Abstract | OBJECTIVES: To evaluate the efficacy of anakinra for patients with acute gout. METHODS: We reviewed the charts of 10 patients who received anakinra for urate crystal-induced arthritis at the Hospital for Special Surgery since 2007. Demographic information, comorbidities, short-term treatment outcomes, and subsequent flares were reviewed. RESULTS: Patients in our study had a high prevalence of comorbidities. All patients received corticosteroids before anakinra treatment. The mean number of anakinra injections was 3.2 per patient (100 mg subcutaneously per day). Six patients had a good response. Three patients had a partial response and 1 patient had no response. Nine patients had documented recurrent flares after discontinuing anakinra (ranging from 3 to 45 days after). CONCLUSION:
Anakinra is a therapeutic option for patients with acute urate crystal-induced arthritis who do not respond to or have a contraindication to traditional treatments. Although a short course of anakinra resulted in favorable outcomes for some of our patients, response rates were poorer in our study than in previously published reports, and relapses were common.
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Authors | Kun Chen, Theodore Fields, Carol A Mancuso, Anne R Bass, Lisa Vasanth |
Journal | Seminars in arthritis and rheumatism
(Semin Arthritis Rheum)
Vol. 40
Issue 3
Pg. 210-4
(Dec 2010)
ISSN: 1532-866X [Electronic] United States |
PMID | 20494407
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2010. Published by Elsevier Inc. |
Chemical References |
- Antirheumatic Agents
- Interleukin 1 Receptor Antagonist Protein
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antirheumatic Agents
(administration & dosage, therapeutic use)
- Dose-Response Relationship, Drug
- Female
- Gout
(drug therapy)
- Humans
- Injections, Subcutaneous
- Interleukin 1 Receptor Antagonist Protein
(administration & dosage, therapeutic use)
- Male
- Middle Aged
- Retrospective Studies
- Treatment Outcome
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