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Ketamine in fibromyalgia: a systematic review.

Jozélio Freire de Carvalho, Eduardo Pondé de Sena

Advances in rheumatology (London, England) July 29, 2024 DOI: 10.1186/s42358-024-00393-9 via PubMed

Summary

AI-generated from the abstract

A systematic review of six studies involving 115 fibromyalgia patients found that ketamine, an anesthetic drug, appears effective and safe for short-term pain relief. Most patients were female (88-100%), aged 23 to 53, with disease duration from one month to 28 years. Ketamine was given intravenously or subcutaneously at doses of 0.1 to 0.5 mg/kg. Pain scores on a visual analog scale dropped from 59-100 mm before treatment to 2-95 mm after. Short-term studies showed good response, but the only eight-week follow-up study did not. Side effects occurred during infusion but resolved quickly. More long-term studies are needed.

Study at a glance

Characteristics Systematic review Peer reviewed
Sample size 115
Population Fibromyalgia patients
Intervention Ketamine
Dose 0.1 mg/kg-0.3-0.5 mg/kg
Topics Depression Ketamine
Keywords Anesthetics Ketamine therapy Chronic pain treatment Fibromyalgia management
Citations 8
Key finding Ketamine provides short-term pain relief in fibromyalgia patients, but long-term efficacy remains unproven.

Abstract

Fibromyalgia (FM) subjects are treated with antidepressant agents; in most cases, these drugs lose efficacy or have adverse effects. Ketamine is an anesthetic drug used in FM in some studies. This article aims to systematically review the safety and efficacy of ketamine in fibromyalgia (FM) patients. We systematically searched articles on FM and ketamine published at Pubmed from 1966 to 2021. This study was registered at PROSPERO. There were only 6 articles published in this field, with a total of 115 patients. The female sex was predominant (88 to 100%). The age varied from 23 to 53 years old. Disease duration ranged from 1 month to 28 years. The dosage of ketamine changed from 0.1 mg/kg-0.3-0.5 mg/kg in intravenous infusion (4/5) and subcutaneous application (1/5). Regarding outcomes, the Visual analog scale (VAS) before ketamine was from 59 to 100 mm and after treatment from 2 to 95 mm. Most short-term studies had a good response. Only the study with 8 weeks of follow-up did not observe a good response. Side effects were common; all appeared during the infusion and disappeared after a few minutes of the ketamine injection. The present study demonstrates the effectiveness and safety of ketamine in FM patients in the short term. Although, more studies, including long-term follow-up studies, are still needed.

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