Rr. Faden et al., ATTITUDES OF PHYSICIANS AND GENETICS PROFESSIONALS TOWARD CYSTIC-FIBROSIS CARRIER SCREENING, American journal of medical genetics, 50(1), 1994, pp. 1-11
With the identification of the cystic fibrosis (CF) gene and its major
mutations in 1989, there has been considerable debate among health pr
ofessionals as to whether population-based carrier testing should be i
nstituted. This paper presents the results of a survey to determine th
e attitudes of physicians and genetics professionals toward CF carrier
testing. Factors associated with differences in attitudes also were e
xamined. A questionnaire was mailed to primary care physicians and psy
chiatrists in 10 states who graduated from medical school between 1950
and 1985. For comparison, medical geneticists and genetic counselors
in the same states also received the questionnaire. A total of 1,140 p
rimary care physicians and psychiatrists (64.8%) and 280 medical genet
icists and genetic counselors (79.1%) responded. Although 92% of respo
ndents believed that a couple should be tested after asking about a te
st that detected 80% of carriers, only 43.9% of respondents believed s
uch a test should be offered routinely. Those specialists most Likely
to have been involved in genetic services were most opposed to routine
screening. The most important reason reported for opposition to routi
ne screening was the consequences of an 80% detection rate. When prese
nted with a hypothetical ''error-free'' test, 75.9% of respondents fav
ored routine testing. Our findings suggest that there was little suppo
rt for routinely offering the CF carrier test available at the time of
this study among the physicians and professionals most involved in th
e provision of genetic services. (C) 1994 Wiley-Liss, Inc.