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常规和超敏快速诊断检测在疟疾诊断中的诊断性能比较:系统评价和荟萃分析。

Comparison of diagnostic performance between conventional and ultrasensitive rapid diagnostic tests for diagnosis of malaria: A systematic review and meta-analysis.

机构信息

Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Department of Biology, Faculty of Natural and Computational Sciences, Woldia University, Woldia, Ethiopia.

出版信息

PLoS One. 2022 Feb 10;17(2):e0263770. doi: 10.1371/journal.pone.0263770. eCollection 2022.

Abstract

BACKGROUND

Successful malaria treatment, control and elimination programs require accurate, affordable, and field-deployable diagnostic tests. A number of studies have directly compared diagnostic performance between the new ultrasensitive rapid diagnostic test (us-RDT) and conventional rapid diagnostic test (co-RDT) for detecting malaria. Thus, we undertook this review to directly compare pooled diagnostic performance of us-RDT and co-RDT for detection of malaria.

METHODS

PubMed, Web of Science, Scopus, Embase, and ProQuest were searched from their inception until 31 January 2021 accompanied by forward and backward citations tracking. Two authors independently assessed the quality of included studies by RevMan5 software (using the QUADAS-2 checklist). Diagnostic accuracy estimates (sensitivity and specificity and others) were pooled using a random-effect model and 95% confidence interval (CI) in Stata 15 software.

RESULTS

Fifteen studies with a total of 20,236 paired co-RDT and us-RDT tests were included in the meta-analysis. Molecular methods (15 studies) and immunoassay test (one study) were used as standard methods for comparison with co-RDT and us-RDT tests. The pooled sensitivity for co-RDT and us-RDT were 42% (95%CI: 25-62%) and 61% (95%CI: 47-73%), respectively, with specificity of 99% (95%CI: 98-100%) for co-RDT, and 99% (95%CI: 96-99%) for us-RDT. In asymptomatic individuals, the pooled sensitivity and specificity of co-RDT were 27% (95%CI: 8-58%) and 100% (95%CI: 97-100%), respectively, while us-RDT had a sensitivity of 50% (95%CI: 33-68%) and specificity of 98% (95%CI: 94-100%). In low transmission settings, pooled sensitivity for co-RDT was 36% (95%CI: 9 76%) and 62% (95%CI: 44 77%) for us RDT, while in high transmission areas, pooled sensitivity for co RDT and us RDT were 62% (95%CI: 39 80%) and 75% (95%CI: 57-87%), respectively.

CONCLUSION

The us-RDT test showed better performance than co-RDT test, and this characteristic is more evident in asymptomatic individuals and low transmission areas; nonetheless, additional studies integrating a range of climate, geography, and demographics are needed to reliably understand the potential of the us-RDT.

摘要

背景

成功的疟疾治疗、控制和消除计划需要准确、负担得起且可在现场部署的诊断检测。许多研究已经直接比较了新的超敏快速诊断检测(us-RDT)和常规快速诊断检测(co-RDT)在检测疟疾方面的诊断性能。因此,我们进行了这项综述,以直接比较 us-RDT 和 co-RDT 检测疟疾的汇总诊断性能。

方法

从成立之初到 2021 年 1 月 31 日,我们在 PubMed、Web of Science、Scopus、Embase 和 ProQuest 上进行了搜索,并进行了前瞻性和回溯性引文追踪。两位作者使用 RevMan5 软件(使用 QUADAS-2 清单)独立评估纳入研究的质量。使用 Stata 15 软件以随机效应模型和 95%置信区间(CI)汇总诊断准确性估计值(敏感性和特异性等)。

结果

15 项研究共纳入 20236 对 co-RDT 和 us-RDT 检测的配对研究,纳入荟萃分析。分子方法(15 项研究)和免疫测定试验(一项研究)被用作与 co-RDT 和 us-RDT 检测比较的标准方法。co-RDT 和 us-RDT 的汇总敏感性分别为 42%(95%CI:25-62%)和 61%(95%CI:47-73%),特异性分别为 99%(95%CI:98-100%)和 99%(95%CI:96-99%)。在无症状个体中,co-RDT 的汇总敏感性和特异性分别为 27%(95%CI:8-58%)和 100%(95%CI:97-100%),而 us-RDT 的敏感性为 50%(95%CI:33-68%),特异性为 98%(95%CI:94-100%)。在低传播环境中,co-RDT 的汇总敏感性为 36%(95%CI:9-76%)和 62%(95%CI:44-77%),而 us-RDT 的敏感性为 62%(95%CI:39-80%)和 75%(95%CI:57-87%)。

结论

us-RDT 检测的性能优于 co-RDT 检测,而在无症状个体和低传播地区,这一特征更为明显;然而,需要进行更多的研究来整合各种气候、地理和人口统计学因素,以可靠地了解 us-RDT 的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de02/8830612/ec37c44399f3/pone.0263770.g001.jpg

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