Literature DB >> 15229006

Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.

Gábor Mezei1, Csaba Papp, Ernö Tóth-Pál, Artúr Beke, Zoltán Papp.   

Abstract

OBJECTIVE: To evaluate factors influencing parental decisions toward continuing or terminating a pregnancy with prenatal diagnosis of sex chromosome aneuploidy.
METHODS: We reviewed the records of patients with fetuses with sex chromosome aneuploidy between 1990 and 2001. A questionnaire survey of women who chose to terminate such pregnancies was designed to examine aspects of their decision-making process.
RESULTS: Forty-nine of 89 pregnancies with sex chromosome aneuploidy were terminated (termination rate 0.55; 95% confidence interval 0.45-0.65). Pregnancies with abnormal ultrasound findings (14/16, 87%), with 45,X or 47,XXY karyotypes (26/36, 72%), and with nonmosaic karyotypes (30/48, 63%) were terminated significantly more often than pregnancies with normal ultrasound findings (35/73, 48%; P <.01), with 47,XXX or 47,XYY karyotypes (4/12, 33%; P <.05), and with mosaic karyotypes (5/25, 20%; P =.01). There was a trend (P =.136) toward a lower rate of termination from 67% to 36% across time, with a significant decrease from 67% to 7% in pregnancies with 47,XXX; 47,XYY; and mosaic karyotypes (P <.01), and no change in cases with 45,X and 47,XXY karyotypes (67% compared with 69%; P = 1.0). Abnormal sexual development and infertility were the greatest parental concerns related to termination.
CONCLUSION: Fear of having a child with abnormal sexual development or infertility remains the major determinant of parental decision toward terminating pregnancy, resulting in consistently high termination rates across time in pregnancies with 45,X and 47,XXY karyotypes. In cases with 47,XXX; 47,XYY; and mosaic karyotypes, the declining termination rate across time is a consequence of recent studies reporting normal sexual development and fertility.

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Year:  2004        PMID: 15229006     DOI: 10.1097/01.AOG.0000128171.14081.eb

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  6 in total

1.  Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy.

Authors:  Patricia Anne Boyd; Maria Loane; Ester Garne; Babak Khoshnood; Helen Dolk
Journal:  Eur J Hum Genet       Date:  2010-08-25       Impact factor: 4.246

2.  Variables influencing pregnancy termination following prenatal diagnosis of fetal chromosome abnormalities.

Authors:  Anne Hawkins; Ana Stenzel; Joanne Taylor; Valerie Y Chock; Louanne Hudgins
Journal:  J Genet Couns       Date:  2012-09-23       Impact factor: 2.537

3.  Parental decisions regarding a prenatally detected fetal chromosomal abnormality and the impact of genetic counseling: an analysis of 38 cases with aneuploidy in Southeast Turkey.

Authors:  Mahmut Balkan; Sevgi Kalkanli; Halit Akbas; Ahmet Yalinkaya; M Nail Alp; Turgay Budak
Journal:  J Genet Couns       Date:  2010-01-30       Impact factor: 2.537

4.  Parental decisions following prenatal diagnosis of chromosomal abnormalities: implications for genetic counseling practice in Japan.

Authors:  Nobuhiro Suzumori; Kyoko Kumagai; Shinobu Goto; Akira Nakamura; Mayumi Sugiura-Ogasawara
Journal:  J Genet Couns       Date:  2014-08-02       Impact factor: 2.537

5.  Pregnancy Outcome following Prenatal Diagnosis of Chromosomal Anomaly: A Record Linkage Study of 26,261 Pregnancies.

Authors:  Myrthe Jacobs; Sally-Ann Cooper; Ruth McGowan; Scott M Nelson; Jill P Pell
Journal:  PLoS One       Date:  2016-12-01       Impact factor: 3.240

6.  Why do parents prefer to know the fetal sex as part of invasive prenatal testing?

Authors:  Angelique J A Kooper; Jacqueline J P M Pieters; Alex J Eggink; Ton B Feuth; Ilse Feenstra; Lia D E Wijnberger; Robbert J P Rijnders; Rik W P Quartero; Peter F Boekkooi; John M G van Vugt; Arie P T Smits
Journal:  ISRN Obstet Gynecol       Date:  2012-12-12
  6 in total

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