4 pregnancy complications
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Transcript of 4 pregnancy complications
Pregnancy With Internal Pregnancy With Internal Medical DiseasesMedical Diseases
Yinglin Liu( 刘颖琳 )MD&PhD, Department of Gyn & Obs
The 2nd Affiliated Hospital of Sun Yat-sen University
EmphasisEmphasis
Pregnancy complicated with:Heart Disease(HD)Viral HepatitisGestational diabetes mellitus(GDM)
Key pointsKey points
Clinical manifestation, diagnosis, and management
Influence between disease & pregnancy(mothers & fetuses)
Types of Heart DiseaseDiagnosis of early heart failure(HF)Maternal-fetal transmission of hepatitis B
virusDefinition of GDM
Part One Part One Cardiovascular DiseasesCardiovascular Diseases
Pregnancy complicated with Heart Disease
Incidence of pregnancies:1-4%
Death rate: 0.6%-2.7%
2nd leading cause of maternal mortality: 8.3%
Influence 0f Pregnancy on Influence 0f Pregnancy on Cardiovascular systemCardiovascular system
During Pregnancy(32-34wks)
During Labor
Puerperium (first 3 days)
Hemodynamic and respiratory Hemodynamic and respiratory change of normal pregnancychange of normal pregnancy
Blood volume: ↑ 25-50% 32-36wksCO: ↑ 30-50% 20-30wksHR: ↑ 10-25bpmVascular resistance: ↓ 40-50%O2 consumption: ↑ 15-30%Tidal volume: ↑ 40%
During laborDuring labor
First stage:
Each ut. Con. CO ↑24%
extrudes 500 ml CVP↑
blood to peripheral cir.
MAP ↑ 10%
(MAP: mean arterial pressure)
During laborDuring labor
Second stage:
Bearing down effort Pulmonary pressure ↑
Congenital heart dis.
Blood shunt(L→R) → Blood shunt(R→L)
During laborDuring labor
Third stage:
1. After placenta elimination→
placental cir. disappears 500ml blood evacuated u. contracts enter circulation
2. u. shrinks → intra-abd. pressure ↓ → blood accumulated in visera
PuerperiumPuerperium
First 3 daysRetension fluid go back to circulationUterus shrinks further
The types of Heart Disease The types of Heart Disease Complication PregnancyComplication Pregnancy
I. Congenital heart diseaseⅡ. Rheumatic heart diseaseⅢ. Cardiovascular disease of hypertensive
disorder complicating pregnancyⅣ. Peripartum cardiomyopathy,PPCMⅤ. Myocarditis
Congenital heart diseaseCongenital heart diseaseBlood shunt only from L to R / No blood shunt
Blood shunt from R to L
Noncyanotic CyanoticAtrial septal defect, ventricular septal defect, Patent ductus arteriosus
Pulmonary stenosis, Coartation of aorta, Marfan’s syndrom
Tetralogy of Fallot
Eisenmenger’s syndrom.
Withstand hemodynamic change of pregnancy and labor with small shunt
Pregnancy is contraindicated
With large L-to-R shunt: pulmonary artery hypertension , right-left shunt , cyanosis
Rheumatic heart diseaseRheumatic heart disease
• Mitral stenosis• Aortic stenosis• Mitral or aortic insufficiency And combinations of those above
Heart Disease of hypertensive Heart Disease of hypertensive disorder complicating pregnancydisorder complicating pregnancy
Heart burthen coronary artery spasm systemic arterial spasm retention of water and sodium viscosity of blood ↑ Contraction force weaken ↓
cardiac muscle ischemic hypoxia systemic arterial spasm
Peripartum cardiomyopathyPeripartum cardiomyopathy (PPCM)(PPCM)
Cause: unknown.(viral infection, genetic factors, autoimmunity, mal-nutrition, etc), no cardiac history before pregnancy.
Period: late trimester ~ 6 months after deliverySymptoms&signs(HF): dyspnea, palpitation, cough,
emptysis, orthopnea, chest pain, hepatomegaly, edema, organic embolism, dyspnea , thoracalgia , edema , hepatomegaly ect
X-ray: dilatation of heart, pulmonary congestionEcho-CG, ECG: Heart chambers dilatation ,left
ventricular hypertrophy, S-T seg. abnormal T waveHF, pulmonary infarction or arrhythmia may cause death.
PPCM
50% recover 6 months postpartum– Recur in the successive pregnancy– Clinical Implications : 10-30% of
fetal death– Therapy
Treatment for heart failureHeart transplantation
Myocarditis and SequelaesMyocarditis and Sequelaes Symptoms may occur after viral infection: enteric virus ,
Coxsackie virus , Rubella virus , cytomegalovirus History of respiratory tract or alimentary infection,
fatigue, palpitation, dyspnea, uncomfortable on anterior chest
Lab.test:CRP ↑ , SR ↑ , enzyme, Ab ↑ (3wks) Abnormal ECG Even heart failure after two-three weeks of infection Not cure with disease for six months——myocarditis
sequelae Acute myocarditis cured——keep on pregnancy
Influence of Heart Diseases Influence of Heart Diseases on Fetuseson Fetuses
Abortion, premature labour, fetal death, FGR(fetal growth retardation) and fetal distress , mortality
Drugs (digoxin) can pass through the placentas and is danger for the fetuses.
Genetic problem Increased caesarean section rate
Symptoms & signs of normal Symptoms & signs of normal pregnancy mimicking HDpregnancy mimicking HD
Symptoms Palpitation, dyspnea / orthopnea, easy fatigability,
dizziness, nocturnal cough
Signs Displacement of apex Sinus tachycardia S1 of apex / S2 on PV ↑ & split, systolic murmur,
third heart sound Prominent jugular venous pulsations
Diagnosis Diagnosis of Heart Diseaseof Heart Disease
HistorySypmtoms: physical dyspnea, emptysis, orthopnea,
palpitationSigns: ≥Ⅱ dia. mur. or≥ III sys. mur, dia. gallop
rhythm,pericardial friction rub,alternating pulse, cyanosis, clubbing of fingers, persistent neck vein distention
ECG: serious arrhythmia (auricular fibrillation or flutter, AVB), abnormal ST
X-ray: Cardiomegaly Echocardiography: movement and construction
Functional Classification of Functional Classification of Heart Disease Heart Disease –– subjective subjective
sym.sym.
Class I: NO limitation to normal active life
Class II: Slight limitation of physical activity
Class III: Marked limitation of physical activity
Class IV: Complete limitation of physical activity
Clinical Classification Clinical Classification –– objective detectionobjective detection
Class A: No evidence of cardiovascular diseas
Class B: minimal cardiovascular disease according to examination
Class C: Moderate cardiovascular disease Class D: Severe cardiovascular disease
According To The PatientsAccording To The Patients’’ Ability Ability To Cope With PregnancyTo Cope With Pregnancy
Conditions allowable for pregnancy: Cardiac function is I or II, slight typesConditions unsuitable for pregnancy : Severe types, class III or IV, history of HF,
pulmonary hypertension, R to L shunt, severe arrhythmia, active rheumatic HD, combined valvar HD, Bac.endocarditis, acute myocarditis, enlargement of heart.
>35ys, long history.
Common complicationCommon complication
Heart failureSubacute infective endocarditisHypoxia & CyanosisVenous & pulmonary embolism
Diagnosis Of The Early Diagnosis Of The Early Cardiac FailureCardiac Failure
1. Stuffy, palpitation, short-breath after slight physical activity, nocturnal cough;
2. HR>110 bpm at rest, R>20 times/min;
3. Paroxysmal nocturnal dyspnea/ Orthopnea may be the very early symptoms;
4. Persistent basilar rales, even after couph.
ManagementManagementI. Prepregnancy
II. During Pregnancy
1. Therapeutic abortion
2. Antenatal examination
3. Prevention of cardiac failure
Prevention of cardiac failurePrevention of cardiac failure• Quiet & rest(>10hrs/d)• Nutrition: pro.& Vit, sodium & fat. weigh gain<10kg,
limited salt intake: <4-5g after 16 weeks, fluid replacement limited in 500~1000ml/d , drop velocity <60ml/h
• Therapy of inducement: prevention of URI.; correct anemia & arrhythmia; therapy of EPH-syn; multiple and small amounts ( 150~200ml ) blood transfused if needed
Therapy of cardiac failure: digoxin (0.25mg, Bid), 2~3d qd. Diuretics. Vessel dilating agents.
