Feasibility and Acceptability Followed by Effectiveness of bCPAP for Treatment of Children Aged 1-59 Months With Severe Pneumonia in Ethiopia

Overview

Principal Investigator: Mohammod Jobayer Chisti Research Protocol Title: Feasibility and Acceptability Followed by Effectiveness of Bubble Continuous Positive Airway Pressure (bCPAP) for Treatment of Children aged 1-59 months with Severe Pneumonia in Ethiopia: A Cluster Randomized Controlled Clinical Trial Proposed start date: 1st July 2018, Estimated end date: 31st December 2022 Background: Feasibility and acceptability followed by effectiveness of bubble continuous positive airway pressure (CPAP) were not evaluated in childhood severe pneumonia in developing countries at a larger scale. Objectives: Stages I and II * To assess the feasibility and acceptability (not only by patients' care-givers but also by physicians and nurses) of bubble CPAP in treating childhood severe pneumonia in two tertiary hospitals in Stage I and in two district hospitals in Stage II * To record adverse events following use of bubble CPAP in these settings * To understand how much resource and time are needed to institutionalize and maintain bubble CPAP as a routine practice in the health system Stage III: * To determine therapeutic efficacy/effectiveness of bubble CPAP compared to WHO standard low flow oxygen in reducing treatment failure in children admitted to hospitals with severe pneumonia and hypoxemia * To determine therapeutic effectiveness of bubble CPAP compared to WHO standard low flow oxygen in reducing treatment failure \& mortality in children aged 1-12 months admitted to hospitals with severe pneumonia and hypoxemia * To record adverse events (pneumothorax, abdominal distension, nasal trauma, aspiration pneumonia) encountered.

Methodology: Cluster randomized controlled clinical trial Methodology: 1. Stages I and II: Feasibility/demonstration stage will be done as an internal pilot in 3 hospitals a. Current treatment practice, facilities, and operational challenges will be evaluated for the introduction, clinical use and maintenance of bubble CPAP 2. Stage III: Implementation of bubble CPAP will be done in 12 hospitals a. It will be done following a cluster randomized design Data collection-socio-demographic and clinical data will be collected using structured questionnaire by trained nurses and physicians. Research Site: St. Paulos Millennium Medical College, Yekatit 12 and Tikur Anbessa Specialized hospitals, 14 district hospitals Number of Participants/Patients: Stage I-30 children in each tertiary hospital (this stage has completed and we enrolled 49 children from two tertiary hospitals; these 49 enrolled children took double of our anticipated time {4 months}) Stage II- 20 children in each general hospital (2 general/district hospitals, we have enrolled total 40 children from this two hospitals from January 2020 to July 2020, which included COVID-19 period) Stage III-1240 children in 12 general/district hospitals (620 in bubble CPAP arm and 620 in WHO standard low flow arm; each hospital will be the cluster and 6 will be randomized to each arm) Main Inclusion Criteria: * Age between 1 month and 59 months * Meet WHO clinical criteria for severe pneumonia with hypoxemia * Hypoxemia (Oxygen saturation \<90% in room air) * Parent/guardian gives informed consent to participate in the study Statistical Analysis: * STATA -14: for initial two phases descriptive analysis of level of feasibility and acceptability will be performed * For the phase III: We shall follow the principle of intention to treat. --Treatment failure and/or death will be analyzed using χ² or Fisher's exact tests as appropriate. * Primary and secondary outcomes will be compared by calculating relative risks (RRs) and their 95% confidence intervals. * Log-linear binomial regression will be applied to adjust for covariates to evaluate the true impact of bubble CPAP in evaluating primary and secondary outcomes and to adjust for baseline differences. * Continuous variables will be analyzed using the Student t-test or the Mann-Whitney test as appropriate. Study Duration: 48 months.