1. To correlate clinical and biochemical profile of pleural effusion: a retrospective study in tertiary care centre of central India.
- Author
-
Pathak H, Pandey S, Dave L, Baradia P, and Srivastava N
- Subjects
- Humans, Retrospective Studies, Middle Aged, India epidemiology, Male, Female, Adult, Aged, Pleural Effusion, Malignant diagnosis, Pleural Effusion, Malignant etiology, Pleural Effusion, Malignant metabolism, Tuberculosis, Pleural diagnosis, Tuberculosis, Pleural epidemiology, Young Adult, Hemoptysis etiology, Hemoptysis epidemiology, Chest Pain etiology, Adolescent, Adenosine Deaminase analysis, Smoking epidemiology, Fever etiology, Tertiary Care Centers, Pleural Effusion etiology, Pleural Effusion diagnosis, Pleural Effusion epidemiology, Pleural Effusion metabolism
- Abstract
Background: Pleural effusion indicates an imbalance between pleural fluid formation and removal. Classified into exudative and transudative, with common symptoms of dry cough, dyspnea and pleuritic chest pain. Confirmed etiology has to be established for effective treatment., Objective: Correlate clinical and biochemical profile of various etiologies of pleural effusion., Materials & Methods: Retrospective observational study of 2 years in the department of respiratory medicine, GMC Bhopal on 280 cases of pleural effusion., Results: Most common etiology was tubercular 202 (72.4%) followed by malignant in 36 (12.8%). With respect to tubercular, malignant pleural effusion has relative risk (RR) of 0.138 (p value < 0.05) in the age group of 51-60 years, which is statistically significant. Patients of tuberculosis complained of fever 158 (78.2%) whereas with malignancy complained of chest pain 16 (44.4%) followed by hemoptysis 12 (33.3%). For hemoptysis, with respect to tubercular, malignant effusion has RR of 5.68 (p value < 0.05) which is significant. History of smoking was significant in malignant effusion with RR of 2.57 (p value < 0.05) as compared to tubercular. Pleural fluid ADA was >70 in 83.7% in tubercular effusion, glucose was <60 mg/dl in 79% tubercular, malignant and bacteriological cause, LDH was >1000 in 88.4% in bacteriological and 72.3% in malignant effusion., Conclusion: Lack of tools for confirming diagnosis leads to diagnostic dilemma and delay in treatment initiation, leading to deterioration and untoward fatality in some cases. Our goal is early diagnosis by correlating clinical symptoms with biochemical profile and help initiate rapid treatment., Competing Interests: Conflicts of interest The authors have none to declare., (Copyright © 2023 Tuberculosis Association of India. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF