Home            Past Issues            About IP            About IAP           Author Information            Subscription            Advertisement              Search  

   
research letter

Indian Pediatr 2020;57: 174-175

Congenital Heart Disease in the Pediatric Population in Eastern India: A Descriptive Study

 

Sharmila Chatterjee1*, Santanu Dutta2, Sumanta Ghosh2, Sanchita Das2 and Nital Bhattachary3

From 1Biomedical Genomics Center, and 2Department of Cardiothoracic Vascular Surgery, IPGMER and SSKM Hospitals; and 3Saha Institute of Nuclear Physics, Salt Lake; Kolkata, West Bengal, India.

Email: [email protected]

   


This cross-sectional study assessed distribution and pattern of echocardiography confirmed congenital heart disease, among 593 pediatric patients in outpatient departments of a tertiary care hospital in eastern India. Commonest defects were ventricular septal defect (43, 40.7%), atrial septal defect (241, 31.7%), and tetralogy of Fallot (125, 21%).

Keywords: Birth defects, Congenital heart failure, Cyanosis.



C
ongenital heart disease (CHD), a common developmental defect among pediatric population, contributes to significant morbidity and mortality [1]. Epidemiological studies show CHD prevalence varying from 4/1000 to 50/1000 live-births [2,3]. This variation is attributed to genetic, environmental and socioeconomic differences. In India, prevalence of CHD ranges from 0.8-26.4/1000 children [4]. However, most studies have been conducted in northern and western parts of India among school children (5–15 years age), and under-represent children from eastern India and those <5 years age [4]. This study aimed to assess proportion and pattern of CHD among pediatric patients attending outpatient department (OPD) of a tertiary care hospital in eastern India.

This cross-sectional study was conducted at Neonatology, Pediatric Medicine, Pediatric Cardiology and Cardiovascular Surgery OPDs of Seth Sukhlal Karnani Memorial (SSKM) Hospital, Kolkata, India, between December, 2016 to June, 2018. Ethical approval was obtained from the Institutional Ethics Committee of SSKM Hospital. Assent and informed consent were obtained from the participants’ and participant’s guardian wherever applicable, prior to study enrollment. All patients (age 0-14 year) attending relevant OPDs were included. The diagnoses were confirmed by echocardiography, and classified according to Q20-Q28 of tenth revision of International Classification of Diseases (ICD) [5], and International Pediatric and Congenital Cardiac Code (IPCCC) [6]. Major CHDs included atrial septal defect (ASD), ventricular septal defect (VSD), patent ductus arteriosus (PDA), pulmonary stenosis (PS) and tetralogy of Fallot (TOF). ASD <4.0 mm diameter was not considered as a cardiac defect. If a patient had more than one lesion, the defect that required treatment or caused hemodynamic effect was considered the main malformation. Standardized, validated questionnaires administered by trained research assistants were used for collecting data. Age-at-diagnosis was considered 0 day if CHD was reported from maternity ward, or age-at-first hospitalization for CHD, or age-at-cardiac procedure.

Proportion of CHD was calculated as number of pediatric patients affected with CHD out of total attendance of pediatric OPDs in hospital. Chi square tests were used to test difference in proportions among categorical variables. Analysis was done using PC-SAS program (V9.2, SAS institute, Cary, NC, USA).

Of 41,236 patients attending pediatric OPDs during study period, 593 (1.4%) had CHD; 51.9% were males. The mean (SD) age was 4 (3.2) years; 225 (37.9%) patients more than one CHD. The commonest types were: VSD (241, 40.7%), ASD (188, 31.7%) and TOF (125, 21%). Others included PDA (44, 7.5%), PS (43, 7.3%) and double outlet right ventricle (DORV) (27, 4.5%). Isolated VSD accounted for 23.2%, both ASD and VSD 7.3%, and VSD combined with other cardiac defects (PS, PDA, DORV) 6.5% of all CHD cases. There was no significant difference in age-group (£5 years and >5 years) (P=0.9) and sex distribution (P=0.3) of CHD. Proportion of CHD did not differ significantly among birth-weight groups (£2.5 kg and >2.5 kg) (P=0.5), gestational age (full-term vs. premature) (P=0.09), maternal age (<18, 18-29 and >29 years) (P=0.9) and maternal weight (normal vs. overweight) (P=0.5). CHD proportion also did not significantly differ with presence/absence of history of spontaneous abortion, maternal co-morbidities, infection and smoking.

