key: cord-0983837-9n2koqu2
authors: Gasparino, Renata Cristina; Lima, Maria Helena Melo; de Souza Oliveira‐Kumakura, Ana Railka; da Silva, Vanessa Abreu; de Jesus Meszaros, Mariana; Antunes, Ivan Rogério
title: Prophylactic dressings in the prevention of pressure ulcer related to the use of personal protective equipment by health professionals facing the COVID‐19 pandemic: A randomized clinical trial
date: 2020-11-28
journal: Wound Repair Regen
DOI: 10.1111/wrr.12877
sha: eda07ce9610eb88183c33c3b5eca05c081da7c29
doc_id: 983837
cord_uid: 9n2koqu2

Device‐related pressure injury (DRPI) is a serious problem that is affecting professionals working on the front lines against COVID‐19 due to the prolonged use of personal protective equipment (PPE). In addition to the physical and psychological integrity of professionals, these injuries can compromise the quality of care. Therefore, using technologies to prevent this adverse effect is an urgent matter. This is a parallel two‐arm randomized clinical trial without the use of a control group to compare the use of foam and extra‐thin hydrocolloid in preventing DRPI associated with the use of PPE by health professionals working on the front lines against coronavirus. In total, 88 professionals were divided into two groups: foam and hydrocolloid. Data were collected using two instruments and related to demographic and professional characteristics and skin evaluation. Each volunteer received one of the dressings, both with the same dimensions and arranged over similar regions, and data were gathered at baseline and after 6 or 12 hours. Descriptive and inferential analytic statistical methods were used; the significance level adopted was 5%. No participant developed DRPI, but four areas with hyperemia were observed in the foam group (two in the forehead, one in the cheeks, and one in the nose bridge), as well as four areas with hyperemia in the hydrocolloid group (two in the nose bridge, one in the right ear, and one in the left ear). There was no difference between the groups regarding skin conditions and discomfort (P > .05). The average cost obtained was $ 5.8/person and $ 4.4/person in the foam group and the hydrocolloid group, respectively, considering the dressing measurements. The results show that foam and extra‐thin hydrocolloid were effective in preventing DRPI associated with the use of PPE.

parallel two-arm randomized clinical trial without the use of a control group to compare the use of foam and extra-thin hydrocolloid in preventing DRPI associated with the use of PPE by health professionals working on the front lines against coronavirus.

In total, 88 professionals were divided into two groups: foam and hydrocolloid. Data were collected using two instruments and related to demographic and professional characteristics and skin evaluation. Each volunteer received one of the dressings, both with the same dimensions and arranged over similar regions, and data were gathered at baseline and after 6 or 12 hours. Descriptive and inferential analytic statistical methods were used; the significance level adopted was 5%. No participant developed DRPI, but four areas with hyperemia were observed in the foam group (two in the forehead, one in the cheeks, and one in the nose bridge), as well as four areas with hyperemia in the hydrocolloid group (two in the nose bridge, one in the right ear, and one in the left ear). There was no difference between the groups regarding skin conditions and discomfort (P > .05). The average cost obtained was $ 5.8/person and $ 4.4/person in the foam group and the hydrocolloid group, respectively, considering the dressing measurements. The results show that foam and extra-thin hydrocolloid were effective in preventing DRPI associated with the use of PPE.

The disease caused by the new coronavirus, COVID-19, is a respiratory tract infection that led the World Health Organization to declare a pandemic on March 11, 2020. 1 Human transmission occurs through droplets of saliva, contact, and air. The recommendation to reduce transmission is effective isolation of the population, meaning that COVID-19 causes not only a disruption in the health system but also a socioeconomic one given the necessary measures needed to control dissemination. 1 Due to its transmission route, 2 high rate of transmissibility, morbidity, and mortality, 3 the availability and correct use of personal protective equipment (PPE) are essential in maintaining the safety of health professionals. 1 However, due to the prolonged use of PPE, frontline professionals in the fight against COVID are at a high risk of developing a Device-related pressure injury (DRPI). [4] [5] [6] Medical devices can cause humidity, heat, and pressure between the device and skin, leading to pressure-related injuries from medical devices. 7 According to the National Pressure Injury Advisory Panel (NPIAP), DRPI is defined as a pressure injury caused by a device applied for therapeutic and diagnostic reasons. The injury may have a similar shape as the device. 8 These skin injuries can compromise the physical and psychological integrity of professionals, which compromises patient safety and the quality of care. 9 According to the literature, DRPI can be avoided with technologies that protect the exposed areas from these adverse events. [4] [5] [6] However, before the pandemic, most studies related to DRPI prevention were carried out with patients. 10, 11 A three-arm clinical trial investigated two different dressings, Tegasorb and Tegaderm, and a control group without dressings for pressure relief on the nose bridge in patients undergoing non-invasive positive pressure ventilation. The results showed that the participants of the two groups that used dressings had a lower occurrence of pressure injury compared to the control group. However, the results were not significant. 10 Another preclinical study on the nasal occurrence of pressure injury induced by nasotracheal intubation found that a combination of Soft Liner and hydrocolloid reduced the size and severity of the injury. 12 Recently, a cross-sectional study conducted with health profes- In evaluating the skin injuries of 1844 participants, 55.0% answered that they did not use preventive treatment and 45.0% received treatment with dressings, oil agents, or other methods.

