of

screening and contraceptive advice has to be established for India, in order to improve the

maternal and foetal health and preventing future diabetes in women with GDM.

Uniform postpartum diabetes screening intervals for the country: Considering the

local factors like high risk of T2DM for Indian women, we have to carry out postpartum

diabetes screening suitable and appropriate for our settings. Postpartum screening at 6-12

weeks after delivery and subsequent screening after one year in women with normal

blood glucose results and 3-6 months in women with abnormal blood glucose results may

be adopted.

Special thrust on contraceptive advice: Hyperglycemia at the time of pregnancy will

affect the baby adversely. Hence advice on using of spacing methods of contraception,

and on the importance of control of blood sugar before the next pregnancy is a must.

Physician education: Training of all health care providers who are managing GDM

affected women on the uniform protocols and the importance of adhering strictly to these

is an urgent priority. Physicians‘ capacity needs to be strengthened in areas such as

counselling for postpartum healthy life style, including physical activity, behavioral

changes, nutrition, breastfeeding and weight loss.

Postpartum referral by the Ob/Gyn conducting delivery to a physician as routine

practice: To ensure uninterrupted support and management of all GDM affected mothers,

the treating obstertician/ gynaecologist should routinely refer them after delivery to a

physician, with a written request.

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Reminder system: Advice regarding future management and follow up should be of

utmost priority at the time of discharge and institution-wise facilities for reminders on

timely postpartum screening must be established under the responsibility of the treating

physician.

Education of physicians of other systems of medicines: Physicians in other systems of

medicine should also be included in the training programme to percolate the message

across all potential health care providers.

Enhancing patient and public awareness: Efforts should be made as part of the NCD

programme as well as the RMNCH+A programme to enhance health awareness on GDM

at various levels: the household, the school and the community.

Building capacity of front-line health workers to play an effective role in the

prevention and management of GDM

Frontline health workers such as the Junior Public Health Nurses, the ASHAs and the

Anganwadi workers and Male Health Workers should receive the appropriate training to

play an effective role in the prevention and management of GDM, as detailed below.

Asking about GDM as a part of routine history taking at the time of antenatal

registration: There should be special emphasis while registering an antenatal case both in

the public and private sector to ask about past history of GDM and family history of

diabetes mellitus. There should be a separate item in the registration system to fill this

detail.

Regular tracking and a system of monitoring GDM patients after delivery: All

pregnant women affected with GDM should be tracked through the local health facility

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(sub-centre, PHC or other) and be registered under the government‘s Non Communicable

Disease Control programme.

Availability of testing at the PHC level: Postpartum screening through PHC and if

possible at sub-centre level. To promote healthy diet and exercise, demonstration at sub

centre level through health workers.

Availability of drugs at the subcentre and PHC level: Availability of drugs and

screening tests closer to home may be helpful for the GDM mothers. We need to set up a

system of regular monitoring similar to the DOTS programme of RNTCP.

Development and validation of a risk screening tool for GDM, and targeted testing

of women found to be high risk based on the tool: To prevent future diabetes in young

women, it is very important to develop an appropriate risk assessment tool, strengthen

screening practices for GDM during pregnancy and take actions for primary prevention.

Encourage studies on GDM and possible interventions to reduce progression to

T2DM.

The present study has identified associated factors and barriers to timely postpartum

diabetes screening. We need intervention studies to evaluate various context-specific

approaches to effective screening.

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Reddy KS, Prabhakaran D, Chaturvedi V, et al. (2006) Methods for establishing a

surveillance system for cardiovascular diseases in Indian industrial populations.

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Seshiah V, Balaji V, Balaji MS, et al. (2008) Prevalence of gestational diabetes mellitus

in South India (Tamil Nadu)--a community based study. The Journal of the

Association of Physicians of India 56: 329–333.

Seshiah V, Balaji V and Balaji MS (2008) Scope for prevention of diabetes--‘focus

intrauterine milieu interieur‘. The Journal of the Association of Physicians of

India 56: 109–113.

Seshiah V, Balaji V, Balaji MS, et al. (2009) Pregnancy and diabetes scenario around the

world: India. International Journal of Gynecology & Obstetrics, Diabetes,

Women and Development: Report and Papers from an Expert Meeting 104,

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Shah B, Lipscombe L, Feig D, et al. (2011) Missed opportunities for type 2 diabetes

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Annexure I

Patterns of and factors associated with postpartum diabetes

screening in women diagnosed with Gestational Diabetes

Mellitus (GDM) in Malappuram district, Kerala

Serial number (for personal use only):

Interview Schedule for the survey

Code For personal use only Main code-M

M1 Participant’s ID

M2 Date of interview

M3 Start time

M4 End time

M5 Number of revisits made to

complete the interview

M6 Contact number of the

participant

Section 1: Background characteristics main code -B

I would like to ask you some questions about yourself and your health

Serial

number

Sub

code

Questions Response

1 B1 How old were you on your

most recent birth day?

DD MM YY

HH MM AM/PM

HH MM AM/PM

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2 B2 What is your educational

qualification?

1 No schooling

2 1-7th standard

3 8-10th standard

4 Higher secondary

5 Post higher

secondary

diploma /

certificate

6 Graduate and

above

7 Others ,specify

3

B3

BMI

1

2

Height in cm

Weight in Kg

4 B4 What is your working status 1 Home maker

2 Daily wage earner

3 Salaried

employment

4 Self-employment

5 Student

6 Others , specify

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Section2:Past Reproductive History(excluding the most recent delivery)

-Main code A

Q5:Order of pregnancy (A1)

Q6:Whether GDM diagnosed (A2) (Yes=1 No=2 )

Q7:Whether miscarriage/ abortions (A3) (Yes=1 No=2 )

Q8:If yes, month of gestations (A4)

If delivered If live birth Remarks Q9:Period of gestation in months (A5)

Q10:Mode of delivery (A6) (Normal=1 C-section=2 Assisted deliver=3)

Q11: Outcome (A7) (Live birth=1, Still birth=2)

Q12:M/F (A8) (male=1,female=2)

Q13:Current status (A9) (Alive +good health=1, Alive+ health problems =2, not alive=3

Q14: (A10)

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Section3:Most recent pregnancy and delivery Main code-D

15 D1 Did you have any health

problems during your most

recent pregnancy?

1 Yes

2 No

16 D2 If yes,

explain……………………………………………….

