Published online September 1, 2006
PEDIATRICS Vol. 118 No. 3 September 2006, pp. e649-e656 (doi:10.1542/peds.2005-2551)

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ARTICLE

Changing Their Minds With Time: A Comparison of Hypothetical and Actual Reproductive Behaviors in Parents of Children With Cystic Fibrosis

Susan M. Sawyer, MD^a,b,c,d, Belinda Cerritelli, BAppSc, BA^a,b,d, Lucy S. Carter, MBBS^a,b,c, Mary Cooke, PhD^a, Judith A. Glazner, MA, RN^a and John Massie, MD^a,d

^a Department of Respiratory Medicine
^b Centre for Adolescent Health, Royal Children's Hospital, Melbourne, Victoria, Australia
^c Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia
^d Murdoch Childrens Research Institute, Melbourne, Victoria, Australia

OBJECTIVE. Newborn screening for cystic fibrosis, with appropriate counseling, enables carrier parents to be informed early about future reproductive choices. Previous studies have assessed attitudes toward reproductive decisions in a hypothetical pregnancy or have measured reproductive behaviors. We aimed to measure parent attitudes to reproductive technologies and to compare prospectively these attitudes with later reproductive behaviors.

METHODS. Parents of children who had cystic fibrosis and were aged 2 to 7 years were surveyed at baseline using a written questionnaire that explored attitudes to prenatal testing and termination of pregnancy in a hypothetical pregnancy. Parent knowledge and access to genetic counseling services also were assessed. Five years later, we compared attitudes with actual reproductive behaviors.

RESULTS. Fifty-six mothers participated at baseline, and 43 were resurveyed 5 years later. Parent knowledge of cystic fibrosis and genetics was very good. A total of 93% had met a genetic counselor at the time of diagnosis, and more than half had on at least 1 subsequent occasion. At baseline, 82% reported that they would be likely to have prenatal diagnosis in a subsequent pregnancy, and 56% reported that they would be likely to terminate an affected pregnancy. Twenty-seven mothers since had been pregnant, with prenatal diagnosis used in 33 of the 55 pregnancies. In 67%, the hypothetically reported behavior regarding use of prenatal testing was the same as their actual behavior. Five of the 33 tested pregnancies were affected; all ended in termination. Reproductive choices in relationship to the number of children wanted, together with attitudes toward prenatal diagnosis and termination of pregnancy, were dynamic over time, with decisions having changed in both directions.

CONCLUSIONS. This cohort of parents has actively used reproductive technologies since the birth of a child who has cystic fibrosis that was diagnosed by newborn screening. The dynamic aspect of reproductive choices highlights the importance of ongoing access to genetic counseling beyond the initial period of diagnosis and education, regardless of whether parents report that they expect to use reproductive technologies.

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Key Words: cystic fibrosis • newborn screening • prenatal diagnosis • termination of pregnancy • genetic counseling • reproductive choices

Abbreviations: NBS—newborn screening • CF—cystic fibrosis • RCH—Royal Children's Hospital

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Accepted Mar 8, 2006.

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