Rickels K, Schweizer E, Csanalosi I, Case W G, Chung H
Department of Psychiatry, Psychopharmacology, University of Pennsylvania, Philadelphia.
Arch Gen Psychiatry. 1988 May;45(5):444-50. doi: 10.1001/archpsyc.1988.01800290060008.
Risk of withdrawal was investigated in a prospective, double-blind comparison of clorazepate dipotassium, a benzodiazepine with a long half-life, and the nonbenzodiazepine buspirone hydrochloride in the long-term treatment of anxious outpatients. Patients were treated with therapeutic doses of clorazepate dipotassium (15 to 60 mg/d) or buspirone hydrochloride (10 to 40 mg/d) for six continuous months before their tranquilizer therapy was blindly and abruptly stopped. There was a significant increase in symptom severity consistent with a withdrawal reaction for the clorazepate group but not the buspirone group. For the clorazepate group, there was a suggestion that previous discontinuous exposure to benzodiazepines might sensitize patients to subsequent withdrawal effects. For the buspirone group, a higher dropout rate raised questions about patient satisfaction with therapy in this rather chronically anxious population.
在一项前瞻性、双盲对照研究中,对氯氮䓬二钾(一种半衰期较长的苯二氮䓬类药物)和非苯二氮䓬类药物盐酸丁螺环酮在长期治疗焦虑门诊患者中的撤药风险进行了调查。患者先接受治疗剂量的氯氮䓬二钾(15至60毫克/天)或盐酸丁螺环酮(10至40毫克/天)连续治疗六个月,然后其镇静剂治疗被盲目且突然地停止。氯氮䓬组出现了与撤药反应一致的症状严重程度显著增加,而丁螺环酮组则未出现。对于氯氮䓬组,有迹象表明先前间断接触苯二氮䓬类药物可能会使患者对随后的撤药效应敏感。对于丁螺环酮组,较高的脱落率引发了对于在这个相当长期焦虑的人群中患者对治疗满意度的疑问。