17

D3 What type of delivery did

you have?

1 Normal delivery

2 C-section

3 Assisted delivery

18 D4 How many months pregnant

were you when you

delivered?

1 Pre term(less

than37weeks)

2 Term(37-41wks)

3 Post

term(>41wks)

19 D5 Did you suffer from any

complications

1 Yes

2 No

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20 D6 If yes, what were they?

Section 4 Child characteristics Main Code: P

21 P1

Birth weight of the child in

kg

22 P2 Sex of the child 1 Male

2 Female

23 P3 *Cried just after delivery 1 Yes

2 No

24 P4 Breast feeding started 1 Less than one hour

2 Less than 24 hours

3 More than 24

hours

4 Others, specify

25 P5 Were there any difficulties in

initiating breast feeding?

1 Yes

2 No

26 P6 Did the child have jaundice

within one week of birth?

1 Yes

2 No

27

P7 Was the child admitted in

ICU before discharge?

1 Yes

2 No

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28 P8 Was blood testing done,

before discharge?

1 Yes

2 No

3 don’t know

29

P9 If yes, for what 1 for routine

screening

2 to test blood

glucose level

3 As part of

investigation

while she/he was

ill

4 Don’t know

5 Any other, specify

30 P10 Is the child immunized for

age?

1 Yes

2 No

31 P11 Has the baby had any health

problems?

1 Yes

2 No

32 P12 If yes, describe ……………………………………….

Section5:Management of GDM in Most Recent Pregnancy

Main code: S

33 S1 Do you have a family history

of diabetes mellitus?

1 Yes

2 No

34 S2 If yes, who has /had

diabetes?

1 Mother

2 Father

3 Siblings

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a)During pregnancy Main Code: SP

35 SP1 I understand that you had

been diagnosed with diabetes

during your pregnancy. Can

you describe how you came

to be diagnosed as having

diabetes during your

pregnancy?

……………………………

…………………………

36

SP2 At which month of gestation

were you diagnosed with

GDM (Prameham)?

1 First trimester

2 Second trimester

3 Third trimester

4 Before pregnancy

37 SP3 Was there a reason for testing

your blood?

1 Routine test

2 One of my

parents/both have

diabetes

3 Previous history

of GDM

4 Previous history

of big baby

(macrosomia)

38 SP4 Did you receive any advice

on this?

1 Yes

2 No

39 SP5 If yes, from whom? 1 Doctor

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2 Nurse(from the

hospital)

3 Friend

4 Others, specify

40 SP6 How did they manage your

condition?

1 Started oral

medicine

2 Advised diet

control

3 Advised exercise

4 Started injection

insulin

5 Any other, specify

41 SP7 What was the reaction of your family members when

you were diagnosed as GDM? Explain

………………………………………………………

b)After delivery Main code :SA

42 SA1 Do you think that blood

glucose testing is necessary

after delivery?

1 Yes

2 No

If no, go to Q:SA4

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43 SA2 If yes, why?

44 SA3 Who told you about this? 1 Doctor

2 Health worker

3 AWW/ASHA

3 Media

5 Others, specify

45 SA4 Have you tested your blood

after delivery to check blood

glucose level?

1 Yes

2 No

(if ,no to Q no:PB1)

46

SA5 If yes, when did you conduct

the test?(period after

delivery)

47 SA6 From where? 1 Public hospital

2

Private hospital

3 Laboratory(self-

referred)

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4 Self(at home)

If answer to SA 6 is 1 or 2 go to SA 10

48 SA7 What was the result of your

blood sugar test?

1 Blood sugar level

was high

(hyperglycemia)

2 Normal

If answer to Q; SA 6, is3 or 4 , then answer SA 8&9.

49 SA8 Did you consult a

doctor(after doing the blood

test- self)

1 Yes

2 No

50

SA 9 If you self-tested, but did not

go to a doctor .What was the

reason?

1 Lack of time

2 No one to

accompany

3 Family does not

support

4 Lack of money

5 Others, specify

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After this question go to FP1

51 SA10 If blood sugar test was

normal and you consulted a

doctor, what did she/he say?

1 Nothing to worry

now

2 Do blood glucose

test at 6 weeks

after delivery

3 Do yearly

screening

4 Any other,

specify?

52

SA11 If the blood glucose level was

high, what did your doctor

advice?

1 To start medicine

2 Diet control

3 Exercise

4 Continue breast

feeding

5 Regular follow-up

6 Any other,

specify?

53 SA12 (a)

Which among the doctor’s advice were you able to

follow?

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54 SA12 (b) Which among these were you

not able to follow?

55 SA12 (c) Why?

If answer to SA 11 is 1,go to SA 14,if not go to FP1

56 SA14 If started medicines , could

you please tell me what these

medicines are ( check

prescriptions)

1 Tablets (Oral

hypoglycemic

agents)

2 Insulin

57 SA15 Are there any difficulties for

you to get medicines

continuously?

1 Yes

2 No

58 SA16 If yes, could you explain me what the difficulties are?

..........................................................................

To be answered by those who have had no postpartum screening

Section 6:Personal Barriers Main code: PB

59

PB1 Why have you not got

yourself tested after delivery

for diabetes mellitus?

1 Lack of time

2 No one to

accompany

3 Family does not

support

4 Lack of money

5 Others, specify

60 PB2 Have you considered getting 1 Yes

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tested anytime in the near

future for diabetes mellitus?

2 No

61 PB3 If yes, when?

Section7:Spacing/family planning Main code: FP

62

FP1 Are you using any

contraceptive methods?

1 Yes

2 No

63 FP2 If yes, what type? 1 IUD

2 Condoms

3 Oral contraceptive

Pills

4 Sterilization

(Vasectomy/

tubectomy)

5 Others, specify

64 FP3 Who told you about this? 1 Doctor

2 Nurse

3 JPHN

4 Husband

5 Friend

6 Self-decision

7 Any other

Section8:Risk Perception Main code: R

65 R1 Women who had developed 1 Yes

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diabetes mellitus during pregnancy are more likely to get diabetes in their life time when compared to those who did not get diabetes mellitus during pregnancy/pregnancies. Do you think you have a higher chance of getting diabetes mellitus in your lifetime? (if No skip Q66 )

2 No

66 R2 If yes, who has told you

about this?

1 Doctor

2 Health worker

3 AWW/ASHA

4 Family members

5 Media

6 Health education

class

7 Others, specify

Section9:Postpartum health Main Code -T

Now I would like to ask you some questions about your health after delivery

67 T1 Have you had any health

problems after delivery(post

discharge)

1 Yes

2 No

68 T2 If yes, describe

69

T3 Have you ever had a feeling

of having little interest or

pleasure in doing things, after

the delivery

1 Yes

2 No

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70 T4 Have you ever had a feeling

of feeling down or having

little energy?

1 Yes

2 No

71 T5 Did you ever experienced

Poor appetite or over eating

1 Yes

2 No

72 T6 Have you ever experienced

feeling bad about yourself or

that you’re a failure or let

yourself or your family down

1 Yes

2 No

*Prolonged labour, especially if macrosomia may lead to foetal distress.

Thank the respondent;take permission to conduct again, if required.

Signature of the PI

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KÀ`Ime {]taltcmKap­mbncp¶ kv{XoIfn {]khm\´c {]taltcmK (Pn.Un.Fw) ]cntim[\bpsS coXnIfpw klmbn¡p¶ LSI§fpw þ ae¸pdw

PnÃ, tIcfw

ANyp-X-ta-t\m³ skâÀ t^mÀ sl¯v kb³kv ÌUo -kv, {ioNn{XXncp-\mÄ C³Ìn-äq«v t^mÀ saUn-¡Â kb³kkv Bâv sSIvt\m-f-Pn, Xncp-h-\- -́]p-cw, 695011, tIcfw

A`n-apJ t^mdw þ KÀ`-Ime {]ta-l-tcm-K-ap-­m-bn-cp¶ A½-amÀ

{Ia \¼À (hyàn]camb Bhiy§Ä¡v am{Xw):

]T\¯n\p th­nbpff A`napJ t^mdw

Code hyàn]camb

Bhiy§Ä¡v am{Xw Main code-M

M1 ]s¦Sp¡p¶bmfpsS

Xncn-̈ -dn-b \¼À

M2 XobXn

M3 XpS§p¶ kabw

M4 Ahkm\n¨ kabw

M5 C³Àhyp

]qÀ¯nbm¡p¶Xn\mbn

F{X XhW aS§n h¶p

M6 ]s¦Sp¯bmfpsS t^m¬

\¼À

Section 1: ]Ým¯e khntijXIÄ main code -B \n§sf Ipdn¨pw \n§fpsS BtcmKys¯¡pdn¨pw GXm\pw tNmZy§Ä

\n§tfmSv tNmZn¡s«

{Ia \w Sub

code

tNmZy§Ä {]XnIcW§Ä

DD MM YY

HH MM AM/PM

HH MM AM/PM

Appendix II

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1 B1 C¡gnª P³aZn\¯n \n§Ä¡v F{X hbÊmbn

2 B2 \n§fpsS hnZym`ymk tbmKyX

1 kvIqfnÂ

t]mbn«nÃ

2 1-7th ¢mÊv

3 8-10th ¢mÊv

4 lbÀ sk¡âdn

5 t]mÌv lbÀ

sk¡âdn

Unt¹ma /

kÀ«n^n¡äv

6 _ncpZhpw

AXn\p apIfnepw

7 asäs´¦nepw,

hyàam¡pI

3

B3

_n. Fw. sF

1

2

s]m¡w (sk.ao)

h®w (In.{Kmw)

4 B4 \nehn \n§fpsS tPmen

F´mWv 1 ho«ptPmen

2 Znhk thX\w

3 amk i¼fw

4 kzbw sXmgnÂ

5 hnZymÀ°n

6 aäpffh

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Section2:Past {]XypXv]mZ\ Ncn{Xw(C¡gnª KÀ`hpw {]khhpw HgnsI) -Main code A

Q5:KÀ`¯n-sâ -{Iaw (A1)

Q6: KÀ`Ime {]talw Is­¯nbncp¶p (A2) (D­v=1 CÃ=2 )

Q7:KÀ`Ñn{Zw / KÀ`w AekÂ

(A3) (D­v=1 CÃ=2 )

Q8:{]khn¡pIbmbncp¶psh¦n F{X amkw (A4)

Pohn¨ncn¡p¶psh¦n Ipdn v̧

Q9: F{X amkw KÀ`nWnbmbncp¶t¸mÄ (A5)

Q10:{]khcoXn

(A6) (kpJ{]khw=1 kntÊdnb³=2 klmbw Bhiyamb

{]khw=3)

Q11: ]cnWnX ^ew

(A7) (Poh\pff

Ipªv=1, Nm]nff=2)

Q12:B¬/s]¬

(A8) (B¬Ipª

v=1, s]¬Ipªv

=2)

Q13:Ct¸ms¯ ØnXn

(A9) (Pohn¨ncn¡p

¶p+ \Ã

BtcmKyw=1, Pohn¨ncn¡p

¶p + BtcmKy {]iv\§fp­v =2, Pohn¨ncn¡p

¶nÃ=3

Q14: (A10)

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15 D1 KÀ` Ime¯v \n§Ä¡v

F´¦nepw BtcmKy

{]iv\§fp­mbncpt¶m?

1 D­v

2 CÃ

16 D2 Ds­¦nÂ

hniZam¡pI

17 D3 GXv Xc¯nepff

{]khambncp¶p

\n§fptSXv?

1 kpJ {]khw

2 kntkdnb³

3 AknÌUv

sUenhdn (klm-

b-t¯m-sS-bpÅ

{]k-hw)

18 D4 F{X amk¯nemWv \n§Ä

{]khn¨Xv 1 {]o tSw(37

BgvNbn Ipdhv)

2 tSw (37-41BgvN)

3 t]mÌv tSw (

>41BgvN Ign-

ªpÅ {]khw)

19 D5 \n§Ä¡v {]khkab¯v

Fs´¦nepw

_p²nap«p­mbn«pt­m?

1 D­v

2 CÃ

20

D6

Ds­¦n Ah F´v?

Section3: C¡gnª KÀ`hpw {]khhpw Main code-D

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Section 4 Ipªnsâ khntijXIÄ Main Code: P

21 P1

P\\ kabs¯ Ipªnsâ

`mcw?

22 P2 Ipªnsâ enwKw 1 B¬

2 s]¬

23 P3 {]khn¨ DSs\ Ipªv

Ictªm?*

1 D­v

2 CÃ

24 P4 {]kh tijw F{X kabw

IgnªmWv Ipªn\v

ape¸m \ÂIm³

XpS§nbXv

1 Hcp

aWn¡qdn\pffnÂ

2 24

aWn¡qdn\pffnÂ

3 24 aWn¡qdn\p

tijw

4 asäs´¦nepw

hyàam¡pI

25 P5 BZyw apebq«nb kab¯v

Fs´¦nepw _p²nap«pIÄ

A\p`hs¸«ncpt¶m ?

1 D­v

2 CÃ

26 P6 \n§fpsS Ipªn\v P\n¨v

HcmgvNbv¡pffnÂ

aª¸n¯w h¶ncp¶pthm?

1 D­v

2 CÃ

27

P7 UnkvNmÀPn\v apt¼ Ipªns\ sF.kn.bphnÂ

{]thin¸n¨ncpt¶m?

1 D­v

2 CÃ

28 P8 UnkvNmÀPn\v ap¼mbn cà

]cntim[\ \S¯nbncpt¶m? 1 D­v

2 CÃ

3 AdnbnÃ

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29

P9 Ds­¦n AXv F´n\v

1 ]Xnhmbpff

]cntim[\bv¡m

bn

2 cà¯nse

]©kmcbpsS

Afhv

]cntim[n¡m³

th­n

3 tcmK_m[nXbmbn

cn¡pt¼mÄ

]cntim[\bv¡m

bn

4 AdnbnÃ

5 asäs´¦nepw

30 P10 Ipªnsâ Ct¸mgs¯

hbkn\\pkcn¨pff FÃm

Ip¯nhbv]pIfpw

FSp¯n«pt­m?

1 D­v

2 CÃ

31 P11 Ipªn\v Fs´¦nepw

BtcmKy

{]iv\§fp­mbn«pt­m?

1 D­v

2 CÃ

32 P12 Ds­¦n hniZam¡pI

……………………………………….

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Section5:KÀ`Ime {]tal \nb{´Ww þ C¡gnª KÀ`¯nepw {]kh¯nepw

Main code: S

33 S1 IpSpw_¯nemÀs¡¦nepw

{]talw Dt­m? 1 D­v

2 CÃ

34 S2 Ds­¦n AXmÀ¡v 1 Aѳ

2 A½

3 _Ôp¡Ä

a)KÀ`Ime¯v Main Code: SP

35 SP1 KÀ`mhØbnembncp¶

kab¯v \n§Ä¡v {]talw

D­mbncp¶sX¶v Rm³

a\knem¡p¶p.

{]talap­mbncp¶psh¶v

\n§Ä F§s\bmWv

a\knem¡nbXv,

hniZam¡mtam?

………………………………

………………………

36

SP2 KÀ`mhØbpsS GXv

amk¯nemWv \n§Ä {]tal

_m[nXbmsW¶v

Is­¯nbXv?

1 BZys¯ aq¶v

amkw

2 c­mas¯ aq¶v

amkw

3 aq¶mas¯ aq¶v

amkw

4 KÀ`nWnbmIp¶Xn

\v apt¼

37 SP3 \n§fpsS càw

]cntimKn¡phm\pff 1 ]Xnhv ]cntim[\

2 amXm]nXm¡fnÂ

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ImcWw? Hcmtfm / c­v

t]tcm {]tal

_m[nXcmtWm?

3 ap³Ime KÀ`

{]talmhØ

4 ap¼s¯

{]kh¯nÂ

henb

Ip«nbmbncpt¶m?

(amt{Im-tkm-anb)

38 SP4 CXn\p th­n \n§Ä¡v

Bcn \ns¶¦nepw D]tZiw

e`n¨ncpt¶m?

1 D­v

2 CÃ

39 SP5 Ds­¦n Bcn \n¶v 1 tUmIvSÀ

2 \gvkv(Bip]{Xnbn

 \n¶pw )

3 kplr¯v

4 aäpffhÀ

40 SP6 \n§fpsS Cu AhØsb

AhÀ F§s\bmWv

]cn]men¨Xv?

1 Ign¡phm\pff

acp¶v

2 `£W \nb{´Ww

3

hymbma \nÀt±iw

4 C³kpen³

C³P£³

5 Asäs´¦nepw,

hyàam¡pI

41 SP7 KÀ`Ime {]talw Ds­¶v Is­¯nbt¸mÄ

F´mbncp¶p IpSpw_mwK§fpsS {]XnIcWw,

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hniZam¡pI.

………………………………………………………

b){]kh tijw Main code :SA

42 SA1 {]kh tijw cà¯nse

¥qt¡mknsâ ]cntim[\

A\nhmcyamsW¶v \n§Ä

IcpXp¶pt­m?

1 D­v

2 CÃ

D¯cw Cà F¶msW¦n tNmZyw SA4 te¡v t]mIpI

43 SA2 BsW¦n F´p sIm­v?

44 SA3 BcmWv Cu

]cntim[\sb¡pdn¨v

\n§tfmSv ]dªXv?

1 tUmIvSÀ

2 BtcmKy

{]hÀ¯I³

3 A¦-W-hmSn

hÀ¡À/Bi

3 ]{X am[ya§Ä

5 asäs´¦nepw

45 SA4 cà¯nse ¥qt¡mknsâ

Afhv Is­¯p¶Xn\pff

cà ]cntim[\ {]kh

tijw \n§Ä

\S¯nbncpt¶m?

1 D­v

2 CÃ

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(D¯cw Cà F¶msW¦n tNmZyw PB1te¡v t]mIpI)

46

SA5 Ds­¦n Ft¸mgmWv

\S¯nbXv?({]kh

tijapff kabw)

47 SA6 sSÌv \S¯nbXv FhnsS

\n¶mbncp¶ppw? 1 Kh.Bip]{Xn

2

kzImcy

Bip]{Xn

3 em_v(kzbw sd -̂

dÂ)

4 kzbw(ho«nÂsh¨v

)

tNmZyw SA 6 sâ D¯cw Ht¶m1 ct­m BsW¦n SA 10 te¡v

t]mhpI

48 SA7 \n§fpsS cà

]cntim[\bpsS ^ew

F´mbncp¶p?

