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无菌听诊器屏障可防止体外传播。

Aseptic Stethoscope Barriers Prevent Transmission In Vitro.

作者信息

Peacock W Frank, Kalra Sarathi, Vasudevan Rajiv S, Torriani Francesca

机构信息

Department of Emergency Medicine, Baylor College of Medicine, Houston, TX.

Department of Emergency Medicine, University of South Alabama, Mobile, AL.

出版信息

Mayo Clin Proc Innov Qual Outcomes. 2021 Jan 13;5(1):103-108. doi: 10.1016/j.mayocpiqo.2020.10.002. eCollection 2021 Feb.

Abstract

OBJECTIVE

To evaluate whether (formerly ) contaminated stethoscope diaphragms remained aseptic by the placement of an aseptic diaphragm barrier.

METHODS

On November 1, 2019, fresh cultures of were diluted to 10 colony-forming units (CFU)/mL and used to inoculate 16 stethoscope diaphragms; 8 had an aseptic diaphragm barrier applied and 8 served as nonbarrier controls. Contaminated stethoscopes were anaerobically incubated, then swabbed at 15 and 30 minutes, 2 and 4 hours, and 1, 2, 3, and 7 days after inoculation and subsequently plated onto blood, chocolate, and cycloserine-cefoxitin fructose agar. Plates were incubated for 48 hours and on November 9, 2019, the resulting colonies were manually counted. Statistical analyses (RStudio, version 1.0.153) used analysis of variance with post hoc Tukey honestly significant difference.

RESULTS

Overall, mean colony count was 33 CFU on stethoscopes without barriers vs zero on those with barriers (≤.05). Growth was greatest at 48 hours, with colony counts as high as 160 CFU. The presence of the barrier resulted in no growth in 100% of stethoscope diaphragms for up to 1 week.

CONCLUSION

We found that stethoscope diaphragm barriers provide an aseptic patient contact point, thus reducing the potential for transmission of  during the physical examination. In critical care environments, in which many hospitals use acoustically inferior disposable stethoscopes, the option of a disposable aseptic stethoscope barrier may allow high-quality auscultation while reducing the potential for pathogen transmission.

摘要

目的

通过设置无菌隔膜屏障来评估曾被(某种病菌)污染的听诊器膜片是否能保持无菌状态。

方法

2019年11月1日,将(某种病菌)的新鲜培养物稀释至每毫升10个菌落形成单位(CFU),并用于接种16个听诊器膜片;其中8个应用了无菌隔膜屏障,8个作为无屏障对照。对接种后的污染听诊器进行厌氧培养,然后在接种后15分钟和30分钟、2小时和4小时、1天、2天、3天和7天进行擦拭,随后接种到血平板、巧克力平板和环丝氨酸-头孢西丁果糖琼脂平板上。平板培养48小时,2019年ll月9日,人工计数所得菌落。统计分析(RStudio,版本1.0.153)采用方差分析及事后Tukey真实显著差异检验。

结果

总体而言,无屏障听诊器的平均菌落数为33 CFU,而有屏障听诊器的平均菌落数为零(P≤0.05)。48小时时生长最为显著,菌落数高达160 CFU。屏障的存在使100%的听诊器膜片在长达1周的时间内均无生长。

结论

我们发现听诊器膜片屏障可提供一个无菌的患者接触点,从而降低体格检查期间(某种病菌)传播的可能性。在许多医院使用声学性能较差的一次性听诊器的重症监护环境中,一次性无菌听诊器屏障这一选择可在减少病原体传播可能性的同时实现高质量听诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da1/7930788/67fa9c903cef/gr1.jpg

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