Are corticosteroid injections needed after needling and lavage of calcific tendinitis? Randomised, double-blind, non-inferiority trial.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
06 2019
Historique:
received: 21 12 2018
revised: 19 03 2019
accepted: 20 03 2019
pubmed: 13 4 2019
medline: 30 1 2020
entrez: 13 4 2019
Statut: ppublish

Résumé

Steroid injections are common after an ultrasound-guided puncture and lavage (UGPL) of calcific tendonitis of the rotator cuff. However, steroids may prevent calcification resorption and negatively affect tendon healing. Our study was designed to determine whether saline solution was non-inferior to steroids in the prevention of acute pain reactions in the week following UGPL. This was a randomised, double-blinded, controlled non-inferiority trial with 12-month follow-up. We included 132 patients (66 in each group) with symptomatic calcification measuring more than 5 mm. Patients received 1 mL of saline or steroid (methylprednisolone 40 mg) in the subacromial bursa at the end of UGPL. Primary outcome was the maximal pain during the week following the procedure with a prespecified non-inferiority margin of 10 mm (0-100 visual analogue scale). Secondary outcomes included pain at rest and during activity, function (disabilities of the arm, shoulder and hand score) and radiological evolution of the calcification over the 12-month follow-up. The estimated mean difference in the first week's maximal pain between these two groups was 11.76 (95% CI 3.78 to 19.75). Steroids significantly improved VAS pain at rest and during activities, as well as function at 7 days and 6 weeks. They did not change the rate of calcification resorption, which occurred in 83% and 74% of patients at 12 months in the saline and steroid groups. Non-inferiority of saline when compared with steroids could not be established. However, steroid injection improved pain in the 6 weeks following the procedure, and function in the 3 months after, with no significant effect on calcification resorption. NTC02403856.

Identifiants

pubmed: 30975645
pii: annrheumdis-2018-214971
doi: 10.1136/annrheumdis-2018-214971
doi:

Substances chimiques

Glucocorticoids 0
Saline Solution 0
Methylprednisolone X4W7ZR7023

Banques de données

ClinicalTrials.gov
['NCT02403856']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

837-843

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Christelle Darrieutort-Laffite (C)

Department of Rheumatology, CHU Nantes, Nantes, France.

Stephane Varin (S)

Department of Rheumatology, CHD Vendée, La Roche sur Yon, France.

Guillaume Coiffier (G)

Department of Rheumatology, CHU de RENNES, Rennes, France.

Jean-David Albert (JD)

Department of Rheumatology, CHU de RENNES, Rennes, France.

Lucie Planche (L)

Biometrics and Statistic Platform, CHU Nantes, Nantes, France.

Yves Maugars (Y)

Department of Rheumatology, CHU Nantes, Nantes, France.

Grégoire Cormier (G)

Department of Rheumatology, CHD Vendée, La Roche sur Yon, France.

Benoit Le Goff (B)

Department of Rheumatology, CHU Nantes, Nantes, France benoit.legoff@chu-nantes.fr.

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Classifications MeSH