BMJ 1994;308:1451-1452 (4 June)

Editorials

Screening for carriers of cystic fibrosis

At the core of genetic management is the principle that once people have been informed about all the options they can then choose. Clinical geneticists facilitate decision making by confirming the diagnosis, providing information non-directively, and arranging counselling that takes account of emotional aspects. Decision making is not always logical, and geneticists (and other doctors) should know this. People's feelings are as important as the facts; decisions should emerge from both.

Two papers in this week's journal concern screening for carriers of cystic fibrosis, although both use quite different models. Can such studies provide an approach to screening that is applicable to other autosomal recessive conditions? If so, and if health authorities were to introduce screening for carriers of the commoner autosomal recessive diseases, which should be chosen? The feelings of health professionals and of those who allocate resources may contribute (alongside the facts) to such strategic decisions.

Livingstone and . . . [Full text of this article]


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This article has been cited by other articles:

  • Boulton, M., Williamson, R. (1995). General practice and new genetics: what do general practitioners know about community carrier screening for cystic fibrosis?. Public Understanding of Science 4: 255-267 [Abstract]  
  • Super, M, Schwarz, M J, Malone, G, Roberts, T, Haworth, A, Dermody, G, Brun, J, Magnay, D (1994). Screening for cystic fibrosis Should begin with cascade screening. BMJ 309: 877c-878 [Full text]  
  • Cooper, J D A, Franks, A J, Brock, D J H, Quereshi, N (1994). Screening for cystic fibrosis Screening before pregnancy is preferred. BMJ 309: 339-340 [Full text]  
  • (1994). SCREENING FOR CYSTIC FIBROSIS ASSESSED. JWatch General 1994: 1-1 [Full text]  
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