Literature DB >> 26535545

[Prevalence of birth defects according to the level of care in two hospitals, Cali, Colombia, 2012-2013].

Harry Pachajoa1, Vania A Villota2, Luz Marina Cruz3, Yoseth Ariza2.   

Abstract

INTRODUCTION: Birth defects are morphologic alterations diagnosed prenatal or postnatally. Surveillance systems have been used to estimate the prevalence in high complexity care centers; however, the variation of the prevalence among different complexity care centers remains unknown.
OBJECTIVE: To compare the prevalence of birth defects among two different complexity care centers in Cali, Colombia.
MATERIALS AND METHODS: A descriptive hospital-based study following the methodology of the Latin American Collaborative Study of Congenital Malformations was conducted during 20 months in a medium complexity hospital and a high complexity hospital.
RESULTS: During the study period, 7,140 births were attended of which 225 had at least one birth defect. The prevalence of these was of 1.7% (IC95% 1.3-2.0) and 7.4% (IC95% 6.2-8.7) for the medium complexity hospital and the high complexity hospital, respectively. The highest frequencies for the high complexity care center were: ventricular septal defect, 10%; congenital hydronephrosis, 7%; abdominal wall defects, 6%, and hydrocephalus, 5%, while for the medium complexity were: polydactyly, 15%; preauricular skin tags, 8%; congenital talipes equino varus, 7%, and hemangioma, 6%.
CONCLUSIONS: The prevalence of birth defects among different complexity care centers varies in quantity, type and severity of the anomaly diagnosed. The surveillance of birth defects is a useful tool for any level of care. It allows estimating more accurately the prevalence of the city, as well being a base for the planning and targeting of resources according to the prevalence of different congenital defects.

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Year:  2015        PMID: 26535545     DOI: 10.1590/S0120-41572015000200011

Source DB:  PubMed          Journal:  Biomedica        ISSN: 0120-4157            Impact factor:   0.935


  2 in total

1.  New PAX2 Mutation Associated with Polycystic Kidney Disease: A Case Report.

Authors:  Jessica Maria Forero-Delgadillo; Vanessa Ochoa; Natalia Duque; Jaime Manuel Restrepo; Hernando Londoño; Jose Antonio Nastasi-Catanese; Harry Pachajoa
Journal:  Clin Med Insights Pediatr       Date:  2021-03-05

2.  Ophthalmic genetics in South America.

Authors:  Malena Daich Varela; Rene Moya; Patricio G Schlottmann; Robert B Hufnagel; Claudia Arberas; Federico M Fernández; M Eugenia Inga; Juliana Lores; Harry Pachajoa; Carlos E Prada; Juliana M Ferraz Sallum
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-08-28       Impact factor: 3.359

  2 in total

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