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1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit
BACKGROUND: Ventilator-associated tracheitis (VAT) is a common intensive-care unit entity considered in febrile patients with endotracheal intubation or with tracheostomy. Prospective-Audit-And-Feedback activities had identified an overall increased and high inter-provider-variability in the use of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6808820/ http://dx.doi.org/10.1093/ofid/ofz360.1006 |
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author | Iacono, Denise Tanweer, Ammara Sweberg, Todd Hagmann, Stefan Chua, Vincent DeCelie-Germana, Joan Tsirilakis, Kalliopi |
author_facet | Iacono, Denise Tanweer, Ammara Sweberg, Todd Hagmann, Stefan Chua, Vincent DeCelie-Germana, Joan Tsirilakis, Kalliopi |
author_sort | Iacono, Denise |
collection | PubMed |
description | BACKGROUND: Ventilator-associated tracheitis (VAT) is a common intensive-care unit entity considered in febrile patients with endotracheal intubation or with tracheostomy. Prospective-Audit-And-Feedback activities had identified an overall increased and high inter-provider-variability in the use of antibiotics for VAT. By developing a VAT-specific guideline, we intended primarily to decrease the amount of respiratory fluid cultures (RFCx) submitted, and secondly decrease the overall antibiotic use (AU) in the PICU, while not increasing the incidence of ventilator-associated events (VAE). METHODS: A multidisciplinary team developed a guideline for patients with fever or change in baseline respiratory support with endotracheal intubation or with tracheostomy who had no radiographic evidence of pneumonia consisting of three parts: A) When to send an RFCx, B) Diagnosis of VAT, C) Antibiotic management of VAT: A) To obtain a RFCx, patient needed to have an abnormal white cell count (WBC) ( <5 K/uL or >14.5 K/uL) AND purulent or increased amount of endotracheal secretions PLUS either abnormal body temperature (T <36°C or ≥38.3°C) or change in baseline respiratory support. B) A diagnosis of VAT is allowed if RFCx shows Gram stain with ≥+3 WBC AND ≥+3 bacteria. C) Empiric antibiotic treatment with antipseudomonal activity (informed by previous RFCx if exist) to be started after RFCx have been obtained. Reassessment and possible modification at 48H based on final RFCx results. Duration of AU to be limited to 5 days. Guideline education was completed at multiple PICU meetings from September 2017 through June 2018. Manual audits were used to analyze adherence to the guideline. Data on RFCx order utilization, ventilator days, and AU from January 2017 to December 2018 were analyzed. RESULTS: Since the initiation of the guideline, we observed a downward trend of RFCx orders (Fig1.A) with an average decrease of 19% after guideline implementation. The overall AU (Fig1.B) in PICU decreased by an average of 24% while the incidence of VAE has remained stable. CONCLUSION: Efforts to standardize diagnosis and treatment of VAT in patients with endotracheal intubation or tracheostomy resulted in a decreased number of RFCx, and reduced overall AU without increasing the risk of VAE. [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6808820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68088202019-10-28 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit Iacono, Denise Tanweer, Ammara Sweberg, Todd Hagmann, Stefan Chua, Vincent DeCelie-Germana, Joan Tsirilakis, Kalliopi Open Forum Infect Dis Abstracts BACKGROUND: Ventilator-associated tracheitis (VAT) is a common intensive-care unit entity considered in febrile patients with endotracheal intubation or with tracheostomy. Prospective-Audit-And-Feedback activities had identified an overall increased and high inter-provider-variability in the use of antibiotics for VAT. By developing a VAT-specific guideline, we intended primarily to decrease the amount of respiratory fluid cultures (RFCx) submitted, and secondly decrease the overall antibiotic use (AU) in the PICU, while not increasing the incidence of ventilator-associated events (VAE). METHODS: A multidisciplinary team developed a guideline for patients with fever or change in baseline respiratory support with endotracheal intubation or with tracheostomy who had no radiographic evidence of pneumonia consisting of three parts: A) When to send an RFCx, B) Diagnosis of VAT, C) Antibiotic management of VAT: A) To obtain a RFCx, patient needed to have an abnormal white cell count (WBC) ( <5 K/uL or >14.5 K/uL) AND purulent or increased amount of endotracheal secretions PLUS either abnormal body temperature (T <36°C or ≥38.3°C) or change in baseline respiratory support. B) A diagnosis of VAT is allowed if RFCx shows Gram stain with ≥+3 WBC AND ≥+3 bacteria. C) Empiric antibiotic treatment with antipseudomonal activity (informed by previous RFCx if exist) to be started after RFCx have been obtained. Reassessment and possible modification at 48H based on final RFCx results. Duration of AU to be limited to 5 days. Guideline education was completed at multiple PICU meetings from September 2017 through June 2018. Manual audits were used to analyze adherence to the guideline. Data on RFCx order utilization, ventilator days, and AU from January 2017 to December 2018 were analyzed. RESULTS: Since the initiation of the guideline, we observed a downward trend of RFCx orders (Fig1.A) with an average decrease of 19% after guideline implementation. The overall AU (Fig1.B) in PICU decreased by an average of 24% while the incidence of VAE has remained stable. CONCLUSION: Efforts to standardize diagnosis and treatment of VAT in patients with endotracheal intubation or tracheostomy resulted in a decreased number of RFCx, and reduced overall AU without increasing the risk of VAE. [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6808820/ http://dx.doi.org/10.1093/ofid/ofz360.1006 Text en © The Author(s) 2019. 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 Iacono, Denise Tanweer, Ammara Sweberg, Todd Hagmann, Stefan Chua, Vincent DeCelie-Germana, Joan Tsirilakis, Kalliopi 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title | 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title_full | 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title_fullStr | 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title_full_unstemmed | 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title_short | 1142. Implementation and Impact of a Tracheitis Diagnosis and Management Guideline in a Pediatric Intensive Care Unit |
title_sort | 1142. implementation and impact of a tracheitis diagnosis and management guideline in a pediatric intensive care unit |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6808820/ http://dx.doi.org/10.1093/ofid/ofz360.1006 |
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