Copyright
©The Author(s) 2025.
World J Clin Cases. Aug 6, 2025; 13(22): 106925
Published online Aug 6, 2025. doi: 10.12998/wjcc.v13.i22.106925
Published online Aug 6, 2025. doi: 10.12998/wjcc.v13.i22.106925
Table 2 Methodology workflow
Step | Content | Key details |
Study design | Retrospective cohort study | Data collected from March 2015 to December 2019 at two hospitals in Rio de Janeiro, Brazil. Total patients: 157 (124 exudates, 33 transudates) |
Inclusion criteria | Confirmed diagnosis of pleural effusion (exudates/transudates) | Exudates: n = 124 (79%); Transudates: n = 33 (21%) |
Exclusion criteria | Absolute contraindications, hemolyzed PF, chronic renal failure, jaundice, unknown etiology, immunosuppressive medication use | Final cohort: 157 patients (after exclusions) |
Sample size calculation | Based on MedCalc software (AUC > 0.50, α = 0.05, β = 0.20) | Required: 57 patients (19 exudates, 38 transudates); Actual: 157 patients |
P-ADA assay | Kinetic method (Diazyme ADA kit) | Linear range: 0–200 U/L; Reference value: < 15 U/L (healthy adults) |
Statistical analysis | ROC curve, Youden index, DeLong test, Hosmer–Lemeshow goodness-of-fit | AUC = 0.8107 (95%CI: 0.7174–0.8754), P < 0.0001 |
- Citation: Shi DD, Tian J, Ding J. Adenosine deaminase in pleural effusion: Bridging diagnosis and the pathophysiology of inflammation. World J Clin Cases 2025; 13(22): 106925
- URL: https://www.wjgnet.com/2307-8960/full/v13/i22/106925.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v13.i22.106925