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Database - (CIANE)

Description of this bibliographical database (CIANE website)
Currently 3108 records
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https://ciane.net/id=867

Created on : 27 Jul 2004
Modified on : 27 Dec 2007

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Bibliographical entry (without author) :

Genetic amniocentesis: a risk factor for preterm delivery? Eur J Obstet Gynecol Reprod Biol. 2003 Oct 10;110(2):153-8.

Author(s) :

Medda E, Donati S, Spinelli A, Di Renzo GC; EUROPOP.

Year of publication :

2003

URL(s) :

http://www.sciencedirect.com/science?_ob=ArticleUR…

Résumé (français)  :

Abstract (English)  :

OBJECTIVE: To determine whether genetic amniocentesis performed in the second trimester of pregnancy is associated with the risk of preterm delivery.

STUDY DESIGN: Case-control study performed in several departments of obstetrics and gynaecology of nine European countries. Three thousand and ninety-one preterm births and 5298 controls randomly selected from singleton births born at term during 1994-1997 were analysed. Logistic regression models were used to compare preterm births altogether and, separately, spontaneous preterm delivery and induced preterm delivery.

RESULTS: An increased risk of preterm delivery was found in women having second trimester genetic amniocentesis after taking account of other risk factors and confounding variables (odds ratios (OR)=1.59, 95% confidence intervals (95% CI): 1.31-1.92). The association was statistically significant and similar for spontaneous preterm delivery and induced preterm delivery.

CONCLUSION: The study shows an association between preterm delivery and genetic amniocentesis. In view of the wide use of amniocentesis, further research on the etiologic role of this prenatal diagnostic technique is needed.

Sumário (português)  :

Resumen (español)  :

Comments :

Argument (français) :

L’amniocentèse au 2nd trimestre augmente le risque de naissances prématurées, spontanées ou déclenchées.

Argument (English):

Argumento (português):

Argumento (español):

Keywords :

➡ evidence-based medicine/midwifery ; premature baby ; amniocentesis ; screening ; trisomy

Author of this record :

Cécile Loup — 27 Jul 2004

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