Awareness, perceptions, and practices regarding transition to adult care for nephropathic cystinosis in Türkiye: a nationwide cross-sectional survey of pediatric nephrologists

Abstract Background Nephropathic cystinosis is a rare multisystem disorder in which transition from pediatric to adult care is particularly a vulnerable period because of lifelong treatment demands and the need for sustained multidisciplinary follow-up. We aimed to assess awareness, perceptions, and self-reported transition practices among pediatric nephrologists in Türkiye caring for patients with nephropathic cystinosis. Methods We conducted a nationwide descriptive cross-sectional web-based survey of pediatric nephrologists in Türkiye who had longitudinally followed at least one patient with nephropathic cystinosis. A 59-item questionnaire covering awareness, perceptions, and self-reported practices was administered via Google Forms, and responses were analysed descriptively at the item level. Results In this nationwide descriptive cross-sectional web-based survey, 48 pediatric nephrologists participated. Respondents worked mainly in university hospitals (47.9%) and training and research hospitals (39.6%) and had a median of 14 years of pediatric nephrology experience (IQR 6–17). Although 66.7% distinguished transition from transfer, familiarity with cystinosis-specific transition models was limited; only 16.7% had ever applied a structured model and 8.3% reported a written transition plan in their center. The most frequently perceived challenges were treatment non-adherence (89.6%) and disruption of multidisciplinary follow-up (87.5%). Most respondents reported marked differences between pediatric and adult services, and the median recommended age for initiating transition planning was 17.5 years (IQR 17–18). Overall, 91.7% supported the development of a national transition model (58.3% considered it definitely necessary and 33.3% necessary but difficult to implement without external support). Conclusions Among pediatric nephrologists in Türkiye, awareness of transition-related risks in nephropathic cystinosis was high, but structured transition practices were uncommon and initiation of transition planning was generally recommended at a later age than suggested by current guidance. These findings indicate an implementation gap and support the development of a feasible national transition framework that can be adapted to local resources.

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2026-08-26
DOI
https://doi.org/10.1186/s13023-026-04557-2
Primary Topic
Biomedical Research and Pathophysiology
Type
article
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article

Awareness, perceptions, and practices regarding transition to adult care for nephropathic cystinosis in Türkiye: a nationwide cross-sectional survey of pediatric nephrologists

Önder Yavaşcan, Songül Yılmaz, Emre Leventoğlu, Burcu Yazıcıoğlu et al.
Orphanet Journal of Rare Diseases
Biomedical Research and Pathophysiology
article

Awareness, perceptions, and practices regarding transition to adult care for nephropathic cystinosis in Türkiye: a nationwide cross-sectional survey of pediatric nephrologists

Önder Yavaşcan, Songül Yılmaz, Emre Leventoğlu, Burcu Yazıcıoğlu, Begüm Avcı, Kenan Yılmaz, Okan Akacı, Sare Gülfem Özlü, Bedriye Nuray Alpman, Erkin Serdaroğlu, Özde Nisa Türkkan, Yeşim Özdemir Atikel, Ayşe Seda Pınarbaşı, Aysun Çaltık Yılmaz, Esra Nagehan Akyol Onder, Aslıhan Kara, Aslı Kavaz Tufan, Seçil Arslansoyu Çamlar, Alev Yılmaz, Yılmaz Tabel, Rezan Topaloğlu, Bahriye Atmış, Hülya Nalçacıoğlu, Serra Sürmeli Döven, Sevcan A. Bakkaloğlu, Aslı Çelebi Tayfur, Ece Demirci Bodur
article en

Abstract

Abstract Background Nephropathic cystinosis is a rare multisystem disorder in which transition from pediatric to adult care is particularly a vulnerable period because of lifelong treatment demands and the need for sustained multidisciplinary follow-up. We aimed to assess awareness, perceptions, and self-reported transition practices among pediatric nephrologists in Türkiye caring for patients with nephropathic cystinosis. Methods We conducted a nationwide descriptive cross-sectional web-based survey of pediatric nephrologists in Türkiye who had longitudinally followed at least one patient with nephropathic cystinosis. A 59-item questionnaire covering awareness, perceptions, and self-reported practices was administered via Google Forms, and responses were analysed descriptively at the item level. Results In this nationwide descriptive cross-sectional web-based survey, 48 pediatric nephrologists participated. Respondents worked mainly in university hospitals (47.9%) and training and research hospitals (39.6%) and had a median of 14 years of pediatric nephrology experience (IQR 6–17). Although 66.7% distinguished transition from transfer, familiarity with cystinosis-specific transition models was limited; only 16.7% had ever applied a structured model and 8.3% reported a written transition plan in their center. The most frequently perceived challenges were treatment non-adherence (89.6%) and disruption of multidisciplinary follow-up (87.5%). Most respondents reported marked differences between pediatric and adult services, and the median recommended age for initiating transition planning was 17.5 years (IQR 17–18). Overall, 91.7% supported the development of a national transition model (58.3% considered it definitely necessary and 33.3% necessary but difficult to implement without external support). Conclusions Among pediatric nephrologists in Türkiye, awareness of transition-related risks in nephropathic cystinosis was high, but structured transition practices were uncommon and initiation of transition planning was generally recommended at a later age than suggested by current guidance. These findings indicate an implementation gap and support the development of a feasible national transition framework that can be adapted to local resources.

Orphanet Journal of Rare Diseases
Aksaray University (TR), Izmir University (TR), Fırat University (TR), Ankara University (TR), University of Health Science (KH), Başkent University (TR), Inonu University (TR), Ondokuz Mayıs University (TR), State Hospital (GB), Zonguldak Bülent Ecevit University (TR), Istanbul Medipol University (TR), Konya Numune Hastanesi (TR), Dr. Behçet Uz Çocuk Hastalıkları Hastanesi (TR), Eskişehir City Hospital (TR), Eskisehir Technical University (TR), Konya Eğitim ve Araştırma Hastanesi (TR), Şanlıurfa Mehmet Akif İnan Eğitim ve Araştırma Hastanesi (TR), Sağlık Bilimleri Üniversitesi (TR), S.B.Ü. Bursa Yüksek İhtisas Eğitim ve Araştırma Hastanesi (TR), Eskişehir Osmangazi University (TR), Mersin Üniversitesi (TR), Cukurova University (TR), Hacettepe University (TR), Istanbul University (TR), Marmara University (TR), Bolu Abant İzzet Baysal University (TR), University of Health Sciences Antigua (AG), Gazi University (TR)
No poverty
Openalex Percentile: Top 11%
Biomedical Research and Pathophysiology
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