Camila N Baldasso, Ruy Teichert-Filho, Daniel R Marinowic, Maria M Campos, Maximiliano S Gomes
{"title":"COVID-19 大流行期间牙科护理中减少气溶胶弥散装置的三种原型的微生物学和人体工程学效果:随机对照临床试验。","authors":"Camila N Baldasso, Ruy Teichert-Filho, Daniel R Marinowic, Maria M Campos, Maximiliano S Gomes","doi":"10.3390/dj13020054","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objectives</b>: This randomized clinical trial evaluated the microbiological efficacy and the ergonomic impact of three prototypes of a device to reduce aerosol dispersion during dental procedures. <b>Methods</b>: Sixty patients undergoing dental care using high-speed turbines and/or ultrasonic tips were randomly assigned to 4 groups (<i>n</i> = 15): CG: control group, with standard personal protective equipment (PPE); G1: PPE + acrylic device (AD) with aspiration; G2: PPE + AD without aspiration; and G3: PPE + polyvinyl chloride device. The device prototypes consisted of a rigid translucent acrylic structure (G1 and G2), or a rigid PVC tube structure surrounded by layers of translucent flexible PVC films (G3), adjusted to the dental chair, involving the patient's head, neck and chest. The main outcome was the microbiological analysis (mean Δ of CFU at 10 different sites), and the secondary outcome was the ergonomic evaluation (questionnaire to dentists and patients). <b>Results</b>: The final sample comprised 59 participants (mean age 38.6 ± 11.4 years, 55.2% male). The overall mean time for dental procedures was 32.4 ± 16.9 min, with no differences between groups (<i>p</i> = 0.348). Microbiological analyses showed that the use of the device significantly reduced contamination in the light reflector (01.46 ± 4.43 ΔCFU in G2 vs. 19.25 ± 36.50 ΔCFU in CG; <i>p</i> = 0.028), apron (09.11 ± 12.05 ΔCFU in G3 vs. 21.14 ± 43.41 ΔCFU in GC; <i>p</i> = 0.044), and face shield (08.80 ± 32.70 ΔCFU in G1 vs. 56.78 ± 76.64 ΔCFU in the GC; <i>p</i> = 0.017). The device was well accepted by patients and increased the dentists' perception of safety and protection (<i>p</i> < 0.001), but significantly decreased ergonomics related to the clinical view, space, agility and access to the patient, and ease of performing procedures (<i>p</i> < 0.001). <b>Conclusions</b>: The tested device can be an additional tool for infection prevention and control in dentistry, not only during the COVID-19 pandemic, but also for the control of future infectious diseases and epidemics.</p>","PeriodicalId":11269,"journal":{"name":"Dentistry Journal","volume":"13 2","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11854043/pdf/","citationCount":"0","resultStr":"{\"title\":\"Microbiological and Ergonomic Effects of Three Prototypes of a Device to Reduce Aerosol Dispersion in Dental Care During the COVID-19 Pandemic: A Randomized Controlled Clinical Trial.\",\"authors\":\"Camila N Baldasso, Ruy Teichert-Filho, Daniel R Marinowic, Maria M Campos, Maximiliano S Gomes\",\"doi\":\"10.3390/dj13020054\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objectives</b>: This randomized clinical trial evaluated the microbiological efficacy and the ergonomic impact of three prototypes of a device to reduce aerosol dispersion during dental procedures. <b>Methods</b>: Sixty patients undergoing dental care using high-speed turbines and/or ultrasonic tips were randomly assigned to 4 groups (<i>n</i> = 15): CG: control group, with standard personal protective equipment (PPE); G1: PPE + acrylic device (AD) with aspiration; G2: PPE + AD without aspiration; and G3: PPE + polyvinyl chloride device. The device prototypes consisted of a rigid translucent acrylic structure (G1 and G2), or a rigid PVC tube structure surrounded by layers of translucent flexible PVC films (G3), adjusted to the dental chair, involving the patient's head, neck and chest. The main outcome was the microbiological analysis (mean Δ of CFU at 10 different sites), and the secondary outcome was the ergonomic evaluation (questionnaire to dentists and patients). <b>Results</b>: The final sample comprised 59 participants (mean age 38.6 ± 11.4 years, 55.2% male). The overall mean time for dental procedures was 32.4 ± 16.9 min, with no differences between groups (<i>p</i> = 0.348). Microbiological analyses showed that the use of the device significantly reduced contamination in the light reflector (01.46 ± 4.43 ΔCFU in G2 vs. 19.25 ± 36.50 ΔCFU in CG; <i>p</i> = 0.028), apron (09.11 ± 12.05 ΔCFU in G3 vs. 21.14 ± 43.41 ΔCFU in GC; <i>p</i> = 0.044), and face shield (08.80 ± 32.70 ΔCFU in G1 vs. 56.78 ± 76.64 ΔCFU in the GC; <i>p</i> = 0.017). The device was well accepted by patients and increased the dentists' perception of safety and protection (<i>p</i> < 0.001), but significantly decreased ergonomics related to the clinical view, space, agility and access to the patient, and ease of performing procedures (<i>p</i> < 0.001). <b>Conclusions</b>: The tested device can be an additional tool for infection prevention and control in dentistry, not only during the COVID-19 pandemic, but also for the control of future infectious diseases and epidemics.</p>\",\"PeriodicalId\":11269,\"journal\":{\"name\":\"Dentistry Journal\",\"volume\":\"13 2\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-01-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11854043/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dentistry Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/dj13020054\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dentistry Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/dj13020054","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
Microbiological and Ergonomic Effects of Three Prototypes of a Device to Reduce Aerosol Dispersion in Dental Care During the COVID-19 Pandemic: A Randomized Controlled Clinical Trial.
Objectives: This randomized clinical trial evaluated the microbiological efficacy and the ergonomic impact of three prototypes of a device to reduce aerosol dispersion during dental procedures. Methods: Sixty patients undergoing dental care using high-speed turbines and/or ultrasonic tips were randomly assigned to 4 groups (n = 15): CG: control group, with standard personal protective equipment (PPE); G1: PPE + acrylic device (AD) with aspiration; G2: PPE + AD without aspiration; and G3: PPE + polyvinyl chloride device. The device prototypes consisted of a rigid translucent acrylic structure (G1 and G2), or a rigid PVC tube structure surrounded by layers of translucent flexible PVC films (G3), adjusted to the dental chair, involving the patient's head, neck and chest. The main outcome was the microbiological analysis (mean Δ of CFU at 10 different sites), and the secondary outcome was the ergonomic evaluation (questionnaire to dentists and patients). Results: The final sample comprised 59 participants (mean age 38.6 ± 11.4 years, 55.2% male). The overall mean time for dental procedures was 32.4 ± 16.9 min, with no differences between groups (p = 0.348). Microbiological analyses showed that the use of the device significantly reduced contamination in the light reflector (01.46 ± 4.43 ΔCFU in G2 vs. 19.25 ± 36.50 ΔCFU in CG; p = 0.028), apron (09.11 ± 12.05 ΔCFU in G3 vs. 21.14 ± 43.41 ΔCFU in GC; p = 0.044), and face shield (08.80 ± 32.70 ΔCFU in G1 vs. 56.78 ± 76.64 ΔCFU in the GC; p = 0.017). The device was well accepted by patients and increased the dentists' perception of safety and protection (p < 0.001), but significantly decreased ergonomics related to the clinical view, space, agility and access to the patient, and ease of performing procedures (p < 0.001). Conclusions: The tested device can be an additional tool for infection prevention and control in dentistry, not only during the COVID-19 pandemic, but also for the control of future infectious diseases and epidemics.