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Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis

There is limited evidence about the prognostic utility of right ventricular dysfunction (RVD) in patients with coronavirus disease 2019 (COVID‐19). We assessed the association between RVD and mortality in COVID‐19 patients. We searched electronic databases from inception to February 15, 2021. RVD wa...

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Autores principales: Diaz‐Arocutipa, Carlos, Saucedo‐Chinchay, Jose, Argulian, Edgar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495092/
https://www.ncbi.nlm.nih.gov/pubmed/34528706
http://dx.doi.org/10.1002/clc.23719
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author Diaz‐Arocutipa, Carlos
Saucedo‐Chinchay, Jose
Argulian, Edgar
author_facet Diaz‐Arocutipa, Carlos
Saucedo‐Chinchay, Jose
Argulian, Edgar
author_sort Diaz‐Arocutipa, Carlos
collection PubMed
description There is limited evidence about the prognostic utility of right ventricular dysfunction (RVD) in patients with coronavirus disease 2019 (COVID‐19). We assessed the association between RVD and mortality in COVID‐19 patients. We searched electronic databases from inception to February 15, 2021. RVD was defined based on the following echocardiographic variables: tricuspid annular plane systolic excursion (TAPSE), tricuspid S′ peak systolic velocity, fractional area change (FAC), and right ventricular free wall longitudinal strain (RVFWLS). All meta‐analyses were performed using a random‐effects model. Nineteen cohort studies involving 2307 patients were included. The mean age ranged from 59 to 72 years and 65% of patients were male. TAPSE (mean difference [MD], −3.13 mm; 95% confidence interval [CI], −4.08–−2.19), tricuspid S′ peak systolic velocity (MD, −0.88 cm/s; 95% CI, −1.68 to −0.08), FAC (MD, −3.47%; 95% CI, −6.21 to −0.72), and RVFWLS (MD, −5.83%; 95% CI, −7.47–−4.20) were significantly lower in nonsurvivors compared to survivors. Each 1 mm decrease in TAPSE (adjusted hazard ratio [aHR], 1.22; 95% CI, 1.08–1.37), 1% decrease in FAC (aHR, 1.09; 95% CI, 1.04–1.14), and 1% increase in RVFWLS (aHR, 1.33; 95% CI, 1.19–1.48) were independently associated with higher mortality. RVD was significantly associated with higher mortality using unadjusted risk ratio (2.05; 95% CI, 1.27–3.31), unadjusted hazard ratio (3.37; 95% CI, 1.72–6.62), and adjusted hazard ratio (aHR, 2.75; 95% CI, 1.52–4.96). Our study shows that echocardiographic parameters of RVD were associated with an increased risk of mortality in COVID‐19 patients.
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spelling pubmed-84950922021-10-08 Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis Diaz‐Arocutipa, Carlos Saucedo‐Chinchay, Jose Argulian, Edgar Clin Cardiol Reviews There is limited evidence about the prognostic utility of right ventricular dysfunction (RVD) in patients with coronavirus disease 2019 (COVID‐19). We assessed the association between RVD and mortality in COVID‐19 patients. We searched electronic databases from inception to February 15, 2021. RVD was defined based on the following echocardiographic variables: tricuspid annular plane systolic excursion (TAPSE), tricuspid S′ peak systolic velocity, fractional area change (FAC), and right ventricular free wall longitudinal strain (RVFWLS). All meta‐analyses were performed using a random‐effects model. Nineteen cohort studies involving 2307 patients were included. The mean age ranged from 59 to 72 years and 65% of patients were male. TAPSE (mean difference [MD], −3.13 mm; 95% confidence interval [CI], −4.08–−2.19), tricuspid S′ peak systolic velocity (MD, −0.88 cm/s; 95% CI, −1.68 to −0.08), FAC (MD, −3.47%; 95% CI, −6.21 to −0.72), and RVFWLS (MD, −5.83%; 95% CI, −7.47–−4.20) were significantly lower in nonsurvivors compared to survivors. Each 1 mm decrease in TAPSE (adjusted hazard ratio [aHR], 1.22; 95% CI, 1.08–1.37), 1% decrease in FAC (aHR, 1.09; 95% CI, 1.04–1.14), and 1% increase in RVFWLS (aHR, 1.33; 95% CI, 1.19–1.48) were independently associated with higher mortality. RVD was significantly associated with higher mortality using unadjusted risk ratio (2.05; 95% CI, 1.27–3.31), unadjusted hazard ratio (3.37; 95% CI, 1.72–6.62), and adjusted hazard ratio (aHR, 2.75; 95% CI, 1.52–4.96). Our study shows that echocardiographic parameters of RVD were associated with an increased risk of mortality in COVID‐19 patients. Wiley Periodicals, Inc. 2021-09-16 /pmc/articles/PMC8495092/ /pubmed/34528706 http://dx.doi.org/10.1002/clc.23719 Text en © 2021 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Diaz‐Arocutipa, Carlos
Saucedo‐Chinchay, Jose
Argulian, Edgar
Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title_full Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title_fullStr Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title_full_unstemmed Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title_short Association between right ventricular dysfunction and mortality in COVID‐19 patients: A systematic review and meta‐analysis
title_sort association between right ventricular dysfunction and mortality in covid‐19 patients: a systematic review and meta‐analysis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495092/
https://www.ncbi.nlm.nih.gov/pubmed/34528706
http://dx.doi.org/10.1002/clc.23719
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