Diagnostic Test Accuracy of the Fungitell Serum (1→3)-β-D-Glucan Assay for the Diagnosis of Pneumocystis jirovecii Pneumonia: A Systematic Review and Meta-Analysis.

IF 10.9 1区 医学 Q1 INFECTIOUS DISEASES
Connor Prosty, Owen Dan Luo, Roy Khalaf, Olivier Del Corpo, Emily G McDonald, Todd C Lee
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引用次数: 0

Abstract

Background: The diagnosis of Pneumocystis jirovecii pneumonia (PCP) can be challenging because of diagnostic tests that are imperfect and/or invasive. The Fungitell serum (1→3)-β-D-glucan (BDG) assay is a non-invasive blood test studied for PCP; however, the manufacturer-recommended cut-off of 80pg/mL is not well validated for this disease.

Objectives: We conducted a systematic review and meta-analysis to determine the diagnostic test accuracy of the Fungitell BDG assay for the diagnosis of PCP.

Methods: Data Sources A search strategy of MEDLINE and Embase from a previous meta-analysis on BDG was updated to January 31, 2024. Test Fungitell BDG assay. Reference Standard One or more of: lung biopsy, bronchoalveolar lavage, induced sputum, or nasopharyngeal swab specimens tested for PCP by histopathology, microscopy using immunofluorescence or staining, or polymerase chain reaction. Assessment of Risk of Bias The QUADAS-2 tool. Methods of Data Synthesis Diagnostic test accuracy data of the Fungitell serum BDG assay across all reported cut-offs were pooled by meta-analysis. We then evaluated a categorical approach using <80pg/mL as a rule-out threshold and ≥400pg/mL as a rule-in threshold.

Results: 26 articles were included comprising 5111 patients and 1150 PCP cases. At the conventional cut-off of 80pg/mL, the overall pooled sensitivity and specificity were 83.5% (95% Confidence Interval [95%CI]=72.8-90.6) and 75.5% (95%CI=66.0-83.0), respectively. At a pre-test probability of <20% and a BDG <80pg/mL, the post-test probability would be <5% (negative predictive value >95%). At 400pg/mL, sensitivity was reduced to 63.5% (95%CI=45.8-78.1) with specificity increased to 93.6% (95%CI=88.6-96.5). At a pre-test probability of 47.5%, a BDG >400pg/mL would have a post-test probability of >90%.

Discussion: A categorical approach using <80pg/mL to rule-out and >400pg/mL to rule-in PCP may allow for a more nuanced interpretation based on pre-test probability. More accurate estimates of pre-test probability and further external validation is required.

Fungitell 血清(1→3)-β-D-葡聚糖测定诊断肺孢子菌肺炎的检验准确性:系统综述与元分析》。
背景:由于诊断测试不完善和/或具有侵入性,因此诊断肺孢子虫肺炎(PCP)具有挑战性。Fungitell血清(1→3)-β-D-葡聚糖(BDG)测定是一种针对PCP的非侵入性血液检验;然而,制造商推荐的80pg/mL临界值并没有得到很好的验证:我们进行了一项系统综述和荟萃分析,以确定 Fungitell BDG 检测法诊断五氯苯酚的准确性:数据来源 从之前关于 BDG 的荟萃分析中提取的 MEDLINE 和 Embase 搜索策略已更新至 2024 年 1 月 31 日。检测方法 Fungitell BDG 检测法。参考标准 肺活检、支气管肺泡灌洗液、诱导痰或鼻咽拭子标本中的一种或多种通过组织病理学、使用免疫荧光或染色的显微镜检查或聚合酶链反应对五氯苯酚进行检测。偏倚风险评估 QUADAS-2 工具。数据综合方法 通过荟萃分析汇集了Fungitell血清BDG测定在所有报告临界值上的诊断检测准确性数据。结果:共纳入 26 篇文章,包括 5111 名患者和 1150 个 PCP 病例。在 80pg/mL 的常规临界值下,汇总的总体灵敏度和特异性分别为 83.5%(95% 置信区间 [95%CI]=72.8-90.6 )和 75.5%(95%CI=66.0-83.0)。检测前概率为 95%)。400pg/mL 时,灵敏度降至 63.5%(95%CI=45.8-78.1),特异性增至 93.6%(95%CI=88.6-96.5)。在检测前概率为47.5%的情况下,BDG>400pg/mL的检测后概率将>90%:讨论:使用 400pg/mL 的分类方法来排除 PCP,可根据检测前概率做出更细致的解释。需要对检测前概率进行更准确的估计,并进一步进行外部验证。
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来源期刊
CiteScore
25.30
自引率
2.10%
发文量
441
审稿时长
2-4 weeks
期刊介绍: Clinical Microbiology and Infection (CMI) is a monthly journal published by the European Society of Clinical Microbiology and Infectious Diseases. It focuses on peer-reviewed papers covering basic and applied research in microbiology, infectious diseases, virology, parasitology, immunology, and epidemiology as they relate to therapy and diagnostics.
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