To Determine The Prevalence, Pattern, Risk Factors Of Congenital Anomalies, And Their Impact On Neonatal Mortality At Georgetown Public Hospital Corporation (Gphc) From January 1st, 2019, To December 31st, 2021..

Authors

  • Ulanda Haynes

Keywords:

Congenital anomalies, neonatal mortality, prevalence, risk factors, cardiovascular defects

Abstract

 Objective: To determine the prevalence, patterns, risk factors, and impact of congenital anomalies (CAs) on neonatal mortality at Georgetown Public Hospital Corporation (GPHC) between January 1st, 2019, and December 31st, 2021.

Design: A facility-based, retrospective, cross-sectional study.

Setting: Georgetown Public Hospital Corporation, the largest and only tertiary hospital in Guyana.

Patients: A total of 17,719 live births over the study period, with 87 neonates diagnosed with congenital anomalies. A control group of 300 neonates without CAs was also included, with 100 neonates selected from each year (2019, 2020, and 2021).

Interventions: Data were collected from neonatal and maternal records, including demographic information, medical history, and outcomes. Data analysis included descriptive statistics, chi-square tests, and logistic regression.

Main Outcome Measures: Prevalence of congenital anomalies, identified patterns of anomalies, risk factors (maternal age, ethnicity, hypertension, infection, folic acid use), and neonatal mortality rates.

Results: The prevalence of CAs was 0.44% in 2019, 0.46% in 2020, and 0.58% in 2021. The most common anomalies were cardiovascular (29.3%), with Patent Ductus Arteriosus being the most frequent condition (16.0%). Maternal risk factors included age >35 years (OR 2.4, 95% CI: 1.4–4.1), East Indian ethnicity (OR 1.8, 95% CI: 1.1–3.0), hypertension (OR 2.1, 95% CI: 1.2–3.7), and no folic acid use (OR 3.2, 95% CI: 1.9–5.4). Preterm birth (OR 5.3, 95% CI: 3.1–9.0) and low birth weight (OR 3.8, 95% CI: 2.3–6.3) were significant neonatal risk factors. Neonatal mortality from CAs decreased from 8% in 2019 to 6% in 2021, but the reduction was not statistically significant (p = 0.35).


Conclusions: Congenital anomalies are prevalent at GPHC, with cardiovascular defects being the most common. Maternal age, ethnicity, hypertension, and lack of folic acid use were significant risk factors. Although neonatal mortality due to CAs decreased slightly, further studies with larger sample sizes are needed to confirm these trends. Public health initiatives focusing on prenatal care and folic acid fortification are recommended to reduce the burden of congenital anomalies in Guyana..

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References

World Health Organization. Congenital anomalies. WHO. 2016. Available from: http://www.who.int/news-room/fact-sheets/detail/congenital-anomalies

2. World Health Organization. Birth defects (fact sheet). WHO. February 2022. Available from: https://www.who.int/news-room/fact-sheets/detail/birth-defects

3. Sitkin NA, Ozgediz D, Donkor P, Farmer DL. Congenital anomalies in low- and middle-income countries: The unborn child of global surgery. World J Surg. 2015;39(1):36–40.

4. Sachdeva S, Nanda S, Bhalla K, Sachdeva R. Gross congenital malformation at birth in a government hospital. Indian J Public Health. 2014;58(1):54.

5. Malcoe LH, Shaw GM, Lammer EJ, Herman AA. The effect of congenital anomalies on mortality risk in white and black infants. Am J Public Health. 1999;89(6):887–92.

6. Ajao AE, Adeoye IA. Prevalence, risk factors and outcome of congenital anomalies among neonatal admissions in Ogbomoso, Nigeria. BMC Pediatr. 2019;19(88). Available from: https://doi.org/10.1186/s12887-019-1471-1

7. Sadler TW. Birth defects and prenatal diagnosis. In: Langman’s Medical Embryology. 13th ed. Wolters Kluwer; 2015. p. 126–40.

8. United Nations Inter-agency Group for Child Mortality Estimation (UN IGME). Levels and trends in child mortality: Report 2020. United Nations Children’s Fund (UNICEF); 2020. Available from: https://childmortality.org/wp-content/uploads/2020/10/UN-IGME-2020-Child-Mortality-Report.pdf

9. Guyana News Room. Nearly 6,000 babies born at GPHC in 2020. Guyana News Room; 2021 Dec 8.

10. Silesh M, Lemma T, Fenta B, Biyazin T. Prevalence and trends of congenital anomalies among neonates at Jimma Medical Center, Jimma, Ethiopia: A three-year retrospective study. Pediatr Health Med Ther. 2021;12:1–10.

