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过氧化氢蒸汽与气溶胶空间消毒系统的头对头比较。

A head-to-head comparison of hydrogen peroxide vapor and aerosol room decontamination systems.

机构信息

Infectious Diseases Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.

出版信息

Infect Control Hosp Epidemiol. 2011 Sep;32(9):831-6. doi: 10.1086/661104.

Abstract

OBJECTIVE

New technologies have emerged in recent years for the disinfection of hospital rooms and equipment that may not be disinfected adequately using conventional methods. There are several hydrogen peroxide-based area decontamination technologies on the market, but no head-to-head studies have been performed.

DESIGN

We conducted a head-to-head in vitro comparison of a hydrogen peroxide vapor (HPV) system (Bioquell) and an aerosolized hydrogen peroxide (aHP) system (Sterinis).

SETTING

The tests were conducted in a purpose-built 136-m(3) test room.

METHODS

One HPV generator and 2 aHP machines were used, following recommendations of the manufacturers. Three repeated tests were performed for each system. The microbiological efficacy of the 2 systems was tested using 6-log Tyvek-pouched Geobacillus stearothermophilus biological indicators (BIs). The indicators were placed at 20 locations in the first test and 14 locations in the subsequent 2 tests for each system.

RESULTS

All BIs were inactivated for the 3 HPV tests, compared with only 10% in the first aHP test and 79% in the other 2 aHP tests. The peak hydrogen peroxide concentration was 338 ppm for HPV and 160 ppm for aHP. The total cycle time (including aeration) was 3 and 3.5 hours for the 3 HPV tests and the 3 aHP tests, respectively. Monitoring around the perimeter of the enclosure with a handheld sensor during tests of both systems did not identify leakage.

CONCLUSION

One HPV generator was more effective than 2 aHP machines for the inactivation of G. stearothermophilus BIs, and cycle times were faster for the HPV system.

摘要

目的

近年来出现了一些新技术,可用于对医院房间和设备进行消毒,而常规方法可能无法充分消毒这些房间和设备。市场上有几种基于过氧化氢的区域去污技术,但尚未进行过直接比较的研究。

设计

我们在一个专门建造的 136 立方米测试室中,对一种过氧化氢蒸气(HPV)系统(Bioquell)和一种雾化过氧化氢(aHP)系统(Sterinis)进行了直接比较的体外测试。

设置

根据制造商的建议,使用了一个 HPV 发生器和 2 个 aHP 机器。每个系统进行了 3 次重复测试。使用 6 对数 Tyvek 包裹的嗜热脂肪芽孢杆菌生物指示剂(BI)测试了这 2 个系统的微生物效能。第一次测试中,将 BI 放在 20 个位置,随后 2 次测试中,每个系统放置在 14 个位置。

结果

HPV 的 3 次测试中所有 BI 都被灭活,而 aHP 的第一次测试中只有 10%被灭活,随后 2 次测试中只有 79%被灭活。HPV 的过氧化氢峰值浓度为 338ppm,aHP 的为 160ppm。HPV 的 3 次测试和 aHP 的 3 次测试的总循环时间(包括通风)分别为 3 小时和 3.5 小时。在测试这两个系统时,用手持式传感器在外壳周围进行监测,未发现泄漏。

结论

与 2 个 aHP 机器相比,1 个 HPV 发生器更有效地使嗜热脂肪芽孢杆菌 BI 失活,HPV 系统的循环时间更快。

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