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ORIGINAL ARTICLE |
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Year : 2022 | Volume
: 19
| Issue : 4 | Page : 554-559 |
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Assessment the risk factors of congenital heart disease among children below 5 years age in Babylon province
Noor Ibraheem Mohammed1, Mohanad Khudhair Shukur Al-ghanimi2
1 Department of family and community medicine, College of Medicine, University of Babylon, Babylon, Iraq 2 Department of Pediatric, College of Medicine, University of Babylon, Babylon, Iraq
Date of Submission | 13-Jul-2022 |
Date of Acceptance | 10-Aug-2022 |
Date of Web Publication | 09-Jan-2023 |
Correspondence Address: Noor Ibraheem Mohammed Babylon Health Directorate, Department of family and community medicine, College of Medicine, University of Babylon Iraq
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/MJBL.MJBL_113_22
Background: Congenital heart diseases (CHDs) account for 25% of all congenital malformations. CHDs are an important cause of morbidity and mortality in children. Prevention of CHDs can be achieved by preventing exposure to modifiable risk factors that affect the cardiac development during pregnancy. Objectives: To assess the sociodemographic and medical risk factors of congenital heart diseases among children below five years in Babylon city, Iraq. Materials and Methods: A retrospective case control study conducted from 1st of February to 1st of May, 2022, at Shaheed Al-Mehrab center, Babylon Maternity/Pediatric Hospital and Al-Imam Al-Sadik General Teaching Hospital, consisted of 100 participants classified to 50 CHDs cases and 50 controls by Echocardiogram, the mother/caregiver of each child was interviewed using a pre-tested questionnaire. Results: The age of the participants ranged from one day to 4.5 years, with a mean age (10.4 ± 13.2) months. (52%) of CHDs cases were females, (68%) of them were below one year age and (54%) of them reside in urban area, 28% of CHDs was VSD and 42% of the cases present with chest infection. BMI percentile was significantly lower in cases of CHDs (P = 0.008) and there was a significant relationship between CHDs and family history of CHDs (P = 0.013). Conclusion: Majority of the cases were females, below one year age and reside in urban area, presented with VSD and chest infection. BMI percentile was lower in cases of CHDs and there was a significant relationship between CHDs and family history of CHDs. Keywords: Children, congenital heart diseases, risk factors
How to cite this article: Mohammed NI, Al-ghanimi MK. Assessment the risk factors of congenital heart disease among children below 5 years age in Babylon province. Med J Babylon 2022;19:554-9 |
How to cite this URL: Mohammed NI, Al-ghanimi MK. Assessment the risk factors of congenital heart disease among children below 5 years age in Babylon province. Med J Babylon [serial online] 2022 [cited 2023 Feb 6];19:554-9. Available from: https://www.medjbabylon.org/text.asp?2022/19/4/554/367322 |
Introduction | |  |
Congenital heart diseases (CHDs) are the abnormalities of the heart`s structure, function or position present from birth and affect the heart or the adjacent blood vessels that are detected in infancy or thereafter.[1] CHDs prevalence is approximately 8/1000 live births, but only 2–3 of them are going to show symptoms within the first year of life. The incidence is higher in stillbirth (3–4%), spontaneous abortions (10–25%), and premature infants (2%), excluding; MVP, PDA in preterm babies, and bicuspid aortic valve (normally presents in 1%–2% of adults).[2] Most CHDs still have unknown causes and many types of CHDs are complex and originate from a mix of genetic predisposition and environmental stimulation, CHDs present in >90% of individuals with trisomy 18, 50% of individuals with trisomy 21, and 40% of individuals with Turner syndrome.[3] It was hypothesized that environmental agents act on the individual’s genetic predisposition to the malformation, and the exposure must occur at the period of cardiac development, which is during the first 8 weeks of gestation.[4] Multiple risk factors are associated with CHDs, including; The teratogenic effects of drugs during pregnancy; for example; many of the anticonvulsant drugs alter the folate metabolism in early pregnancy that lead to neural tube defects and congenital heart diseases.[5] First trimester fever in general, especially if by viral infection carries an increased risk of offspring CHDs, mainly coarctation of aorta, tricuspid atresia, d-TGA, VSD,[6] especially maternal infection with Rubella (congenital rubella syndrome) that cause pulmonic stenosis, patent ductus arteriosus, and, less frequently, tetralogy of Fallot.[7] Parental consanguinity.[8] Family history of congenital heart defects,[9] especially if first-degree relative (parent or sibling) is affected.[3] Low birth weight.[9] Age related maternal factors.[10] Maternal Diabetes mellitus is associated with aterio-ventricular septal defects.[11] Environmental and behavioral factors, such as cigarette smoking have also been associated with risk of CHDs, especially septal defects.[12] Some studies show that periconceptional intake of folic acid may reduce the risk of CHDs in offspring, and folic acid consumption during pregnancy may result in a 50% reduction in the risk of CHDs, which similar to the risk reduction for neural tube defects.[13],[14]
Objective of the study
To assess the sociodemographic and medical risk factors of congenital heart diseases among children below five years in Babylon city, Iraq.
