Editorial
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
Table 2 Methodology workflow
Step
Content
Key details
Study designRetrospective cohort studyData collected from March 2015 to December 2019 at two hospitals in Rio de Janeiro, Brazil. Total patients: 157 (124 exudates, 33 transudates)
Inclusion criteriaConfirmed diagnosis of pleural effusion (exudates/transudates)Exudates: n = 124 (79%); Transudates: n = 33 (21%)
Exclusion criteriaAbsolute contraindications, hemolyzed PF, chronic renal failure, jaundice, unknown etiology, immunosuppressive medication useFinal cohort: 157 patients (after exclusions)
Sample size calculationBased on MedCalc software (AUC > 0.50, α = 0.05, β = 0.20)Required: 57 patients (19 exudates, 38 transudates); Actual: 157 patients
P-ADA assayKinetic method (Diazyme ADA kit)Linear range: 0–200 U/L; Reference value: < 15 U/L (healthy adults)
Statistical analysisROC curve, Youden index, DeLong test, Hosmer–Lemeshow goodness-of-fitAUC = 0.8107 (95%CI: 0.7174–0.8754), P < 0.0001