Cesaren section. Timing is important.• Observe
To choose suitable birth wayTo choose suitable birth way
Trial labour: class ~ of cardiac function, Ⅰ Ⅱmoderate fetal size, normal fetal position, cervical condition is good enough.
Cesaren section: class ~ of cardiac Ⅲ Ⅳfunction, large fetal size, obstetric condition is not so good.
Management During DeliveryManagement During Delivery
• 1st stage: sedatives; surveillance (BP, P,R,HR); O2; digitalis; antibiotics
• 2nd stage : Bearing down effort should be avoid -- episiotomy, elective forceps and vacuums extraction
• 3rd stage: Sand bag, Oxytocin (ergometrine should be avoid)
• Who has torpidity labor or cephalopelvic disproportion or grade heart function should undergo cesarean section
Management During Management During PuerperiumPuerperium
• Careful observation (first 3 days)• Antibiotics (7 days after labour)• Breast feeding should be avoid in some
patients(III or IV cardiac function) : natrii sulfas , not estrogen• Contraception and sterilization (1 week
after labour)
Heart SurgeryHeart Surgery
• Should not be done during pregnancy • <12 weeks of gestation• Prevention of abortion & infection
Part Two Acute Viral Hepatitis
Physiological Changes of Physiological Changes of Liver During PregnancyLiver During Pregnancy
Blood flow, size
AST/ALP
ALP, fibrinogen↑, Coagulative factors ↑ ,
A/G
The Effect Of Pregnancy On The Effect Of Pregnancy On HepatitisHepatitis
• More nutrition is needed• Hyperemesis gravidarum • The liver burden (maternal & fetal metabolism). • Endocrine change (estrogen )• Hypertensive disorder complicating
pregnancy,ICP,AFLP• During labor Postpartum hemorrhage Maternal mortality rate elevated
The Effect Of Viral Hepatitis On The Effect Of Viral Hepatitis On Pregnancy: For Gravidas Pregnancy: For Gravidas
• Mortality ↑18.3%• Worsen pregnant reaction• Hypertensive disorder complicating
pregnancy↑ (Aldosterone)• Postpartum hemorrhage , DIC↑
(coagulative factors)
The Effect Of Viral Hepatitis The Effect Of Viral Hepatitis On Pregnancy: For FetusesOn Pregnancy: For Fetuses
Malformation
Abortion
Premature labor
Fetal demise / still birth
Fetal malfromation
Perinatal mortality ↑ 46 ‰
Perinatal transmission
Materno-Fetal Transmission Materno-Fetal Transmission (HBV)(HBV)
• Intrauterine infection (9.1%~36.7%)
Impaired placental barrier, penetrability , leakage
• During delivery (40%~60%)
Mother’s blood or vaginal secretion• Postpartum
Sweat, saliva & milk
DiagnosisDiagnosis
• History• Symptoms• Sign• Laboratory examination: HBsAg, HBeAg,
HBVDNA, HBc-IgM
HBsAg: Active HBV infection; may be acute or chronic
HBeAg: High infectivity, active viral replication
HBcAg: Active copying, undetectable in serum
Anti-HBcAg IgM: Acute HBV infection (newer and more sensitive assays may also be positive during reactivation of chronic infections)
HBV-DNA and DNA polymerase: Direct measure of infectivity or replicative state; becoming increasingly available
Anti-HBsAg: Immune to HBV; may be natural immunity or following vaccination
Anti-HBeAg: Low or no infectivity; need only be measured in chronic HBV
Differential DiagnosisDifferential Diagnosis
• Hyperemesis gravidarum: ketosurine(+)• Hypertensive disorder complicating
pregnancy: hypertension, proteinuria, edema, renal function . HELLP Syn.
