Randomized Controlled Trial to Compare Clinical Efficacy of Surgical and Filtering Facepiece 2 Masks for Care Home Workers Treating COVID-19 Patients
Randomized Controlled Trial to Compare Clinical Efficacy of Surgical and Filtering Facepiece 2 Masks for Care Home Workers Treating COVID-19 Patients
Recent results demonstrated an increased risk of COVID-19 infection among healthcare workers (HCW), particularly when access to personal protective equipment (PPE) was inadequate. (ref). During the COVID-19 pandemic, access to PPE has become complicated by a surge in worldwide demand combined with production limitations and logistical barriers. Since their introduction in hospitals in the 1990s, filtering facepiece (FFP) masks, mostly of the FFP2 type, are used by HCWs to protect themselves against bioaerosols due to tuberculosis, measles, and selected respiratory viruses. The COVID-19 pandemic has sparked debate around reasonable and safe use of the different types of face masks to protect the HCWs who provide direct care for COVID-19 patients. At the heart of the discussion are the respective contributions to SARS-CoV-2 transmissions by droplets and aerosols, and the corresponding risk levels resulting in COVID-19 infection.
The objective is to perform a cluster-randomized, parallel, controlled, non-inferiority study among Swiss nursing and retirement homes to evaluate the efficacy of surgical masks vs. FFP2 masks during patient care and prospectively observe possible infections amongst both vaccinated and unvaccinated staff.
Staff in nursing homes will be randomized to use either surgical or FFP2 masks for patient care consistently. Considering an attack rate of 0.8% over three months among healthcare workers, a non-inferiority margin of 5%, and an intracluster variability of 0.01, - we require a minimum of 625 participants per group. The COVID-19 attack rate will be tested by initial serology testing and weekly pooled saliva specimen for SARS-CoV-2 testing. (Re)-Infections will be tracked by weekly pooled saliva-based PCR testing. Exposure to COVID-19 other than during work time will be explored by questionnaires and focus group discussions.
Project summary Recent results demonstrated an increased risk of COVID-19 infection among healthcare workers (HCW), particularly when access to personal protective equipment (PPE) was inadequate. (ref) During the COVID-19 pandemic, access to PPE has become complicated by a surge in worldwide demand combined with production limitations and logistical barriers. Since their introduction in hospitals in the 1990s, filtering facepiece (FFP) masks, mostly of the FFP2 type, are used by HCWs to protect themselves against bioaerosols due to tuberculosis, measles, and selected respiratory viruses. The COVID-19 pandemic has sparked debate around reasonable and safe use of the different types of face masks to protect the HCWs who provide direct care for COVID-19 patients. At the heart of the discussion is whether droplets or aerosols transmit SARS-CoV-2, and which of the two is responsible for what risk level of SARS-CoV-2 transmission resulting in disease.
The objective is to perform a cluster-randomized, parallel, controlled, non-inferiority study among Swiss nursing and retirement homes (homes) to evaluate the efficacy of surgical masks vs. FFP2 masks during patient care and prospectively observe possible infections amongst both vaccinated and unvaccinated staff.
Staff in nursing homes will be randomized to use either surgical or FFP2 masks for patient care consistently. Considering an attack rate of 0.8%[1] over three months among healthcare workers, a non-inferiority margin of 5%, and an intracluster variability of 0.01,[2] - we require a minimum of 625 participants per group.[3] The COVID-19 attack rate will be tested by initial serology testing and weekly pooled saliva specimen for SARS-CoV-2 testing. (Re)-Infections will be tracked by weekly pooled Saliva based PCR testing. Exposure to COVID-19 other than during work time will be explored by questionnaires and focus group discussions.
