Pda Part 2 Epidemiology

17
EPIDEMIOLOGY OF PDA DR. NURE ISHRAT NAZME HMO, MU-1 DHAKA SHISHU HOSPITAL

description

persia

Transcript of Pda Part 2 Epidemiology

Page 1: Pda Part 2 Epidemiology

EPIDEMIOLOGY OF PDA

DR. NURE ISHRAT NAZME HMO, MU-1

DHAKA SHISHU HOSPITAL

Page 2: Pda Part 2 Epidemiology

Patent ductus arterisus is a congenital heart

abnormality wherein ductus arteriosus fails

to close after birth.

Page 3: Pda Part 2 Epidemiology

As an isolated defect, PDA is the 5th - 6th most

common congenital cardiovascular lesion.

It represents 5-10% of all types of Congenital

Heart Diseases, excluding those in premature

infants.

Page 4: Pda Part 2 Epidemiology

It occurs in approximately 8 per 1000 live

premature births.

Isolated PDA is found in around 1 in 2000 full

term infants.

Page 5: Pda Part 2 Epidemiology

A higher prevalence is found in preterm infants.

50–80% incidence was found in preterm infants

<26 wks gestation. Douglas J et al, Circulation. 2006;114:1873-1882.

In babies who are less than 1500 g at birth,

many studies show the incidence of a patent

ductus arteriosus >30%.

Page 6: Pda Part 2 Epidemiology

The female to male ratio is 2:1.

In patients in whom the PDA is associated

with a specific teratogenic exposure, e.g.

congenital rubella, the incidence is equal

between the sexes.

Page 7: Pda Part 2 Epidemiology

PDA occurs more commonly in

populations that  live at high altitude.

The incidence is as much as 30 times greater in

populations that live higher than 5000 m.

Page 8: Pda Part 2 Epidemiology

As many as 20% of neonates with respiratory

distress syndrome have a patent ductus

arteriosus.

Rubella infection during the first trimester of

pregnancy, particularly in the first 4 weeks, is

associated with a high incidence of PDA.

Page 9: Pda Part 2 Epidemiology

PDA is also associated with-

single-gene mutations

(such as Carpenter’s

syndrome and Holt-

Oram syndrome).

X-linked mutations

(such as incontinentia

pigmenti).

asphyxia at birth.

fetal alcohol syndrome.

maternal amphetamine

use and

maternal phenytoin use.

Page 10: Pda Part 2 Epidemiology

Occasional cases are associated with specific genetic defects, such as-

Trisomy 21

Trisomy 18

Rubinstein-Taybi syndrome and

CHARGE syndrome.

Page 11: Pda Part 2 Epidemiology

Familial occurrence of PDA is uncommon.

The usual mechanism of inheritance is

considered to be polygenic with a recurrence

risk of 3%.

In some patients genetic mechanism of PDA

may be autosomal recessive inheritance with

incomplete penetrance.

Page 12: Pda Part 2 Epidemiology

PDA cases undergo spontaneous closure in a

rate of 0.6% per year.

It is estimated that if left untreated, the mortality

rate is-

-20% by age 20 years.

-45% by age 45 years.

-60% by age 60 years.

Page 13: Pda Part 2 Epidemiology

Incidence of CHD in Bangladesh: in 80s(Jan’82 – Dec’91)

ASD VSD PDA Others TOF TOF+ TGA Others

Total = 2636

N1245

N888

N162

N341

N446

N448

N9

N3

1500

1250

1000

750

500

250

0

500

400

300

200

100

0

39.88%

28.44%

5.19%

10.92%

14.28%14.35%

0.29%

0.096%

Acyanotic Cyanotic OthersTotal = 3

5

4

3

2

1

0

Note: ASD was the majority,<10 year VSD was highest.Ref.:The Incidence of CHD diagnosed by non-invasive technique-ten years study in Bangladesh

Sufia Rahman et all. DS (Child) HJ Vol8(1992):No1&2

Total = 903

Prof. Manzoor Hussain

PDA

5.19%

Page 14: Pda Part 2 Epidemiology

Past & Present comparison of CHD at Dhaka Shishu Hospital from Nov. 1989 to Oct. 1990 with that of June, 2007 to Sept, 2009

& June 2007 to Sept.2009.

VSD TOF ASD PDA P/S Others

Nov. 1989 – Oct. 1990

June 2007 – Sept. 2009

19 8 4 3 1 1

52.78%

22.22%

11.11%8.33%

2.78% 2.78%

26.90%

20

15

10

5

0

150

125

100

75

50

25

0

N = 36

Jan’ 2005 – Apr’ 2007

38 114 47 2624

9.09%7.05%

21.15%

8.71%

4.82%4.45%

4 24 3 58

0.74%4.45%

1.29% 0.55%

10.76%

VSD TOF ASD PDA PS TGA DORD A-V TAPVD Si VE M C Others7145 49

N = 537

N = 539

175

150

125

100

75

50

25

0

142 64127 30 22 12

26.44%

11.91%

23.64%

5.58%4.09%

2.23%612 2 2 55

01.11%2.23% 0.37%00.37%

10.24%

63

11.73%

142

VSD ASD PDA TOF TGA P/S A-V DORV HLHS Si VE M. C.Others

Prof. Manzoor HussainCourtesy: Echo lab experience, DSH, Dr. Sayeed

Jan.2005 – Apr.2007

Page 15: Pda Part 2 Epidemiology

Past & Present comparison of CHD at Dhaka Shishu Hospital from Nov. 1989 to Oct. 1990 with that of Jan, 2005 to Apr, 2007

& June 2007 to Sept.2009.

VSD TOFASD PDA P/S Others

Nov. 1989 – Oct. 1990

June 2007 – Sept. 2009

8 4 3 1 1

52.78%

22.22%

11.11%

8.33%2.78% 2.78%

26.90%150

125

100

75

50

25

0

N = 36

Jan’ 2005 – Apr’ 2007

38 114 47 2624

9.09%7.05%

21.15%

8.71%4.82%

4 24 3 580.74%

4.45%1.29% 0.55%

10.76%

VSD TOFASD PDAPS TGA DORD A

-V TAPVD Si VE M C Others7145 49

N = 537

N = 539

175

150

125

100

75

50

25

0

142 64127 30 22 12

26.44%

11.91%

23.64%

5.58% 4.09%

2.23%612 2 2 55

01.11%2.23% 0.37%00.37%

10.24%

63

11.73%

142

VSD ASD PDA TOF TGA P/S A-V DORV HLHS Si VE M. C.Others

Manzoor HussainCourtesy: Echo lab experience, DSH, Dr. Sayeed

Page 16: Pda Part 2 Epidemiology

Reference

1.Nelson text book of pediatrics-18th edition.

2.Professional guide to disease-8th edition.

3.Pediatric cardiology-2nd edition by Benson LN .

4.The 5 minutes Pediatric consult,2008.

5. Forsey et al Orphanet journal of rare diseases, 2009,4:17,1172-74

6. Douglas J et al, Circulation. 2006;114:1873-1882

Page 17: Pda Part 2 Epidemiology