Screening for carriers of cystic fibrosis through primary health care services

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Abstract

Objective - To evaluate the uptake of cystic fibrosis carrier testing offered through primary health care services. Design - Carrier testing for cystic fibrosis was offered to patients of reproductive age through primary health care services. Setting - Three general practice surgeries and four family planning clinics in South West Hertfordshire District Health Authority. Subjects - Over 1000 patients aged 16-44 attending two general practices and four family planning clinics and a stratified random sample of patients aged 16-44 from one general practice's age-sex register. Results - When screening was offered opportunistically the uptake was 66% in general practice and 87% in family planning clinics. Ten per cent of those offered a screening appointment by letter took up the invitation. Of the screened population, 76% had previously heard of cystic fibrosis, 35% realised it is inherited, and 18% realised that carriers need not have any family history. If they found themselves in an "at risk" partnership 39% would consider not having children and 26% would consider terminating an affected pregnancy, but in each case most people were unsure how they would react. Conclusions - Most people offered a cystic fibrosis test opportunistically wish to be tested, and the responses of those tested indicate that knowledge of carrier state would be considered in future reproductive decisions.

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APA

Watson, E. K., Mayall, E., Chapple, J., Dalziel, M., Harrington, K., Williams, C., & Williamson, R. (1991). Screening for carriers of cystic fibrosis through primary health care services. British Medical Journal, 303(6801), 504–507. https://doi.org/10.1136/bmj.303.6801.504

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