Literature DB >> 11680963

[Congenital malformations in Chile. An emerging problem (period 1995-1999)].

J Nazer1, T Aravena, L Cifuentes.   

Abstract

BACKGROUND: The Latin American collaborative study of congenital malformations (ECLAMC) is a surveillance program designed to monitor the frequency of congenital malformations and detect abrupt changes in their frequency, look for the cause of such change and implement primary prevention measures. AIM: To construct a secular trend curve with the frequency of congenital malformations in Chile.
MATERIAL AND METHODS: Using the ECLAMC protocol, every malformed newborn or stillbirth, weighting more than 500 g at birth is registered using a standard protocol, and the next non malformed child of the same sex born in the same hospital is assigned as control. Using the gathered data, secular trend curves of congenital malformations were constructed.
RESULTS: Between 1982 and 1999, there is a secular tendency in the rate of congenital malformations and maternal age, with a correlation coefficient of 0.8 and slope of 13.5 (p < 0.05). The rates of congenital malformations at the moment of birth are higher at the University of Chile Clinical Hospital than in the rest of Chilean hospitals and other Latin American Hospitals. Anencephaly is a defect with a high frequency in Concepción and spina bifida has a high frequency in Rancagua, Viña del Mar, Concepción and Valdivia. There is an impressive increase in malformations dependent on prenatal diagnosis such as kidney agenesis, polycystic kidney and diaphragmatic hernia.
CONCLUSIONS: Congenital malformations are having an increasing importance as causes of morbidity or mortality in the newborn.

Entities:  

Mesh:

Year:  2001        PMID: 11680963

Source DB:  PubMed          Journal:  Rev Med Chil        ISSN: 0034-9887            Impact factor:   0.553


  1 in total

1.  Conceptions on genetics in a group of college students.

Authors:  Patrícia Santana Correia; Pedro Vitiello; Maria Helena Cabral de Almeida Cardoso; Dafne Dain Gandelman Horovitz
Journal:  J Community Genet       Date:  2012-11-01
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.