No influence of ibuprofen on bone healing after Colles' fracture - A randomized controlled clinical trial.


Journal

Injury
ISSN: 1879-0267
Titre abrégé: Injury
Pays: Netherlands
ID NLM: 0226040

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 26 02 2019
revised: 30 04 2019
accepted: 04 06 2019
pubmed: 13 6 2019
medline: 25 2 2020
entrez: 13 6 2019
Statut: ppublish

Résumé

Nonsteroidal anti-inflammatory drugs (NSAIDs) may delay bone healing. This knowledge is mainly derived from retrospective uncontrolled clinical studies and from animal experiments. The purpose of this prospective controlled study was to investigate whether ibuprofen influences pain, function, and bone healing after a Colles' fracture. A single center, triple-blind, randomized clinical trial. 95 patients, 80 females and 15 males, with displaced Colles' fracture aged median 65 (range 40-85) years old were included and operated by external fixation from June 2012 through June 2015. 89 participants received interventional medicine and 83 completed the one-year follow-up. The 7-day ibuprofen group received 600 mg of ibuprofen three times a day, the 3-day ibuprofen group received ibuprofen for three days and a placebo for the following four days, and finally, the placebo group received a placebo for seven days. All patients received paracetamol 1000 mg four times a day and 50 mg tramadol if needed. The primary outcome were radiological changes in radius tilt, length, and inclination observed during and 6 weeks after the surgery. The analgesic outcome were 14 days experience of pain, and registered use of tramadol. The functional outcomes were the percentage differences in the motion between the injured and non-injured wrist, and the DASH score at 3 and 12 months. All analyses were performed according to the intention to treat. No clinically relevant difference was observed in the radiological migration between the treatment groups, 0.064≤P ≤ 0.81. There was no difference in the pain score between the treatment groups, P = 0.13. The use of tramadol was lower in the ibuprofen groups than in the placebo group, P = 0.035. Ibuprofen treatment did not affect the range of motion, 0.148 ≤P ≤ 0.963. Patients in all groups demonstrated DASH score, and wrist motion improvement, close to 90% of normal amplitude. The complication rate was higher in the 7-day ibuprofen group compared to the placebo group, P = 0.043. Ibuprofen treatment demonstrated a tramadol-sparing effect during the postoperative period. Neither wrist function nor radiological migration were influenced. The complication rate was higher in the ibuprofen-treated group compared the placebo-treated group.

Identifiants

pubmed: 31186121
pii: S0020-1383(19)30342-0
doi: 10.1016/j.injury.2019.06.011
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Ibuprofen WK2XYI10QM

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1309-1317

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Marius Aliuskevicius (M)

Department of Orthopedic Surgery, Clinic Head-Orto, Aalborg University Hospital, Hobrovej 18-22, 9000 Aalborg, Denmark. Electronic address: marali@rn.dk.

Svend Erik Østgaard (SE)

Department of Orthopedic Surgery, Clinic Head-Orto, Aalborg University Hospital, Hobrovej 18-22, 9000 Aalborg, Denmark. Electronic address: sveo@rn.dk.

Sten Rasmussen (S)

Department of Orthopedic Surgery, Clinic Head-Orto, Aalborg University Hospital, Hobrovej 18-22, 9000 Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Denmark. Electronic address: sten.rasmussen@rn.dk.

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