• AFLP (Acute fatty liver of pregnancy)• Liver lesion caused by medicine:
wintermin, luminal, erythromycin, rimifon,
Viral hepatitis ICP Acute fatty liver of pregnancy
HELLP syndrome
Hyperemesis gravidarum
Drug induced hepatitis
onset All time Late Late Late Early All time
Inducement - - - PIH - Drug use
symptoms Gastrointestinal, jaundice
pruritus-jaundice
epigastric pain, vomiting, acute liver failure
epigastric pain, jaundice, bleeding
Prolonged vomiting
Jaundice and prutitus after drug intake
Lab findings Hepatitis virus positive
Cholic acid serum bilirubin urine bilirubin(-)
Hemolysis, coagulopathy, BPC
Water, salt and ph imbalance
acidophil
Hepatic disfunction
Light-severe light Acute and severe
severe light light
pathology Hepatocyte damage
Intrahepatic cholestasis
Fat filled in cytoplasm
ischemia light light
fetus Malformation,demise
distress death death light light
prognosis prolonged Recover after delivery
poor Recover after delivery
recover Recover
Management Of Hepatitis
• Slight type: nutrition & rest• Severe type:
Liver protection (glucagon-insulin-glucose)
Prevention & therapy of hepatic coma, DIC & renal failure
Obstetric Management Obstetric Management • 1st trimester : artificial abortion• 2nd / 3rd trimester: avoid operation & drug,
fetal surveillance, prevention of EPH-syndrome
• During labor: Vit K, fresh blood; avoid bleeding; oxytocin; antibiotics
serious case --- Cesarean section 24hrs after• Puerperium: antibiotics; Stop Breast feeding (
HBVDNA /HBeAg+ in milk) disuse estrogen
PreventionPrevention
Enhence peripartum health care: surveillance, nutrition, serological screening
Prophylaxis of HAV: -globulin 2~3 ml im. within 7 days
Prophylaxis of HCV: diminish nosocomial transmission. γ- globulin
HBV Immunoprophylaxis
• Active immunity: HB vac (vaccine) 30 μg im. (<24hr, 10 μg 1st, 6 th month)
• Passive immunity: HBIG 0.5ml im.(just born), 0.16ml/kg (1, 3 months)
• Combined immunity:
active immunity plus HBIG 0.5ml im.(<24hr after birth)
Part IIIPart III Diabetes Mellitus Diabetes Mellitus
Gestational Diabetes Gestational Diabetes Mellitus(GDM)Mellitus(GDM)
Definition: It is the first time for D.M. to be found just during pregnancy.
Diagnostic standard: ①At least two values are abnormal in OGTT
(oral glucose tolerance test). (5.6-10.3-8.6-6.7mmol/l)② Fasting plasma glucose ≥5.8 mmol/L (105mg/dl) twice.
Effects of Pregnancy on Effects of Pregnancy on DiabetesDiabetes
Placentas →E3, HPL,…↑→antagonize insulin:• Latent D.M. →apparent type• Situation → worse →coma• More and more insulin is needed to be used.
Effects of Diabetes on Effects of Diabetes on Pregnancy Pregnancy (Gravidas)(Gravidas)
1. Natural abortion ↑ 15%~30%.
2. EPH-syn. 3-5 times ↑
3. Infection ↑ (WBC function ↓)
4. Prolonged labor and postpartum hemorrhage
5. Hydramnios and macrosomia
6. Ketoacidosis
Effects of Diabetes on Effects of Diabetes on Pregnancy Pregnancy (Fetuses)(Fetuses)
1. Fetal macrosomia: 25%~40%.
2. FGR: 21%.
3. Premature labour: 10%~25%
4. Fetal malformation: 6%~8%
5. Perinatal death rate ↑
Effects of Diabetes on Effects of Diabetes on Pregnancy Pregnancy (Neonates)(Neonates)
1. Respiratory distress syndrome (RDS) : mothers Glu.↑→ fetuses → Insulin↑ → antagonize the glucocorticoid (promote synthesis of surfactant) →surfactant↓.