Materials and Methods | |  |
This is a retrospective case control study, carried out from the 1st of February to the 1st of May 2022, at Shaheed Al-Mehrab center for cardiac catheterization and surgery, Babylon Maternity and Pediatric Hospital and Al-Imam Al-Sadik General Teaching Hospital in Babylon city, Iraq. The mother or the caregiver of each child was interviewed using a pre-tested questionnaire, including socio-demographic information of the child and the mother, clinical presentation and the possible risk factors of CHDs, including: parental consanguinity, rubella and COVID-19 infections during pregnancy, maternal history of hypertension, diabetes and abortion, intake of folic acid, hormonal medications, aspirin and tetanus vaccine during pregnancy and family history of congenital heart diseases. BMI of the children was calculated by measuring the weight of each child (in kilograms) by beam balance or electronic scale and measuring the height/length of each child (in centimeters) using length board with full extension for any child below two years age and by fixed board on the wall in standing position for any child above two years age.
The inclusion criteria
The mother or the caregiver of children below five years age, who attended or were admitted to the general wards, the intensive care unit, respiratory care unit and the emergency unit of the mentioned hospitals and who are living in Babylon governorate.
The exclusion criteria
The mother or the caregiver who refused to participate in the study, whose children are above five years age, whose children with syndromes and who are living in other governorate.
The limitations of the study
Short duration of the study, relative small sample size and this study is retrospective case control study so it is inefficient for rare exposures, the temporal relationship between the exposure and the disease may be difficult to established and it is prone to the selection and recall bias.
Data analysis
The data were analyzed using the SPSS IBM, version 27. Data entered and managed using descriptive statistics (frequency distribution and percentage) and inferential statistic (the Chi-square test was used to test association between categorical variables, while t student test was used to compare the means of quantitative continuous variables). P-value of <0.05 considered statistically significant and Odd’s ratio was calculated.
Ethical approval
The study was conducted in accordance with the ethical principles that have their origin in the Declaration of Helsinki. It was carried out with patients verbal and analytical approval before sample was taken. The study protocol and the subject information and consent form were reviewed and approved by a local ethics committee according to the document number 52 (including the number and the date in 11/4/2022) to get this approval. Verbal consent was obtained from the participants, after explaining to them the purpose of the study.
