How do cystic fibrosis patients experience parenthood? A systematic review
Anne Jacob1, Jonathan Journiac1, Lotte Fischer1,2
1Laboratoire de Psychopathologie et Processus de Santé (LPPS), Université de Paris, Institut de Psychologie, Boulogne-Billancourt, France.
Abstract:
Improved treatments for cystic fibrosis allow more patients to become parents. This article presents a systematic review of literature on cystic fibrosis patients' experience of parenthood. Five databases (Cairn, Cochrane Library, PsycINFO, PubMed and ScienceDirect) produced 2335 documents that were screened. In total, 13 documents were retained and assessed with validated criteria. Five themes related to cystic fibrosis parenthood were discovered: population presentation, health and treatment adherence, adjustments, role of professionals and pressured temporality. Parenthood requires an important reorganisation of daily life in order to remain capable of childcare. Regardless of negative health impacts, cystic fibrosis parents have a positive outlook on parenthood.
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