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Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience

BACKGROUND: Congenital malformations contribute significantly to the disease burden among children globally. A study conducted in Kenya on understanding the burden of surgical congenital anomalies, highlights the need for Kenyan health systems to go beyond the medical dimensions of illness. This cou...

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Autores principales: Onyambu, Callen Kwamboka, Tharamba, Norah Mukiri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966855/
https://www.ncbi.nlm.nih.gov/pubmed/29792180
http://dx.doi.org/10.1186/s12884-018-1824-z
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author Onyambu, Callen Kwamboka
Tharamba, Norah Mukiri
author_facet Onyambu, Callen Kwamboka
Tharamba, Norah Mukiri
author_sort Onyambu, Callen Kwamboka
collection PubMed
description BACKGROUND: Congenital malformations contribute significantly to the disease burden among children globally. A study conducted in Kenya on understanding the burden of surgical congenital anomalies, highlights the need for Kenyan health systems to go beyond the medical dimensions of illness. This could be achieved by linking knowledge of the severe congenital anomalies (CAs) and their impact of varying disability to the delivery of local health services and public health program planning. Subsequently, early detection of these congenital anomalies is vital and can be achieved through fetal ultrasonography. Studies have proven that antenatal ultrasound can successfully diagnose fetal abnormalities in many cases and therefore aid in counseling of parents and planning for early intervention. Although there are studies on screening of congenital anomalies in various populations, very few have been done in the African population and none to the best of our knowledge has been done in Kenya. METHODS: The patients, who underwent routine obstetric ultrasounds, were recruited into the study. The study population comprised patients who were referred from the obstetric clinic, casualty and other clinics within the hospital vicinity. Data of antenatal ultrasounds was statistically analyzed on structured data collection form to determine the prevalence of congenital anomalies. RESULTS: Fifteen fetal anomalies were diagnosed in 500 women who came for routine ultrasound (3%). The mean age of the mothers was 28.2 years (SD ± 4.5) with an age range from 15 to 44 years. 400 (80%) of the mothers were aged between 27 and 34 years. The most frequently observed fetal anomalies involved the head (8/ 500; 1.6%). Each of the remaining anomalies affected less than 1% of the fetuses and included anomalies of the spine (2/ 500; 0.4%), pulmonary (2/ 500; 0.4%), renal and urinary tract (2/ 500; 0.4%) and skeletal systems (2/ 500; 0.4%). Majority, 9 of 15 (60%) of the fetuses with anomalies detected on prenatal ultrasound resulted in postnatal mortality within days of delivery. CONCLUSION: Congenital anomalies prevalence in our setting compares with those found in other studies. From this study, major birth defects are a major cause of perinatal mortality.
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spelling pubmed-59668552018-05-24 Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience Onyambu, Callen Kwamboka Tharamba, Norah Mukiri BMC Pregnancy Childbirth Research Article BACKGROUND: Congenital malformations contribute significantly to the disease burden among children globally. A study conducted in Kenya on understanding the burden of surgical congenital anomalies, highlights the need for Kenyan health systems to go beyond the medical dimensions of illness. This could be achieved by linking knowledge of the severe congenital anomalies (CAs) and their impact of varying disability to the delivery of local health services and public health program planning. Subsequently, early detection of these congenital anomalies is vital and can be achieved through fetal ultrasonography. Studies have proven that antenatal ultrasound can successfully diagnose fetal abnormalities in many cases and therefore aid in counseling of parents and planning for early intervention. Although there are studies on screening of congenital anomalies in various populations, very few have been done in the African population and none to the best of our knowledge has been done in Kenya. METHODS: The patients, who underwent routine obstetric ultrasounds, were recruited into the study. The study population comprised patients who were referred from the obstetric clinic, casualty and other clinics within the hospital vicinity. Data of antenatal ultrasounds was statistically analyzed on structured data collection form to determine the prevalence of congenital anomalies. RESULTS: Fifteen fetal anomalies were diagnosed in 500 women who came for routine ultrasound (3%). The mean age of the mothers was 28.2 years (SD ± 4.5) with an age range from 15 to 44 years. 400 (80%) of the mothers were aged between 27 and 34 years. The most frequently observed fetal anomalies involved the head (8/ 500; 1.6%). Each of the remaining anomalies affected less than 1% of the fetuses and included anomalies of the spine (2/ 500; 0.4%), pulmonary (2/ 500; 0.4%), renal and urinary tract (2/ 500; 0.4%) and skeletal systems (2/ 500; 0.4%). Majority, 9 of 15 (60%) of the fetuses with anomalies detected on prenatal ultrasound resulted in postnatal mortality within days of delivery. CONCLUSION: Congenital anomalies prevalence in our setting compares with those found in other studies. From this study, major birth defects are a major cause of perinatal mortality. BioMed Central 2018-05-23 /pmc/articles/PMC5966855/ /pubmed/29792180 http://dx.doi.org/10.1186/s12884-018-1824-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Onyambu, Callen Kwamboka
Tharamba, Norah Mukiri
Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title_full Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title_fullStr Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title_full_unstemmed Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title_short Screening for congenital fetal anomalies in low risk pregnancy: the Kenyatta National Hospital experience
title_sort screening for congenital fetal anomalies in low risk pregnancy: the kenyatta national hospital experience
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966855/
https://www.ncbi.nlm.nih.gov/pubmed/29792180
http://dx.doi.org/10.1186/s12884-018-1824-z
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