11. Taye M, Afework M, Fantaye W, Diro E, Worku A. Magnitude of birth defects in Central and Northwest Ethiopia from 2010-2014: A descriptive retrospective study. PLoS One. 2016;11(10):e0161998. Available from: https://doi.org/10.1371/journal.pone.0161998

12. Muga R, Mumah S, Juma P. Congenital malformations among newborns in Kenya. Afr J Food Agric Nutr Dev. 2009;9(3):815–29.

13. Radu R, Molnar A, Mirza T, Tigan SI. Congenital malformation prevalence in Cluj district between 2003–2007. Appl Med Inform. 2009;25(3–4):37–46.

14. Abdou MSM, Sherif AAR, Wahdan IMH, Ashour KSE. Pattern and risk factors of congenital anomalies in a pediatric university hospital, Alexandria, Egypt. J Egypt Public Health Assoc. 2019;94(3). Available from: https://doi.org/10.1186/s42506-019-0032-7

15. Etemad L, Moshiri M, Moallem S. Epilepsy drugs and effects on fetal development: Potential mechanisms. J Res Med Sci. 2012;17(9):876–81.

16. Czeizel AE. Birth defects are preventable. Int J Med Sci. 2005;2(3):91–2.

17. Yakoob MY, Bateman BT, Ho E, Hernandez-Diaz S, Franklin JM, Goodman JE, et al. The risk of congenital malformations associated with exposure to beta-blockers early in pregnancy: A meta-analysis. Hypertension. 2013;62(2):375–81.

18. Lawal TA, Yusuf B, Fatiregun AA. Knowledge of birth defects among nursing mothers in a developing country. Afr Health Sci. 2015;15(1):180–7.

19. Mashuda F. Patterns and factors associated with congenital anomalies among young infants admitted at Bugando Medical Centre, Mwanza-Tanzania [Master’s thesis]. Catholic University of Health and Allied Sciences; 2013.

20. Liete SB, Acosta M, Macchi ML. Congenital malformations associated with pesticides in Encarnacion, Paraguay. Pediatrics. 2008;121:107.

21. Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE, et al. Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: An updated systematic analysis. Lancet. 2015;385(9966):430–40.

22. Macintosh MC, Fleming KM, Bailey JA, Doyle P, Modder J, Acolet D, et al. Perinatal mortality and congenital anomalies in babies of women with type 1 or type 2 diabetes in England, Wales, and Northern Ireland: Population based study. BMJ. 2006;333:177.

23. Ndibazza J, Lule S, Nampijja M, Mpairwe H, Oduru G, Kiggundu M, et al. A description of congenital anomalies among infants in Entebbe, Uganda. Birth Defects Res A Clin Mol Teratol. 2011;91(10):857–61.

24. Oestergaard MZ, Inoue M, Yoshida S, Mahanani WR, Gore FM, Cousens S, et al. Neonatal mortality levels for 193 countries in 2009 with trends since 1990: A systematic analysis of progress, projections, and priorities. PLoS Med. 2011;8(8):e1001080.

25. Robins J. Congenital anomalies surveillance 2012–2013. NHS Greater Glasgow and Clyde; 2014.

26. Samina S, Nadeem S. Pattern of congenital malformations and their neonatal outcome. J Surg Pak. 2010;15(1):34–7.

27. Zhang X, Li S, Wu S, Hao X, Guo S, Suzuki K, et al. Prevalence of birth defects and risk-factor analysis from a population-based survey in Inner Mongolia, China. BMC Pediatr. 2012;12(125). Available from: http://www.biomedcentral.com/1471-2431/12/125

28. Rasmussen SA, Erickson JD, Reef SE, Ross DS. Teratology: From science to birth defects prevention. Birth Defects Res A Clin Mol Teratol. 2009;85(1):82–92.

29. Kishimba RS, Mpembeni R, Mghamba J. Factors associated with major structural birth defects among newborns delivered at Muhimbili National Hospital and Municipal Hospitals in Dar Es Salaam, Tanzania 2011–2012. Pan Afr Med J. 2015;20(153). Available from: http://www.panafrican-med-journal.com/content/article/20/153/full/.

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Published

2026-04-13

How to Cite

1.
Haynes U. To Determine The Prevalence, Pattern, Risk Factors Of Congenital Anomalies, And Their Impact On Neonatal Mortality At Georgetown Public Hospital Corporation (Gphc) From January 1st, 2019, To December 31st, 2021. J Neonatal Surg [Internet]. 2026 Apr. 13 [cited 2026 Apr. 18];15(1s):85-94. Available from: https://jneonatalsurg.com/index.php/jns/article/view/10201