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The Research Gap in Non-tuberculous Mycobacterium (NTM) and Reusable Medical Devices

机译:非结核分枝杆菌(NTM)和可重复使用的医疗器械的研究差距

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Patient infections with Non-tuberculous Mycobacterium (NTM) have been attributed to somereusable medical devices (1, 2), such as heater cooler devices (3–5), dental unit waterlines (6),bronchoscopes (7), and automated endoscope reprocessors (8, 9). Such incidents can be relatedto insufficient reprocessing or growth of resistant organisms. For example, NTM infections canarise from patient exposure to contaminated water from established biofilms in water systems, andin some cases, aerosolization of the contaminated water (10). These medical devices are regulatedby the U.S. Food and Drug Administration (FDA) and the Agency seeks to better understand themechanism by which devices can transmit NTM. Some NTM-specific challenges include potentiallyyears-long incubation period to clinical infection, subsequent difficulty identifying the bacteria tothe species-level and extended duration of treatment (11).
机译:具有非结核分枝杆菌(NTM)的患者感染已归因于可令人毛的医疗装置(1,2),例如加热器冷却器装置(3-5),牙科单位水线(6),支气管镜(7)和自动内窥镜后备 (8,9)。 这种事件可以与抗性生物的再加工或生长相关。 例如,NTM感染从患者暴露于来自水系统中成立的生物膜的污染水中的污染水,以及一些情况,污染水的雾化(10)。 这些医疗器械被规定,美国食品和药物管理局(FDA)和原子能机构寻求更好地了解设备可以传输NTM的机制。 一些特定的NTM特定挑战包括临床感染的潜在般的潜伏期,随后难以识别细菌,抑制物种水平和延长的治疗持续时间(11)。

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