ANALYSIS OF CONGENITAL ANOMALY TRENDS AND IMPLICATIONS IN A TERTIARY CARE HOSPITAL: A STUDY FROM PESHAWAR, PAKISTAN

Authors

  • W SYED Department of Gynecology & Obstetrics Medical Teaching Institute Lady Reading Hospital, Peshawar, Pakistan
  • N LIAQAT Department of Gynecology & Obstetrics Medical Teaching Institute Lady Reading Hospital, Peshawar, Pakistan
  • S RAFIQ Department of Gynecology & Obstetrics Medical Teaching Institute Lady Reading Hospital, Peshawar, Pakistan
  • N HASSAN Department of Gynecology & Obstetrics Medical Teaching Institute Lady Reading Hospital, Peshawar, Pakistan
  • F ABID Department of Gynecology & Obstetrics Medical Teaching Institute Lady Reading Hospital, Peshawar, Pakistan

DOI:

https://doi.org/10.54112/bcsrj.v2023i1.592

Keywords:

Congenital anomalies, Tertiary care hospital, Prevalence, Consanguinity

Abstract

This research, conducted at a tertiary care hospital in Peshawar, Pakistan, aimed to examine the trends and rates of congenital malformations. The study was a cross-sectional study that took place from January 2021 to January 2022 at the Department of Gynaecology & OBs MTI, LRH Peshawar. The study's objectives were to determine the frequency and trends of congenital disabilities in infants, identify risk factors associated with these conditions, and suggest prevention and early intervention measures. The study excluded stillbirths but included newborns with congenital disabilities diagnosed through clinical examinations such as chromosomal analysis, radiography, and ultrasound. Information on kinship, maternal and prenatal history, and other risk factors were gathered through records and interviews. Statistical analysis was conducted using Fisher's exact test and chi-square test. The most common congenital anomaly identified was musculoskeletal abnormalities, accounting for 3.8% of cases. The study highlights the importance of prenatal diagnosis and treatment for prevention and timely intervention. The study's limitations include its hospital-based setting and exclusion of stillbirths, which may have led to an underestimation of prevalence. Nonetheless, the research sheds light on the need for early detection and prevention of congenital anomalies and associated risk factors. According to the report, congenital abnormalities affect 3.8% of babies at Lady Reading Hospital in Peshawar. Consanguinity and fetal abnormalities were significantly correlated (p<0.05). Five occurrences of anencephaly were reported, making central nervous system (CNS) abnormalities the most common kind. Gastrointestinal tract (GIT) abnormalities accounted for 15% of cases, whereas musculoskeletal anomalies accounted for 33.2%. The genitourinary (10.5%), cardiovascular (9.1%), and cutaneous (8.7%) systems were also impacted. Although these results are consistent with other studies, if abortions and stillbirths had been taken into account, the frequency may have been greater. Prenatal diagnosis and early antenatal care are essential for intervention and prevention. The analysis shows that congenital abnormalities were 3.8% common throughout the study period at Lady Reading Hospital in Peshawar. Fetal abnormalities were substantially correlated with consanguinity. Anomalies in the central nervous system showed the most significant occurrence. Prenatal diagnosis and early antenatal care are crucial for intervention and prevention.

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References

Akhter, Z., Rankin, J., Ceulemans, D., Ngongalah, L., Ackroyd, R., Devlieger, R., Vieira, R., and Heslehurst, N. (2019). Pregnancy after bariatric surgery and adverse perinatal outcomes: a systematic review and meta-analysis. PLoS medicine 16, e1002866.

Christianson, A. L., Howson, C. P., and Modell, B. (2006). "Global report on birth defects: the hidden toll of dying and disabled children," March of Dimes Birth Defects Foundation.

Control, C. f. D., and Prevention (2011). State-specific trends in lung cancer incidence and smoking--United States, 1999-2008. MMWR. Morbidity and mortality weekly report 60, 1243-1247.

D’Amato, G., Holgate, S. T., Pawankar, R., Ledford, D. K., Cecchi, L., Al-Ahmad, M., Al-Enezi, F., Al-Muhsen, S., Ansotegui, I., and Baena-Cagnani, C. E. (2015). Meteorological conditions, climate change, new emerging factors, and asthma and related allergic disorders. A statement of the World Allergy Organization. World allergy organization journal 8, 1-52.

Dolk, H., Loane, M., and Garne, E. (2010). The prevalence of congenital anomalies in Europe. Rare diseases epidemiology, 349-364.

