Addressing the psychosocial aspects of transition to adult care in patients with cystinosis

Other authors

Institut Català de la Salut

[Stabouli S] 1st Department of Pediatrics, Aristotle University Thessaloniki, Hippokratio Hospital, Thessaloniki, Greece. [Sommer A, Kraft S, Schweer K] Department of Pediatric Nephrology, University Hamburg-Eppendorf, Hamburg, Germany. [Bethe D] Division of Pediatric Nephrology, Center for Pediatrics and Adolescent Medicine, University Hospital, Heidelberg, Germany. [Bertholet Thomas A] Pediatric Nephrology, Rheumatology and Dermatology Unit, Reference Center for Rare Renal Diseases, Hospices Civils de Lyon & INSERM1033 Research Unit, Hospital Femme Mere Enfant, Lyon 1 University, Lyon, France. [Ariceta G] Servei de Nefrologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-09-27T11:28:16Z

2024-09-27T11:28:16Z

2024-03



Abstract

Adolescents; Cystinosis; Psychologists


Adolescentes; Cistinosis; Psicólogos


Adolescents; Cistinosi; Psicòlegs


Cystinosis is a rare autosomal-recessive lysosomal storage disease that progressively affects multiple organs beginning with the kidneys. Patients require lifelong multidisciplinary care for the management of kidney disease and progressive extra-renal manifestations, and thus, they are especially fragile and vulnerable during transition from pediatric to adult care. Previous documents have provided guidance to help the medical transition of these highly burdened patients. Patients and their families often experience great psychological distress and face significant social challenges; for these reasons, they often need help from psychologists, social workers, and other psychosocial professionals. Due to the rarity of the disease, most psychosocial professionals have no expertise in this disorder and require advice. To this end, a steering committee (SC) composed of six experts, including pediatric nephrologists, psychologists, and social workers with experience in the care for patients with cystinosis, have identified and addressed seven key questions related to psychosocial challenges of the disease and the burden of treatment. Ten additional international experts (the extended faculty, EF) were invited to answer these questions. Since robust evidence is lacking, as in many rare diseases, conclusions were based on collective agreement between members of the SC and the EF, and the consolidated answers were summarized into expert opinion statements. The present document contains information on the concerns and psychosocial burden of patients with cystinosis and of their caregivers, and provides practical advice for timely and appropriate support to facilitate the transition to adult care.


Open access funding provided by HEAL-Link Greece. The program was supported by Chiesi Farmaceutici S.p.A. Chiesi was not involved in the content or outcome of the manuscript, which were solely determined by the SC and EF experts.

Document Type

Article


Published version

Language

English

Publisher

Springer

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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