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Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis
IMPORTANCE: Efforts to quantify the burden of SARS-CoV-2–associated sepsis have been limited by inconsistent definitions and underrecognition of viral sepsis. OBJECTIVE: To describe the incidence and outcomes of SARS-CoV-2–associated sepsis vs presumed bacterial sepsis using objective electronic cli...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543118/ https://www.ncbi.nlm.nih.gov/pubmed/37773495 http://dx.doi.org/10.1001/jamanetworkopen.2023.35728 |
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author | Shappell, Claire N. Klompas, Michael Chan, Christina Chen, Tom Kanjilal, Sanjat McKenna, Caroline Rhee, Chanu |
author_facet | Shappell, Claire N. Klompas, Michael Chan, Christina Chen, Tom Kanjilal, Sanjat McKenna, Caroline Rhee, Chanu |
author_sort | Shappell, Claire N. |
collection | PubMed |
description | IMPORTANCE: Efforts to quantify the burden of SARS-CoV-2–associated sepsis have been limited by inconsistent definitions and underrecognition of viral sepsis. OBJECTIVE: To describe the incidence and outcomes of SARS-CoV-2–associated sepsis vs presumed bacterial sepsis using objective electronic clinical criteria. DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study included adults hospitalized at 5 Massachusetts hospitals between March 2020 and November 2022. EXPOSURES: SARS-CoV-2–associated sepsis was defined as a positive SARS-CoV-2 polymerase chain reaction test and concurrent organ dysfunction (ie, oxygen support above simple nasal cannula, vasopressors, elevated lactate level, rise in creatine or bilirubin level, and/or decline in platelets). Presumed bacterial sepsis was defined by modified US Centers for Disease Control and Prevention adult sepsis event criteria (ie, blood culture order, sustained treatment with antibiotics, and organ dysfunction using identical thresholds as for SARS-CoV-2–associated sepsis). MAIN OUTCOMES AND MEASURES: Trends in the quarterly incidence (ie, proportion of hospitalizations) and in-hospital mortality for SARS-CoV-2–associated and presumed bacterial sepsis were assessed using negative binomial and logistic regression models. RESULTS: This study included 431 017 hospital encounters from 261 595 individuals (mean [SD] age 57.9 [19.8] years, 241 131 (55.9%) females, 286 397 [66.5%] from academic hospital site). Of these encounters, 23 276 (5.4%) were from SARS-CoV-2, 6558 (1.5%) had SARS-CoV-2–associated sepsis, and 30 604 patients (7.1%) had presumed bacterial sepsis without SARS-CoV-2 infection. Crude in-hospital mortality for SARS-CoV-2–associated sepsis declined from 490 of 1469 (33.4%) in the first quarter to 67 of 450 (14.9%) in the last (adjusted odds ratio [aOR], 0.88 [95% CI, 0.85-0.90] per quarter). Crude mortality for presumed bacterial sepsis was 4451 of 30 604 patients (14.5%) and stable across quarters (aOR, 1.00 [95% CI, 0.99-1.01]). Medical record reviews of 200 SARS-CoV-2–positive hospitalizations confirmed electronic health record (EHR)–based SARS-CoV-2–associated sepsis criteria performed well relative to sepsis-3 criteria (90.6% [95% CI, 80.7%-96.5%] sensitivity; 91.2% [95% CI, 85.1%-95.4%] specificity). CONCLUSIONS AND RELEVANCE: In this retrospective cohort study of hospitalized adults, SARS-CoV-2 accounted for approximately 1 in 6 cases of sepsis during the first 33 months of the COVID-19 pandemic. In-hospital mortality rates for SARS-CoV-2–associated sepsis were high but declined over time and ultimately were similar to presumed bacterial sepsis. These findings highlight the high burden of SARS-CoV-2–associated sepsis and demonstrate the utility of EHR-based algorithms to conduct surveillance for viral and bacterial sepsis. |
format | Online Article Text |
