Abstract
Purpose: To summarize a conference convened to examine how cystic fibrosis screening might appropriately be introduced into routine prenatal practice. Methods: Participants included experts from various relevant disciplines. Systematic reviews and data from individual trials were presented; issues were identified and discussed. Results: Judged by published criteria, prenatal cystic fibrosis screening is suitable for introduction. Screening can be performed cost-effectively by identifying racial/ethnic groups at sufficient risk and then using either of two models for delivering laboratory services. Validated educational materials exist. Ethical issues are not unique. Conclusions: Once adequate facilities for patient and provider education, testing, counseling, quality control, and monitoring are in place, individual programs can begin prenatal screening for cystic fibrosis.
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Haddow, J. E., Bradley, L. A., Palomaki, G. E., Doherty, R. A., Bernhardt, B. A., Brock, D. J. H., … Witt, D. R. (1999). Issues in implementing prenatal screening for cystic fibrosis: Results of a working conference. Genetics in Medicine, 1(4), 129–135. https://doi.org/10.1097/00125817-199905000-00003
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