1 cà¯nse

]©kmcbpsS

Afhv IqSpXÂ

(ssl¸À

Kvssfko-anb)

2 km[mcWw

tNmZyw SA 6 sâ D¯cw, aqt¶m \mtem BsW¦n tNmZyw SA 8 sâbpw

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9sâbpw D¯cw ]dbpI

49 SA8 cà ]cntim[\bv¡v tijw

\n§Ä tUmIvSsd

I­ncpt¶m? (cà

]cntim[\bv¡v tijw)

1 D­v

2 CÃ

50

SA 9 \n§Ä tUmIvSsd ImWmsX

kzbw ]cntim[\

\S¯pIbmbncp¶pthm? F¦n F´mWv ImcWw?

Cu tNmZy¯n\p tijw FPI te¡v t]mhpI

1 kab¡pdhp aqew

2 IqsS hcm³

BcpanÃm¯Xv

sIm­v

3 IpSpw_¯nsâ

klmbw

CÃmXncp¶Xv

sIm­v

4 ]WanÃm¯Xp

sIm­v

5 asäs´¦nepw,

hyàam¡pI

51 SA10 ]cntim[\m ^ew t\mÀaÂ

Bbncn¡pIbpw tUmIvSsd

ImWpIbpw sNbvXp,

F´mWv tUmIvSÀ ]dªXv?

1 Ct¸mÄ

t]Snt¡­

ImcyanÃ

2 {]kh¯n\v

BdmgvNbv¡v

tijw ho­pw

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càw

]cntim[n¡pI

3 hÀjmhÀjw

càw

]cntim[n¡pI

4 asäs´¦nepw,

hyàam¡pI

52

SA11 cà¯nse ¥qt¡mknsâ

Afhv IqSpXembncn¡pIbpw

tUmIvSsd ImWpIbpw

sNbvXp, tUmIvSdpsS

D]tZiw F´mbncp¶p ?

1 acp¶v

Bcw`n¡pI

2 `£W

\nb{´Ww

3 hymbmaw

4 apebq«p¶Xv

XpScpI

5 IrXyamb

]cnNcWw

6 asäs´¦nepw,

hyàam¡pI

53 SA12 (a)

tUmIvSdpsS GXv D]tZiamWv \n§Ä¡v ]n´pScm³

IgnªXv.?

54 SA12 (b) GXp]tZiamWv \n§Ä¡v

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]n³XpScm³

IgnbmXncp¶Xv?

55 SA12 (c) F´psIm­v?

SA 11 sâ D¯cw 1 BsW¦n tNmZyw SA 14 Asæn FP1te¡v

t]mhpI

56 SA14 acp¶v Bcw`n¨ncp¶psh¦nÂ

GsXms¡bmbncp¶psh¶v

]dbmtam (No«v

]cntim[n¡pI)

1 KpfnIIÄ(HmdÂ

sslt¸m

ss¥koanIv

GPâvkv)

2 C³kpen³

57 SA15 XpSÀ¨bmbn acp¶v

e`n¡p¶Xn Fs´¦nepw

_p²nap«p­mbncpt¶m ?

1 D­v

2 CÃ

58 SA16 D­v F¶msW¦n F´mbncp¶p _p²nap«v F¶v

]dbmtam?

..........................................................................

{]k-hm-\-́ -c-c-à-]-cn-tim-[\ sN¿m-̄ -hÀ am{Xw D¯cw \ÂIpI

Section 6:hyàn]camb XS椀 Main code: PB

59

PB1 {]kh¯n\p tijw

{]tal¯n\v ]cntim[\

tXSmXncp¶Xv F´p

sIm­v?

1

kab¡pdhp aqew

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2 IqsS hcm³

BcpanÃm¯Xv

sIm­v

3 IpSpw_¯nsâ

klmbw

CÃmXncp¶Xv

sIm­v

4 ]WanÃm¯Xp

sIm­v

5 asäs´¦nepw,

hyàam¡pI

60 PB2 kao] `mhnbn {]tal

]cntim[\ \S¯phm³

Dt±in¡p¶pt­m?

1 D­v

2 CÃ

61 PB3 D­v F¦n Ft¸mÄ?

Section7: {]kh§Ä X½n AIew/ IpSpw_mkq{XWw Main code: FP

62

FP1 \nehn GsX¦nepw

KÀ`\ntcm[\ amÀK§Ä

kzoIcn¡p¶pt­m?

1 D­v

2 CÃ

63 FP2 D­v F¦n GXv? 1 IUD

2 tIm­w

3 HmdÂ

tIm¬{Smsk]väo

hv KpfnIIÄ

4 sÌdnssetkj³

(hmkIvSan/Syq_

IvSan)

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5 asäs´¦nepw,

hyàam¡pI

64 FP3 \n§tfmSnXnt\¡pdn¨v

BcmWv ]dªXv? 1 tUmIvSÀ

2 \gvkv

3 sP.]n.F¨v.F³

4 `À¯mhv

5 kplr¯v

6 kz´w Xocpam\w

7 asäs´¦nepw

Section8:A]ISkm[yXsb¡pdn¨pff Aht_m[w/ Úm\w

Main code: R

65 R1 KÀ`n-Wn-bm-Ip¶ kab¯v {]tal _m[nXcmIp¶ kv{XoIÄ¡v XpSÀ¶v PohnX¯n {]talap­mIphm\pff km[yX KÀ`n-Wn-bm-Ip¶ kab¯v {]tal _m[nXcmIm¯ kv{XoItf¡mfpw IqSpXemWv. \n§Ä¡v XpSÀ¶pff PohnX¯n {]talw _m[n¡m\pff km[yX IqSpXemsW¶v

IcpXp¶pt­m? (CÃ

F¶msW¦n Q: 66

Hgnhm¡pI )

1

2

D­v

66 R2 D¯cw D­v F¶msW¦nÂ

BcmWv CXns\¡pdn¨v

Xm¦tfmSv ]dªXv

1 tUmIvSÀ

2 BtcmKy

{]hÀ¯I³

3 AwK\hmSn

hÀ¡À/Bi

4 IpSpw_w

5 ]{X am[ya§Ä

6 BtcmKy

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¢mÊpIÄ

7 asäs´¦nepw

Section9: {]khm\´c BtcmKyw Main Code -T {]khm\´capff \n§fpsS BtcmKys¯¡pdn¨pff tNmZy§fmWv C\n

67 T1 {]kh¯n\p tijw

Fs´¦nepw BtcmKy

{]iv\§fp­mtbm?(UnkvNm

ÀPn\v tijw)

1 D­v

2 CÃ

68 T2 Ds­¦n hyàam¡pI

69

T3 {]kh¯n\p tijw

Imcy§Ä sN¿p¶XnÂ

sNdnb kt´mjtam

Xm¸cytam am{Xta \n§Ä

ImWn¡p¶pÅpthm

1 D­v

2 CÃ

70 T4 ISp¯ \ncmitbm

DuÀÖkzeX¡pdthm

\n§sf Ae«p¶pt­m?

