author_facet Wang, Amanda Y
Trongtrakul, Konlawij
Bellomo, Rinaldo
Li, Qiang
Cass, Alan
Gallagher, Martin
Wang, Amanda Y
Trongtrakul, Konlawij
Bellomo, Rinaldo
Li, Qiang
Cass, Alan
Gallagher, Martin
author Wang, Amanda Y
Trongtrakul, Konlawij
Bellomo, Rinaldo
Li, Qiang
Cass, Alan
Gallagher, Martin
spellingShingle Wang, Amanda Y
Trongtrakul, Konlawij
Bellomo, Rinaldo
Li, Qiang
Cass, Alan
Gallagher, Martin
Nephrology
HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
Nephrology
General Medicine
author_sort wang, amanda y
spelling Wang, Amanda Y Trongtrakul, Konlawij Bellomo, Rinaldo Li, Qiang Cass, Alan Gallagher, Martin 1320-5358 1440-1797 Wiley Nephrology General Medicine http://dx.doi.org/10.1111/nep.13597 <jats:title>ABSTRACT</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Mortality in intensive care unit (ICU) patients with acute kidney injury (AKI) remains high. Previous studies have explored the role of HMG‐CoA reductase inhibitors (statins) with variable findings.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The Randomized Evaluation of Normal <jats:italic>versus</jats:italic> Augmented Level Replacement Therapy (RENAL) Study recruited 1508 participants requiring dialysis in ICU between 2006 and 2009. Statin use was recorded at study baseline. Multivariate Cox modelling was used to assess associations of such statin use and all‐cause mortality. Propensity score analysis was performed for sensitivity analysis. The primary outcome was all‐cause mortality at 90 days.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Of the 1462 participants with the available data on statin usage, 187 (12.8%) received statin therapy at baseline. Participants who receiving statins were older (<jats:italic>P</jats:italic> &lt; 0.001), less likely to have sepsis or require mechanical ventilation (<jats:italic>P</jats:italic> &lt; 0.001). Multivariable analysis showed statin use did not have significant associations with mortality at both day 28 (hazard ratio (HR) = 1.053, 95% confidence interval (CI) = 0.784–1.415, <jats:italic>P</jats:italic> = 0.730) and day 90 (HR = 1.091, 95% CI = 0.836–1.424, <jats:italic>P</jats:italic> = 0.520). Propensity score analysis confirmed the lack of association between statin use and mortality at day 90 (HR = 1.042, 95% CI = 0.734–1.479, <jats:italic>P</jats:italic> = 0.819). However, in septic patients, multivariable analysis suggested statin therapy was associated with a trend to higher mortality at day 90 (HR = 1.688, 95% CI = 1.132–2.519, <jats:italic>P</jats:italic> = 0.010) and continuation of statins was associated with higher mortality (HR = 2.160, 95% CI = 1.296–3.599, <jats:italic>P</jats:italic> = 0.003), compared with statin withdrawal.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>In the RENAL study cohort, baseline statin use was not associated with mortality. Our findings do not support a protective role of statins in ICU patients with severe AKI.</jats:p><jats:p>Clinical Trials registration number for the RENAL study: NCT00221013, the date of registration: September 14, 2005.</jats:p></jats:sec> HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes Nephrology
doi_str_mv 10.1111/nep.13597
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title HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_unstemmed HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_full HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_fullStr HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_full_unstemmed HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_short HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_sort hmg‐coa reductase inhibitors (statins) and acute kidney injury: a secondary analysis of renal study outcomes
topic Nephrology
General Medicine
url http://dx.doi.org/10.1111/nep.13597
publishDate 2019
physical 912-918