Results
This study included (100) children under 5 years: (50) CHDs cases and (50) controls. [Table 1] is comparison between the cases and controls regarding socio-demographic characteristics showed that no significant differences were observed between them regarding age, gender, residence, maternal education and occupation (P-value >0.05). [Table 2]: Chest infection alone was the commonest presentation, accounting for (42.0%) of the cases, and the commonest type of congenital heart disease was VSD (28.0%) as detailed in [Table 3]. [Table 4]: BMI percentile was found to be significantly lower in cases with CHDs (23.65 ± 29.95) compared to controls (41.88 ± 37.34), with (P-value of 0.008). [Table 5]: Relationship between CHDs and family history of CHDs was found to be significant, with (P-value of 0.013), Odds ratio was calculated to be 3.22, which means that children with family history of CHDs were 3 times more likely to have CHDs compared to those with no family history of CHDs. [Table 6]: summarize the possible risk factors; including: consanguinity, rubella infection (fever, headache, myalgia and rash) and COVID-19 infection during pregnancy, maternal previous history (hypertension, diabetes and abortion) and history of medications and vaccinations during pregnancy (folic acid, hormonal medications, aspirin, and tetanus vaccine), no significant relationship was observed between congenital heart disease and any of these risk factors.
Discussion | |  |
This study compared between CHDs cases and controls regarding socio-demographic characteristics and showed that females were more than males (52%, 48%, respectively), another study conducted in Karbala/Babylon, Iraq, also showed female predominance (56.6% of the cases),[15] but in this study, there was no significant difference between cases and controls regarding their gender, this is consistent with[16] study, (68%) of the cases were below 1 year age, another study was done in in Ramadi city, Iraq, reported that (71.76%) of the cases were below 1 year age,[17] however, there was no significant difference regarding the age of participants of the current study, which agrees with another study in Mosul city, Iraq,[18] 54% of the cases reside in urban area, a study was done in china found that (69.7%) of the cases were living in urban area,[19] anyway, there was no significant difference regarding the residence of the participants of this study, which goes in line with[20] study, also there was no significant differences between the cases and controls regarding maternal education and occupation, which is similar to another study.[19] The commonest type of CHDs in this study was VSD (28% of the cases), this is consistent with a study conducted in Karbala/Babylon, Iraq, which found that VSD was the commonest type (38.3% of the cases).[15] This study found that chest infection was the commonest presentation, accounts for (42% of the cases presentation), which is similar to the finding of a study in Al-Diwanyia city, Iraq,[21] in which chest infection accounts for (36% of the cases presentation), as many subtypes of CHDs cause pulmonary over circulation and pulmonary edema, which is a good nidus for the infection for the lower respiratory tract.[22] BMI percentile in CHDs cases was found to be significantly lower than controls, this is similar to the result of another study,[23] as impaired hemodynamic status in children with CHDs lead to impair growth and lower BMI,[24] while another study reported that decrease energy intake, malabsorption and increase energy requirements lead to underweight in children with CHDs.