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杀微生物剂凝胶黏附监测方法的评价。

Evaluation of microbicide gel adherence monitoring methods.

机构信息

ReProtect, Inc., Baltimore, MD, USA.

出版信息

Sex Transm Dis. 2012 May;39(5):335-40. doi: 10.1097/OLQ.0b013e31824790bb.

Abstract

BACKGROUND

An objective and accurate method that measures adherence to vaginal microbicide gel regimens during clinical trials could provide more accurate estimates of microbicide efficacy, aid in targeting adherence promotion resources, and enable objective assessment of adherence promotion strategies.

METHODS

We evaluated 4 methods to assess whether or not gel applicators had been vaginally inserted. At the study site, 50 women inserted hydroxyethylcellulose universal placebo gel through a polypropylene vaginal applicator and handled, but did not insert a second "sham-inserted" applicator. Applicators were discarded into a container capped with a medical event monitor system (MEMS) that recorded the time and date of opening. Fifteen additional participants did likewise at 2 study site visits, and administered gel on 6 intervening days at home. Applicators were scored as inserted, or not, by direct inspection under ambient light, ultraviolet (UV) light, staining with Alcian blue, and microscopic detection of vaginal cells stained with iodine.

RESULTS

Mean sensitivity/specificity of 2 readings each by 3 test readers for UV, Alcian blue, ambient light, and iodine methods were 84/83, 79/83, 76/63, and 65/80%, respectively. Sensitivity of all methods was significantly higher in applicators inserted after one or more prior insertions of gel, with the highest sensitivity (95%) obtained with UV. MEMS caps accurately recorded applicator disposal time.

CONCLUSIONS

The modest accuracy of all 4 methods for applicator insertions without prior gel applications may limit their accuracy in monitoring coital regimens. However, for daily dosing regimens, MEMS monitoring and UV inspection should provide a rapid, reliable, and quantitative assessment of adherence.

摘要

背景

一种客观准确的方法,可以衡量临床试验中阴道杀微生物剂凝胶方案的依从性,这可以更准确地估计杀微生物剂的疗效,有助于针对依从性促进资源,并能够客观评估依从性促进策略。

方法

我们评估了 4 种方法来评估凝胶涂药器是否已插入阴道。在研究现场,50 名女性通过聚丙烯阴道涂药器插入羟乙基纤维素通用安慰剂凝胶,并处理但未插入第二个“假插入”涂药器。涂药器被丢弃到一个容器中,该容器的盖子上装有一个医疗事件监测系统(MEMS),该系统记录了打开的时间和日期。另外 15 名参与者在 2 次研究现场访问中也这样做了,并在 6 天的间隔在家中使用凝胶。通过在环境光、紫外线(UV)光下、用阿尔辛蓝染色和用碘染色的阴道细胞的显微镜检测下直接检查,将涂药器标记为插入或未插入。

结果

3 名测试读者每人对 2 次读数的平均敏感性/特异性为 UV、Alcian blue、环境光和碘方法分别为 84/83、79/83、76/63 和 65/80%。所有方法的敏感性在涂药器插入后,在前一次或多次插入凝胶后均明显更高,其中 UV 的敏感性最高(95%)。MEMS 帽准确记录了涂药器处置时间。

结论

在没有先前凝胶应用的情况下,所有 4 种涂药器插入方法的准确性都适中,这可能限制了它们在监测性行为方案中的准确性。然而,对于每日剂量方案,MEMS 监测和 UV 检查应该提供快速、可靠和定量的依从性评估。

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