1 D­v

2 CÃ

71 T5 hni¸nÃmbvatbm AanXamb

`£W {]nbtam \n§sf

Ae«p¶pt­m?

1 D­v

2 CÃ

72 T6 \n§fpsS PohnXw Hcp

]cmPbamsWt¶m

IpSpw_s¯ \n§Ä

\ncmis¸Sp¯nsbt¶m

tXm¶p¶pt­m?

1 D­v

2 CÃ

* kpZoÀLamb {]khw, {]tXyIn¨pw henb Ip«n BIpt¼mÄ izmk

XSʯn\pff km[yX hfsc IqSpXemWv.

]s¦Sp¯bmtfmSv \µn ]dbpI, X¶ hnhc§fn hniZoIcWw

Bhiyaps­¦n ho­pw ImWm\pff A\phmZw tNmZn¡pI.

{][m\ At\zjIsâ H¸v.

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Annexure III

Achutha Menon Centre for Health Science Studies,

Sree Chitra Tirunal Institute for Medical Sciences & Technology,

Trivandrum 695011

Patterns of and factors associated with postpartum diabetes screening in women diagnosed with Gestational Diabetes Mellitus (GDM) in Malappuram district, Kerala.

Research Subject Information Sheet for Mothers Who Had GDM

Namaskaram, I am ***, Master of Public Health student of Achutha Menon

Centre for Health Science Studies of the Sree Chitra Tirunal Institute for

Medical Sciences and Technology, Trivandrum. This study is being carried

out as a part of the course requirement for the Master in Public Health (MPH

course) that I am currently undertaking. This study is being done under the

supervision of ***, Professor of Achutha Menon Centre for Health Science

Studies. Please feel free to ask any questions or doubts related to this study.

Purpose of the study:

This study is being done to understand the kind of medical care that is being

provided to pregnant women who may have diabetes during their pregnancy

and their management afterwards. Understanding this may contribute to

preventing the development of diabetes mellitus in women. That is why we

want to learn about your experiences during pregnancy, child birth and after

delivery.

This study is being conducted in three private and one public hospital of

Malappuram district, and you have been chosen from the hospital delivery

register based on the eligibility criteria for participating in this study, as per

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the procedure. A total of 200 participants will be included and interviewed in

this study.

Procedure:

The survey would take approximately 30-45 minutes of your valuable time.

You will be asked a few questions regarding your pregnancy experiences,

about your delivery, and the postpartum period. The collected data will be

used for research purpose only. If you will permit, I would like to contact

you for clarifications related to the information collected during the present

interview.

Benefits:

There may not be any direct benefit for you from this study. But the

information provided by you may prove to be of great importance with

respect to understanding the factors influencing postpartum GDM

management, the patterns of seeking care and your morbidity experiences as

well as the provider’s role in the management of care. As this is an important

public health issue, this study may contribute to policies that help to ensure a

standardized protocol for management of GDM and incorporation of GDM

management to the National programs for controlling non communicable

diseases.

Confidentiality:

Utmost priority will be given to protect the privacy and confidentiality of

your personal information. The collected information will not be shared with

anyone not involved in the study and reporting will be done in aggregate

form only. At no stage shall your identity be revealed for this. Complete

anonymity will be maintained and you will be assigned a participant

identification number. All hard copies of filled interview schedules and

consent forms will be kept under my custody and will be destroyed properly

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when they are deemed no longer needed after one year of dissertation report

submission, whichever comes first.

Voluntary participation:

Your participation in this study is voluntary and you have the right to

withdraw your participation at any time during the interview without any

explanation. Refusal to participate will not involve any penalty or loss of

benefits to which you are otherwise entitled. There might be certain

questions which you may find stressful. You can choose to decline

answering these questions. If you have additional questions about this

research you may contact me, the supervisor or the

IEC Member Secretary.

*** ******* ******* Contact details of guide Contact details of the (Principal investigator’s IEC Member Secretary contact details)

Signature of Principal investigator

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Annexure IV

ANyp-X-ta-t\m³ skâÀ t^mÀ sl¯v kb³kv ÌUo-kv,

{ioNn{XXncp-\mÄ C³Ìn-äq«v t^mÀ saUn-¡Â kb³kkv

& sSIvt\m-f-Pn, Xncp-h-\-´-]p-cw, 695011, tIcfw

KÀ`Ime {]taltcmKap­mbncp¶ A½-amÀ¡pÅ hnh-cW ]{XnI

KÀ`Ime {]taltcmKap­mbncp¶ kv{XoIfn {]khm\´c {]taltcmK (Pn.Un.Fw) ]cntim[\bpsS coXnIfpw klmbn¡p¶ LSI§fpw þ ae¸pdw PnÃ, tIcfw

\akvImcw,

Rm³ tUm. k¡o\ {io Nn¯ncXncp\mÄ C³Ìnäyq«v Hm^v saUn¡Â kb³kkv Bâv sSIvt\m-f-Pn, {Snhm³{U-̄ nsâ Iognse ANypXtat\m³ skâÀ t^mÀ sl¯v kb³kv ÌUoknÂ, amÌÀ Hm^v ]»nIv sl¯v hnZymÀ°n\nbmWv. Fsâ _ncpZm\´c _ncpZ tImgvkn\v Bhiyamb {]_Ôw kaÀ¸n¡p¶Xnte¡mbn«mWv {]kvXpX KthjWw \S¯p¶Xv. Cu ]T\w ANypX tat\m³ skâÀ t^mÀ sl¯v kb³knse s{]m^. kpµ-co-c-ho-{µsâ t\XrXz¯nemWv \S¶p hcp¶Xv.

Cu ]T\s¯¡pdn¨v Fs´¦nepw kwib§tfm tNmZy§tfm Ds­¦n tNmZn¡m³ aSn¡cpsX¶v A`yÀ°n¡p¶p.

