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New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis

BACKGROUND: The aims of this study were to prospectively assess the prevalence of sustained (lasting more than 30 s) new-onset supraventricular arrhythmia (NOSVA) during septic shock, identify the associated factors (including septic myocardial dysfunction), and evaluate its impact on hemodynamics a...

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Autores principales: Seemann, Aurélien, Boissier, Florence, Razazi, Keyvan, Carteaux, Guillaume, de Prost, Nicolas, Brun-Buisson, Christian, Mekontso Dessap, Armand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Paris 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579158/
https://www.ncbi.nlm.nih.gov/pubmed/26395899
http://dx.doi.org/10.1186/s13613-015-0069-5
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author Seemann, Aurélien
Boissier, Florence
Razazi, Keyvan
Carteaux, Guillaume
de Prost, Nicolas
Brun-Buisson, Christian
Mekontso Dessap, Armand
author_facet Seemann, Aurélien
Boissier, Florence
Razazi, Keyvan
Carteaux, Guillaume
de Prost, Nicolas
Brun-Buisson, Christian
Mekontso Dessap, Armand
author_sort Seemann, Aurélien
collection PubMed
description BACKGROUND: The aims of this study were to prospectively assess the prevalence of sustained (lasting more than 30 s) new-onset supraventricular arrhythmia (NOSVA) during septic shock, identify the associated factors (including septic myocardial dysfunction), and evaluate its impact on hemodynamics and prognosis. METHODS: Patients with a diagnosis of septic shock were screened in a medical intensive care unit of a tertiary hospital center in France with a continuous 12-lead EKG for the occurrence of NOSVA. Biological and clinical data (including septic myocardial dysfunction characterized by echocardiography) were collected. We also assessed the hemodynamic tolerance and prognosis of NOSVA. RESULTS: Among the 71 septic shock episodes assessed during the study, NOSVA occurred in 30 [prevalence of 42 %, 95 % confidence interval (CI) 30–53 %]. Among all recorded factors, only renal failure (as assessed by renal SOFA score at day 1) was associated with NOSVA and this difference persisted by multivariable analysis (odds ratio of 1.29, 95 % CI 1.03–1.62, p = 0.03). There was a significant increase in norepinephrine dosage during the first hour after SVA onset. NOSVA was associated with longer catecholamine use during septic shock as compared with patients in sinus rhythm, whereas ICU mortality was identical between groups. CONCLUSIONS: We found a high prevalence of sustained NOSVA during septic shock. NOSVA was not related to septic myocardial dysfunction, but rather to acute renal failure, raising the hypothesis of an acute renocardiac syndrome.
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spelling pubmed-45791582015-09-25 New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis Seemann, Aurélien Boissier, Florence Razazi, Keyvan Carteaux, Guillaume de Prost, Nicolas Brun-Buisson, Christian Mekontso Dessap, Armand Ann Intensive Care Research BACKGROUND: The aims of this study were to prospectively assess the prevalence of sustained (lasting more than 30 s) new-onset supraventricular arrhythmia (NOSVA) during septic shock, identify the associated factors (including septic myocardial dysfunction), and evaluate its impact on hemodynamics and prognosis. METHODS: Patients with a diagnosis of septic shock were screened in a medical intensive care unit of a tertiary hospital center in France with a continuous 12-lead EKG for the occurrence of NOSVA. Biological and clinical data (including septic myocardial dysfunction characterized by echocardiography) were collected. We also assessed the hemodynamic tolerance and prognosis of NOSVA. RESULTS: Among the 71 septic shock episodes assessed during the study, NOSVA occurred in 30 [prevalence of 42 %, 95 % confidence interval (CI) 30–53 %]. Among all recorded factors, only renal failure (as assessed by renal SOFA score at day 1) was associated with NOSVA and this difference persisted by multivariable analysis (odds ratio of 1.29, 95 % CI 1.03–1.62, p = 0.03). There was a significant increase in norepinephrine dosage during the first hour after SVA onset. NOSVA was associated with longer catecholamine use during septic shock as compared with patients in sinus rhythm, whereas ICU mortality was identical between groups. CONCLUSIONS: We found a high prevalence of sustained NOSVA during septic shock. NOSVA was not related to septic myocardial dysfunction, but rather to acute renal failure, raising the hypothesis of an acute renocardiac syndrome. Springer Paris 2015-09-22 /pmc/articles/PMC4579158/ /pubmed/26395899 http://dx.doi.org/10.1186/s13613-015-0069-5 Text en © Seemann et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Seemann, Aurélien
Boissier, Florence
Razazi, Keyvan
Carteaux, Guillaume
de Prost, Nicolas
Brun-Buisson, Christian
Mekontso Dessap, Armand
New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title_full New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title_fullStr New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title_full_unstemmed New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title_short New-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
title_sort new-onset supraventricular arrhythmia during septic shock: prevalence, risk factors and prognosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579158/
https://www.ncbi.nlm.nih.gov/pubmed/26395899
http://dx.doi.org/10.1186/s13613-015-0069-5
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