The high proportion of VSD in our study is in agreement with reported range of 21-53% from other studies [4,7,8]. ASD was the second most common CHD (31.7%), and was higher compared to reported figures of 10-23% in Indian studies [4,7]. TOF was the most common cyanotic heart disease and its proportion (21%) was higher compared to reported figures of 4.6-18.3% [9]. Though our study did not document detailed history on socioeconomic and nutritional background of mothers, our study population comprised mostly middle- and low socioeconomic class, and our findings seem consistent with studies that report premature birth, low socio-economic status and poor nutrition as important factors associated with CHDs among Asian population [10].

Most studies state that 50% of all cases of CHD are detected by 1 month, 75% by 3 months and 100% by 3-4 years age [9]. This variation at CHD detection occurs due to hemodynamic alterations occurring after birth. Our study showed that about 5% of cases were detected by 1 month, majority (83.1%) by 5 years and diagnosis was delayed beyond 10 years in 11.7% of cases. The delay in diagnosis of CHD can be explained by lack of awareness, and less health facilities and pediatric cardiac care programs in India.

The nature of survey only provided us with an estimation of proportion and pattern of CHD and no conclusions can be drawn on prevalence and causality of CHD from this study. Nevertheless, this is the first survey from eastern India providing an up-to-date data on CHD, and filling some gaps in knowledge of CHD from this geographical region.

Contributors: SC, SD, NB: study conception, analysis and interpretation of data, and manuscript writing; SG, SD: data collection and manuscript revision. All authors approved the final version of manuscript and agree to be accountable for all aspects of this work.

Funding: Department of Health Research, Ministry of Health and Family Welfare, Government of India as HRD Fellowship – Start-up grant.

Competing Interest: None stated.

References

1. Boneva RS, Botto LD, Moore CA, Yang Q, Correa A, Erickson JD. Mortality associated with congenital heart defects in the United States: Trends and racial disparities, 1979 -1997. Circulation. 2001;103:2376-81.

2. Hoffman JI, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol. 2002;39:1890-900.

3. Chen YLS, Zuhlke L, Black GC, Choy M, Li N, Keavney BD. Global birth prevalence of congenital heart defects 1970–2017: Updated systematic review and meta-analysis of 260 studies. Int J Epidemiol. 2019;48:455-63.

4. Bhardwaj R, Rai SK, Yadav AK, Lakhotia S, Agrawal D, Kumar A, et al. Epidemiology of congenital heart disease in India. Congenit Heart Dis. 2015;10:437-46.

5. International Statistical Classification of Diseases and Related Health Problems 10th revision 2016. Available from: http://apps.who.int/classifications/icd10/browse/ 2016/en. Accessed March 21, 2018.

6. International Pediatric and Congenital Cardiac Code (IPCCC). 2005. Available from: http://ipccc.net/. Accessed 21 March 2018.

7. Misra M, Mittal M, Verma AM, Rai R, Chandra G, Singh DP, et al. Prevalence and pattern of congenital heart disease in school children of eastern Uttar Pradesh. Indian Heart J. 2009;61:58-60.

8. Wu MH, Chen HC, Lu CW, Wang JK, Huang SC, Huang SK. Prevalence of congenital heart disease at live birth in Taiwan. J Pediatr. 2010;156:782-5.

9. Bernier PL, Stefanescu A, Samoukovic G, Tchervenkov CI. The challenge of congenital heart disease worldwide: Epidemiologic and demographic facts. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2010;13:26-34.

9. Sadiq M, Stümper O, Wright JG, De Giovanni JV, Billingham C, Silove ED. Influence of ethnic origin on the pattern of congenital heart defects in the first year of life. Br Heart J. 1995;73:173-6.

 

Copyright © 1999-2020 Indian Pediatrics