[25] The current study had observed that the relationship between CHDs and family history of CHDs was found to be significant and odds ratio was calculated to be (3.22), this is consistent with the result of another study, which found that there was significant relationship between CHDs and family history of CHDs with odd’s ratio of (3.4),[26] the result of both studies means that parents with family history of CHDs were 3 times more likely to have offspring with CHDs compared to those with no family history. This study reported that there was no significant relationship between CHDs and consanguinity, this is similar to the result of another study conducted in India,[27] both studies found that the consanguineous marriage was the common pattern of marriage between the parents of cases and controls, which lead to this non-significant result. This study discussed the effect of rubella infection (fever, headache, myalgia and rash) and COVID-19 (positive PCR/chest CT scan) as a risk of CHDs, and showed that there was no significant relationship between CHDs and infection with rubella/COVID-19 during pregnancy, another study conducted in Mosel city, Iraq, found that there was no significant relationship between CHDs and rubella infection.[26] Cardiac malformations are the most common congenital anomaly in diabetic pregnant woman,[28] but this study found that there was no significant difference between CHD and maternal diabetes, this result agrees with another study conducted in Saudi Arabia,[29] in both studies, just few cases reported diagnosed maternal diabetes, so we need to screen for chronic diabetes through the preconception counselling and to screen for gestational diabetes in pregnant woman with risk factors by glucose tolerance test at 24–28 weeks of gestation through antenatal care. The current study reported no significant difference between CHDs and maternal hypertension, this is consistent with the finding of another study.[18] Complex CHDs may cause spontaneous abortion or stillbirth.[30] This study found that 32% of the cases’ mother and 22% of the controls’ mother reported history of abortion, so there was no significant difference between CHDs and maternal history of abortion, which agrees with the result of a study conducted in China, in which history of abortion in the cases’ and controls’ mother was 28%,25% respectively, so there was no significant difference between CHDs and maternal history of abortion.[31] This study found that 74% of CHDs cases’ mother and 72% of controls’ mother reported use of folic acid supplements during pregnancy, so there was no significant relationship between CHD and folic acid intake as these percentages are convergent, another study demonstrated that folic acid intake among the mothers of CHDs children was significantly lower in corresponding to mothers of children without CHDs, so there was a significant relationship between CHDs and lack of folic acid intake during pregnancy.[26] Intake of progesterone in the early pregnancy increases the risk (5 times) of CHDs in the offspring, especially VSD.[32] This study reported that 40% of the cases and 48% of the controls confirmed the maternal hormone use during pregnancy, thus there was no significant relationship between CHDs and hormonal treatment, while another study was done in Gaza Strip identified 37% of the mothers of children with CHDs and 18% of the controls’ mothers were exposed to hormonal treatment during pregnancy, so there was a positive association between hormonal treatment and CHDs in the offspring,[33] thus it is mandatory to improve the knowledge of the healthcare providers and pregnant women about the risks of progesterone for and limit it’s usage during first trimester unless where a clear indication existed. The use of NSAIDs during pregnancy especially in the third trimester poses a potential threat to the myocardium and cause persistent pulmonary hypertension and premature closure of the ductus arteriosus.[34] The current study reported no significant relationship between CHDs and aspirin intake, this result is similar to the result of a study conducted in Basra city, Iraq,[35] both studies found that just few cases reported the use of aspirin during pregnancy. Several studies have pointed to Tdap vaccine safety in pregnancy to both maternal and newborn health,[37],[38] and the risk of birth defects in general is minimal.[36] The current study found that no significant relationship was observed between CHDs and tetanus toxoid vaccine, while another study conducted in Boston, USA; discussed the Tdap vaccine in pregnancy and risk of major birth defects in the offspring also reported that there was no significant relationship between CHDs and tetanus vaccine.[39] However, other studies also discussed vaccine in pregnancy and its relation to the risk of major birth defects.[40],[41]