Study protocol 2.1 State of research in the field 2.1.1 Transmission of COVID-19 by droplets or aerosols Since the beginning of the COVID-19 pandemic, more than 110 million cases were confirmed with almost 2.4 million deaths as of February 22nd, 2020. Given that SARS-CoV-2 is a respiratory virus, its spread is expected to occur mainly by droplets (diameter >5µm) and via contact; however, laboratory tests suggest that SARS-CoV-2 may remain viable and infectious also in aerosols (diameter <5 µm).1,2. Both droplets and aerosols are naturally produced by humans when breathing, talking, coughing, or sneezing. A cough and a sneeze can generate between 3000 and 40,000 droplets of diameters between 0.5 to 12 µm, respectively 3-5; furthermore, droplets and aerosols can both contain SARS-CoV-2 virus if produced by COVID-19 patients. Aerosols are small-size droplets remaining in the air, and thus may travel beyond 2m from a source the respiratory tract bypassing surgical masks. Therefore, healthcare workers have been advised to wear FFP2 masks in procedures that generate aerosols. It remains to be clarified if surgical masks are inferior to FFP2 masks in the care of COVID-19 patients other than being exposed to aerosol-generating procedures. Recent data suggests that if worn correctly by both patient and exposed staff, surgical masks are able of filtering over 90% of particles generated 6.
Specifics about COVID-19 disease transmission and infectious dose are currently lacking. However, numbers in the order of 1000 droplets and more are realistic assumptions.7 The infection risk by one virus copy in viral shedding is about 1.5×10-6 to 1.6×10-5. Thus the infection risk due to aerosols at distances larger than 1-2 meters is substantially lower than that due to close interaction within 1 meter.
Consequently, protection from COVID-19 patients must focus on close interaction where droplets play a significant role, which could be addressed by wearing a surgical mask.
The added protective benefit of FFP2 masks outside so-called "aerosol-generating procedures" where aerosols are believed to be produced in large quantities is meager. Thus, recommending FFP2 masks for non-aerosol-generating procedures with regard to COVID-19 is not justified. Hence, a randomized trial to test the non-inferiority of surgical masks in COVID-19 care (other than during aerosol-generating procedures) is ethically sound.
With logistical challenges arising to vaccinate the greater public8, many people refusing vaccinations, a significant percent of the population having contracted COVID-19 since the beginning of the pandemic, and new mutations emerging with growing amounts of reports of reinfections,9 we are facing a reality in which, regarding their infection and vaccination status, non-homogenous groups of people will have to learn to co-exist for months and possibly years to come.
In Switzerland, there is currently a lot of discordance between hospitals when it comes to the choice of mask for healthcare workers, making recruitment of sufficient participants basically impossible. We decided to focus on including retirement homes and homes for the elderly. The homes have designated wards for COVID-19 and separate wards for patients requiring aerosol generating procedures. They also require more nursing and support staff to take care of the elderly, making them ideal candidates for our study design and tracking infections based on the mask type. In the United States a third of all COVID-19 related deaths in the United States are believed to be linked to nursing homes10, highlighting the importance to have unanimous guidelines as to the most important basic measures such as mask wearing, to reduce infections and mortality across populations.
2.1.2 Face masks and their appropriate use
Two different types of face masks are distinguished for patient care:
Surgical masks (usually II and IIR) have the main role of limiting the transmission of infective agents from HCWs to patients, mainly during surgical procedures. In specific situations such as colonization with multidrug-resistant microorganisms in the respiratory tract or during outbreaks with respiratory pathogens, wearing them is also recommended for infected patients as source control to limit transmission. The fitting of these masks is loose and leakage occurs around the edges of the mask. While IIR masks protect the wearer from projected splashes of biological fluids, they do not provide the wearer with a reliable protection level from inhaling smaller airborne particles unless modified by e.g. knotting the edges. Ref 6
Class 2 filtering facepiece (FFP 2) masks offer respiratory protection for the wearer. They have tight-fitting and minimal leakage occurs around the edges of the mask. Filtering facepiece masks were initially intended to protect workers from dust exposure. However, FFP2 masks were introduced to healthcare predominantly to protect healthcare workers exposed to patients with tuberculosis or measles. (ref) Their appropriate use during the COVID-19 pandemic in healthcare units remains controversial, as explained above. A recent meta-analysis pooling five randomized-controlled trials showed no difference between surgical masks and FFP masks for outcomes such as clinical respiratory illness or laboratory-confirmed influenza. 11 2.2 Aims Primary outcome: The aim of this study is to test the hypothesis that surgical masks are not inferior to FFP2 masks in patient care (in situations outside of aerosol-generating procedures).
