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通过定量病毒载量检测监测冠状病毒病的进展和临床影响。

Monitoring coronavirus disease progression and clinical impact through quantitative viral load testing.

机构信息

Division of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.

Division of Infectious Diseases and Tropical Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

Clin Chim Acta. 2024 Jun 15;560:119731. doi: 10.1016/j.cca.2024.119731. Epub 2024 May 15.

Abstract

BACKGROUND

The viral load (VL) in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected individuals is critical for improving clinical treatment strategies, care, and decisions. Several studies have reported that the initial SARS-CoV-2 VL is associated with disease severity and mortality. Cycle threshold (Ct) values and/or copies/mL are often used to quantify VL. However, a multitude of platforms, primer/probe sets of different SARS-CoV-2 target genes, and reference material manufacturers may cause inconsistent interlaboratory interpretations. The first International Standard for SARS-CoV-2 RNA quantitative assays has allowed diagnostic laboratories to transition SARS-CoV-2 VL results into international units per milliliter (IU/mL). The Cobas SARS-CoV-2 Duo quantitative assay provides VL results expressed in IU/mL.

MATERIALS AND METHODS

We enrolled 145 and 50 SARS-CoV-2-positive, hospitalized and 50-negative individuals at the Tri-Service General Hospital, Taiwan from January to May 2022. Each participant's electronic medical record was reviewed to determine asymptomatic, mild, moderate, and severe cases. Nasopharyngeal swabs were collected using universal transport medium. We investigated the association of SARS-CoV-2 VL with disease severity using the Cobas SARS-CoV-2 Duo quantitative assay and its functionality in clinical assessment and decision making to further improve clinical treatment strategies. Limit of detection (LOD) was assessed.

RESULTS

All 50 SARS-CoV-2-negative samples confirmed negative for SARS-CoV-2, demonstrating 100 % specificity of the Cobas SARS-CoV-2 Duo assay. Patients with severe symptoms had longer hospital stays, and the length of hospital stay (30.56 days on average) positively correlated with the VL (8.22 ± 1.21 log IU/mL). Asymptomatic patients had the lowest VL (5.54 ± 2.06 log IU/mL) at admission and the shortest hospital stay (14.1 days on average).

CONCLUSIONS

VL is associated with disease severity and duration of hospitalization; therefore, its quantification should be considered when making clinical care decisions and treatment strategies. The Cobas SARS-CoV-2 Duo assay provides a commutable unitage IU/mL for interlaboratory interpretations.

摘要

背景

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染个体的病毒载量(VL)对于改善临床治疗策略、护理和决策至关重要。多项研究报告称,SARS-CoV-2 的初始 VL 与疾病严重程度和死亡率相关。Ct 值和/或拷贝/ml 通常用于定量 VL。然而,众多平台、不同 SARS-CoV-2 靶基因的引物/探针集和参考物质制造商可能导致实验室间解释不一致。首个 SARS-CoV-2 RNA 定量检测国际标准允许诊断实验室将 SARS-CoV-2 VL 结果转换为每毫升国际单位(IU/mL)。Cobas SARS-CoV-2 Duo 定量检测提供以 IU/mL 表示的 VL 结果。

材料和方法

我们在 2022 年 1 月至 5 月期间从台湾三军总医院招募了 145 名 SARS-CoV-2 阳性住院患者和 50 名 SARS-CoV-2 阴性个体。每位参与者的电子病历均经过审查,以确定无症状、轻症、中度和重症病例。使用通用转运培养基采集鼻咽拭子。我们使用 Cobas SARS-CoV-2 Duo 定量检测研究了 SARS-CoV-2 VL 与疾病严重程度的关系,以及其在临床评估和决策中的功能,以进一步改善临床治疗策略。评估了检测限(LOD)。

结果

所有 50 名 SARS-CoV-2 阴性样本均确认为 SARS-CoV-2 阴性,表明 Cobas SARS-CoV-2 Duo 检测的特异性为 100%。症状严重的患者住院时间更长,住院时间(平均 30.56 天)与 VL(8.22±1.21 log IU/mL)呈正相关。无症状患者入院时 VL 最低(5.54±2.06 log IU/mL),住院时间最短(平均 14.1 天)。

结论

VL 与疾病严重程度和住院时间有关;因此,在制定临床护理决策和治疗策略时,应考虑对其进行定量分析。Cobas SARS-CoV-2 Duo 检测为实验室间解释提供了可互换的单位 IU/mL。

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