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Doxepin's effects on chronic pain and depression: a controlled study
The Journal of Clinical Psychiatry
|March 1, 1984
Summary
Doxepin significantly improved chronic pain and depression symptoms in patients compared to placebo over six weeks. This treatment demonstrated effectiveness without significant adverse effects.
Area of Science:
- Psychiatry
- Pain Management
- Pharmacology
Background:
- Chronic pain, particularly of the low back or cervical spine, frequently co-occurs with clinical depression, complicating treatment.
- Effective management strategies for patients experiencing both chronic pain and depression are crucial.
Purpose of the Study:
- To evaluate the efficacy and safety of doxepin in treating patients with chronic low back or cervical spine pain and concomitant depression.
- To compare the effects of doxepin versus placebo on depression scores, pain severity, and related functional impairments.
Main Methods:
- A 6-week, randomized, double-blind, placebo-controlled trial involving sixty patients with chronic pain and depression.
- Patients received either doxepin or a placebo, with assessments including Hamilton depression scores and Global Assessment Scale scores.
- Pain severity, duration, and impact on activity, sleep, and muscle tension were also evaluated.
Main Results:
- The doxepin group showed significant improvements in Hamilton depression scores and Global Assessment Scale scores compared to placebo.
- Significant reductions in pain severity, percentage of time pain was felt, and improvements in activity, sleep, and muscle tension were observed in the doxepin group.
- Improvements were noted as early as week 1, with maximal effects at week 6, at a mean doxepin dosage of approximately 200 mg/day.
Conclusions:
- Doxepin is an effective and safe treatment option for patients suffering from chronic pain and co-existing depression.
- The study supports the use of doxepin in managing multifaceted symptoms associated with chronic pain and depressive disorders.
- No significant changes in plasma beta-endorphin or enkephalin-like activity were observed, suggesting the therapeutic effects are not mediated by these pathways.
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