SELECTIVE MISCARRIAGE OF DOWNS-SYNDROME FETUSES IN WOMEN AGED 35 YEARS AND OLDER

被引:48
作者
MACINTOSH, MCM
WALD, NJ
CHARD, T
HANSEN, J
MIKKELSEN, M
THERKELSEN, AJ
PETERSEN, GB
LUNDSTEEN, C
机构
[1] UNIV LONDON ST BARTHOLOMEWS HOSP & MED COLL,WOLFSON INST PREVENT MED,LONDON EC1A 7BE,ENGLAND
[2] PSYCHIAT HOSP AARHUS,DANISH CYTOGENET REGISTRY,AARHUS,DENMARK
来源
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY | 1995年 / 102卷 / 10期
关键词
D O I
10.1111/j.1471-0528.1995.tb10845.x
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective To estimate the fetal loss of Down's syndrome fetuses between the time of chorionic villus sampling (10 weeks gestation) and the time of amniocentesis (16 weeks gestation) and term in women aged 35 years and older. Design The age specific prevalence rates in the first trimester of Down's syndrome were estimated using the Danish cytogenetic register in combination with results from four published studies. These were compared with the reported prevalence at the time of amniocentesis and at birth. Subjects 5927 singleton pregnancies undergoing chorionic villus sampling (71 cases of Down's syndrome and 5856 unaffected cases). This was combined with published data on a further 231 cases of Down's syndrome and 16620 unaffected cases. Main outcome measures Age specific prevalences at the time of chorionic villus sampling. Proportion of pregnancies lost between the time of chorionic villus sampling and the time of amniocentesis and term. Results Thirty-two percent of Down's syndrome pregnancies are lost between the time of chorionic villus sampling (10 weeks) and the time of amniocentesis (16 weeks) and 54 % are lost by term. Conclusions The high fetal loss rates of Down's syndrome between the time of chorionic villus sampling and term introduce problems when evaluating first trimester screening tests with respect to their effective detection rates at term. A recommendation for quoting term risks is made.
引用
收藏
页码:798 / 801
页数:4
相关论文
共 12 条
[1]   ESTIMATING A WOMANS RISK OF HAVING A PREGNANCY ASSOCIATED WITH DOWNS-SYNDROME USING HER AGE AND SERUM ALPHA-FETOPROTEIN LEVEL [J].
CUCKLE, HS ;
WALD, NJ ;
THOMPSON, SG .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1987, 94 (05) :387-402
[2]  
CUCKLE HS, 1990, PRENATAL DIAGNOSIS P, P67
[3]   MATERNAL AGE SPECIFIC RATES FOR CHROMOSOME-ABERRATIONS AND FACTORS INFLUENCING THEM - REPORT OF A COLLABORATIVE EUROPEAN STUDY ON 52965 AMNIOCENTESES [J].
FERGUSONSMITH, MA ;
YATES, JRW .
PRENATAL DIAGNOSIS, 1984, 4 :5-44
[4]  
HOOK EB, 1988, AM J HUM GENET, V42, P797
[5]  
HOOK EB, 1983, AM J HUM GENET, V35, P110
[6]   THE FREQUENCY OF 47,+21, 47,+18, AND 47,+13 AT THE UPPERMOST EXTREMES OF MATERNAL AGES - RESULTS ON 56,094 FETUSES STUDIED PRENATALLY AND COMPARISONS WITH DATA ON LIVEBIRTHS [J].
HOOK, EB ;
CROSS, PK ;
REGAL, RR .
HUMAN GENETICS, 1984, 68 (03) :211-220
[7]   CYTOGENETIC EVIDENCE FOR ENHANCED SELECTIVE MISCARRIAGE OF TRISOMY 21-PREGNANCIES WITH ADVANCING MATERNAL AGE [J].
KRATZER, PG ;
GOLBUS, MS ;
SCHONBERG, SA ;
HEILBRON, DC ;
TAYLOR, RN .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (05) :657-663
[8]   CYTOGENETIC FINDINGS IN 1250 CHORIONIC VILLUS SAMPLES OBTAINED IN THE 1ST TRIMESTER WITH CLINICAL FOLLOW-UP OF THE 1ST 1000 PREGNANCIES [J].
LESCHOT, NJ ;
WOLF, H ;
VANPROOIJENKNEGT, AC ;
VANASPEREN, CJ ;
VERJAAL, M ;
SCHURINGBLOM, GH ;
BOER, K ;
KANHAI, HHH ;
CHRISTIAENS, GCML .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1989, 96 (06) :663-670
[9]  
MACINTOSH MCM, 1993, FETAL MATERNAL MED R, V5, P181
[10]   FETAL NUCHAL TRANSLUCENCY - ULTRASOUND SCREENING FOR CHROMOSOMAL DEFECTS IN 1ST TRIMESTER OF PREGNANCY [J].
NICOLAIDES, KH ;
AZAR, G ;
BYRNE, D ;
MANSUR, C ;
MARKS, K .
BRITISH MEDICAL JOURNAL, 1992, 304 (6831) :867-869