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. 2020 Nov 27;10(11):e040547.
doi: 10.1136/bmjopen-2020-040547.

Mask shortage during epidemics and pandemics: a scoping review of interventions to overcome limited supply

Affiliations

Mask shortage during epidemics and pandemics: a scoping review of interventions to overcome limited supply

Abirami Kirubarajan et al. BMJ Open. .

Abstract

Objective: To characterise published evidence regarding preclinical and clinical interventions to overcome mask shortages during epidemics and pandemics.

Design: Systematic scoping review.

Settings: All healthcare settings relevant to epidemics and pandemics.

Search strategy: English peer-reviewed studies published from January 1995 to June 2020 were included. Literature was identified using four databases (Medline-OVID, EMBASE, CINAHL, Cochrane Library), forwards-and-backwards searching through Scopus and an extensive grey literature search. Assessment of study eligibility, data extraction and evidence appraisal were performed in duplicate by two independent reviewers.

Results: Of the 11 220 database citations, a total of 47 articles were included. These studies encompassed six broad categories of conservation strategies: decontamination, reusability of disposable masks and/or extended wear, layering, reusable respirators, non-traditional replacements or modifications and stockpiled masks. Promising strategies for mask conservation in the context of pandemics and epidemics include use of stockpiled masks, extended wear of disposable masks and decontamination.

Conclusion: There are promising strategies for overcoming face mask shortages during epidemics and pandemics. Further research specific to practical considerations is required before implementation during the COVID-19 pandemic.

Keywords: infection control; public health; risk management.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Preferred Reporting Items for Systematic Reviews and Meta-Analysis diagram.
Figure 2
Figure 2
Cochrane risk of bias tool. Seven randomised controlled trials were evaluated using the Cochrane risk of bias tool. The majority (n=6) were noted to be intermediate risk, with one study graded as low risk.
Figure 3
Figure 3
RoBANS risk of bias tool. Eight non-randomised studies were evaluated with the RoBANS tool. Seven studies were graded as low risk, with one study graded as intermediate risk to high risk.
Figure 4
Figure 4
Preclinical risk of bias grading. Twenty-seven preclinical studies were evaluated using markers previously described in literature (see ‘Methods’ section). All studies were ranked as medium to high risk for bias.

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