Conclusion | |  |
CHDs are one of the most important causes of fetal deaths, thus to prevent CHDs, it is mandatory to understand CHDs’ risk factors. This study had observed that majority of the cases were females, below one year age, reside in urban area, presented with VSD and chest infection and there was a significant relationship between CHDs and family history of CHDs, also BMI percentile was found to be lower in cases of CHDs compared to controls.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | Chelo D, Nguefack F, Menanga AP, Um SN, Gody JC, Tatah SA,Ndombo POK Spectrum of heart diseases in children: An echocardiographic study of 1,666 subjects in a pediatric hospital, YAOUNDE, Cameroon. Cardiovasc Diagn 2016;6:10-9. |
2. | Kliegman RM, St Geme JW, Blum NJ, Shah SS,Tasker RC, Wilson KM, Behrman RE Nelson textbook of pediatric. In: Bernstein D, editor. Epidemiology and Genetic Basis of Congenital Heart Disease. Philadelphia: Elsevier Inc; 2020. p. 9336. |
3. | Kliegman RM, St Geme JW, Blum NJ, Shah SS,Tasker RC, Wilson KM, Behrman RE Nelson textbook of pediatric. In: Bernstein D, editor. Epidemiology and Genetic Basis of Congenital Heart Disease. Philadelphia: Elsevier Inc; 2020. p. 9338. |
4. | Balat MS, Sahu SK Congenital heart disease: Factor affecting it and role of RBSK India ling with situation. International Journal of Community Medicin and Public Health 2018;5:4437-0. |
5. | Kliegman RM, St Geme JW, Blum NJ, Shah SS,Tasker RC, Wilson KM, et al. Nelson textbook of pediatric In: Bernstein D, editor. Epidemiology and Genetic Basis of Congenital Heart Disease. Philadelphia: Elsevier Inc; 2020. p. 9345. |
6. | Dreier JW, Andersen AM, Berg-Beckhoff G Systematic review and meta-analyses: Fever in pregnancy and health impacts in the offspring. Pediatrics 2014;133:e674–88. |
7. | Karen G,editor. Pediatric Physical Examination Anillu Strated Hand Book. 3th ed. St. Louis, MO: Elsevier, lnc; 2019. p. 233-5. |
8. | Tadmouri GO, Nair P, Obeid T, Al Ali MT, Al Khaja N, Hamamy HA Consanguinity and reproductive health among Arabs. Reprod Health 2009;6:17. |
9. | Nicoll R Environmental contaminants, and congenital heart defects: Are evaluation of the evidence. International Journal of Environmental Research and Public Health 2018;15: 2096. |
10. | Schulkey CE, Regmi SD, Magnan RA, Danzo MT, Luther H, Hutchinson AK, et al. The maternal-age-associated risk of congenital heart disease is modifiable. Nature 2015;520:230–3. |
11. | Hoang TT, Marengo LK, Mitchell LE, Canfield MA, Agopian AJ Original findings and updated meta-analysis for the association between maternal diabetes and risk for congenital heart disease phenotypes. Am J Epidemiol 2017;186:118–28. |
12. | Zhu Z, Cheng Y, Yang W, Li D, Yang X, Liu D, et al. Who should be targeted for the prevention of birth defects? A latent class analysis based on a large, population-based, cross-sectional study in Shaanxi province, Western China. PLoS One 2016;11:e0155587. |
13. | Mao B, Qiu J, Zhao N, Shao Y, Dai W, He X, et al. Maternal folic acid supplementation and dietary folate intake and congenital heart defects. PLoS One 2017;12:e0187996. |
14. | Feng Y, Cai J, Tong X, Chen R, Zhu Y, Xu B, et al. Non-inheritable risk factors during pregnancy for congenital heart defects in offspring: A matched case-control study. Int J Cardiol 2018;264:45-52. |
15. | Tuky HS, Alghanimi MK, Semender BA Comparing certain echocardiographic measurements with catheterization in children with pulmonary hypertension due to left-to-right cardiac shunt. Med J Babylon 2020;17:79-83. |
16. | Mecklin M, Heikkilä P, Korppi M Low age, low birthweight and congenital heart disease are risk factors for intensive care in infants with bronchiolitis. Acta Paediatr 2017;106:2004-10. |
17. | Al-Dalla Ali FJ, Hammood MD, Al-Dulaimy KM, Salman BM Pattern of congenital heart disease among children referred for echocardiography in Ramadi city, West of Iraq. ANB MED J 2019;15:40-4. |
18. | Attia QA, Al-Obeidi RA Risk factors for congenital heart disease among infants in mosul city. Mosul Journal of Nursing 2020;8:176-85. |
19. | Li H, Luo M, Zheng J, Luo J, Zeng R, Feng N, et al. An artificial neural network prediction model of congenital heart disease based on risk factors, a hospital-based case-control study. Medicine 2017;96:e6090. |
