Comparison of Amitriptyline and US Food and Drug Administration-Approved Treatments for Fibromyalgia A Systematic Review and Network Meta-analysis

被引:45
作者
Farag, Hussein M. [1 ]
Yunusa, Ismaeel [1 ,2 ]
Goswami, Hardik [1 ,3 ]
Sultan, Ihtisham [1 ,4 ]
Doucette, Joanne A. [1 ]
Eguale, Tewodros [1 ,5 ]
机构
[1] Massachusetts Coll Pharm & Hlth Sci, Dept Pharmaceut Econ & Policy, 179 Longwood Ave, Boston, MA 02115 USA
[2] Univ South Carolina, Coll Pharm, Dept Clin Pharm & Outcomes Sci, Columbia, SC 29208 USA
[3] Merck & Co Inc, Biostat & Res Decis Sci & Hlth Econ & Decis Sci, N Wales, PA USA
[4] AbbVie, Hlth Econ & Outcomes Res Neurosci, Cambridge, MA USA
[5] McGill Univ, Hlth Ctr, Dept Med, Montreal, PQ, Canada
关键词
PLACEBO-CONTROLLED TRIAL; PHASE-III TRIAL; DOUBLE-BLIND; MILNACIPRAN TREATMENT; THERAPEUTIC RESPONSE; COMPARATIVE EFFICACY; CLINICAL-TRIAL; DULOXETINE; PREGABALIN; PAIN;
D O I
10.1001/jamanetworkopen.2022.12939
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Amitriptyline is an established medication used off-label for the treatment of fibromyalgia, but pregabalin, duloxetine, and milnacipran are the only pharmacological agents approved by the US Food and Drug Administration (FDA) to treat fibromyalgia. OBJECTIVE To investigate the comparative effectiveness and acceptability associated with pharmacological treatment options for fibromyalgia. DATA SOURCES Searches of PubMed/MEDLINE, Cochrane Library, Embase, and Clinicaltrials.gov were conducted on November 20, 2018, and updated on July 29, 2020. STUDY SELECTION Randomized clinical trials (RCTs) comparing amitriptyline or any FDA-approved doses of investigated drugs. DATA EXTRACTION AND SYNTHESIS This study follows the Preferred Reporting Items for Systematic Reviews and Meta-analyses reporting guideline. Four independent reviewers extracted data using a standardized data extraction sheet and assessed quality of RCTs. A random-effects bayesian network meta-analysis (NMA) was conducted. Data were analyzed from August 2020 to January 2021. MAIN OUTCOMES AND MEASURES Comparative effectiveness and acceptability (defined as discontinuation of treatment owing to adverse drug reactions) associated with amitriptyline (off-label), pregabalin, duloxetine, and milnacipran (on-label) in reducing fibromyalgia symptoms. The following doses were compared: 60-mg and 120-mg duloxetine; 150-mg, 300-mg. 450-mg, and 600-mg pregabalin; 100-mg and 200-mg milnacipran; and amitriptyline. Effect sizes are reported as standardized mean differences (SMDs) for continuous outcomes and odds ratios (ORs) for dichotomous outcomes with 95% credible intervals (95% CrIs). Findings were considered statistically significant when the 95% CrI did not include the null value (0 for SMD and 1 for OR). Relative treatment ranking using the surface under the cumulative ranking curve (SUCRA) was also evaluated. RESULTS A total of 36 studies (11930 patients) were included. The mean (SD) age of patients was 48.4 (10.4) years, and 11 261 patients (94.4%) were women. Compared with placebo, amitriptyline was associated with reduced sleep disturbances (SMD, -0.97; 95% CrI, -1.10 to -0.83). fatigue (SMD, 0.64; 95% CrI, -0.75 to -0.53), and improved quality of life (SMD, -0.80; 95% CrI, -0.94 to -0.65). Duloxetine 120 mg was associated with the highest improvement in pain (SMD, -0.33; 95% CrI, - 0.36 to -0.30) and depression (SMD, -0.25; 95% CrI, -0.32 to -0.17) vs placebo. All treatments were associated with inferior acceptability (higher dropout rate) than placebo, except amitriptyline (OR, 0.78; 95% CrI, 0.31 to 1.66). According to the SUCRA-based relative ranking of treatments, duloxetine 120 mg was associated with higher efficacy for treating pain and depression, while amitriptyline was associated with higher efficacy for improving sleep, fatigue, and overall quality of life. CONCLUSIONS AND RELEVANCE These findings suggest that clinicians should consider how treatments could be tailored to individual symptoms, weighing the benefits and acceptability, when prescribing medications to patients with fibromyalgia.
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页数:15
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