Among those who did not present skin injuries, 17.7% of the participants reported the use of prophylactic dressing for the prevention of skin injuries, including foam, hydrocolloids, oil, or cream, among others. 13 A systematic review of the use of prophylactic dressings to prevent pressure injuries suggested that their use decreased the incidence of this medical device-associated event. However, there was no clinical evidence of which type of dressing was the most effective. 14 Given this context, DRPI prevention among professionals at the front lines of the fight against COVID is crucial, mainly to reduce the contamination risk due to the absence of cutaneous integrity and the inability to use PPE in the presence of pressure injury. However, the best dressing for preventing skin injuries remains unknown.

This study this aimed to compare the use of foam and extra-thin hydrocolloid in the prevention of DRPI associated with the use of PPE by health professionals working on the front line against coronavirus.

This is a parallel two-arm randomized clinical trial without a control group. The following steps were carried out: consultation of the Consolidated Statement of Reporting Trials (CONSORT) for randomization, group follow-up, blinding, and data analysis. 15 The study was registered on the Brazilian Clinical Trials platform (ReBEC), available at http://www.ensaiosclinicos.gov.br, under number RBR-7 drpyr.

The study participants were professionals working in the Adult Intensive Care Units of a teaching hospital at the University of Campinas, Brazil. The sample size was calculated considering the objective of comparing prophylactic dressing groups (foam × hydrocolloid), according to the presence of a pressure ulcer (without ulcer, with ulcer). The calculation was made considering the methodology of a sample calculation for a Pearson's Chi-square test. 14 In this estimate, a 5% significance level, an 80% test power, a 0.30 of freedom, and effect size were assumed, which can be considered a medium degree effect size. 16 The sample size obtained was 88 professionals (44 per group). The software PASS 13 17 was used.

The study included professionals who provided direct care (nurses, physicians, and physical therapists) or indirect care (cleaning staff) to patients with suspected or diagnosed coronavirus and needed to use PPE (face shield, gloves, caps, and particulate respirator) for six or 12 consecutive hours.

The following professionals were excluded from the sample: those who did not finish the shift, those who needed to remove the dressing due to discomfort or signs of allergy, the presence of skin damage in the region of the face, and those who did not complete the checklist received along with the dressing to prevent DRPI resulting from the use of PPE. Despite the professionals' skill and knowledge levels, all the participants received theoretical and practical training about the personal protective device before this research.

The selection of participants was random and considered the inclusion criteria. Eighty-eight opaque envelopes were prepared by a team member who had no contact with the participants. The envelopes contained the dressing to be used by the professional and were then randomly distributed using the website http://www.randomization. com/. The professionals were then allocated to the respective groups.

The statistician who performed the data analysis was blind to the denomination of the groups.

This study used an instrument for personal and professional characterizations of the sample that included the variables: age, sex, skin color, presence of comorbidities, profession, and time of experience in the profession and the unit.

The data on skin characteristics were collected using a form specifically designed for this study after reviewing the literature. This form had its face validity evaluated by three specialists, selected for convenience. The form included the following information: characteristics of the skin (intact without hyperemia, intact with hyperemia that pales with digit pressure, or pressure injury classified by I to IV stages 

For the foam group, the participants received a material based on polyurethane foam, which was placed over the forehead (15 cm × 3 cm), nose bridge and cheeks (15 cm × 3 cm), and ears (5 cm × 3 cm). In the hydrocolloid group, the participant received extra-thin hydrocolloid plates with the same dimensions, which were installed over the same regions. The areas for installing the dressings and the cuts that were made on the plates were chosen according to recommendations from the literature. 18, 19 The outcome was the evaluation of the presence or absence of skin injuries in the regions covered with foam or hydrocolloid.

Both groups were approached only once, and, to maintain the safety requirements established in the guidelines, 20,21 the following guidelines and care were reinforced when installing the dressing before entering the work environment: hand hygiene, installation of the technology in the recommended places, placing the N95 mask on the face, and performing the sealing test according to the manufacturer's recommendations. For analyzing the costs related to the dressings, the cost for the purchase of products and the measurement of cuts established for each participant were considered. When asked about the discomfort related to the use of the dressings, the participants reported difficulties when removing the dressing, as well as itching, problems with the mask moving and sealing, among others ( Table 3) .

