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首页> 外文期刊>Sexually transmitted diseases >Validation of a dye stain assay for vaginally inserted hydroxyethylcellulose-filled microbicide applicators.
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Validation of a dye stain assay for vaginally inserted hydroxyethylcellulose-filled microbicide applicators.

机译:阴道插入羟乙基纤维素填充的杀菌剂施加器的染料染色试验的验证。

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BACKGROUND: The reliability and validity of self-reports of vaginal microbicide use are questionable given the explicit understanding that participants are expected to comply with study protocols. Our objective was to optimize the use of Population Council's previously validated dye stain assay (DSA) and related procedures, and to establish predictive values for the DSAs ability to identify vaginally inserted single-use, low-density polyethylene microbicide applicators filled with hydroxyethylcellulose gel. METHODS: Applicators, inserted by 252 female sex workers enrolled in a microbicide feasibility study in Southern India, served as positive controls for optimization and validation experiments. Before validation, optimal dye concentration and staining time were ascertained. Three validation experiments were conducted to determine sensitivity, specificity, and negative and positive predictive values. RESULTS: The dye concentration of 0.05% (wt/vol) FD&C Blue No. 1 Granular Food Dye (Prime Ingredients, Inc, Saddlebrook, NJ) and staining time of 5 seconds were determined to be optimal and were used for the 3 validation experiments. There were a total of 1848 possible applicator readings across validation experiments; 1703 (92.2%) applicator readings were correct. On average, the DSA performed with 90.6% sensitivity, 93.9% specificity, and had a negative predictive value of 93.8% and a positive predictive value of 91.0%. No statistically significant differences between experiments were noted. CONCLUSIONS: The DSA was optimized and successfully validated for use with single use, low-density polyethylene applicators filled with hydroxyethylcellulose gel. We recommend including the DSA in future microbicide trials involving vaginal gels so as to identify participants who have low adherence to dosing regimens. In doing so, we can develop strategies to improve adherence as well as investigate the association between product use and efficacy.
机译:背景:鉴于明确了解参与者应遵守研究方案,因此阴道杀菌剂使用自我报告的可靠性和有效性令人质疑。我们的目标是优化人口委员会先前验证的染料染色测定(DSA)和相关程序的使用,并确定DSA识别阴道插入的一次性使用的低密度聚乙烯杀微生物剂涂抹器的羟乙基纤维素凝胶的预测值。方法:在印度南部进行的杀菌剂可行性研究中,由252名女性性工作者插入了涂药器,作为优化和验证实验的阳性对照。在验证之前,确定最佳染料浓度和染色时间。进行了三个验证实验以确定敏感性,特异性以及阴性和阳性预测值。结果:确定染料浓度为0.05%(wt / vol)的FD&C蓝色1号颗粒食品染料(Prime Ingredients,Inc,Saddlebrook,NJ)的染色时间为5秒是最佳的,并用于3个验证实验。在验证实验中,总共有1848个可能的涂药器读数。 1703(92.2%)涂药器读数正确。平均而言,DSA的敏感性为90.6%,特异性为93.9%,阴性预测值为93.8%,阳性预测值为91.0%。实验之间没有统计上的显着差异。结论:对DSA进行了优化,并成功验证了其可用于一次性,低密度聚乙烯填充器中,该填充器装有羟乙基纤维素凝胶。我们建议将DSA纳入涉及阴道凝胶的未来杀菌剂试验中,以识别对给药方案依从性较低的参与者。在此过程中,我们可以制定策略来提高依从性,并研究产品使用与功效之间的关联。

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