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快速分子诊断检测对出现病毒性呼吸道症状患者的临床影响:一项系统文献综述

Clinical impact of rapid molecular diagnostic tests in patients presenting with viral respiratory symptoms: A systematic literature review.

作者信息

Mojebi Ali, Wu Ping, Keeping Sam, Hale Braden, Chase Jordan G, Beaubrun Anne

机构信息

Evidence Synthesis, PRECISIONheor, Vancouver, BC, Canada.

Global Health Economics & Outcomes Research, Cepheid, Sunnyvale, CA, United States of America.

出版信息

PLoS One. 2024 Jun 13;19(6):e0303560. doi: 10.1371/journal.pone.0303560. eCollection 2024.

Abstract

BACKGROUND

Molecular tests can detect lower concentrations of viral genetic material over a longer period of respiratory infection than antigen tests. Delays associated with central laboratory testing can result in hospital-acquired transmission, avoidable patient admission, and unnecessary use of antimicrobials, all which may lead to increased cost of patient management. The aim of this study was to summarize comparisons of clinical outcomes associated with rapid molecular diagnostic tests (RMDTs) versus other diagnostic tests for viral respiratory infections.

METHODS

A systematic literature review (SLR) conducted in April 2023 identified studies evaluating clinical outcomes of molecular and antigen diagnostic tests for patients suspected of having respiratory viral infections.

RESULTS

The SLR included 21 studies, of which seven and 14 compared RMDTs (conducted at points of care or at laboratories) to standard (non-rapid) molecular tests or antigen tests to detect SARS-CoV-2 and influenza, respectively. In studies testing for SARS-CoV-2, RMDTs led to reductions in time to test results versus standard molecular tests (range of the reported medians: 0.2-3.8 hours versus 4.3-35.9 hours), with similar length of emergency department stay (3.2-8 hours versus 3.7-28.8 hours). Similarly, in studies testing for influenza, RMDTs led to reductions in time to test results versus standard molecular tests (1-3.5 hours versus 18.2-29.2 hours), with similar length of emergency department stay (3.7-11 hours versus 3.8-11.9 hours). RMDTs were found to decrease exposure time of uninfected patients, rate of hospitalization, length of stay at the hospitals, and frequency of unnecessary antiviral and antibacterial therapy, while improving patient flow, compared to other tests.

CONCLUSIONS

Compared to other diagnostic tests, RMDTs improve clinical outcomes, test turnaround time, and stewardship by decreasing unnecessary use of antibiotics and antivirals. They also reduce hospital admission and length of stay, which may, in turn, reduce unnecessary exposure of patients to hospital-acquired infections and their associated costs.

摘要

背景

与抗原检测相比,分子检测在呼吸道感染的较长时间内能够检测到更低浓度的病毒遗传物质。与中心实验室检测相关的延迟可能导致医院获得性传播、不必要的患者住院以及抗菌药物的不必要使用,所有这些都可能导致患者管理成本增加。本研究的目的是总结与快速分子诊断检测(RMDT)和其他用于病毒性呼吸道感染的诊断检测相关的临床结果比较。

方法

2023年4月进行的一项系统文献综述(SLR)确定了评估疑似呼吸道病毒感染患者分子和抗原诊断检测临床结果的研究。

结果

该SLR纳入了21项研究,其中7项和14项分别将RMDT(在护理点或实验室进行)与标准(非快速)分子检测或抗原检测进行比较,以检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和流感。在检测SARS-CoV-2的研究中,与标准分子检测相比,RMDT缩短了检测结果的时间(报告的中位数范围:0.2 - 3.8小时对4.3 - 35.9小时),急诊留观时间相似(3.2 - 8小时对3.7 - 28.8小时)。同样,在检测流感的研究中,与标准分子检测相比(1 - 3.5小时对18.2 - 29.2小时),RMDT缩短了检测结果的时间,急诊留观时间相似(3.7 - 11小时对3.8 - 11.9小时)。与其他检测相比,发现RMDT减少了未感染患者的暴露时间、住院率、住院时间以及不必要的抗病毒和抗菌治疗频率,同时改善了患者流程。

结论

与其他诊断检测相比,RMDT通过减少抗生素和抗病毒药物的不必要使用,改善了临床结果、检测周转时间和管理。它们还减少了住院率和住院时间,这反过来可能减少患者不必要地暴露于医院获得性感染及其相关成本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb0/11175541/f6df54aab216/pone.0303560.g001.jpg

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