The mean cost was $5.8/person for the foam group and $4.4/ person for the hydrocolloid group, based on the dressing measures used to prevent skin injuries in each studied region (nose bridge, right and left ears, cheeks, and forehead).

Until now, research about the use of prophylactic dressing in the prevention of skin injuries by medical devices was done in patients. 10, 11 However, the current situation caused the development of DRPI related PPE use by health professionals to become a concern; thus, research on this topic has recently started.

This study showed that both prophylactic dressings were effective in preventing DRPI on the nose bridge, forehead, cheeks, and ears since no participant had skin injuries. Nevertheless, four occurrences of hyperemia were observed in each group (foam and hydrocolloid).

Even though there was no difference between the groups examined in this study, who used the dressing for 6-to 12-hour periods, hyperemia must be highlighted as a signal within the development chain of the DRPI.

Previous research to investigating the use of PPE and the occurrence of DRPI showed that the prevalence of skin injuries was higher in physicians, people who sweat more, males, aged over 35 years old, and who used PPE for more than 4 hours. 13 However, since no participant developed skin injuries in our study, it is impossible to compare the findings.

Most professionals in the institution where this study was conducted continuously used the N95 mask during their shift. Considering a series of cases that demonstrated the relationship between the occurrence of pressure injuries on the nose bridge and the use of N95 mask over 4 hours, 22 we can infer that the use of prophylactic dressing led to the prevention of this occurrence.

Although these prophylactic dressings were initially developed to prevent pressure ulcers in bone prominences of bedridden patients, 23,24 they also had positive effects when adapted to prevent this event in professionals working in health settings, perhaps because the mechanical forces involved in the development of skin injuries are the same for patients and professionals who use PPE for prolonged periods. 3, 4, 25, 26 The literature presents a divergence of opinion among researchers regarding the use of these dressings to prevent DRPI by using PPE. 3, 18, 19, 27 The most cautious ones emphasize the increased risk of professional contamination by coronavirus when a dressing is placed under a particulate respirator. 3 However, to reduce this risk, those in favor recommend using dressings that are thin, nontraumatic in the removal, absorbent, and adaptable to the contours of the facial structures, thus ensuring the correct sealing of the mask. 18, 19, 27 Although authors claim that these characteristics are found in thin foam dressings with silicone, hydrocolloid, and film, 18,28 the absence of some of these attributes reported by the professionals who participated in this study was noted.

Despite being known for having a better capacity to absorb, retain, and release moisture, thus maintaining the proper balance in preserving dry skin, 28 the polyurethane foam had several reports of detachments that even culminated in the exclusion of three participants.

In the group that used hydrocolloid, the reports of discomfort were higher compared to the foam group, highlighting the difficulty in removing the dressing, followed by the sensation of itching and pain.

One can assume that such discomforts may contribute to increasing the risk of contamination by COVID-19 or other diseases, as there may be greater contact between the professionals' hands and their face. However, there are no studies that have analyzed discomfort regarding the use of prophylactic dressing in healthcare professionals.

On the other hand, a study that compared two dressings, Tegasorb and Tegaderm, in the prevention of pressure injury on the nose bridge and around the mask concluded that the dressings prevented these injuries and increased the patients' tolerance and comfort. 10 The choice of an efficient and safe dressing is crucial since the development of skin injuries increases the risk of infection, 18 in addition to being uncomfortable and causing pain. Furthermore, the development of DRPI in professionals can lead to a public health problem as it can cause not only physical, but also financial, emotional, psychological, and social impacts. 4, 29 Although both dressings demonstrated effectiveness in preventing DRPI, we have to consider the small sample size in this study. Future research should on a larger sample size can lead to a better understanding of the effectiveness of these dressing and preventing DRPI. The cost of these materials is also a factor that should be considered by health managers to incorporate these dressings into clinical practice. Furthermore, one must emphasize the need to pay attention to the quality of the PPE used, particularly face masks, respirators, and goggles, since the anatomical characteristics of the face can influence the development of skin injuries. 4 Limitations of this study include being conducted without a control group and using professionals from a single health institution who were only followed up with once. Another characteristic that requires careful evaluation is the facial anatomical characteristics of each individual, which may have influenced the reports of discomfort. Therefore, the products must be rethought to meet the specificities of each audience.

In conclusion, foam and extra-thin hydrocolloid proved to be effective in preventing the DRPI associated with the use of PPE by health professionals working on the front line against coronavirus.

Discomfort related to the use of the dressing was reported in both groups, but no significant differences were found.

This study was supported by grants from the University of Campinas

Research Fund -Faepex (Grant No. 2374/20).

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The authors declare no conflicts of interest.

https://orcid.org/0000-0001-8729-4707Maria Helena Melo Lima https://orcid.org/0000-0001-6521-8324