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QT prolongation is associated with increased mortality in end stage liver disease

AIM: To determine the prevalence of QT prolongation in a large series of end stage liver disease (ESLD) patients and its association to clinical variables and mortality. METHODS: The QT interval was measured and corrected for heart rate for each patient, with a prolonged QT cutoff defined as QT >...

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Autores principales: Kim, Sun Moon, George, Bennet, Alcivar-Franco, Diego, Campbell, Charles L, Charnigo, Richard, Delisle, Brian, Hundley, Jonathan, Darrat, Yousef, Morales, Gustavo, Elayi, Samy-Claude, Bailey, Alison L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411969/
https://www.ncbi.nlm.nih.gov/pubmed/28515853
http://dx.doi.org/10.4330/wjc.v9.i4.347
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author Kim, Sun Moon
George, Bennet
Alcivar-Franco, Diego
Campbell, Charles L
Charnigo, Richard
Delisle, Brian
Hundley, Jonathan
Darrat, Yousef
Morales, Gustavo
Elayi, Samy-Claude
Bailey, Alison L
author_facet Kim, Sun Moon
George, Bennet
Alcivar-Franco, Diego
Campbell, Charles L
Charnigo, Richard
Delisle, Brian
Hundley, Jonathan
Darrat, Yousef
Morales, Gustavo
Elayi, Samy-Claude
Bailey, Alison L
author_sort Kim, Sun Moon
collection PubMed
description AIM: To determine the prevalence of QT prolongation in a large series of end stage liver disease (ESLD) patients and its association to clinical variables and mortality. METHODS: The QT interval was measured and corrected for heart rate for each patient, with a prolonged QT cutoff defined as QT > 450 ms for males and QT > 470 ms for females. Multiple clinical variables were evaluated including sex, age, serum sodium, international normalized ratio, creatinine, total bilirubin, beta-blocker use, Model for End-Stage Liver Disease (MELD), MELD-Na, and etiology of liver disease. RESULTS: Among 406 ESLD patients analyzed, 207 (51.0%) had QT prolongation. The only clinical variable associated with QT prolongation was male gender (OR = 3.04, 95%CI: 2.01-4.60, P < 0.001). During the study period, 187 patients (46.1%) died. QT prolongation was a significant independent predictor of mortality (OR = 1.69, 95%CI: 1.03-2.77, P = 0.039). In addition, mortality was also associated with viral etiology of ESLD, elevated MELD score and its components (P < 0.05 for all). No significant reversibility in the QT interval was seen after liver transplantation. CONCLUSION: QT prolongation was commonly encountered in an ESLD population, especially in males, and served as a strong independent marker for increased mortality in ESLD patients.
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spelling pubmed-54119692017-05-17 QT prolongation is associated with increased mortality in end stage liver disease Kim, Sun Moon George, Bennet Alcivar-Franco, Diego Campbell, Charles L Charnigo, Richard Delisle, Brian Hundley, Jonathan Darrat, Yousef Morales, Gustavo Elayi, Samy-Claude Bailey, Alison L World J Cardiol Retrospective Study AIM: To determine the prevalence of QT prolongation in a large series of end stage liver disease (ESLD) patients and its association to clinical variables and mortality. METHODS: The QT interval was measured and corrected for heart rate for each patient, with a prolonged QT cutoff defined as QT > 450 ms for males and QT > 470 ms for females. Multiple clinical variables were evaluated including sex, age, serum sodium, international normalized ratio, creatinine, total bilirubin, beta-blocker use, Model for End-Stage Liver Disease (MELD), MELD-Na, and etiology of liver disease. RESULTS: Among 406 ESLD patients analyzed, 207 (51.0%) had QT prolongation. The only clinical variable associated with QT prolongation was male gender (OR = 3.04, 95%CI: 2.01-4.60, P < 0.001). During the study period, 187 patients (46.1%) died. QT prolongation was a significant independent predictor of mortality (OR = 1.69, 95%CI: 1.03-2.77, P = 0.039). In addition, mortality was also associated with viral etiology of ESLD, elevated MELD score and its components (P < 0.05 for all). No significant reversibility in the QT interval was seen after liver transplantation. CONCLUSION: QT prolongation was commonly encountered in an ESLD population, especially in males, and served as a strong independent marker for increased mortality in ESLD patients. Baishideng Publishing Group Inc 2017-04-26 2017-04-26 /pmc/articles/PMC5411969/ /pubmed/28515853 http://dx.doi.org/10.4330/wjc.v9.i4.347 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Retrospective Study
Kim, Sun Moon
George, Bennet
Alcivar-Franco, Diego
Campbell, Charles L
Charnigo, Richard
Delisle, Brian
Hundley, Jonathan
Darrat, Yousef
Morales, Gustavo
Elayi, Samy-Claude
Bailey, Alison L
QT prolongation is associated with increased mortality in end stage liver disease
title QT prolongation is associated with increased mortality in end stage liver disease
title_full QT prolongation is associated with increased mortality in end stage liver disease
title_fullStr QT prolongation is associated with increased mortality in end stage liver disease
title_full_unstemmed QT prolongation is associated with increased mortality in end stage liver disease
title_short QT prolongation is associated with increased mortality in end stage liver disease
title_sort qt prolongation is associated with increased mortality in end stage liver disease
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411969/
https://www.ncbi.nlm.nih.gov/pubmed/28515853
http://dx.doi.org/10.4330/wjc.v9.i4.347
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