The evidence reviewed was considered to be of generally low quality because of small sample sizes, imprecise results, and bias risk from limited study designs. Intended subgroup analyses, such as those with and without depression, could not be completed because of an insufficient number of studies. Quality of evidence was also downgraded because of indirectness (exclusions of patients with disease) and imprecision (fewer than 400 patients analyzed). Larger and more methodologically sound studies will be needed to verify the conclusions.
Quetiapine was the only antipsychotic the authors found that was studied in adults with fibromyalgia. Doses of quetiapine ranged from 50 to 300 mg at bedtime. The review concluded that quetiapine may be considered for a limited period (less than 12 weeks) to improve pain, sleep, and depression in fibromyalgia, while considering the potential for weight gain.
A reduction of at least 50% in pain is used by the Cochrane Pain, Palliative and Supportive Care Review Group as a threshold because it correlates with improvements in morbidity, function, and quality of life.
The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the U.S. Army Medical Department or the U.S. Army.
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