20. | Pei L, Kang , Zhao Y, Yan H Prevalence and risk factors of congenital heart defects among live births: In Shaanxi province, Northwestern China. BMC Pediatr 2017;17:18. |
21. | Al-Jeboori RK, Abdul Hassan SD, Farhan TH Presentations of congenital heart disease in children. Indian Journal of Public Health Research & Development 2019;10:36. |
22. | Hajela S Profile of congenital heart disease in childhood. Int J. Med Res Rev 2014;2:15-19. |
23. | Schwartz S, Olsen M, Woo JG, Madsen N Congenital heart disease and the prevalence of underweight and obesity from age 1 to 15 years: Data on a nationwide sample of children. BMJ Paediatrics Open 2017;1:e000127. |
24. | Polat S, Okuyaz C, Hallioğlu O, Mert E, Makharoblidze K Evaluation of growth and neurodevelopment in children with congenital heart disease. Pediatr Int 2011;53:345-9. |
25. | Daymont C, Neal A, Prosnitz A, Cohen MS Growth in children with congenital heart disease. Pediatrics 2013;131:e236-42. |
26. | Gh E Al-Hyali S Prevalence and risk factors for congenital heart anomalies among hospital attendees in Mosul city. The Iraqi Postgraduate Medical Journal 2015;14:2. |
27. | Abqari S, Gupta A, Shahab T, Rabbani MU, Ali SM, Firdaus U Profile and risk factors for congenital heart defects: A study in a tertiary care hospital. Annals of Pediatric Cardiology 2016;9:3. |
28. | Ali AI, Nori W Gestational diabetes mellitus: A narrative review. Med J Babylon 2021;18:163-8. |
29. | Shoukri MM, AlJufan M, Subhani S, Baig M, Al-Mohanna F, et al. Consanguinity, maternal age, and maternal diabetes as potential risk factors for congenital heart diseases: A nested case control study from Saudi Arabia. J Epidemiol Public Health Rev 2017;2:2. |
30. | Tegnander E, Williams W, Johansen OJ, Blaas HG, Eik-Nes SH Prenatal detection of heart defects in a non-selected population of 30,149 fetuses–detection rates and outcome. Ultrasound Obstet Gynecol 2006;27:252-65. |
31. | Zhang Y, Zhao Q, Ma X, Hu X, Wang H, Sun L, et al. Peri-Conceptuarl and antenatal parental factors and neonatal congenital heart disease: A case-control study. Pediatr Med 2019;2:1-6. |
32. | Steinberg ZL, Dominguez-Islas CP, Otto CM, Stout KK, Krieger EV Maternal and fetal outcomes of anticoagulation in pregnant women with mechanical heart valves. J Am Coll Cardiol 2017;69:2681-91. |
33. | Zaqout M, Aslem E, Abughazza O, Abuqamar M, Panzer J, de wolf D The impact of oral intake of dydrogesterone on fetal heart development during early pregnancy. Pediatric Cardiology 2015;36:1483-8. |
34. | Mone SM, Gillman MW, Miller TL, Herman EH, Lipshultz SE Effects of environmental exposures on the cardiovascular system: Prenatal period through adolescence. Pediatrics 2004;113:1058–69. |
35. | Abood GM, Hassan MK Environmental risk factors for congenital cardiovascular defects among infants and children in Basra, Southern Iraq. Iraqi J Med Sci 2014;12:9-17. |
36. | Liang JL, Tiwari T, Moro P, Messonnier NE, Reingold A, Sawyer M, et al. Prevention of pertussis, tetanus, and diphtheria with vaccines in the United States. Recommendations and Reports 2018;67:1-4. |
37. | DeSilva M, Vazquez-Benitez G, Nordin JD, Lipkind HS, Klein NP, Cheetham TC, et al. Maternal tdap vaccination and risk of infant morbidity. Vaccine 2017;35:3655-60. |
38. | Campbell H, Gupta S, Dolan GP, Kapadia SJ, Kumar Singh A, Andrews N, et al. Review of vaccination in pregnancy to prevent pertussis in early infancy. J Med Microbiol 2018;67:1426-56. |
39. | Kerr SM, Van Bennekom CM, Mitchell AA Tetanus, diphtheria, and pertussis vaccine (Tdap) in pregnancy and risk of major birth defects in the offspring. Birth Defects Res 2020;112:393-403. |
40. | Nsaif AK, Al-Joborae SFF Medical and social analysis of preschool children under the age of six years at secondary and tertiary care after home accidents in Hilla City. Med J Babylon 2022;19:169-75. |
41. | Kotwal SK, Charak G, Rafiq N, Shekhar S, Nabi T Effect of isometric exercise on heart rate variability in prehypertensive young adults. Med J Babylon 2022;19:275-80. |
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]
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