Piroxicam and paracetamol in the prevention of early recurrent pain and emergency department readmission after renal colic: Randomized placebo‐controlled trial

Author:

Jaballah Rahma12ORCID,Toumia Marwa13ORCID,Youssef Rym2,Ali Khaoula Bel Haj13,Bakir Arij2,Sassi Sarra13,Yaakoubi Hajer2,Kouraichi Cyrine13,Dhaoui Randa13,Sekma Adel13ORCID,Zorgati Asma2,Beltaief Kaouthar13,Mezgar Zied4,Khrouf Mariem4,Bouida Wahid13,Grissa Mohamed Habib13,Saad Jamel5,Boubaker Hamdi13,Boukef Riadh12ORCID,Msolli Mohamed Amine13ORCID,Nouira Semir13

Affiliation:

1. Research Laboratory LR12SP18 Monastir University Monastir Tunisia

2. Emergency Department Sahloul University Hospital Sousse Tunisia

3. Emergency Department Fattouma Bourguiba University Hospital Monastir Tunisia

4. Emergency Department Hached University Hospital Sousse Tunisia

5. Department of Imaging and Interventional Radiology Fattouma Bourguiba University Hospital Monastir Tunisia

Abstract

AbstractObjectiveRenal colic (RC) is a common urologic emergency often leading to significant pain and recurrent hospital visits. This study aimed to compare the efficacy and safety of piroxicam versus paracetamol in preventing pain recurrence and hospital readmission in patients treated for RC and discharged from the emergency department (ED).MethodsA prospective, randomized, single‐blind trial was conducted in four EDs. Eligible adults with RC were randomized to receive oral piroxicam, paracetamol, or placebo for 5 days post–ED discharge. Primary outcomes included pain recurrence and ED readmission within 7 days. Secondary outcomes included time to recurrence and treatment‐related side effects.ResultsOf 1383 enrolled patients, no significant differences were observed among the groups regarding baseline characteristics. Pain recurrence rates within 7 days were 29% (95% confidence interval [CI] 24.9%–33.2%) for piroxicam, 30.3% (95% CI 26.1%–34.5%) for paracetamol, and 30.8% (95% CI 26.6%–35.0%) for placebo, with no significant between‐group differences (p = 0.84). Among patients experiencing recurrence, the majority encounter it within the initial 2 days following their discharge (86% in the piroxicam group, 84.1% in the paracetamol group, and 86% in the placebo group, respectively). ED readmission rates were similar across groups: 20.8% (95% CI 17.1%–24.5%) in the piroxicam group, 23.8% (95% CI 19.9%–27.7%) in the paracetamol group, and 22.9% (95% CI 19.1%–26.8%) in the placebo group (p = 0.52). The piroxicam group reported significantly higher adverse effects compared to others.ConclusionsPiroxicam and paracetamol did not demonstrate efficacy in preventing pain recurrence or ED readmission within the first week following RC treatment.

Publisher

Wiley

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