Back to Search Start Over

Cystinosis in adult and adolescent patients: Recommendations for the comprehensive care of cystinosis

Authors :
Gema Ariceta
Juan Antonio Camacho
Matilde Fernández-Obispo
Aurora Fernández-Polo
Josep Gamez
Judit García-Villoria
Enrique Lara Monteczuma
Pere Leyes
Nieves Martín-Begué
Federico Oppenheimer
Manel Perelló
Guillem Pintos Morell
Roser Torra
Anna Vila Santandreu
Ana Güell
Grupo T-CiS.bcn
Source :
Nefrología (English Edition), Vol 35, Iss 3, Pp 304-321 (2015)
Publication Year :
2015
Publisher :
Elsevier, 2015.

Abstract

Introduction: Cystinosis is a rare systemic lysosomal storage disease that mainly affects the kidney and the eye. Renal replacement therapy is started in patients with cystinosis during the first decade of life in the absence of treatment. The prognosis of cystinosis depends on early diagnosis and the prompt start of and good compliance with cysteamine treatment. Kidney disease progression, extra-renal complications and shorter life expectancy are more pronounced in patients who do not adhere to treatment. Objective: The aim of this work was to establish recommendations for the comprehensive care of cystinosis and facilitate patient transition from paediatric to adult medicine, based on clinical experience. The goal is to reduce the impact of the disease and improve prognosis and patient quality of life. Methods: Bibliographic research and consensus meetings with a multidisciplinary professional team of clinical experts in cystinosis (T-CiS.bcn group) from 5 hospitals in Barcelona. Results: This consensus document gathers specific recommendations for the diagnosis, treatment and multidisciplinary care of cystinotic patients in the following areas: nephrology, dialysis, kidney transplantation, ophthalmology, endocrinology, neurology, laboratory, genetic counselling, nursing and pharmacy. Conclusions: Guidelines for the comprehensive care of cystinosis provide a support tool for health professionals who look after these patients. They are based on the following main pillars: (a) a multidisciplinary approach; (b) appropriate disease monitoring and control of white blood cell (WBC) cystine levels; (c) the importance of adherence to cysteamine treatment; and (d) the promotion of patient self-care by means of disease education programmes. All these recommendations will lead us, in a second phase, to create a coordinated model of transition from paediatric to adult care services which will cover the specific needs of cystinosis.

Details

Language :
English
ISSN :
20132514
Volume :
35
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Nefrología (English Edition)
Publication Type :
Academic Journal
Accession number :
edsdoj.b7f2601834a4bd1809ae5488fa06f86
Document Type :
article
Full Text :
https://doi.org/10.1016/j.nefroe.2015.06.010