Perspectives of Patients and Clinicians on Reproductive Health Care and ADPKD

Publication date

2024-11

Authors

Gosselink, Margriet E.ORCID 0000-0001-7682-3685
Mooren, Robin
Snoek, Rozemarijn
Crombag, Neeltje M T HORCID 0000-0002-6808-0874
Vos, Paul
Keijzer-Veen, Mandy GISNI 000000038749480X
van Eerde, Albertien MORCID 0000-0001-5953-5956ISNI 0000000393754858
Lely, A TitiaISNI 0000000387328449

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Advisors

Supervisors

Document Type

Article

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License

cc_by_nc_nd

Abstract

Introduction: Family planning and reproductive care are essential but complex aspects of lifecycle management for individuals with autosomal dominant polycystic kidney disease (ADPKD), given the potential genetic transmission and pregnancy-related complications. In this qualitative study, we studied the experiences and perspectives of patients with ADPKD and clinicians to identify areas for potential improvement in reproductive lifecycle care. Methods: Focus group discussions (FGDs) were conducted in the Netherlands with patients with ADPKD, both men and women, who had children through varied reproductive choices; and clinicians, including (pediatric) nephrologists, obstetric gynecologists and geneticists. Thematic analysis, utilizing a grounded theory approach, was performed on verbatim transcriptions of recordings, followed by consensus discussions to finalize themes. Results: Nine focus groups involving 31 participants (16 patients and 15 physicians) identified 6 key themes. These included the need for timely and comprehensive information dissemination from puberty on, understanding patient-specific decision-making factors, improving tailored psychosocial guidance and communication, the need for systematic efforts to take care of missed (minor) at-risk patients, addressing inequities in access to care, and improving multidisciplinary collaboration. Conclusions: This study represents the first qualitative study of patient and physician perspectives on reproductive lifecycle care for ADPKD. We present valuable insights into factors influencing patients’ reproductive decision-making, a comprehensive comparison between the perspectives of patients and clinicians on family planning and follow-up care of minors at risk for ADPKD, and recommendations for enhancing overall care quality. Incorporating these insights into clinical care could enhance patient-centered care and foster interdisciplinary collaborations to further improve the quality of reproductive health care services for individuals with ADPKD.

Keywords

autosomal dominant polycystic kidney disease (ADPKD), family planning, focus group, qualitative study, reproductive care, Nephrology, Journal Article

Citation

Gosselink, M E, Mooren, R, Snoek, R, Crombag, N M T H, Vos, P, Keijzer-Veen, M G, van Eerde, A M & Lely, A T 2024, 'Perspectives of Patients and Clinicians on Reproductive Health Care and ADPKD', Kidney International Reports, vol. 9, no. 11, pp. 3190-3203. https://doi.org/10.1016/j.ekir.2024.08.028