Perceived Workload Using Separate (Filtering Facepiece Respirator and Face Shield) and Powered Air-Purifying Respirator and Integrated Lightweight Protective Air-Purifying Respirator: Protocol for an International Multisite Human Factors Randomized Crossover Feasibility Study

  • Amy PRICE
  • , Ying Ling LIN
  • , Anna S. LEVIN
  • , Fabio TUMIETTO
  • , Rodrigo ALMEIDA
  • , Ana ALMEIDA
  • , Caroline Lopes CIOFI-SILVA
  • , Luca FONTANA
  • , Naila OLIVEIRA
  • , Nicola Francesco PARISI
  • , Giulia Marcelino MAINARDI
  • , Luciana CORDEIRO
  • , Marco ROSELLI
  • , Paul SHEPHERD
  • , Luana MORELLI
  • , Najmeh MEHRABI
  • , Kathleen PRICE
  • , Whitney CHAN
  • , Shrinidhy SRINIVAS
  • , T. Kyle HARRISON
  • May CHU, Maria Clara PADOVEZE, Larry CHU*
*Corresponding author for this work

Research output: Journal PublicationsJournal Article (refereed)peer-review

1 Citation (Scopus)

Abstract

Background: The design of personal protective equipment (PPE) may affect well-being and clinical work. PPE as an integrated item may improve usability and increase adherence by healthcare professionals. Human factors design and safety may reduce occupational-acquired diseases. As an integrated PPE, a lightweight protective air-purifying respirator (L-PAPR) could be used during health procedures where healthcare professionals are exposed to airborne pathogens. The human factors affecting the implementation of alternative PPE such as L-PAPR have not been thoroughly studied. The population of interest is health care professionals, the intervention is the performance by PPE during tasks across the three PPE types 1.) N95 respirators and face shields, 2.)traditional powered air-purifying respirator(PAPR), and 3.) L-PAPR. The outcomes are user error, communications, safety, and end-user preferences. Objective: This study will assess whether the L-PAPR improves health care professionals’ comfort in terms of perceived workload and physical and psychological burden during direct patient care when compared with the traditional PAPR or N95 and face shield. This study also aims to evaluate human factors during the comparison of the use of L-PAPR with a combination of N95 respirators plus face shields or the traditional PAPRs. Methods: This is an interventional randomized crossover quality improvement feasibility study consisting of a 3-site simulation phase with 10 participants per site and subsequent field testing in 2 sites with 30 participants at each site. The 3 types of respiratory PPE will be compared across medical tasks and while donning and doffing. We will evaluate the user’s perceived workload, usability, usage errors, and heart rate. We will conduct semistructured interviews to identify barriers and enablers to implementation across each PPE type over a single continuous wear episode and observe interpersonal communications across conditions and PPE types. Results: We expect the research may highlight communication challenges and differences in usability and convenience across PPE types along with error frequency during PPE use across PPE types, tasks, and time. Conclusions: The design of PPE may affect overall well-being and hinder or facilitate clinical work. Combining 2 pieces of PPE into a single integrated item may improve usability and reduce occupational-acquired diseases. The human factors affecting the implementation of an alternative PPE such as L-PAPR or PAPR have not been thoroughly studied. International Registered Report Identifier (IRRID): PRR1-10.2196/36549

Original languageEnglish
Article numbere36549
Number of pages13
JournalJMIR Research Protocols
Volume11
Issue number12
DOIs
Publication statusPublished - Dec 2022
Externally publishedYes

Bibliographical note

Edited by T Leung
Publisher Copyright:
©Amy Price, Ying Ling Lin, Anna S Levin, Fabio Tumietto, Rodrigo Almeida, Ana Almeida, Caroline Lopes Ciofi-Silva, Luca Fontana, Naila Oliveira, Nicola Francesco Parisi, Giulia Marcelino Mainardi, Luciana Cordeiro, Marco Roselli, Paul Shepherd, Luana Morelli, Najmeh Mehrabi, Kathleen Price, Whitney Chan, Shrinidhy Srinivas, T Kyle Harrison, May Chu, Maria Clara Padoveze, Larry Chu.

Funding

The authors acknowledge that funds for the project were provided by WHO based on a grant from the German Federal Ministry of Health. We acknowledge the support and administration staff at each of our sites. MC is our principal investigator for the DeMaND2 bundle of which Stanford is a part. We are thankful to Aishini Damaris and Adam Soomro of the Stanford Anesthesia Summer Institute Research Track 2020 for their contributions to the background and their comments on our study design and human factors. We are thankful to Hexoskin Corporation who supplied us with wearables for comparisons with the smartwatch, to Withings for their technology and database assistance, and to 3M for donating PAPRs to Bologna and Stanford. We appreciate the improvements to the L-PAPRs and regular PAPRs provided by 3M and TIKI based on our preliminary feedback and their generous provision of training and media materials.

Keywords

  • N95
  • SARS-CoV-2
  • personal protective equipment
  • human factors simulation
  • human factors field study
  • human factors
  • health care workers
  • health care
  • safety
  • patient care

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