PT - JOURNAL ARTICLE AU - Luigi Pisani AU - Anna Geke Algera AU - Ary Serpa Neto AU - Areef Ahsan AU - Abigail Beane AU - Kaweesak Chittawatanarat AU - Abul Faiz AU - Rashan Haniffa AU - Reza Hashemian AU - Madiha Hashmi AU - Hisham Ahmed Imad AU - Kanishka Indraratna AU - Shivakumar Iyer AU - Gyan Kayastha AU - Bhuvana Krishna AU - Hassan Moosa AU - Behzad Nadjm AU - Rajyabardhan Pattnaik AU - Sriram Sampath AU - Louise Thwaites AU - Ni Ni Tun AU - Nor’azim Mohd Yunos AU - Salvatore Grasso AU - Frederique Paulus AU - Marcelo Gama de Abreu AU - Paolo Pelosi AU - Arjen M Dondorp AU - Marcus J Schultz ED - , TI - PRactice of VENTilation in Middle-Income Countries (PRoVENT-iMIC): rationale and protocol for a prospective international multicentre observational study in intensive care units in Asia AID - 10.1136/bmjopen-2017-020841 DP - 2018 Apr 01 TA - BMJ Open PG - e020841 VI - 8 IP - 4 4099 - http://bmjopen.bmj.com/content/8/4/e020841.short 4100 - http://bmjopen.bmj.com/content/8/4/e020841.full SO - BMJ Open2018 Apr 01; 8 AB - Introduction Current evidence on epidemiology and outcomes of invasively mechanically ventilated intensive care unit (ICU) patients is predominantly gathered in resource-rich settings. Patient casemix and patterns of critical illnesses, and probably also ventilation practices are likely to be different in resource-limited settings. We aim to investigate the epidemiological characteristics, ventilation practices and clinical outcomes of patients receiving mechanical ventilation in ICUs in Asia.Methods and analysis PRoVENT-iMIC (study of PRactice of VENTilation in Middle-Income Countries) is an international multicentre observational study to be undertaken in approximately 60 ICUs in 11 Asian countries. Consecutive patients aged 18 years or older who are receiving invasive ventilation in participating ICUs during a predefined 28-day period are to be enrolled, with a daily follow-up of 7 days. The primary outcome is ventilatory management (including tidal volume expressed as mL/kg predicted body weight and positive end-expiratory pressure expressed as cm H2O) during the first 3 days of mechanical ventilation—compared between patients at no risk for acute respiratory distress syndrome (ARDS), patients at risk for ARDS and in patients with ARDS (in case the diagnosis of ARDS can be made on admission). Secondary outcomes include occurrence of pulmonary complications and all-cause ICU mortality.Ethics and dissemination PRoVENT-iMIC will be the first international study that prospectively assesses ventilation practices, outcomes and epidemiology of invasively ventilated patients in ICUs in Asia. The results of this large study, to be disseminated through conference presentations and publications in international peer-reviewed journals, are of ultimate importance when designing trials of invasive ventilation in resource-limited ICUs. Access to source data will be made available through national or international anonymised datasets on request and after agreement of the PRoVENT-iMIC steering committee.Trial registration number NCT03188770; Pre-results.