]T\¯nsâ Dt±iyw

KÀ`Ime {]tal tcmKnIÄ¡v KÀ`mhØbnepw {]kh tijhpw \ÂInb NnInÕsb¡pdn¨v a\knem¡p¶Xn\mWv Cu ]T\w \S¯p¶Xv. CXvv a\knem¡p¶Xv kv{XoIfn {]talw XSbp¶Xn\v klmbn¡pw. AXpsIm­mWv KÀ`Ime {]talapffhcpsS KÀ`mhØbnepw {]kh kab¯pw {]khm\´capff ]cnNcW§fn \n§fpsS A\p`h§Ä Rm³ ]T\hnt[bam¡m³ Dt±in¡p¶Xv.

ae¸pdw PnÃbn 3 kzImcy Bip]{Xnbnepw Hcp kÀ¡mÀ Bip]{XnbnepamWv Cu ]T\w \S¯p¶Xv. Bip]{XnIfnse enÌn \n¶pamWv \n§sf R§Ä XncsªSp¯Xv. GI-tZiw 200 t]scbmWv Cu ]T-\-̄ n DÄs -̧Sp-̄ n-bn-cn-¡p-¶Xpw CâÀhyq-\-S-̄ p-¶Xpw.

]T\ coXn

30 apX 45 an\n«mWv \n§Ä Cu kÀthbv¡mbn Nnehgnt¡­Xv. A`napJ kw`mjW coXnbn \n§fpsS KÀ`Imes¯bpw {]khImes¯bpw {]khm\´c Imes¯bpw A\p`h§Ä tNmZn¡p¶Xmbncn¡pw. {]kvXpX hnhc§Ä KthjW Dt±i§Ä¡v am{Xambncn¡pw D]tbmKn¡p¶Xv F¶v Dd¸v Xcp¶p. \n§fpsS k½Xw Ds­¦n Cu hnhc§sf Ipdn¨v kwibw D­mhp¶ ]£w \n§sf XpSÀ¶v _Ôs¸Sp¶Xmbncn¡pw.

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KpW§Ä

{]kvXpX ]T\¯neqsS \n§Ä¡mbn am{Xw bmsXmcp hn[ B\pIqey§tfm KpW§tfm e`n¡p¶Xmbncn¡nÃ. F¶m \n§Ä Xcp¶ hnhc§Ä {]tal _m[nXcmb KÀ`nWnIfpsS NnInÕsb¡pdn¨pw AhÀ¡v e`n¡p¶ ip{iqjsb¡pdn¨pw Adnbphm³ klmbn¡pw. Hcp s]mXpP\mtcmKy hnjbsa¶ coXnbn Cu ]T\w {]tal_m[nXcmb KÀ`nWnIÄ¡p anI¨ ip{iqj e`n¡p¶Xn\mhiyamb ]²XnIÄ cq]s¸Sp¯p¶Xnt\m {]tXyI Kh¬saâv ]²Xn cq]s¸Sp¯p¶Xnt\m klmbnt¨¡pw.

kzImczX

\n§Ä Xcp¶ FÃm hnhc§fpw kzImcyambn kq£n¡p¶XmWv. {]tXyIn¨v \n§fpsS hyàn]camb hnhc§Ä ]T\hpambn _ÔanÃm¯hÀ¡v bmsXmcp ImcWhimepw \ÂIpIbnÃ. IqSmsX hnh-c-§Ä dnt¸mÀ«v sN¿p¶Xv kw{K-l-cq-]-̄ n-em-bn-cn-¡pw. \n§fpsS A`napJ¯nsâ tcJIfpw k½X]{Xhpw Rm³ `{Zambn kq£n¡p¶XmWv. KthjW Bhiyw Ignªm AX-sÃ-¦n ]T-\-dn-t¸mÀ«v kaÀ¸n-̈ mÂ, GXmWv BZyw hcp-¶Xv F¶-X-\p-k-cn-̈ v, Hcp hÀj¯n\p tijw icn-bmb coXn-bn \in¸n¡p¶-Xm-Wv.

kzta[bm Dff ]s¦Sp¡Â

Cu ]T\¯n \n§Ä ]s¦Sp¡p¶Xv kzta[bm BWv. bmsXmcp ImcWhpw IqSmsX GXv kab¯pw ]T\¯n \n¶v ]n´ncnbm\pff kzmX{´yw \n§Ä¡v D­mbncn¡p¶XmWv. ]T\¯n ]s¦Sp¡mXncp¶Xv sIm­v Xm¦Ä¡v bmsXmcp hn[¯nepff \jvS§tfm ]ngtbm D­mbncn¡p¶XÃ. ]T\hpambn _Ôs¸«v A[nIambn Fs´¦nepw tNmZy§fps­¦n \n§Ä¡v Fs¶tbm Asæn F¯n¡Â I½nän sk{I«dnbpamtbm _Ôs¸Smhp¶XmWv.

{][m-\-K-th-j-Isb _Ô-s¸tS­ hnh-c-§Ä

ssKUns\ _Ô-s¸tS­ hnh-c-§Ä

sF. C. kn saw¼Àsk-{I-«dn _Ô-s¸tS­ hnh-c-§Ä

{][m-\-K-th-j-IbpsS H v̧

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Annexure V

Patterns of and factors associated with seeking postpartum health care

including diabetes screening in women diagnosed with Gestational

Diabetes Mellitus (GDM) in Malappuram district , Kerala

CONSENT STATEMENT

Participant’s Unique Identification (UID) Number:

I have read/been read the details of the information sheet. The nature of the

study and my involvement has been explained and all my questions

regarding the study have been answered satisfactorily. By signing /

providing thumb impression on this consent form, I indicate that I

understand what is expected from me and that I am willing to participate in

this study. I have also been informed as to whom I should contact for further

clarifications. I know that I can withdraw my participation at any time during

the interview without any explanations.

