期刊论文详细信息
PLoS One
Evaluation of PCR on Bronchoalveolar Lavage Fluid for Diagnosis of Invasive Aspergillosis: A Bivariate Metaanalysis and Systematic Review
Yi Shi1  Xin Su2  Wenkui Sun2  Yong Song2  Xin Lu3  Yaling Guo3  Wei Gao3  Qian Qian4  Ke Wang5 
[1] Department of Respiratory Diseases, Nursing School, Guangxi Medical University, Nanning, China;Department of Respiratory Medicine, Jinling Hospital, Clinical School of Nanjing, Second Military Medical University, Nanjing, China;Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China;First Department of Respiratory Medicine, Nanjing Chest Hospital, Nanjing, China;Institute of Respiratory Diseases, First Affiliated Hospital, Guangxi Medical University, Nanning, China
关键词: Polymerase chain reaction;    Aspergillus fumigatus;    Aspergillus;    DNA extraction;    Diagnostic medicine;    Proteases;    Aspergillus flavus;    Adults;   
DOI  :  10.1371/journal.pone.0028467
学科分类:医学(综合)
来源: Public Library of Science
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【 摘 要 】

Background Nucleic acid detection by polymerase chain reaction (PCR) is emerging as a sensitive and rapid diagnostic tool. PCR assays on serum have the potential to be a practical diagnostic tool. However, PCR on bronchoalveolar lavage fluid (BALF) has not been well established. We performed a systematic review of published studies to evaluate the diagnostic accuracy of PCR assays on BALF for invasive aspergillosis (IA). Methods Relevant published studies were shortlisted to evaluate the quality of their methodologies. A bivariate regression approach was used to calculate pooled values of the method sensitivity, specificity, and positive and negative likelihood ratios. Hierarchical summary receiver operating characteristic curves were used to summarize overall performance. We calculated the post-test probability to evaluate clinical usefulness. Potential heterogeneity among studies was explored by subgroup analyses. Results Seventeen studies comprising 1191 at-risk patients were selected. The summary estimates of the BALF-PCR assay for proven and probable IA were as follows: sensitivity, 0.91 (95% confidence interval (CI), 0.79–0.96); specificity, 0.92 (95% CI, 0.87–0.96); positive likelihood ratio, 11.90 (95% CI, 6.80–20.80); and negative likelihood ratio, 0.10 (95% CI, 0.04–0.24). Subgroup analyses showed that the performance of the PCR assay was influenced by PCR assay methodology, primer design and the methods of cell wall disruption and DNA extraction. Conclusions PCR assay on BALF is highly accurate for diagnosing IA in immunocompromised patients and is likely to be a useful diagnostic tool. However, further efforts towards devising a standard protocol are needed to enable formal validation of BALF-PCR.

【 授权许可】

CC BY   

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