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Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction

BACKGROUND: Over five million Americans suffer from heart failure (HF), and this is associated with multiple chronic comorbidities and recurrent decompensation. Currently, there is an increased incidence in vaccine‐preventable diseases (VPDs). We aim to investigate the impact of HF with reduced ejec...

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Autores principales: Del Cid Fratti, Juan, Salazar, Miguel, Argueta‐Sosa, Erwin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045068/
https://www.ncbi.nlm.nih.gov/pubmed/35266175
http://dx.doi.org/10.1002/clc.23800
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author Del Cid Fratti, Juan
Salazar, Miguel
Argueta‐Sosa, Erwin E.
author_facet Del Cid Fratti, Juan
Salazar, Miguel
Argueta‐Sosa, Erwin E.
author_sort Del Cid Fratti, Juan
collection PubMed
description BACKGROUND: Over five million Americans suffer from heart failure (HF), and this is associated with multiple chronic comorbidities and recurrent decompensation. Currently, there is an increased incidence in vaccine‐preventable diseases (VPDs). We aim to investigate the impact of HF with reduced ejection fraction (HFrEF) in patients hospitalized with VPDs. HYPOTHESIS: Patient with HFrEF are at higher risk for VPDs and they carry a higher risk for in‐hospital complications. METHODS: Retrospective analysis from all hospital admissions from the 2016‐2018 National Inpatient Sample (NIS) using the ICD‐10CM codes for patients admitted with a primary diagnosis of VPDs with HFrEF and those without reduced ejection fraction. Outcomes evaluated were in‐hospital mortality, length of stay (LOS), healthcare utilization, frequency of admissions, and in‐hospital complications. Multivariate regression analysis was conducted to adjust for confounders. RESULTS: Out of 317 670 VPDs discharges, we identified 12 130 (3.8%) patients with HFrEF as a comorbidity. The most common admission diagnosis for VPDs was influenza virus (IV) infection (75.0% vs. 64.1%; p < .01), followed by pneumococcal pneumonia (PNA) (13% vs. 9.4%; p < .01). After adjusting for confounders, patients with HFrEF had higher odds of having diagnosis of IV (adjusted [aOR], 1.42; p < .01) and PNA (aOR, 1.27; p < .01). Patients with VPDs and HFrEF had significantly higher odds of mortality (aOR, 1.76; p < .01), LOS, respiratory failure requiring mechanical ventilation, and mechanical ventilation for less than 96 h. CONCLUSION: Influenza and PNA were the most common VPDs admitted to the hospital in patients with a concomitant diagnosis of HFrEF. They were associated with increased mortality and in‐hospital complications.
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spelling pubmed-90450682022-04-28 Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction Del Cid Fratti, Juan Salazar, Miguel Argueta‐Sosa, Erwin E. Clin Cardiol Clinical Investigations BACKGROUND: Over five million Americans suffer from heart failure (HF), and this is associated with multiple chronic comorbidities and recurrent decompensation. Currently, there is an increased incidence in vaccine‐preventable diseases (VPDs). We aim to investigate the impact of HF with reduced ejection fraction (HFrEF) in patients hospitalized with VPDs. HYPOTHESIS: Patient with HFrEF are at higher risk for VPDs and they carry a higher risk for in‐hospital complications. METHODS: Retrospective analysis from all hospital admissions from the 2016‐2018 National Inpatient Sample (NIS) using the ICD‐10CM codes for patients admitted with a primary diagnosis of VPDs with HFrEF and those without reduced ejection fraction. Outcomes evaluated were in‐hospital mortality, length of stay (LOS), healthcare utilization, frequency of admissions, and in‐hospital complications. Multivariate regression analysis was conducted to adjust for confounders. RESULTS: Out of 317 670 VPDs discharges, we identified 12 130 (3.8%) patients with HFrEF as a comorbidity. The most common admission diagnosis for VPDs was influenza virus (IV) infection (75.0% vs. 64.1%; p < .01), followed by pneumococcal pneumonia (PNA) (13% vs. 9.4%; p < .01). After adjusting for confounders, patients with HFrEF had higher odds of having diagnosis of IV (adjusted [aOR], 1.42; p < .01) and PNA (aOR, 1.27; p < .01). Patients with VPDs and HFrEF had significantly higher odds of mortality (aOR, 1.76; p < .01), LOS, respiratory failure requiring mechanical ventilation, and mechanical ventilation for less than 96 h. CONCLUSION: Influenza and PNA were the most common VPDs admitted to the hospital in patients with a concomitant diagnosis of HFrEF. They were associated with increased mortality and in‐hospital complications. John Wiley and Sons Inc. 2022-03-10 /pmc/articles/PMC9045068/ /pubmed/35266175 http://dx.doi.org/10.1002/clc.23800 Text en © 2022 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 Clinical Investigations
Del Cid Fratti, Juan
Salazar, Miguel
Argueta‐Sosa, Erwin E.
Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title_full Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title_fullStr Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title_full_unstemmed Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title_short Vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
title_sort vaccine‐preventable disease hospitalized patients with heart failure with reduced ejection fraction
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045068/
https://www.ncbi.nlm.nih.gov/pubmed/35266175
http://dx.doi.org/10.1002/clc.23800
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