Gilbert-Barness, E. (2010). Teratogenic causes of malformations. Annals of Clinical & Laboratory Science 40, 99-114.

Jones, J., and Smith, J. (2017). Ethnography: challenges and opportunities. Evidence-Based Nursing 20, 98-100.

Kalter, H., and Warkany, J. (1983). Congenital malformations: etiologic factors and their role in prevention. New England journal of medicine 308, 424-431.

Kumar, M. R., Bhat, B. V., and Oumachigui, A. (1996). Perinatal mortality trends in a referral hospital. The Indian Journal of Pediatrics 63, 357-361.

MacLennan, D. H., and Zvaritch, E. (2011). Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1813, 948-964.

Malherbe, H. L., Aldous, C., Woods, D., and Christianson, A. (2016). The contribution of congenital disorders to child mortality in South Africa. South African Health Review 2016, 137-152.

Morris, J. K., Garne, E., Loane, M., Barisic, I., Densem, J., Latos-Bieleńska, A., Neville, A., Pierini, A., Rankin, J., and Rissmann, A. (2021). EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies. BMJ open 11, e047859.

Olsen, J., Nøhr, E. A., Thomsen, R. W., and Støvring, H. (2013). Non-communicable disease epidemic: epidemiology in action (EuroEpi 2013 and NordicEpi 2013) Aarhus, Denmark from 11 August to 14 August 2013. European Journal of Epidemiology 28, S1-S270.

Pinzon-Morales, R.-D., Baquero-Duarte, K.-A., Orozco-Gutierrez, A.-A., and Grisales-Palacio, V.-H. (2011). Pattern recognition of surface EMG biological signals by means of hilbert spectrum and fuzzy clustering. In "Software Tools and Algorithms for Biological Systems", pp. 201-209. Springer.

Rajab, A., Vaishnav, A., Freeman, N., and Patton, M. (1998). Neural tube defects and congenital hydrocephalus in the Sultanate of Oman. Journal of tropical pediatrics 44, 300-303.

Ramakrishnan, R., Rao, S., and He, J.-R. (2021). Perinatal health predictors using artificial intelligence: a review. Women's Health 17, 17455065211046132.

Salemi, J. L., Tanner, J. P., Kennedy, S., Block, S., Bailey, M., Correia, J. A., Watkins, S. M., and Kirby, R. S. (2012). A comparison of two surveillance strategies for selected birth defects in Florida. Public health reports 127, 391-400.

Singh, A., and Gupta, R. K. (2009). Pattern of congenital anomalies in newborn: a hospital based prospective study. JK science 11.

Ten Kate, L. P., Teeuw, M. E., Henneman, L., and Cornel, M. C. (2014). Consanguinity and endogamy in the Netherlands: demographic and medical genetic aspects. Human Heredity 77, 161-166.

Tinanoff, N., Baez, R. J., Diaz Guillory, C., Donly, K. J., Feldens, C. A., McGrath, C., Phantumvanit, P., Pitts, N. B., Seow, W. K., and Sharkov, N. (2019). Early childhood caries epidemiology, aetiology, risk assessment, societal burden, management, education, and policy: Global perspective. International journal of paediatric dentistry 29, 238-248.

Van Der Linde, D., Konings, E. E., Slager, M. A., Witsenburg, M., Helbing, W. A., Takkenberg, J. J., and Roos-Hesselink, J. W. (2011). Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis. Journal of the American College of Cardiology 58, 2241-2247.

Webber, D. M., MacLeod, S. L., Bamshad, M. J., Shaw, G. M., Finnell, R. H., Shete, S. S., Witte, J. S., Erickson, S. W., Murphy, L. D., and Hobbs, C. (2015). Developments in our understanding of the genetic basis of birth defects. Birth Defects Research Part A: Clinical and Molecular Teratology 103, 680-691.

Yngwe, M. Å., Fritzell, J., Lundberg, O., Diderichsen, F., and Burström, B. (2003). Exploring relative deprivation: is social comparison a mechanism in the relation between income and health? Social science & medicine 57, 1463-1473.

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Published

2023-12-12

How to Cite

SYED , W., LIAQAT , N., RAFIQ , S., HASSAN , N., & ABID , F. (2023). ANALYSIS OF CONGENITAL ANOMALY TRENDS AND IMPLICATIONS IN A TERTIARY CARE HOSPITAL: A STUDY FROM PESHAWAR, PAKISTAN. Biological and Clinical Sciences Research Journal, 2023(1), 592. https://doi.org/10.54112/bcsrj.v2023i1.592