Despite it being a frequent practice, there is limited evidence supporting the prescription of antidepressant drugs to help treat pain conditions.
In new data from an overview of systematic reviews conducted by an international team of investigators, approximately 1 in every 4 comparison trials showed an efficacy of antidepressants in the treatment of pain conditions including back, neuropathic and fibromyalgia pain.1 The findings elucidate a need to improve guidance and rationale behind the use of drug classes including serotonin-norepinephrine reuptake inhibitors (SNRIs) in matters of pain management.
Key Highlights
- Antidepressant drugs are frequently prescribed to treat pain conditions, but limited evidence supports their efficacy.
- An international team of investigators reviewed the efficacy, safety, and tolerability of antidepressants for treating pain based on the condition
- The findings showed that 11 out of 42 trial comparisons had at least moderate evidence of efficacy, including SNRIs for forms of chronic pain.
- The rest of the comparisons (74%) showed either inefficacy or inconclusive evidence on the efficacy of antidepressants for pain.
Led by Dr. Giovanni E. Ferreira, a research fellow at the Sydney School of Public Health’s Faculty of Medicine and Health, investigators sought to review the efficacy, safety and tolerability of antidepressants for treating pain, based on the pain condition itself. With most common pain conditions being difficult to treat, management strategies are “suboptimal” and dependent on individual benefit-risk profiles (i.e, the utility of opioid analgesics or non-steroidal anti-inflammatory drugs [NSAIDs]).
Antidepressants have globally become more commonplace among chronic pain patients, despite 2021 National Institute for Health and Care Excellence guidelines for chronic primary pain “explicitly” recommended against their use in such circumstances.
“Given the heterogeneity in the types of pain conditions for which the efficacy of antidepressants has been documented by existing systematic reviews, we chose to conduct an overview of systematic reviews to appraise efficacy estimates for each condition individually,” they wrote.
The team conducted the review of research comparing any antidepressant with a placebo control for any pain condition in adults. A pair of independent reviewers had extracted data from relevant trials at the time point closes to end of treatment. They sought a primary outcome measure of pain for standard trials, and frequency of headaches for trials involving headache disorders.
The investigators converted continuous pain outcomes on a scale of 0-100 for severity and presented as mean differences. Dichotomous trial outcomes were presented as risk ratios. They additionally sought secondary outcomes for safety and tolerability based on adverse event withdrawals. Findings were defined as either efficacious, non-efficacious or inconclusive.