Literature DB >> 20466293

Informed consent for antenatal serum screening for Down syndrome.

Hsiao-Lin Hwa1, Lian-Hua Huang, Fon-Jou Hsieh, Song-Nan Chow.   

Abstract

OBJECTIVE: Respect for patients' autonomy is a principle issue in medical ethics. Patients' understanding of antenatal serum screening for Down syndrome upon informed consent has barely been assessed. Our objective was to evaluate pregnant women's perceived level of understanding of this serum screening.
MATERIALS AND METHODS: Pregnant women between the 15(th) and 21(st) gestational week were randomized into control and experimental groups, and were asked to complete a questionnaire before and after genetic counselling provided by researchers. The primary endpoints were the perceived level of understanding of serum screening for Down syndrome and the autonomy of the decision making for this serum screening. The secondary endpoints were the anxiety and depression levels of these women.
RESULTS: Participants in the experimental group (n = 96) had a significantly higher perceived level of understanding of antenatal serum screening for Down syndrome than participants in the control group (n = 97). There were significantly more respondents in the experimental group making the decision themselves to undergo serum screening than women in the control group. Anxiety and depression levels were not significantly different between the women in the two groups.
CONCLUSION: Pregnant women should be offered more information to allow them to make an informed decision before they undergo antenatal serum screening for Down syndrome. Comprehensive genetic counseling improved pregnant women's autonomy in deciding whether to participate in serum screening. Health service providers should make effort to fulfill the ethical requirements of informed consent.

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Year:  2010        PMID: 20466293     DOI: 10.1016/S1028-4559(10)60009-5

Source DB:  PubMed          Journal:  Taiwan J Obstet Gynecol        ISSN: 1028-4559            Impact factor:   1.705


  5 in total

Review 1.  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

Review 2.  A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.

Authors:  Barbara A Athens; Samantha L Caldwell; Kendall L Umstead; Philip D Connors; Ethan Brenna; Barbara B Biesecker
Journal:  J Genet Couns       Date:  2017-03-02       Impact factor: 2.537

3.  Impact of increased risk for fetal aneuploidy on maternal mood: a prospective longitudinal study.

Authors:  Dayna L Nevay; Catriona Hippman; Angela Inglis; Arianne Albert; Jehannine Austin
Journal:  Acta Obstet Gynecol Scand       Date:  2016-08-17       Impact factor: 3.636

4.  Effect of pre-test genetic counseling for deaf adults on knowledge of genetic testing.

Authors:  Erin E Baldwin; Patrick Boudreault; Michelle Fox; Janet S Sinsheimer; Christina G S Palmer
Journal:  J Genet Couns       Date:  2011-08-05       Impact factor: 2.537

5.  A comparison of face to face and group education on informed choice and decisional conflict of pregnant women about screening tests of fetal abnormalities.

Authors:  Masoumeh Kordi; Sahar Riyazi; Marziyeh Lotfalizade; Mohammad Taghi Shakeri; Hoseyn Jafari Suny
Journal:  J Educ Health Promot       Date:  2018-01-10
  5 in total

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