Nefrología (English Edition) (May 2015)

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

  • 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

DOI
https://doi.org/10.1016/j.nefroe.2015.06.010
Journal volume & issue
Vol. 35, no. 3
pp. 304 – 321

Abstract

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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.

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