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Congenital anomalies in Ibadan, Nigeria

Background: There is a need for a multidisciplinary database that can be used as a potential source for developing a protocol and a guideline for a possible nationwide prospective surveillance of congenital anomalies in Nigeria. Methods: This five-year cross-sectional retrospective survey of data f...

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Published: 2016
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LEADER 00000njm a2000000a 4500
001 oai:repository.ui.edu.ng:123456789/12200
042 |a dc 
720 |a Ayede, A. I.  |e author 
720 |a Adeleye, A. O.  |e author 
720 |a Olusanya, A. A.  |e author 
720 |a Ademola, A. D.  |e author 
720 |a Olayemi, O.  |e author 
720 |a Ogbole, G. I.  |e author 
720 |a Akinmoladun, J. A.  |e author 
720 |a Agunloye, A. M.  |e author 
720 |a Akinrinoye, O. O.  |e author 
720 |a Takure, A. O.  |e author 
720 |a Oyewole, O. B.  |e author 
720 |a Oluwatosin, O. M.  |e author 
720 |a Omokhodion, S. I.  |e author 
260 |c 2016 
520 |a Background: There is a need for a multidisciplinary database that can be used as a potential source for developing a protocol and a guideline for a possible nationwide prospective surveillance of congenital anomalies in Nigeria. Methods: This five-year cross-sectional retrospective survey of data from January 2009 to December 2013 was done at the University College Hospital, Ibadan. Data were collected from the admission records on the wards in 8 specialty units with the most workable documented clinical records of congenital anomalies in their care using a predesigned proforma. Proportions of congenital anomalies were determined based on systemic classification of the anomalies and the descriptive terms used were according to the ICD_10-chapter XVIII_RCPCH extension. Result: The total number of patients with congenital anomalies whose records were obtained from the ward registers was 1311, there were 75 (5.7%) missing case notes while information was obtained on 1236 (94.3%) patients. There were a total of 1479 anomalies with multiple anomalies seen in 16.1% of the patients. The male/female ratio was 2:1 and multiple births as well as positive family history of birth defects were seen in about 2.4% and 2.2% of cases respectively. Prenatal diagnosis of the anomalies was documented in only 11 cases (0.9%). Only about one in five cases presented within the neonatal period, and defects of the abdominal wall as well as the cranial-facial-orbital regions were the most prevalent. Next were those in the cardiovascular, spinal column, anorectal and genital, as well as musculoskeletal systems. Conclusion: The size and pan-systemic profiles of the birth defects documented in this study calls for further action on this all-important cause of childhood mortality and significant life-long morbidity in our country. 
024 8 |a 0309-3913 
024 8 |a ui_art_ayede_congenital_2016 
024 8 |a African journal of medicine and medical sciences 45, pp. 433-438 
024 8 |a https://repository.ui.edu.ng/handle/123456789/12200 
653 |a Congenital 
653 |a anomaly 
653 |a Ibadan 
245 0 0 |a Congenital anomalies in Ibadan, Nigeria