Respiratory Health Division, National Institute for Occupational Safety and Health, Morgantown, West Virginia.
School of Dentistry, West Virginia University, Morgantown, West Virginia.
J Occup Environ Hyg. 2022 May;19(5):281-294. doi: 10.1080/15459624.2022.2053140. Epub 2022 Apr 6.
Dental personnel are ranked among the highest risk occupations for exposure to SARS-CoV-2 due to their close proximity to the patient's mouth and many aerosol generating procedures encountered in dental practice. One method to reduce aerosols in dental settings is the use of intraoral evacuation systems. Intraoral evacuation systems are placed directly into a patient's mouth and maintain a dry field during procedures by capturing liquid and aerosols. Although multiple intraoral dental evacuation systems are commercially available, the efficacy of these systems is not well understood. The objectives of this study were to evaluate the efficacy of four dental evacuation systems at mitigating aerosol exposures during simulated ultrasonic scaling and crown preparation procedures. We conducted real-time respirable (PM) and thoracic (PM) aerosol sampling during ultrasonic scaling and crown preparation procedures while using four commercially available evacuation systems: a high-volume evacuator (HVE) and three alternative intraoral systems (A, B, C). Four trials were conducted for each system. Respirable and thoracic mass concentrations were measured during procedures at three locations including (1) near the breathing zone (BZ) of the dentist, (2) edge of the dental operatory room approximately 0.9 m away from the mannequin mouth, and (3) hallway supply cabinet located approximately 1.5 m away from the mannequin mouth. Respirable and thoracic mass concentrations measured during each procedure were compared with background concentrations measured in each respective location. Use of System A or HVE reduced thoracic (System A) and respirable (HVE) mass concentrations near the dentist's BZ to median background concentrations most often during the ultrasonic scaling procedure. During the crown preparation, use of System B or HVE reduced thoracic (System B) and respirable (HVE or System B) near the dentist's BZ to median background concentrations most often. Although some differences in efficacy were noted during each procedure and aerosol size fraction, the difference in median mass concentrations among evacuation systems was minimal, ranging from 0.01 to 1.48 µg/m across both procedures and aerosol size fractions.
牙科医务人员由于与患者口腔近距离接触,以及在牙科实践中经常进行许多产生气溶胶的程序,因此被列为感染 SARS-CoV-2 的最高风险职业之一。减少牙科环境中气溶胶的一种方法是使用口腔内抽吸系统。口腔内抽吸系统直接放置在患者口中,并通过捕获液体和气溶胶在手术过程中保持干燥区域。尽管有多种商业上可用的口腔内牙科抽吸系统,但这些系统的效果并不清楚。本研究的目的是评估四种牙科抽吸系统在模拟超声洁牙和牙冠预备过程中减少气溶胶暴露的效果。我们在进行超声洁牙和牙冠预备过程中进行了实时可吸入(PM)和胸内(PM)气溶胶采样,同时使用了四种市售的抽吸系统:高容量抽吸器(HVE)和三种替代的口腔内系统(A、B、C)。每个系统进行了四次试验。在程序过程中在三个位置测量可吸入和胸内质量浓度,包括(1)牙医的呼吸区(BZ)附近,(2)距模型口腔约 0.9 m 的牙科手术室边缘,以及(3)距模型口腔约 1.5 m 的走廊供应柜。每次程序中测量的可吸入和胸内质量浓度与各自位置测量的背景浓度进行比较。使用系统 A 或 HVE 通常在超声洁牙过程中减少牙医 BZ 附近的胸内(系统 A)和可吸入(HVE)质量浓度至中位数背景浓度。在牙冠预备过程中,使用系统 B 或 HVE 通常减少牙医 BZ 附近的胸内(系统 B)和可吸入(HVE 或系统 B)的浓度至中位数背景浓度。尽管在每个程序和气溶胶粒径分数中都注意到了一些效果差异,但抽吸系统之间的中位数质量浓度差异很小,在两个程序和气溶胶粒径分数中范围从 0.01 至 1.48μg/m。