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Renal Registries play a key role in assessing quality of care and outcomes of renal replacement therapy and comparisons of outcomes between groups should adjust for differences in comorbidities. This study aimed to describe patterns of missing comorbidity data and differences in survival between patients with comorbidity data returned and those with missing comorbidity data.

Patterns and effects of missing comorbidity data for patients starting renal replacement therapy in England, Wales and Northern Ireland