

* Department of Psychiatry
School of Nursing
Department of Biostatistics and Medical Informatics
|| Medical School, University of Wisconsin, Madison, Wisconsin
Background. The psychosocial effects on parents of infants with abnormal results in cystic fibrosis (CF) newborn screening (NBS) that uses genetic testing remain unclear.
Methods. Twenty-eight individuals representing 14 families participated in grounded theory interviews
6 months after their childs positive NBS results for CF. Participants also completed the Center for Epidemiologic Studies Depression Scales (CES-D) at their infants sweat-test appointment (n = 51) and/or
6 months after the sweat test (n = 35).
Results. Most parents experienced high levels of emotional distress during their wait for the sweat-test appointment (CES-D score, mean ± SD: 16.5 ± 6.7; 43.1% in the clinical range; median wait: 7 days; range: 335 days). CES-D scores of these parents were also significantly higher than those of comparison parents. Interviews showed that parental cognitive uncertainty and emotional distress were influenced by the parents prior knowledge of NBS, CF, and their carrier status; parents adjustment to their new baby; and the physicians approach to informing parents. Parents coping strategies involved requesting a sweat test as soon as possible, searching for information, assessing the infants risk/health, seeking support, praying, or not talking with others.
Conclusions. The waiting period from notification regarding positive NBS results to diagnostic test results can be psychologically distressing to parents, causing depressive symptoms that vary depending on their perceptions about the likelihood that their infant has CF. Implications for future research examining psychosocial interventions for NBS are discussed.
Key Words: cystic fibrosis newborn screening psychosocial risk
Abbreviations: CES-D, Center for Epidemiological Studies Depression Scales CF, cystic fibrosis CFTR, cystic fibrosis transmembrane conductance regulator NBS, newborn screening
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