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

nonsteroidal anti‐inflammatory drugs paracetamol readmission recurrent pain renal colic

Journal

Academic emergency medicine : official journal of the Society for Academic Emergency Medicine
ISSN: 1553-2712
Titre abrégé: Acad Emerg Med
Pays: United States
ID NLM: 9418450

Informations de publication

Date de publication:
19 Aug 2024
Historique:
revised: 09 07 2024
received: 10 04 2024
accepted: 24 07 2024
medline: 20 8 2024
pubmed: 20 8 2024
entrez: 20 8 2024
Statut: aheadofprint

Résumé

Renal 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). A 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. Of 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. Piroxicam and paracetamol did not demonstrate efficacy in preventing pain recurrence or ED readmission within the first week following RC treatment.

Identifiants

pubmed: 39161087
doi: 10.1111/acem.14996
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Academic Emergency Medicine published by Wiley Periodicals LLC on behalf of Society for Academic Emergency Medicine.

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Auteurs

Rahma Jaballah (R)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Marwa Toumia (M)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Rym Youssef (R)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Khaoula Bel Haj Ali (KBH)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Arij Bakir (A)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Sarra Sassi (S)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Hajer Yaakoubi (H)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Cyrine Kouraichi (C)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Randa Dhaoui (R)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Adel Sekma (A)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Asma Zorgati (A)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Kaouthar Beltaief (K)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Zied Mezgar (Z)

Emergency Department, Hached University Hospital, Sousse, Tunisia.

Mariem Khrouf (M)

Emergency Department, Hached University Hospital, Sousse, Tunisia.

Wahid Bouida (W)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Mohamed Habib Grissa (MH)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Jamel Saad (J)

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

Hamdi Boubaker (H)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Riadh Boukef (R)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Mohamed Amine Msolli (MA)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Semir Nouira (S)

Research Laboratory LR12SP18, Monastir University, Monastir, Tunisia.
Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Classifications MeSH