Sumpton J E, Moulin D E
Pharmacy Department, London Health Sciences Centre, Ontario, Canada.
Ann Pharmacother. 2001 May;35(5):557-9. doi: 10.1345/aph.10206.
To report a case of successful treatment of neuropathic pain with venlafaxine.
A 39-year-old white woman presented with neuropathic back pain. The patient obtained 50% pain relief with consecutive use of amitriptyline, desipramine, and imipramine. Anticholinergic effects prompted a switch to extended-release venlafaxine 75 mg/d. Pain relief was as effective with this therapy as with the tricyclic antidepressants. The absence of adverse effects allowed the patient to discontinue all laxatives.
Venlafaxine is an antidepressant that inhibits reuptake of norepinephrine and serotonin. This is the major mechanism by which tricyclic antidepressants relieve neuropathic pain. Venlafaxine does not bind to muscarinic-cholinergic, histaminic or alpha1-adrenergic receptors responsible for the common adverse effects seen with tricyclic antidepressants.
This report describes the efficacious use of venlafaxine in the treatment of neuropathic pain. Double-blind, randomized, controlled trials are needed to explore this further.
报告1例用文拉法辛成功治疗神经性疼痛的病例。
一名39岁白人女性,患有神经性背痛。该患者连续使用阿米替林、地昔帕明和丙咪嗪后疼痛缓解了50%。抗胆碱能效应促使改用文拉法辛缓释片,75毫克/天。这种治疗的止痛效果与三环类抗抑郁药相同。无不良反应使患者停用了所有泻药。
文拉法辛是一种抑制去甲肾上腺素和5-羟色胺再摄取的抗抑郁药。这是三环类抗抑郁药缓解神经性疼痛的主要机制。文拉法辛不与三环类抗抑郁药常见不良反应所涉及的毒蕈碱-胆碱能、组胺或α1-肾上腺素能受体结合。
本报告描述了文拉法辛在治疗神经性疼痛中的有效应用。需要进一步开展双盲、随机、对照试验进行探究。