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Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction

BACKGROUND: The role of an impaired estimated glomerular filtration rate (eGFR) at hospital admission in the outcome of acute kidney injury (AKI) after acute myocardial infarction (AMI) has been underreported. The aim of this study was to assess the influence of an admission eGFR<60 mL/min/1.73 m...

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Autores principales: Bruetto, Rosana G., Rodrigues, Fernando B., Torres, Ulysses S., Otaviano, Ana P., Zanetta, Dirce M. T., Burdmann, Emmanuel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335121/
https://www.ncbi.nlm.nih.gov/pubmed/22539974
http://dx.doi.org/10.1371/journal.pone.0035496
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author Bruetto, Rosana G.
Rodrigues, Fernando B.
Torres, Ulysses S.
Otaviano, Ana P.
Zanetta, Dirce M. T.
Burdmann, Emmanuel A.
author_facet Bruetto, Rosana G.
Rodrigues, Fernando B.
Torres, Ulysses S.
Otaviano, Ana P.
Zanetta, Dirce M. T.
Burdmann, Emmanuel A.
author_sort Bruetto, Rosana G.
collection PubMed
description BACKGROUND: The role of an impaired estimated glomerular filtration rate (eGFR) at hospital admission in the outcome of acute kidney injury (AKI) after acute myocardial infarction (AMI) has been underreported. The aim of this study was to assess the influence of an admission eGFR<60 mL/min/1.73 m(2) on the incidence and early and late mortality of AMI-associated AKI. METHODS: A prospective study of 828 AMI patients was performed. AKI was defined as a serum creatinine increase of ≥50% from the time of admission (RIFLE criteria) in the first 7 days of hospitalization. Patients were divided into subgroups according to their eGFR upon hospital admission (MDRD formula, mL/min/1.73 m(2)) and the development of AKI: eGFR≥60 without AKI, eGFR<60 without AKI, eGFR≥60 with AKI and eGFR<60 with AKI. RESULTS: Overall, 14.6% of the patients in this study developed AKI. The admission eGFR had no impact on the incidence of AKI. However, the admission eGFR was associated with the outcome of AMI-associated AKI. The adjusted hazard ratios (AHR, Cox multivariate analysis) for 30-day mortality were 2.00 (95% CI 1.11–3.61) for eGFR<60 without AKI, 4.76 (95% CI 2.45–9.26) for eGFR≥60 with AKI and 6.27 (95% CI 3.20–12.29) for eGFR<60 with AKI. Only an admission eGFR of <60 with AKI was significantly associated with a 30-day to 1-year mortality hazard (AHR 3.05, 95% CI 1.50–6.19). CONCLUSIONS: AKI development was associated with an increased early mortality hazard in AMI patients with either preserved or impaired admission eGFR. Only the association of impaired admission eGFR and AKI was associated with an increased hazard for late mortality among these patients.
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spelling pubmed-33351212012-04-26 Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction Bruetto, Rosana G. Rodrigues, Fernando B. Torres, Ulysses S. Otaviano, Ana P. Zanetta, Dirce M. T. Burdmann, Emmanuel A. PLoS One Research Article BACKGROUND: The role of an impaired estimated glomerular filtration rate (eGFR) at hospital admission in the outcome of acute kidney injury (AKI) after acute myocardial infarction (AMI) has been underreported. The aim of this study was to assess the influence of an admission eGFR<60 mL/min/1.73 m(2) on the incidence and early and late mortality of AMI-associated AKI. METHODS: A prospective study of 828 AMI patients was performed. AKI was defined as a serum creatinine increase of ≥50% from the time of admission (RIFLE criteria) in the first 7 days of hospitalization. Patients were divided into subgroups according to their eGFR upon hospital admission (MDRD formula, mL/min/1.73 m(2)) and the development of AKI: eGFR≥60 without AKI, eGFR<60 without AKI, eGFR≥60 with AKI and eGFR<60 with AKI. RESULTS: Overall, 14.6% of the patients in this study developed AKI. The admission eGFR had no impact on the incidence of AKI. However, the admission eGFR was associated with the outcome of AMI-associated AKI. The adjusted hazard ratios (AHR, Cox multivariate analysis) for 30-day mortality were 2.00 (95% CI 1.11–3.61) for eGFR<60 without AKI, 4.76 (95% CI 2.45–9.26) for eGFR≥60 with AKI and 6.27 (95% CI 3.20–12.29) for eGFR<60 with AKI. Only an admission eGFR of <60 with AKI was significantly associated with a 30-day to 1-year mortality hazard (AHR 3.05, 95% CI 1.50–6.19). CONCLUSIONS: AKI development was associated with an increased early mortality hazard in AMI patients with either preserved or impaired admission eGFR. Only the association of impaired admission eGFR and AKI was associated with an increased hazard for late mortality among these patients. Public Library of Science 2012-04-23 /pmc/articles/PMC3335121/ /pubmed/22539974 http://dx.doi.org/10.1371/journal.pone.0035496 Text en Bruetto et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bruetto, Rosana G.
Rodrigues, Fernando B.
Torres, Ulysses S.
Otaviano, Ana P.
Zanetta, Dirce M. T.
Burdmann, Emmanuel A.
Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title_full Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title_fullStr Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title_full_unstemmed Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title_short Renal Function at Hospital Admission and Mortality Due to Acute Kidney Injury after Myocardial Infarction
title_sort renal function at hospital admission and mortality due to acute kidney injury after myocardial infarction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335121/
https://www.ncbi.nlm.nih.gov/pubmed/22539974
http://dx.doi.org/10.1371/journal.pone.0035496
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