Name of the participant: ________________________________________

Signature / left thumb print:

Date of consent: D D M M Y Y

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If the participant is willing to participate but unwilling to provide signature

or thumb impression

(Verbal consent):

Name of witness: ________________________________________

Signature of the witness:

Signature of the investigator:

Date:

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Annexure VI KÀ`Ime {]taltcmKap­mbncp¶ kv{XoIfn {]khm\´c {]taltcmK (Pn.Un.Fw) ]cntim[\bpsS coXnIfpw klmbn¡p¶ LSI§fpw þ ae¸pdw PnÃ, tIcfw

k½-X-]{Xw

]s¦-Sp-¡p-¶-bm-fpsS \w¼À

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Annexure VII Achutha Menon Centre for Health Science Studies,

Sree Chitra Tirunal Institute for Medical Sciences & Technology,

Trivandrum 695011

Patterns of and factors associated with postpartum diabetes screening in women diagnosed with Gestational Diabetes Mellitus (GDM) in Malappuram district, Kerala.

Research Subject Information Sheet for Providers

Namaskaram, I am ***, Master of Public Health student of Achutha Menon

Centre for Health Science Studies of the Sree Chitra Tirunal Institute for

Medical Sciences and Technology, Trivandrum. This study is being carried

out as a part of the course requirement for the Master in Public Health (MPH

course) that I am currently undertaking. This study is being done under the

supervision of ***, Professor of Achutha Menon Centre for Health Science

Studies. Please feel free to ask any questions or doubts related to this study.

Purpose of the study:

This study is being done among providers who give direct obstetric care and

manage women affected with gestational diabetes mellitus (GDM) during

pregnancy, delivery and postpartum period. Hence understanding their

perspectives regarding various aspects of gestational diabetes management

and postpartum diabetes screening and management based on their

experiences will help to guide future policy formulations. This will

contribute to improving postpartum screening status of GDM affected

women and reduce progression to Type2DM. This is why we would like to

interview you to learn about your experiences of management of gestational

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diabetes mellitus (GDM) during pregnancy, child birth and after delivery. If

you will permit we would like to audio record the interview.

This study is being conducted in three private and one public hospitals of

Malappuram district, and you have been chosen from the available list in the

hospital for participating in this study. A total of 6-7 providers, who provide

direct obstetric care to the GDM affected mothers will be interviewed in the

study.

Procedure:

The survey would take approximately 20-25 minutes of your valuable time.

You will be asked a few questions regarding the management of GDM. The

collected data will be used for research purpose only. If you will permit, I

would like to contact you for clarifications related to the information

collected during the present interview.

Benefits:

There may not be any direct benefit for you from this study. But the

information provided by you may prove to be of great importance with

respect to understanding the factors influencing postpartum GDM

management, the patterns of seeking care and as well as the provider’s role

in the management of care. As this is an important public health issue, this

study may contribute to policies that help to ensure a standardized protocol

for management of GDM and incorporation of GDM management to the

National programs for controlling non communicable diseases.

Confidentiality:

Utmost priority will be given to protect the privacy and confidentiality of the

information given by you. The collected information will not be shared with

anyone not involved in the study. At no stage shall your identity be revealed

for this. Complete anonymity will be maintained and you will be assigned a

participant identification number. All audio recordings and transcripts of the

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interview and consent forms will be kept under my custody and will be

destroyed properly when they are deemed no longer needed after one year of

dissertation report submission, whichever comes first.

Voluntary participation:

Your participation in this study is voluntary and you have the right to

withdraw your participation at any time during the interview without any

explanation. Refusal to participate will not involve any penalty or loss of

benefits to which you are otherwise entitled. There might be certain

questions which you may find stressful. You can choose to decline

answering these questions. If you have additional questions about this

research you may contact me, the supervisor or the

IEC Member Secretary.

*** ******* ******* Contact details of guide Contact details of the (Principal investigator’s IEC Member Secretary contact details)

Signature of Principal investigator

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Annexure VIII

Achutha Menon Centre for Health Science Studies,

Sree Chitra Tirunal Institute for Medical Sciences & Technology,

Trivandrum 695011

Patterns of and factors associated with seeking postpartum health care

including diabetes screening in women diagnosed with Gestational

Diabetes Mellitus (GDM) in Malappuram district , Kerala

CONSENT STATEMENT

Participant’s Unique Identification (UID) Number: I have read/been read the details of the information sheet. The nature of the

study and my involvement has been explained and all my questions

regarding the study have been answered satisfactorily. By signing /

providing thumb impression on this consent form, I indicate that I

understand what is expected from me and that I am willing to participate in

this study. I have also been informed as to whom I should contact for further

clarifications. I know that I can withdraw my participation at any time during

the interview without any explanations.

Name of the participant: ________________________________________

Consent for interview Consent for audio recording Signature Date of consent:

D D M M Y Y

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Annexure IX

Achutha Menon Centre for Health Science Studies,

Sree Chitra Tirunal Institute for Medical Sciences & Technology,

Trivandrum 695011

Patterns of and factors associated with postpartum diabetes

screening in women diagnosed with Gestational Diabetes

Mellitus (GDM) in Malappuram district, Kerala

Interview Guide-Provider

1. How often in your practice do you come across pregnant women

affected by GDM? 2. What do you do when one of your patient diagnosed with GDM comes to

you with the test results? (Probe if not mentioned: What information do

you give them, how do you manage them, information regarding future

risk of progression to T2 diabetes, advice to come frequently for

Antenatal check up, /postpartum screening/risk to baby).

3. Can you tell me about the management of GDM during labour and the

immediate postpartum period? (Probe if not mentioned about : any

special precautions like admissions before EDD, frequent blood sugar

level monitoring, delivery from a hospital with paediatrician & physician,

and facility to give advance life care support to both mother and child)

4. Can you tell me about the situation where you take decisions regarding C-

sections (probe-do you prefer C-sections to all or specific ones).

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5. What advice do you give when a GDM patient is discharged after

delivery? (probe if not mentioned: regarding diet, breast feeding,

exercise(for normal delivery),about medicines ,about returning for

postpartum screening)

6. Do you prescribe any medicines for them while discharging them after

delivery from your institution?

7. In your experience, roughly what proportion of the GDM affected women

come for follow-up after delivery?

8. Out of this how many come for follow up even if you have not

specifically told them?

9. What according to you are the best methods to ensure follow up visits by

the patients?(probe if not mentioned :written advice along with discharge

card/message alert system/telephonic reminders)

10. In your experience, what proportion of the women diagnosed with GDM

progress to Type 2 DM in future? (Probe if not mentioned: about

possibility of conversion of these cases to type 2 DM in future? Is it

common or not?)

11. What is your practice regarding family planning advice for women

affected by GDM?

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