Comparison of reproductive outcome, including the pattern of loss, between couples with chromosomal abnormalities and those with unexplained repeated miscarriages

Adult Chromosome Aberrations Male Abortion, Habitual Family Characteristics Heterozygote Translocation, Genetic 3. Good health Pregnancy, Ectopic 03 medical and health sciences 0302 clinical medicine Pregnancy Embryo Loss Humans Female Embryo Implantation Fetal Death Live Birth Retrospective Studies
DOI: 10.1111/jog.12133 Publication Date: 2013-09-05T08:32:40Z
ABSTRACT
AbstractAimChromosomal abnormalities are an important cause of repeated miscarriage. Several studies have discussed the association between chromosomal abnormalities and repeated miscarriage. This study attempts to describe the pattern of miscarriage in this group of women and the eventual pregnancy outcome of couples with chromosomal abnormalities compared with couples with unexplained repeated pregnancy loss.Material and MethodsThis was a retrospective study involving 795 couples with repeated miscarriages.ResultsOut of 795 couples, 28 (3.52%) were found to have a chromosomal abnormality (carrier group). Over half (65.5%) of the chromosomal abnormalities were balanced reciprocal translocations. After referral, this carrier group had a total of 159 pregnancies, leading to 36 live births (22.6%) among 18 couples. The after referral miscarriage rate in the chromosomal anomaly group (55.6%) was significantly (P < 0.01) higher than that in the unexplained recurrent miscarriage group (28.1%). In couples with chromosomal anomaly, the miscarriages were more likely to occur between 6 and 12 weeks' gestation.ConclusionsThe encouraging cumulative live birth rate of 64.3% for couples with chromosomal anomaly and repeated miscarriage suggests that further attempts at natural conception are a viable option.
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