id | pubmed-10543118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-105431182023-10-03 Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis Shappell, Claire N. Klompas, Michael Chan, Christina Chen, Tom Kanjilal, Sanjat McKenna, Caroline Rhee, Chanu JAMA Netw Open Original Investigation IMPORTANCE: Efforts to quantify the burden of SARS-CoV-2–associated sepsis have been limited by inconsistent definitions and underrecognition of viral sepsis. OBJECTIVE: To describe the incidence and outcomes of SARS-CoV-2–associated sepsis vs presumed bacterial sepsis using objective electronic clinical criteria. DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study included adults hospitalized at 5 Massachusetts hospitals between March 2020 and November 2022. EXPOSURES: SARS-CoV-2–associated sepsis was defined as a positive SARS-CoV-2 polymerase chain reaction test and concurrent organ dysfunction (ie, oxygen support above simple nasal cannula, vasopressors, elevated lactate level, rise in creatine or bilirubin level, and/or decline in platelets). Presumed bacterial sepsis was defined by modified US Centers for Disease Control and Prevention adult sepsis event criteria (ie, blood culture order, sustained treatment with antibiotics, and organ dysfunction using identical thresholds as for SARS-CoV-2–associated sepsis). MAIN OUTCOMES AND MEASURES: Trends in the quarterly incidence (ie, proportion of hospitalizations) and in-hospital mortality for SARS-CoV-2–associated and presumed bacterial sepsis were assessed using negative binomial and logistic regression models. RESULTS: This study included 431 017 hospital encounters from 261 595 individuals (mean [SD] age 57.9 [19.8] years, 241 131 (55.9%) females, 286 397 [66.5%] from academic hospital site). Of these encounters, 23 276 (5.4%) were from SARS-CoV-2, 6558 (1.5%) had SARS-CoV-2–associated sepsis, and 30 604 patients (7.1%) had presumed bacterial sepsis without SARS-CoV-2 infection. Crude in-hospital mortality for SARS-CoV-2–associated sepsis declined from 490 of 1469 (33.4%) in the first quarter to 67 of 450 (14.9%) in the last (adjusted odds ratio [aOR], 0.88 [95% CI, 0.85-0.90] per quarter). Crude mortality for presumed bacterial sepsis was 4451 of 30 604 patients (14.5%) and stable across quarters (aOR, 1.00 [95% CI, 0.99-1.01]). Medical record reviews of 200 SARS-CoV-2–positive hospitalizations confirmed electronic health record (EHR)–based SARS-CoV-2–associated sepsis criteria performed well relative to sepsis-3 criteria (90.6% [95% CI, 80.7%-96.5%] sensitivity; 91.2% [95% CI, 85.1%-95.4%] specificity). CONCLUSIONS AND RELEVANCE: In this retrospective cohort study of hospitalized adults, SARS-CoV-2 accounted for approximately 1 in 6 cases of sepsis during the first 33 months of the COVID-19 pandemic. In-hospital mortality rates for SARS-CoV-2–associated sepsis were high but declined over time and ultimately were similar to presumed bacterial sepsis. These findings highlight the high burden of SARS-CoV-2–associated sepsis and demonstrate the utility of EHR-based algorithms to conduct surveillance for viral and bacterial sepsis. American Medical Association 2023-09-29 /pmc/articles/PMC10543118/ /pubmed/37773495 http://dx.doi.org/10.1001/jamanetworkopen.2023.35728 Text en Copyright 2023 Shappell CN et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Shappell, Claire N. Klompas, Michael Chan, Christina Chen, Tom Kanjilal, Sanjat McKenna, Caroline Rhee, Chanu Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title | Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title_full | Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title_fullStr | Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title_full_unstemmed | Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title_short | Use of Electronic Clinical Data to Track Incidence and Mortality for SARS-CoV-2–Associated Sepsis |
title_sort | use of electronic clinical data to track incidence and mortality for sars-cov-2–associated sepsis |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543118/ https://www.ncbi.nlm.nih.gov/pubmed/37773495 http://dx.doi.org/10.1001/jamanetworkopen.2023.35728 |
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