The analytical and clinical aspects pleural fluid analysis

IF 1.4
Zhi-De Hu
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Abstract

Etiological diagnosis of pleural effusion (PE) remains a challenge for clinicians. Although thoracoscopy has high diagnostic accuracy in patients with undiagnosed PE, it has some limitations, such as invasiveness and the requirement for special training. Pleural fluid analysis shows a high diagnostic accuracy in undiagnosed PE. Compared with thoracoscopy, pleural fluid analysis has the advantages of noninvasiveness, low cost, no requirement for special training, and objectivity. PE can be categorized into transudate and exudate according to the underlying etiology. Transudates are caused by systemic disorders, such as cardiac failure and liver cirrhosis, and exudates are associated with local inflammation of the pleura. The first step in the etiological diagnosis of pleural effusion is separating transudates from exudates. The landmark work in separating exudates and transudate is the Light’s criteria (1). The most common causes of exudate are malignancy, pneumonia, and tuberculous pleurisy. Additional biomarkers beyond the Light’s criteria are needed to verify the underlying causes of exudate. In this special issue of pleural fluid analysis, some issues in the pleural fluid analysis were discussed. The diagnostic accuracy of tumor markers for malignant pleural effusion (MPE) is controversial, and the results from the available studies are always inconsistent. Consequently, systematic reviews and meta-analyses are needed to ascertain the diagnostic accuracy of a given marker. In this special issue, the diagnostic accuracy of pleural endostatin for MPE was investigated by a meta-analysis. The results indicate that the endostatin’s diagnostic accuracy for MPE is low (doi: 10.21037/ jlpm-20-91). Machine learning (ML) represents a novel and promising strategy for investigating the diagnostic accuracy of multiple biomarkers (2). A previous study showed that ML improved the diagnostic accuracy of conventional biomarkers for tuberculosis pleural effusion (TPE) (3). In this special the of for (MPM) was evaluated. to findings in indicated accuracy of tumor markers for MPM (doi: 10.21037/jlpm-20-90).
胸腔积液分析的分析与临床
胸腔积液(PE)的病因诊断仍然是临床医生面临的挑战。尽管胸腔镜对未确诊的PE患者有很高的诊断准确性,但它也有一些局限性,如侵入性和需要特殊训练。胸腔积液分析对未确诊的PE具有较高的诊断准确率。与胸腔镜相比,胸腔积液分析具有无创、成本低、无需特殊训练和客观性的优点。PE根据病因可分为渗出液和渗出液。渗出物是由系统性疾病引起的,如心力衰竭和肝硬化,渗出物与胸膜的局部炎症有关。胸腔积液病因诊断的第一步是从渗出物中分离渗出物。分离渗出物和渗出物的里程碑式工作是光的标准(1)。渗出物最常见的原因是恶性肿瘤、肺炎和结核性胸膜炎。需要光标准之外的其他生物标志物来验证渗出物的潜在原因。在本期胸膜液分析专刊中,对胸膜液分析中的一些问题进行了讨论。肿瘤标志物对恶性胸腔积液(MPE)的诊断准确性存在争议,现有研究的结果总是不一致。因此,需要系统综述和荟萃分析来确定给定标记物的诊断准确性。在本期特刊中,通过荟萃分析研究了胸膜内皮抑素对MPE的诊断准确性。结果表明,内皮抑素对MPE的诊断准确率较低(doi:10.21037/jlpm-20-91)。机器学习(ML)代表了一种新的、有前途的策略,用于研究多种生物标志物的诊断准确性(2)。先前的一项研究表明,ML提高了传统生物标志物对结核性胸腔积液(TPE)的诊断准确性(3)。在此特殊情况下,对(MPM)的进行了评估。肿瘤标志物对MPM的指示准确性的发现(doi:10.21037/jlpm-20-90)。
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CiteScore
1.70
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