Timing of referral for prenatal genetic counselling

被引:6
作者
Schmid, Maximilian [1 ]
Drahonsky, Regina [1 ]
Fast-Hirsch, Christa [1 ]
Baumuehlner, Konstantin [1 ]
Husslein, Peter [1 ]
Blaicher, Wibke [1 ]
机构
[1] Med Univ Vienna Gen Hosp, Dept Obstet & Fetomaternal Med, A-1090 Vienna, Austria
关键词
prenatal genetic counselling; pregnancy rate; timing; FAMILIAL CONDITIONS; TESTING SERVICES; PREGNANCY; DEFICIENCY; DIAGNOSIS; CARE;
D O I
10.1002/pd.2201
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective To evaluate the timing of referrals for prenatal genetic counselling. Method The data of 406 consecutive patients referred because of a family history of genetic disease or a suspected risk factor for genetic disease other than an unfavourable first trimester screening outcome were retrospectively analysed. Results In 37.2% (151/406) of included patients, a pregnancy was already ongoing. The mean gestational age at first contact was 1'3.6 weeks (SD 5.5 weeks). The main counselling issues were previous pregnancy with abortive outcome (ICD O00-O08) 23.9% (97/406), chromosomal abnormalities (ICD Q90-Q99) 16.7% (68/406) and metabolic disorders (ICD E70-E90) 9.9% (40/406). As a result of prenatal genetic counselling, invasive prenatal diagnostic procedures were performed in 11.3% (46/406) of all patients. Conclusion Patients are often referred to prenatal genetic counselling when prenatal diagnosis of a familial genetic condition is no longer feasible, preventive measures are limited and alternative reproductive options have become impossible. Healthcare providers are challenged to improve services so prenatal genetic counselling can take place before conception. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:156 / 159
页数:4
相关论文
共 16 条
[1]   Genetic counselling for familial conditions during pregnancy: A review of the literature published during the years 1989-2004 [J].
Aalfs, C. M. ;
Smets, E. M. A. ;
Leschot, N. J. .
COMMUNITY GENETICS, 2007, 10 (03) :159-168
[2]   Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics [J].
Aalfs, CM ;
Mollema, ED ;
Oort, FJ ;
de Haes, JCJM ;
Leschot, NJ ;
Smets, EMA .
CLINICAL GENETICS, 2004, 66 (02) :112-121
[3]   Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs [J].
Aalfs, CM ;
Smets, EMA ;
de Haes, HCJM ;
Leschot, NJ .
FAMILY PRACTICE, 2003, 20 (02) :135-141
[4]   Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem [J].
Baars, MJH ;
Henneman, L ;
ten Kate, LP .
GENETICS IN MEDICINE, 2005, 7 (09) :605-610
[5]   EuroGentest - a European Network of Excellence aimed at harmonizing genetic testing services [J].
Cassiman, JJ .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (10) :1103-1105
[6]   Genetic testing and counselling in Europe: health professionals current educational provision, needs assessment and potential strategies for the future [J].
Coviello, Domenico A. ;
Skirton, Heather ;
Ceratto, Nadia ;
Lewis, Celine ;
Kent, Alastair .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (12) :1203-1204
[7]   National Confidential Enquiry into counselling for genetic disorders by non-geneticists: general recommendations and specific standards for improving care [J].
Harris, R ;
Lane, B ;
Harris, H ;
Williamson, P ;
Dodge, J ;
Modell, B ;
Ponder, B ;
Rodeck, C ;
Alberman, E .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1999, 106 (07) :658-663
[8]   Preconception genetic counseling [J].
Hogge, JS ;
Hogge, WA .
CLINICAL OBSTETRICS AND GYNECOLOGY, 1996, 39 (04) :751-762
[9]  
Hopwood P, 2003, Community Genet, V6, P192, DOI 10.1159/000079381
[10]   Towards quality assurance and harmonization of genetic testing services in the European Union [J].
Ibarreta, D ;
Elles, R ;
Cassiman, JJ ;
Rodriguez-Cerezo, E ;
Dequeker, E .
NATURE BIOTECHNOLOGY, 2004, 22 (10) :1230-1235