Literature DB >> 12128276

Mothers' knowledge of screening for trisomy 21 in 1999: a survey in Paris maternity units.

C De Vigan1, V Vodovar, J Goujard, M Garel, C Vayssière, F Goffinet.   

Abstract

OBJECTIVE: To assess mothers' knowledge of screening tests for trisomy 21. STUDY
DESIGN: Interview of all women who had recently delivered a healthy child and were present in 15 Paris maternity units during one of the two non-consecutive days in June 1999 (N = 734).
RESULTS: Two-third said that they had access to a nuchal translucency measurement (NTM) and to maternal serum screening (MSS), and 16% to amniocentesis. Thirty-eight percent of the women who had NTMs and 69% of those who had serum screening said that they had been informed of the need for amniocentesis if the results were abnormal. Among the women who had amniocentesis, 20% did not know the risk of miscarriage and 41% had not been informed about the possibility of terminating the pregnancy if trisomy 21 was diagnosed.
CONCLUSIONS: Mothers' knowledge about the screening tests for trisomy 21 remains fragmentary. Providing comprehensive information about all these tests should be considered in early pregnancy so that women can make informed choices.

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Year:  2002        PMID: 12128276     DOI: 10.1016/s0301-2115(01)00559-0

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  5 in total

1.  A population-based evaluation of the impact of antenatal screening for Down's syndrome in France, 1981-2000.

Authors:  Babak Khoshnood; Catherine De Vigan; Véronique Vodovar; Janine Goujard; François Goffinet
Journal:  BJOG       Date:  2004-05       Impact factor: 6.531

2.  Socioeconomic barriers to informed decisionmaking regarding maternal serum screening for down syndrome: results of the French National Perinatal Survey of 1998.

Authors:  Babak Khoshnood; Béatrice Blondel; Catherine de Vigan; Gérard Bréart
Journal:  Am J Public Health       Date:  2004-03       Impact factor: 9.308

Review 3.  Measuring informed choice in population-based reproductive genetic screening: a systematic review.

Authors:  Alice Grace Ames; Sylvia Ann Metcalfe; Alison Dalton Archibald; Rony Emily Duncan; Jon Emery
Journal:  Eur J Hum Genet       Date:  2014-05-21       Impact factor: 4.246

4.  Evaluation of a decision aid for prenatal testing of fetal abnormalities: a cluster randomised trial [ISRCTN22532458].

Authors:  Cate Nagle; Sharon Lewis; Bettina Meiser; Sylvia Metcalfe; John B Carlin; Robin Bell; Jane Gunn; Jane Halliday
Journal:  BMC Public Health       Date:  2006-04-13       Impact factor: 3.295

5.  Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: a qualitative focus group study.

Authors:  Cate Nagle; Sharon Lewis; Bettina Meiser; Jane Gunn; Jane Halliday; Robin Bell
Journal:  BMC Health Serv Res       Date:  2008-05-28       Impact factor: 2.655

  5 in total

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