End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases

<p>Abstract</p> <p>Background</p> <p>The aim of this study was to investigate the characteristics and outcomes of patients receiving renal replacement therapy for end-stage kidney disease (ESKD) secondary to haemolytic uraemic syndrome (HUS).</p> <p>Methods&...

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Main Authors: Tang Wen, Mohandas Janaki, McDonald Stephen P, Hawley Carmel M, Badve Sunil V, Boudville Neil, Brown Fiona G, Clayton Philip A, Wiggins Kathryn J, Bannister Kym M, Campbell Scott B, Johnson David W
Format: Article
Language:English
Published: BMC 2012-12-01
Series:BMC Nephrology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2369/13/164
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spelling doaj-46467e93ef174874809e05433305d1712020-11-25T00:33:28ZengBMCBMC Nephrology1471-23692012-12-0113116410.1186/1471-2369-13-164End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry casesTang WenMohandas JanakiMcDonald Stephen PHawley Carmel MBadve Sunil VBoudville NeilBrown Fiona GClayton Philip AWiggins Kathryn JBannister Kym MCampbell Scott BJohnson David W<p>Abstract</p> <p>Background</p> <p>The aim of this study was to investigate the characteristics and outcomes of patients receiving renal replacement therapy for end-stage kidney disease (ESKD) secondary to haemolytic uraemic syndrome (HUS).</p> <p>Methods</p> <p>The study included all patients with ESKD who commenced renal replacement therapy in Australia and New Zealand between 15/5/1963 and 31/12/2010, using data from the ANZDATA Registry. HUS ESKD patients were compared with matched controls with an alternative primary renal disease using propensity scores based on age, gender and treatment era.</p> <p>Results</p> <p>Of the 58422 patients included in the study, 241 (0.4%) had ESKD secondary to HUS. HUS ESKD was independently associated with younger age, female gender and European race. Compared with matched controls, HUS ESKD was not associated with mortality on renal replacement therapy (adjusted hazard ratio [HR] 1.14, 95% CI 0.87-1.50, p = 0.34) or dialysis (HR 1.34, 95% CI 0.93-1.93, p = 0.12), but did independently predict recovery of renal function (HR 54.01, 95% CI 1.45-11.1, p = 0.008). 130 (54%) HUS patients received 166 renal allografts. Overall renal allograft survival rates were significantly lower for patients with HUS ESKD at 1 year (73% vs 91%), 5 years (62% vs 85%) and 10 years (49% vs 73%). HUS ESKD was an independent predictor of renal allograft failure (HR 2.59, 95% CI 1.70-3.95, p < 0.001). Sixteen (12%) HUS patients experienced failure of 22 renal allografts due to recurrent HUS. HUS ESKD was not independently associated with the risk of death following renal transplantation (HR 0.92, 95% CI 0.35-2.44, p = 0.87).</p> <p>Conclusions</p> <p>HUS is an uncommon cause of ESKD, which is associated with comparable patient survival on dialysis, an increased probability of renal function recovery, comparable patient survival post-renal transplant and a heightened risk of renal transplant graft failure compared with matched ESKD controls.</p> http://www.biomedcentral.com/1471-2369/13/164Haemolytic uraemic syndromeKidney FailureChronicOutcomesRenal function recoveryRenal transplantationThrombotic microangiopathy
collection DOAJ
language English
format Article
sources DOAJ
author Tang Wen
Mohandas Janaki
McDonald Stephen P
Hawley Carmel M
Badve Sunil V
Boudville Neil
Brown Fiona G
Clayton Philip A
Wiggins Kathryn J
Bannister Kym M
Campbell Scott B
Johnson David W
spellingShingle Tang Wen
Mohandas Janaki
McDonald Stephen P
Hawley Carmel M
Badve Sunil V
Boudville Neil
Brown Fiona G
Clayton Philip A
Wiggins Kathryn J
Bannister Kym M
Campbell Scott B
Johnson David W
End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
BMC Nephrology
Haemolytic uraemic syndrome
Kidney Failure
Chronic
Outcomes
Renal function recovery
Renal transplantation
Thrombotic microangiopathy
author_facet Tang Wen
Mohandas Janaki
McDonald Stephen P
Hawley Carmel M
Badve Sunil V
Boudville Neil
Brown Fiona G
Clayton Philip A
Wiggins Kathryn J
Bannister Kym M
Campbell Scott B
Johnson David W
author_sort Tang Wen
title End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
title_short End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
title_full End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
title_fullStr End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
title_full_unstemmed End-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive ANZDATA registry cases
title_sort end-stage kidney disease due to haemolytic uraemic syndrome – outcomes in 241 consecutive anzdata registry cases
publisher BMC
series BMC Nephrology
issn 1471-2369
publishDate 2012-12-01
description <p>Abstract</p> <p>Background</p> <p>The aim of this study was to investigate the characteristics and outcomes of patients receiving renal replacement therapy for end-stage kidney disease (ESKD) secondary to haemolytic uraemic syndrome (HUS).</p> <p>Methods</p> <p>The study included all patients with ESKD who commenced renal replacement therapy in Australia and New Zealand between 15/5/1963 and 31/12/2010, using data from the ANZDATA Registry. HUS ESKD patients were compared with matched controls with an alternative primary renal disease using propensity scores based on age, gender and treatment era.</p> <p>Results</p> <p>Of the 58422 patients included in the study, 241 (0.4%) had ESKD secondary to HUS. HUS ESKD was independently associated with younger age, female gender and European race. Compared with matched controls, HUS ESKD was not associated with mortality on renal replacement therapy (adjusted hazard ratio [HR] 1.14, 95% CI 0.87-1.50, p = 0.34) or dialysis (HR 1.34, 95% CI 0.93-1.93, p = 0.12), but did independently predict recovery of renal function (HR 54.01, 95% CI 1.45-11.1, p = 0.008). 130 (54%) HUS patients received 166 renal allografts. Overall renal allograft survival rates were significantly lower for patients with HUS ESKD at 1 year (73% vs 91%), 5 years (62% vs 85%) and 10 years (49% vs 73%). HUS ESKD was an independent predictor of renal allograft failure (HR 2.59, 95% CI 1.70-3.95, p < 0.001). Sixteen (12%) HUS patients experienced failure of 22 renal allografts due to recurrent HUS. HUS ESKD was not independently associated with the risk of death following renal transplantation (HR 0.92, 95% CI 0.35-2.44, p = 0.87).</p> <p>Conclusions</p> <p>HUS is an uncommon cause of ESKD, which is associated with comparable patient survival on dialysis, an increased probability of renal function recovery, comparable patient survival post-renal transplant and a heightened risk of renal transplant graft failure compared with matched ESKD controls.</p>
topic Haemolytic uraemic syndrome
Kidney Failure
Chronic
Outcomes
Renal function recovery
Renal transplantation
Thrombotic microangiopathy
url http://www.biomedcentral.com/1471-2369/13/164
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