Registry of dialysis patients (RDP) is an activity of the Czech Nephrological Society (CNS), which is the sole owner of the collected data. Since 2006, the RDP serves the purpose of newly conceived collection of data from patients on regular dialysis treatment. It is based on prospective anonymized (both in terms of patient and centre identification) follow-up of individual patients with quarterly collection of periodical data. Primary aim of the RDP is to get basic and also some additional data on epidemiology and treatment of renal failure and to contribute in this way towards quality assurance of the treatment and its further development.

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