Establishing Healthcare Worker Performance and Safety in Providing Critical Care for Patients in a Simulated Ebola Treatment Unit: Non-Randomized Pilot Study

Peter Kiiza(Sunnybrook Health Science Centre), Sarah Mullin(University of Toronto), Koren Teo(Canadian Armed Forces), Len Goodman(Defence Research and Development Canada), Adic Pérez(Sunnybrook Health Science Centre), Ruxandra Pinto(Sunnybrook Health Science Centre), Kelly Thompson(UNSW Sydney), Dominique Piquette(Sunnybrook Health Science Centre), Trevor Hall(University of Toronto), Elhadj Ibrahima Bah(Donka Hospital), Christian Sandrock(Island Health), Jan Hájek(University of British Columbia), Raymond Kao(Western University), François Lamontagne(Université de Sherbrooke), John C. Marshall(St. Michael's Hospital), Sharmistha Mishra(St. Michael's Hospital), Srinivas Murthy(University of British Columbia), Abel Vanderschuren(Université Laval), Robert Fowler(Sunnybrook Health Science Centre), Neill K. J. Adhikari(Sunnybrook Health Science Centre)
Viruses
November 2, 2021
Cited by 3Open Access
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Abstract

Improving the provision of supportive care for patients with Ebola is an important quality improvement initiative. We designed a simulated Ebola Treatment Unit (ETU) to assess performance and safety of healthcare workers (HCWs) performing tasks wearing personal protective equipment (PPE) in hot (35 °C, 60% relative humidity) or thermo-neutral (20 °C, 20% relative humidity) conditions. In this pilot phase to determine the feasibility of study procedures, HCWs in PPE were non-randomly allocated to hot or thermo-neutral conditions to perform peripheral intravenous (PIV) and midline catheter (MLC) insertion and endotracheal intubation (ETI) on mannequins. Eighteen HCWs (13 physicians, 4 nurses, 1 nurse practitioner; 2 with prior ETU experience; 10 in hot conditions) spent 69 (10) (mean (SD)) minutes in the simulated ETU. Mean (SD) task completion times were 16 (6) min for PIV insertion; 33 (5) min for MLC insertion; and 16 (8) min for ETI. Satisfactory task completion was numerically higher for physicians vs. nurses. Participants’ blood pressure was similar, but heart rate was higher (p = 0.0005) post-simulation vs. baseline. Participants had a median (range) of 2.0 (0.0–10.0) minor PPE breaches, 2.0 (0.0–6.0) near-miss incidents, and 2.0 (0.0–6.0) health symptoms and concerns. There were eight health-assessment triggers in five participants, of whom four were in hot conditions. We terminated the simulation of two participants in hot conditions due to thermal discomfort. In summary, study tasks were suitable for physician participants, but they require redesign to match nurses’ expertise for the subsequent randomized phase of the study. One-quarter of participants had a health-assessment trigger. This research model may be useful in future training and research regarding clinical care for patients with highly infectious pathogens in austere settings.


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