How do cystic fibrosis patients experience parenthood? A systematic review
Bibliographic Data
| ID | 15084782 |
|---|---|
| Authors | Anne Jacob (0000-0002-2644-6479, Université Paris Cité), Jonathan Journiac (Université Paris Cité), Lotte Fischer (Université Paris Cité), Lisa Astrologo (Concordia University), Cécile Flahault (0000-0001-7930-205X, Université Paris Cité) |
| Year | 2021 |
| Volume | 26 |
| Issue | 1 |
| Pages | 60-81 |
| Publication date | 2021-01-01 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Journal of Health Psychology (JOURNAL) |
| Journal identifiers | ISSN: 1359-1053 • E-ISSN: 1461-7277 |
| Publisher | SAGE Publications (PUBLISHER • US) |
| DOI | 10.1177/1359105320916539 |
| Language | EN |
| Citations received | 3 |
| References cited | 26 |
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
| Citations per year | 1.5 |
|---|---|
| Citation span | 2024 - 2025 (2) |
| Highly cited | No |