Application of ventilator-associated events (VAE) in ventilator-associated pneumonia (VAP) notified in Brazil (IMPACTO MR-PAV): a protocol for a cohort study

Author:

Nascimento Giovanna Marssola,Gomes Rodrigues Daniela Laranja,Mangas Catarino Daniela Ghidetti,Piastrelli Filipe Teixeira,Cheno Maysa Yukari,Braz Katia Cristina Camonda,Oliveira Alves Lucas Bassolli,Avezum Álvaro,Veiga Viviane CORCID,Zavascki Alexandre Prehn,Tomazini Bruno,Besen BrunoORCID,Pereira Adriano José,Marques de Pinho Ana Paula Neves,De Oliveira Junior Haliton AlvesORCID

Abstract

IntroductionCertain criteria for ventilator-associated events (VAE) definition might influence the type of an event, its detection rate and consequently the resource expenditure in intensive care unit. TheImpact of Infections by Antimicrobial-Resistant Microorganisms - Ventilator-Associated Pneumonia(IMPACTO MR-PAV) aims to evaluate the incidence and diagnostic accuracy of ventilator-associated pneumonia (VAP) using the current criteria for VAP surveillance in Brazil versus the VAE criteria defined by the US National Healthcare Safety Network-Center for Diseases Control and Prevention (CDC) criteria.Methods and analysisThe study will be conducted in around 15 centres across Brazil from October 2022 to December 2023. Trained healthcare professionals will collect data and compare the incidence of VAP using both the current criteria for VAP surveillance in Brazil and the VAE criteria defined by the CDC. The accuracy of the two criteria for identifying VAP will also be analysed. It will also characterise other events associated with mechanical ventilation (ventilator-associated condition, infection-related ventilator-associated complication) and adjudicate VAP reported to the Brazilian Health Regulatory Agency (ANVISA) using current epidemiological diagnostic criteria.Ethics and disseminationThis study was approved by the Institutional Review Board under the number 52354721.0.1001.0070. The study’s primary outcome measure will be the incidence of VAP using the two different surveillance criteria, and the secondary outcome measures will be the accuracy of the two criteria for identifying VAP and the adjudication of VAP reported to ANVISA. The results will contribute to the improvement of VAP surveillance in Brazil and may have implications for other countries that use similar criteria.Trial registration numberNCT05589727; Clinicaltrials.gov.

Funder

PROADI-SUS

Publisher

BMJ

Subject

General Medicine

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