Secondary outcome: By including staff who may have received vaccination we want to track possible infections
2.3 Methods
A cluster-randomized, parallel, controlled, non-inferiority study among Swiss nursing- and retirement homes hosting COVID-19 patients will evaluate the benefits of wearing surgical masks vs. FFP2 masks during COVID-19 patient care (outside aerosol-generating procedures).
2.3.1 Settings: Any Swiss nursing- and retirement home offering COVID-19 care is eligible to be included. The homes will be recruited through direct contact. Each home will have an appointed onsite investigator for communication with the study team.
2.3.2 Study duration We will recruit homes between January 1 and March 10th. During three months, the intervention will last until no later than June 30, 2021.
2.3.3.Randomization: Home wards will be computer-randomized before starting the intervention, stratified by ward size.
Intervention: Interventions include either universal FFP2-masking for every healthcare worker with patient contact, compared to selective FFP2-masking, which means that FFP2 masks are worn only during aerosol-generating procedures such as tube manipulation; for all other procedures, healthcare workers wear a surgical mask of the IIR type. Furthermore, weekly saliva-based pooling will be conducted to track possible (re)-infections.
2.3.4 Outcomes: Primary outcomes are new SARS-CoV-2 infections among healthcare workers appointed to deliver care to COVID-19 patients, measured by a baseline seroprevalence testing and a weekly pooled saliva specimen-based SARS-CoV-2 testing. Secondary outcomes are newly identified SARS-CoV-2 infections among healthcare workers by rtPCR; questionnaires on monthly activity for healthcare workers; focus group discussions on workplace vs. private exposure to COVID-19 patients. Serology testing and saliva-based testing for healthcare workers are voluntary and are performed upon written informed consent.
2.3.5 Sample collection and laboratory testing: Sample size calculation: We hypothesize an attack rate of 0.8 % among healthcare workers (0.8% of the participating healthcare workers become SARS-CoV-2 positive by the end of the study period), the surgical masks are non-inferior to FFP2 masks by 5%. Considering an attack rate of 0.8 %, an inferiority margin of 5%, and an intra-cluster correlation coefficient of 0.01, 1250 participants (625 per group) have to be included (one-sided and with 80% power). The study will be conducted in a cross-over design.
2.3.6 Outcome measurements SARS-CoV-2 serology at baseline and weekly saliva-based specimen pooled SARS-CoV-2 tests. Exposure to COVID-19 patients and risk behavior by questionnaire. Qualitative interpretation of focus group discussions.
2.3.7 Data analysis A non-inferiority difference of proportions test will model the primary outcome. Secondary outcomes will be analyzed descriptively.
2.4 Expected Results
We expect that selective FFP2-masking is not inferior to universal FFP-2 masking; however, selecting when and how FFP-2 masks are to be worn by HCWs is not trivial. This project aims to inform those decisions with improvements in our understanding of the issues involved and the generation of on-site data to guide decision-making.
2.5 Project milestones and timeline[15]
2.6 The potential impact of the research Recent research and government regulations6,12 have shown a significant disparity in opinions regarding the appropriate usage of surgical masks / FFP2 masks. In light of new regulations enforcing FFP2 mask usage by the general population in neighboring countries such as Germany and the diverging opinions amongst health care professionals - we expect this study to help elucidate appropriate use and clear up possible misconceptions. Given the lack of research in this area, this study's outcome will potentially have a world-wide public health impact and aid regulatory bodies to make founded decisions and recommendations to both healthcare workers and the public alike.
2.7 Budget (see Excel)
3 References
Study inclusion criteria;
Additional inclusion criteria for primary objective 2 (reinfection after vaccination)
- SARS-CoV-2 vaccination
List the study exclusion criteria:
michel.bielecki@uzh.ch+41798990584
walter.zingg@usz.ch+41764194018