2. Neonatal hypoglycemia:
intrauterine Glu.↑→ fetuses’ Insulin↑ → after birth → no Glu. → hypoglycemia
Minor adverse health effects for offspring in GDM
Birth Wt (g) 3303±64 3649±51 3849±72 <0.01
Macrosomia(%) 8 36 47 <0.01
C-S 5 10 14 <0.01
Hypoglycemia 2 28 52 <0.01
Hypocalcemia 0 4 7 <0.01
Hyperbilirubinemia 15 23 21 <0.01
Polycythemia 0 7 11 <0.01
Cord C-Pep 1.18±0.1 2.07±0.12 2.98±0.22 <0.01
Cord Glu 100±3.6 103±2.9 114±5.5 <0.01
Normal GDM DM P
DiagnosisDiagnosis• History• Laboratory examination:Fasting blood sugar ≥5.8 mmol/L at least
twice can be diagnosed as D.M.Screening test— Glu.50g →1hr.plasma
glucose ≥7.8 mmol/L (140mg/dl).OGTT -- Glu.75g →0, 1, 2, 3hrs (5.6, 10.3,
8.6, 6.7 mmol/L ) 2 values↑→GDM; 1 values↑→GIGT
White grouping
class description
A Abnormal OGTT treat only by diet therapy
B Onset at age 20years or older and duration of less than 10 years
C Onset at age 10-19 years or duration of 10-19years
D Onset before 10 years of age, duration over 20 years, exudative retinopathy
E Calcification of pelvic cavity vasculopathy by X-ray
F Nephropathy
R proliferative retinopathy
RF proliferative retinopathy and Nephropathy
G Many pregnancy failure
H coronary heart disease
T Prior renal transplantation
ManagementManagement
Ⅰ. To Estimate the Patients’ Ability to Cope With Pregnancy:
Class D, F, R → artificial abortion
Ⅱ. Dietotherapy
Balance diet: supply = consumption
With adequate proportion of various components (pro., Glucose, fat, vit, mineral)
Standard of blood glucose controled
Time blood glucose
fasting blood glucose 3.3~5.6mmol/L
two hours after meal 4.4~6.7mmol/L
at night
Before three meals4.4~6.7mmol/L
3.3~5.8mmol/L
ManagementManagement
Ⅲ. Medicinal therapy• Oral heparopen→pass placenta→fetal damage.• Insulin is the only drug to be used in gravidas.
The dosage should be moderated according to the blood glucose.
32~33 weeks: dosage reach maximum
postpartum dosage: 1/2 ~ 1/3 of maximum
Ⅳ. Materno-fetal Surveillance
Management Management ( . Termination of Ⅴ( . Termination of Ⅴpregnancy)pregnancy)
TimingIf blood glucose remain normal, pregnancy
can be prolonged as long as usual.Cesaren section: blood glucose can’t be
controlled ideally, serious EPH-syn., severe infection, FGR, fetal distress. Stop insulin 3 hours before operation
Amnionic fluid should be detected the indexs of fetal maturity by amniocentesis
Management Management (During labour & (During labour & puerperium)puerperium)
• Blood glucose and electrolytic level must be kept normal. (Glucose 4g + 1 U.) Glucose monitoring: >5.6mmol/L (100mg/dL)
• Labour and fetal monitoring maintain in whole period(12hrs). Vaginal delivery– Control the whole course within 12 hours
• Epidural anesthesia• After labour, dose of Insulin 1/2(< 24 hrs)• Puerperium: prevention of postpartum hemorrhage
& infection. insulin requirements recover at progestation dose post partum1~2weeks
Low-dosage constant insulin infusion for the intrapartum period
blood-glucose (mg/100ml )
Insulin dosage ( U/h )
fluids ( 125ml/h )
<100 0 5%dextrose/lactated Ringer’s solution
100~140 1.0 5%dextrose/lactated Ringer’s solution
141~180 1.5 Normal saline
181~220 2.0 Normal saline
>220 2.5 Normal saline
dilution is 25U regular insulin in 250ml normal saline, administerd intravenously
Management of NeonatesManagement of Neonates
Treat them as preterm infants!Prevention of hypoglycemia(<2.22mmol/L),
hypocalcemia, jaundice & RDS.
Feeding them with 25% Glucose solusion.
(beginning from 30 minutes after birth.)
Prognosis
tendency to recur next pregnancythe risk of type diabetes riseⅡdevelop obesity and typeⅡ diabetes easily in
adult
Key pointsKey points Clinical manifestation, diagnosis, and
management of Pregnancy With Internal Medical Diseases(HD, Viral Hepatitis, GDM)
Influence between disease & pregnancy(mothers & fetuses)
3 danger phases in pregnancy with HD Types of Heart Disease Diagnosis, prophylaxis/treatment of early HF Maternal-fetal transmission of hepatitis B virus Definition of GDM
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