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中国和尼日利亚三种HIV和梅毒双重快速诊断检测的实验室评估。

Laboratory evaluation of three dual rapid diagnostic tests for HIV and syphilis in China and Nigeria.

作者信息

Yin Yue-Ping, Ngige Evelyn, Anyaike Chukwuma, Ijaodola Gbenga, Oyelade Taiwo A, Vaz Rui Gama, Newman Lori M, Chen Xiang-Sheng

机构信息

National Center for STD Control and Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.

National AIDS and STIs Control Program, Federal Ministry of Health, Abuja, Nigeria.

出版信息

Int J Gynaecol Obstet. 2015 Jun;130 Suppl 1:S22-6. doi: 10.1016/j.ijgo.2015.04.004. Epub 2015 Apr 29.

Abstract

OBJECTIVE

To determine the laboratory-based performance and operational characteristics of three dual rapid diagnostic tests (RDTs) for testing HIV and syphilis.

METHODS

Three dual RDTs (SD Bioline, Chembio, and MedMira) were evaluated using 1514 serum specimens archived at laboratories or collected from clinics in China and Nigeria to determine sensitivity and specificity, with 95% confidence intervals. Concordance of testing results read by two technicians, stability of testing results read at two time points, and test operation characteristics were also assessed.

RESULTS

All three of the evaluated RDTs gave excellent performance with a combined sensitivity ranging from 99.0%-99.6% for HIV and 98.3%-99.0% for syphilis, and a combined specificity ranging from 97.9%-99.0% for HIV and 97.2%-99.6% for syphilis. Concordance of testing results between two technicians and stability of testing results read within and one hour past the recommended reading period showed excellent agreement, with Kappa greater than or equal to 0.98.

CONCLUSIONS

All the tests were found to be very or fairly easy to use and easy to interpret the results. Further evaluations of these dual RDTs with whole blood in field settings, and more studies on the implication of introduction of these tests in HIV and syphilis control programs are needed.

摘要

目的

确定三种用于检测HIV和梅毒的双重快速诊断检测(RDT)基于实验室的性能和操作特征。

方法

使用在中国和尼日利亚的实验室存档或从诊所收集的1514份血清标本对三种双重RDT(SD Bioline、Chembio和MedMira)进行评估,以确定敏感性和特异性,并给出95%置信区间。还评估了两名技术人员读取的检测结果的一致性、在两个时间点读取的检测结果的稳定性以及检测操作特征。

结果

所有三种评估的RDT均表现出色,HIV的综合敏感性为99.0%-99.6%,梅毒的综合敏感性为98.3%-99.0%;HIV的综合特异性为97.9%-99.0%,梅毒的综合特异性为97.2%-99.6%。两名技术人员之间检测结果的一致性以及在推荐读取时间内和之后一小时内读取的检测结果的稳定性显示出极佳的一致性,Kappa大于或等于0.98。

结论

发现所有检测都非常或相当易于使用且易于解释结果。需要在现场环境中对这些双重RDT进行全血进一步评估,以及更多关于在HIV和梅毒控制项目中引入这些检测的影响的研究。

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