description <jats:title>ABSTRACT</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Mortality in intensive care unit (ICU) patients with acute kidney injury (AKI) remains high. Previous studies have explored the role of HMG‐CoA reductase inhibitors (statins) with variable findings.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The Randomized Evaluation of Normal <jats:italic>versus</jats:italic> Augmented Level Replacement Therapy (RENAL) Study recruited 1508 participants requiring dialysis in ICU between 2006 and 2009. Statin use was recorded at study baseline. Multivariate Cox modelling was used to assess associations of such statin use and all‐cause mortality. Propensity score analysis was performed for sensitivity analysis. The primary outcome was all‐cause mortality at 90 days.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Of the 1462 participants with the available data on statin usage, 187 (12.8%) received statin therapy at baseline. Participants who receiving statins were older (<jats:italic>P</jats:italic> &lt; 0.001), less likely to have sepsis or require mechanical ventilation (<jats:italic>P</jats:italic> &lt; 0.001). Multivariable analysis showed statin use did not have significant associations with mortality at both day 28 (hazard ratio (HR) = 1.053, 95% confidence interval (CI) = 0.784–1.415, <jats:italic>P</jats:italic> = 0.730) and day 90 (HR = 1.091, 95% CI = 0.836–1.424, <jats:italic>P</jats:italic> = 0.520). Propensity score analysis confirmed the lack of association between statin use and mortality at day 90 (HR = 1.042, 95% CI = 0.734–1.479, <jats:italic>P</jats:italic> = 0.819). However, in septic patients, multivariable analysis suggested statin therapy was associated with a trend to higher mortality at day 90 (HR = 1.688, 95% CI = 1.132–2.519, <jats:italic>P</jats:italic> = 0.010) and continuation of statins was associated with higher mortality (HR = 2.160, 95% CI = 1.296–3.599, <jats:italic>P</jats:italic> = 0.003), compared with statin withdrawal.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>In the RENAL study cohort, baseline statin use was not associated with mortality. Our findings do not support a protective role of statins in ICU patients with severe AKI.</jats:p><jats:p>Clinical Trials registration number for the RENAL study: NCT00221013, the date of registration: September 14, 2005.</jats:p></jats:sec>
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author Wang, Amanda Y, Trongtrakul, Konlawij, Bellomo, Rinaldo, Li, Qiang, Cass, Alan, Gallagher, Martin
author_facet Wang, Amanda Y, Trongtrakul, Konlawij, Bellomo, Rinaldo, Li, Qiang, Cass, Alan, Gallagher, Martin, Wang, Amanda Y, Trongtrakul, Konlawij, Bellomo, Rinaldo, Li, Qiang, Cass, Alan, Gallagher, Martin
author_sort wang, amanda y
container_issue 9
container_start_page 912
container_title Nephrology
container_volume 24
description <jats:title>ABSTRACT</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Mortality in intensive care unit (ICU) patients with acute kidney injury (AKI) remains high. Previous studies have explored the role of HMG‐CoA reductase inhibitors (statins) with variable findings.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The Randomized Evaluation of Normal <jats:italic>versus</jats:italic> Augmented Level Replacement Therapy (RENAL) Study recruited 1508 participants requiring dialysis in ICU between 2006 and 2009. Statin use was recorded at study baseline. Multivariate Cox modelling was used to assess associations of such statin use and all‐cause mortality. Propensity score analysis was performed for sensitivity analysis. The primary outcome was all‐cause mortality at 90 days.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Of the 1462 participants with the available data on statin usage, 187 (12.8%) received statin therapy at baseline. Participants who receiving statins were older (<jats:italic>P</jats:italic> &lt; 0.001), less likely to have sepsis or require mechanical ventilation (<jats:italic>P</jats:italic> &lt; 0.001). Multivariable analysis showed statin use did not have significant associations with mortality at both day 28 (hazard ratio (HR) = 1.053, 95% confidence interval (CI) = 0.784–1.415, <jats:italic>P</jats:italic> = 0.730) and day 90 (HR = 1.091, 95% CI = 0.836–1.424, <jats:italic>P</jats:italic> = 0.520). Propensity score analysis confirmed the lack of association between statin use and mortality at day 90 (HR = 1.042, 95% CI = 0.734–1.479, <jats:italic>P</jats:italic> = 0.819). However, in septic patients, multivariable analysis suggested statin therapy was associated with a trend to higher mortality at day 90 (HR = 1.688, 95% CI = 1.132–2.519, <jats:italic>P</jats:italic> = 0.010) and continuation of statins was associated with higher mortality (HR = 2.160, 95% CI = 1.296–3.599, <jats:italic>P</jats:italic> = 0.003), compared with statin withdrawal.