The impact of first-trimester screening on AMA patients' uptake of invasive testing

被引:28
作者
Wray, AM [1 ]
Ghidini, A [1 ]
Alvis, C [1 ]
Hodor, J [1 ]
Landy, HJ [1 ]
Poggi, SH [1 ]
机构
[1] Georgetown Univ Hosp, Dept Obstet & Gynecol, Washington, DC 20007 USA
关键词
decision making; genetic counseling; prenatal diagnosis; prenatal screening;
D O I
10.1002/pd.1144
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective Prenatal testing for AMA includes invasive procedures such as CVS and amniocentesis, which have risks. We sought to determine the effects of first-trimester screening (FTS) on referrals for genetic counseling and patients' decisions to pursue invasive testing after FTS was offered in 2002. Methods We compared AMA patients presenting for prenatal care Who underwent early genetic counseling (<13 weeks' gestation) from 2001 to those from 2003, Charts were reviewed for maternal age, gestational age, past obstetric history, prior CVS or amniocentesis, abnormal ultrasound findings and decision to proceed with invasive testing. The two groups were compared using Student t-test and chi-square tests. Results In 2001, 552 AMA women enrolled in prenatal care. 68 presented for early genetic counseling, In 2003, 728 AMA women enrolled in prenatal care; 172 presented for early genetic counseling, More counseled women chose genetic testing in 2003 than in 2001 (95% vs 79%. p < 0.01). More patients elected in invasive procedure in 2001 compared to 2003 (71% vs 26%, p < 0.01). Conclusion Availability of FTS results in more AMA women having early prenatal genetic counseling and choosing some form of genetic testing. Such women are less likely to choose invasive tests than those without access to FTS. Copyright (C) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:350 / 353
页数:4
相关论文
共 15 条
[1]  
American College of Obstetricians and Gynecologists, 2001, Obstet Gynecol, V97, P1
[2]   Changes in the utilization of prenatal diagnosis [J].
Benn, PA ;
Egan, JFX ;
Fang, M ;
Smith-Bindman, R .
OBSTETRICS AND GYNECOLOGY, 2004, 103 (06) :1255-1260
[3]   CHROMOSOME FINDINGS IN 2,500 2ND TRIMESTER AMNIOCENTESES [J].
CRANDALL, BF ;
LEBHERZ, TB ;
RUBINSTEIN, L ;
ROBERTSON, RD ;
SAMPLE, WF ;
SARTI, D ;
HOWARD, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 5 (04) :345-356
[4]  
Hahnemann JM, 1997, PRENATAL DIAG, V17, P801, DOI 10.1002/(SICI)1097-0223(199709)17:9<801::AID-PD153>3.0.CO
[5]  
2-E
[6]   Cost utility of prenatal diagnosis and the risk-based threshold [J].
Harris, RA ;
Washington, AE ;
Nease, RF ;
Kuppermann, M .
LANCET, 2004, 363 (9405) :276-282
[7]   First-trimester Down syndrome screening using dried blood biochemistry and nuchal translucency [J].
Krantz, DA ;
Hallahan, TW ;
Orlandi, F ;
Buchanan, P ;
Larsen, JW ;
Macri, JN .
OBSTETRICS AND GYNECOLOGY, 2000, 96 (02) :207-213
[8]   GENETIC-COUNSELING - POST-COUNSELING PERIOD .2. MAKING REPRODUCTIVE CHOICES [J].
LIPPMANHAND, A ;
FRASER, FC .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 4 (01) :73-87
[9]   Decisions about amniocentesis by advanced maternal age patients following maternal serum screening may not always correlate clinically with screening results: Need for improvement in informed consent process [J].
Marini, T ;
Sullivan, J ;
Naeem, R .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 109 (03) :171-175
[10]   Sonographic markers of fetal trisomies - Second trimester [J].
Nyberg, DA ;
Souter, VL .
JOURNAL OF ULTRASOUND IN MEDICINE, 2001, 20 (06) :655-674