Efficacy of anakinra in acute hydroxyapatite calcification-induced joint pain: A retrospective study of 23 cases.


Journal

Joint bone spine
ISSN: 1778-7254
Titre abrégé: Joint Bone Spine
Pays: France
ID NLM: 100938016

Informations de publication

Date de publication:
01 2019
Historique:
received: 23 01 2018
accepted: 14 05 2018
pubmed: 9 6 2018
medline: 18 2 2020
entrez: 9 6 2018
Statut: ppublish

Résumé

Hydroxyapatite (HA) crystal calcifications in or around the joint can induce acute flares with severe pain. A previous pilot study suggested that the interleukin-1β (IL-1β) inhibitor anakinra was effective. The goal of this observational study was to confirm these results in a larger set of patients and to report on the long-term follow-up. Flare was defined as acute pain for<10 days. Calcification in or around a joint (rotator cuff: 15/23 patients) was confirmed by conventional radiography and/or ultrasonography (US). Anakinra 100mg daily was administered subcutaneously for 1 to 3 consecutive days. Clinical data collected before the injection and on days 3 and 21 included pain score on a visual analog scale (VAS, 0-10cm) and C-reactive protein (CRP) level. When available, US baseline and follow-up findings were compared. Long-term follow-up data were collected from patient charts and/or after a phone call. 23 patients (15 males, mean [SD] age 58 [11] years) were included. Baseline mean (SD) VAS pain was 7.7 (1) cm and CRP level was elevated in half of the patients. After therapy, mean (SD) VAS pain score decreased rapidly in the first 3 days to 1.6 (1.4) cm (P<0.001) and remained stable for 3 weeks at 1.8 (2.1) cm. US assessment revealed decreased Doppler intensity but no significant change in size of calcifications. No significant side effects were noted. After long-term follow-up (median duration 24 months), half of the patients still had some chronic pain, but only 4 experienced acute relapse. This study suggests that IL-1β inhibition may be an efficient therapeutic approach for acute HA flare, with a good safety profile.

Identifiants

pubmed: 29883768
pii: S1297-319X(18)30108-8
doi: 10.1016/j.jbspin.2018.05.008
pii:
doi:

Substances chimiques

Antirheumatic Agents 0
Interleukin 1 Receptor Antagonist Protein 0
Durapatite 91D9GV0Z28

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-88

Informations de copyright

Copyright © 2018 Société française de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Pascal Zufferey (P)

RHU/DAL/CHUV Lausanne, 4, avenue Pierre-Decker, 1005 Lausanne, Switzerland. Electronic address: Pascal.zufferey@chuv.ch.

Roxana Valcov (R)

RHU/DAL/CHUV Lausanne, 4, avenue Pierre-Decker, 1005 Lausanne, Switzerland.

Marion Thomas (M)

Service de rhumatologie, CHU de Bichat-Claude Bernard, AP-HP, 75018 Paris, France.

Alexandre Dumusc (A)

RHU/DAL/CHUV Lausanne, 4, avenue Pierre-Decker, 1005 Lausanne, Switzerland.

Marine Forien (M)

Service de rhumatologie, CHU de Bichat-Claude Bernard, AP-HP, 75018 Paris, France.

Alexander So (A)

RHU/DAL/CHUV Lausanne, 4, avenue Pierre-Decker, 1005 Lausanne, Switzerland.

Sebastien Ottaviani (S)

Service de rhumatologie, CHU de Bichat-Claude Bernard, AP-HP, 75018 Paris, France.

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Classifications MeSH