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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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. |
format | Online Article Text |
id | pubmed-6252506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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