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A tolerability assessment of new respiratory protective devices developed for health care personnel: A randomized simulated clinical study

机译:对医疗保健人员开发的新呼吸保护装置的可耐受性评估:随机模拟临床研究

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摘要

BackgroundU.S. health care personnel (HCP) have reported that some respiratory protective devices (RPD) commonly used in health care have suboptimal tolerability. Between 2012 and 2016, the U.S. National Institute for Occupational Safety and Health, and the Veterans Health Administration collaborated with two respirator manufacturers, Company A and B, to bring new RPD with improved tolerability to the U.S. health care marketplace. The purpose of this study was to compare the tolerability of four new prototype RPD to two models commonly used in U.S. health care delivery.MethodsA randomized, simulated workplace study was conducted to compare self-reported tolerability of four new prototype RPD (A1, A2, B1, and B2) worn by HCP and two N95 control respirators commonly used in U.S. health care delivery, the 1870 and 1860, manufactured by 3M Corporation. A new survey tool, the Respirator Comfort, Wearing Experience, and Function Instrument (R-COMFI), developed previously in part for the current study, was used as the primary outcome metric. With a maximum total score of 47, lower R-COMFI scores reflected better self-reported tolerability. Poisson regression analyses were used to estimate prototype relative risks compared to controls.ResultsConducted between 2014 and 2015 in two inpatient care rooms at the North Florida/South Georgia Veterans Health System, among 383 participants who enrolled, 335 (87.5%) completed the study. Mean total R-COMFI scores for the 3M 1870, 3M 1860, and prototypes A1, A2, B1, and B2 were 8.26, 9.36, 5.79, 7.70, 6.09, and 5.71, respectively. Compared to the 3M 1870, total R-COMFI unadjusted relative risks (RR) and 95 percent confidence intervals (CI) were A1 (RR 0.70, CI 0.60, 0.82), A2 (RR 0.93, CI 0.82, 1.06), B1 (RR 0.74, CI 0.64, 0.85), and B2 (RR 0.69, CI 0.60, 0.80). Compared to the 3M 1860, prototype total R-COMFI unadjusted RR and 95 percent CI were A1 (RR 0.62, CI 0.53, 0.72), A2 (RR 0.82, CI 0.73, 0.93), B1 (RR 0.65, CI 0.57, 0.74), and B2 (RR 0.61, CI 0.53, 0.70). Similarly, models adjusted for demographic characteristics showed that prototypes A1, B1, and B2 significantly improved tolerability scores compared to both controls, while prototype A2 was significantly improved compared to the 3M 1860.ConclusionsCompared to the 3M 1870 and 3M 1860, two RPDs commonly used in U.S. health care delivery, tolerability improved for three of four newly developed prototypes in this simulated workplace study. The R-COMFI tool, used in this study to assess tolerability, should be useful for future comparative studies of RPD.
机译:butckstucku.s。医疗保健人员(HCP)报告说,常用于医疗保健的一些呼吸保护装置(RPD)具有次优耐受性。 2012年至2016年间,美国国家职业安全和卫生研究院,以及与两家呼吸器制造商,A和B公司合作的退伍军人卫生行政促进了新的RPD,以提高美国医疗保健市场的耐受性。本研究的目的是将四种新型原型RPD的可耐受性进行比较,常用于美国医疗送货上的两种型号。方法进行了随机的模拟工作场所研究,以比较四种新型原型RPD的自我报告的可耐受性(A1,A2, HCP和B2)和B1和B2常用于美国医疗保健交付的两种N95控制呼吸器,由3M公司制造的1870年和1860年。新的测量工具,呼吸器舒适性,佩戴经验和功能仪器(R-Comfi),主要用于目前的研究,用作主要的结果指标。最大总得分为47,较低的R-COMFI分数反映了更好的自我报告的可耐受性。泊松回归分析用于估算与控制的原型相对风险。在佛罗里达州/南格丽亚退伍军人卫生系统的两个住院护理室,2014年和2015年间,在北佛罗里达州/南乔治亚退伍军人卫生系统中,383名注册,335名(87.5%)完成了这项研究。为3M 1870,3M 1860和原型A1,A2,B1和B2分别为8.26,9.36,5.79,7.70,6.09和5.71分别为3M 1870,3M 1860和原型的总R-COMFI分数。与3M 1870相比,总R-COMFI不调整的相对风险(RR)和95%置信区间(CI)是A1(RR 0.70,CI 0.60,0.82),A2(RR 0.93,CI 0.82,1.06),B1(RR 0.74,CI 0.64,0.85)和B2(RR 0.69,CI 0.60,0.80)。与3M 1860相比,原型总R-COMFI不调整的RR和95%CI为A1(RR 0.62,CI 0.53,0.72),A2(RR 0.82,CI 0.73,0.93),B1(RR 0.65,CI 0.57,0.74) ,B2(RR 0.61,CI 0.53,0.70)。类似地,针对人口统计学特性调整的模型显示,与两种控制相比,原型A1,B1和B2显着提高了可耐受性评分,而原型A2与3M 1860相比显着提高。与3M 1870和3M 1860相比,两个RPD相比,常用在美国医疗保健交付中,在这项模拟工作场所研究中的四种新开发的原型中的三种新开发的原型中的三种耐受性提高。在本研究中用于评估耐受性的R-Comfi工具应该对RPD的未来比较研究应该有用。

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