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>In the RENAL study cohort, baseline statin use was not associated with mortality. Our findings do not support a protective role of statins in ICU patients with severe AKI.</jats:p><jats:p>Clinical Trials registration number for the RENAL study: NCT00221013, the date of registration: September 14, 2005.</jats:p></jats:sec>
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spelling Wang, Amanda Y Trongtrakul, Konlawij Bellomo, Rinaldo Li, Qiang Cass, Alan Gallagher, Martin 1320-5358 1440-1797 Wiley Nephrology General Medicine http://dx.doi.org/10.1111/nep.13597 <jats:title>ABSTRACT</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Mortality in intensive care unit (ICU) patients with acute kidney injury (AKI) remains high. Previous studies have explored the role of HMG‐CoA reductase inhibitors (statins) with variable findings.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The Randomized Evaluation of Normal <jats:italic>versus</jats:italic> Augmented Level Replacement Therapy (RENAL) Study recruited 1508 participants requiring dialysis in ICU between 2006 and 2009. Statin use was recorded at study baseline. Multivariate Cox modelling was used to assess associations of such statin use and all‐cause mortality. Propensity score analysis was performed for sensitivity analysis. The primary outcome was all‐cause mortality at 90 days.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Of the 1462 participants with the available data on statin usage, 187 (12.8%) received statin therapy at baseline. Participants who receiving statins were older (<jats:italic>P</jats:italic> &lt; 0.001), less likely to have sepsis or require mechanical ventilation (<jats:italic>P</jats:italic> &lt; 0.001). Multivariable analysis showed statin use did not have significant associations with mortality at both day 28 (hazard ratio (HR) = 1.053, 95% confidence interval (CI) = 0.784–1.415, <jats:italic>P</jats:italic> = 0.730) and day 90 (HR = 1.091, 95% CI = 0.836–1.424, <jats:italic>P</jats:italic> = 0.520). Propensity score analysis confirmed the lack of association between statin use and mortality at day 90 (HR = 1.042, 95% CI = 0.734–1.479, <jats:italic>P</jats:italic> = 0.819). However, in septic patients, multivariable analysis suggested statin therapy was associated with a trend to higher mortality at day 90 (HR = 1.688, 95% CI = 1.132–2.519, <jats:italic>P</jats:italic> = 0.010) and continuation of statins was associated with higher mortality (HR = 2.160, 95% CI = 1.296–3.599, <jats:italic>P</jats:italic> = 0.003), compared with statin withdrawal.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>In the RENAL study cohort, baseline statin use was not associated with mortality. Our findings do not support a protective role of statins in ICU patients with severe AKI.</jats:p><jats:p>Clinical Trials registration number for the RENAL study: NCT00221013, the date of registration: September 14, 2005.</jats:p></jats:sec> HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes Nephrology
spellingShingle Wang, Amanda Y, Trongtrakul, Konlawij, Bellomo, Rinaldo, Li, Qiang, Cass, Alan, Gallagher, Martin, Nephrology, HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes, Nephrology, General Medicine
title HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_full HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_fullStr HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_full_unstemmed HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_short HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
title_sort hmg‐coa reductase inhibitors (statins) and acute kidney injury: a secondary analysis of renal study outcomes
title_unstemmed HMG‐CoA reductase inhibitors (statins) and acute kidney injury: A secondary analysis of renal study outcomes
topic Nephrology, General Medicine
url http://dx.doi.org/10.1111/nep.13597