3.8 Article

Efficacy of procalcitonin and pentraxin-3 as early biomarkers for differential diagnosis of pleural effusions

期刊

PLEURA AND PERITONEUM
卷 6, 期 2, 页码 83-90

出版社

WALTER DE GRUYTER GMBH
DOI: 10.1515/pp-2021-0111

关键词

malignant effusions; parapneumonic effusions; pentraxin-3; pleural effusion; procalcitonin; tuberculous effusions

资金

  1. Himalaya Institute of Medical Science, Swami Rama Himalaya University [SRHU/HIMS/RC/2017/23]

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The study aimed to evaluate the predictive accuracy of PCT and PTX-3 in the differential diagnosis of pleural effusions compared to other biochemical markers, and found that PCT and PTX-3 have favorable discrimination ability in predicting different types of pleural effusions.
Objectives: Pleural effusion, defined as an abnormal accumulation of fluid in pleural space, can be of two types: transudative and exudative. The primary aim of the study was to assess the predictive accuracy of procalcitonin (PCT) and pentraxin-3 (PTX-3) in comparison to other biochemical markers such as C-reactive protein (CRP), and adenosine deaminase (ADA) in the differential diagnosis of pleural effusions. Methods: Across-sectional analytical study was conducted on patients with pleural effusion. Multiple comparisons and receiver-operating characteristics (ROC) analyses were made to evaluate the diagnostic significance of biochemical markers. Results: Sixty-six patients with exudative pleural effusion classified as malignant, tuberculous, and parapneumonic effusions (malignant pleural effusion [MPE], tuberculous [TPE], and parapneumonic [PPE]) were included. Significant differences in pleural fluid levels in both PCT (p-value: 0.001) and PTX-3(p-value: 0.001), as well as serum levels of PCT (p-value: 0.001), were observed between the three groups. ROC analysis showed both PTX-3 and PCT having favorable discrimination ability with high sensitivity (>= 90%) and specificity to predict PPE from TPE and MPE. Conclusions: Evaluation of serum and pleural fluid PCT and levels of PTX-3 in the pleural fluid may be used as an early biomarker to differentiate the etiology of pleural effusion.

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