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1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients

BACKGROUND: Pneumonia is the most common hospital-acquired infection; most cases occur in nonventilated patients, yet the majority of hospitals do not track nonventilator hospital-acquired pneumonia (NV-HAP) given the complexity and subjectivity of CDC’s current surveillance definition and large num...

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Autores principales: Ji, Wenjing, Smith, Cara, Zhang, Zilu, Ochoa, Aileen, Young, Jessica, Rhee, Chanu, Klompas, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252506/
http://dx.doi.org/10.1093/ofid/ofy210.1305
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author Ji, Wenjing
Smith, Cara
Zhang, Zilu
Ochoa, Aileen
Young, Jessica
Rhee, Chanu
Klompas, Michael
author_facet Ji, Wenjing
Smith, Cara
Zhang, Zilu
Ochoa, Aileen
Young, Jessica
Rhee, Chanu
Klompas, Michael
author_sort Ji, Wenjing
collection PubMed
description BACKGROUND: Pneumonia is the most common hospital-acquired infection; most cases occur in nonventilated patients, yet the majority of hospitals do not track nonventilator hospital-acquired pneumonia (NV-HAP) given the complexity and subjectivity of CDC’s current surveillance definition and large number of patients at risk. We sought to develop objective, electronically computable surveillance definitions for NV-HAP to facilitate routine surveillance. METHODS: We developed ten candidate definitions based on different combinations of 6 clinical indicators and applied them to 60,725 adult admissions of ≥3 days to Brigham and Women’s Hospital between July 2015 and June 2017. Potential indicators included worsening oxygenation, new antibiotics given for ≥3 days, fever, abnormal white blood cell count, chest imaging orders, and respiratory cultures on hospital day ≥3. Worsening oxygenation was defined as ≥2 days of decreased oxygen saturation or escalation in supplemental oxygen following ≥2 days of stable oxygenation. We calculated incidence and mortality rates for each definition. We then matched each case with up to four controls on the basis of clinical service and duration of hospitalization and measured associations between each definition and increased mortality and length of stay, adjusting for patients’ demographics, comorbidities, and severity of illness. RESULTS: The incidence of NV-HAP ranged from 7.6 events per 100 admissions with the least restrictive definition (worsening oxygenation alone), to 0.7 events per 100 admissions (worsening oxygenation, fever or leukocytosis, and new antibiotics), to 0.2 events per 100 admissions (all signs present). Crude mortality rates ranged from 17% to 30%. Odds ratios for mortality in cases vs. controls ranged from 4.3 (95% CI 3.8–5.0) to 8.5 (95% CI 6.3–11.4). Odds ratios for days-until-discharge in cases vs. controls ranged from 1.7 (95% CI 1.5–1.9) to 2.1 (95% CI 2.0–2.2). CONCLUSION: We demonstrate the feasibility of applying electronically computable objective surveillance definitions for NV-HAP. These definitions yield incidence and mortality rates comparable to existing estimates based on manual surveillance Methods. Further work is needed to better understand the clinical correlates of these events and their potential preventability. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62525062018-11-28 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients Ji, Wenjing Smith, Cara Zhang, Zilu Ochoa, Aileen Young, Jessica Rhee, Chanu Klompas, Michael Open Forum Infect Dis Abstracts BACKGROUND: Pneumonia is the most common hospital-acquired infection; most cases occur in nonventilated patients, yet the majority of hospitals do not track nonventilator hospital-acquired pneumonia (NV-HAP) given the complexity and subjectivity of CDC’s current surveillance definition and large number of patients at risk. We sought to develop objective, electronically computable surveillance definitions for NV-HAP to facilitate routine surveillance. METHODS: We developed ten candidate definitions based on different combinations of 6 clinical indicators and applied them to 60,725 adult admissions of ≥3 days to Brigham and Women’s Hospital between July 2015 and June 2017. Potential indicators included worsening oxygenation, new antibiotics given for ≥3 days, fever, abnormal white blood cell count, chest imaging orders, and respiratory cultures on hospital day ≥3. Worsening oxygenation was defined as ≥2 days of decreased oxygen saturation or escalation in supplemental oxygen following ≥2 days of stable oxygenation. We calculated incidence and mortality rates for each definition. We then matched each case with up to four controls on the basis of clinical service and duration of hospitalization and measured associations between each definition and increased mortality and length of stay, adjusting for patients’ demographics, comorbidities, and severity of illness. RESULTS: The incidence of NV-HAP ranged from 7.6 events per 100 admissions with the least restrictive definition (worsening oxygenation alone), to 0.7 events per 100 admissions (worsening oxygenation, fever or leukocytosis, and new antibiotics), to 0.2 events per 100 admissions (all signs present). Crude mortality rates ranged from 17% to 30%. Odds ratios for mortality in cases vs. controls ranged from 4.3 (95% CI 3.8–5.0) to 8.5 (95% CI 6.3–11.4). Odds ratios for days-until-discharge in cases vs. controls ranged from 1.7 (95% CI 1.5–1.9) to 2.1 (95% CI 2.0–2.2). CONCLUSION: We demonstrate the feasibility of applying electronically computable objective surveillance definitions for NV-HAP. These definitions yield incidence and mortality rates comparable to existing estimates based on manual surveillance Methods. Further work is needed to better understand the clinical correlates of these events and their potential preventability. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6252506/ http://dx.doi.org/10.1093/ofid/ofy210.1305 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Ji, Wenjing
Smith, Cara
Zhang, Zilu
Ochoa, Aileen
Young, Jessica
Rhee, Chanu
Klompas, Michael
1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title_full 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title_fullStr 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title_full_unstemmed 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title_short 1476. Objective Surveillance Definitions for Hospital-Acquired Pneumonia in Non-Ventilated Patients
title_sort 1476. objective surveillance definitions for hospital-acquired pneumonia in non-ventilated patients
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252506/
http://dx.doi.org/10.1093/ofid/ofy210.1305
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