Lepola Ulla, Arató Mihaly, Zhu Young, Austin Carol
Kuopio Psychiatric Research Clinic, Kuopio, Finland.
J Clin Psychiatry. 2003 Jun;64(6):654-62. doi: 10.4088/jcp.v64n0606.
To evaluate the efficacy and tolerability of sertraline and imipramine in patients with comorbid panic disorder and major depressive disorder.
Outpatients meeting a DSM-IV diagnosis of panic disorder and concurrent major depressive disorder were randomized in a 2:1 ratio to 26 weeks of double-blind treatment with either sertraline, in daily doses of 50 to 100 mg, or imipramine, in daily doses of 100 to 200 mg. Primary outcome measures were panic attack frequency (derived from patient diaries) and the Montgomery-Asberg Depression Rating Scale (MADRS).
138 patients were treated with sertraline (76% female; mean age = 40 years) and 69 with imipramine (70% female; mean age = 40 years). The symptoms of both major depressive disorder and panic disorder responded significantly and equivalently to both drugs. Endpoint improvement with sertraline versus imipramine, respectively, on the MADRS was 11.1 +/- 10.8 versus 11.2 +/- 10.4, and on the Clinical Global Impressions-Improvement scale (CGI-I) was 2.1 +/- 1.3 versus 2.4 +/- 1.6. Among study completers, CGI-I responder rates were 88% with sertraline and 91% with imipramine. Treatment outcome was concordant for both diagnoses in approximately 70% of patients and discordant in approximately 30%. Overall, sertraline was significantly better tolerated with significantly fewer discontinuations due to adverse events (11% vs. 22%; chi(2) = 4.39, df = 1, p =.04).
Both sertraline and imipramine were found to be highly effective treatments for both major depressive disorder and panic disorder, with sertraline showing significantly greater tolerability and compliance during long-term treatment than imipramine.
评估舍曲林和丙咪嗪对伴有惊恐障碍和重度抑郁症患者的疗效及耐受性。
符合DSM-IV惊恐障碍诊断标准且并发重度抑郁症的门诊患者按2:1比例随机分组,接受为期26周的双盲治疗,一组服用舍曲林,每日剂量50至100毫克,另一组服用丙咪嗪,每日剂量100至200毫克。主要疗效指标为惊恐发作频率(源自患者日记)和蒙哥马利-阿斯伯格抑郁评定量表(MADRS)。
138例患者接受舍曲林治疗(76%为女性;平均年龄 = 40岁),69例接受丙咪嗪治疗(70%为女性;平均年龄 = 40岁)。重度抑郁症和惊恐障碍的症状对两种药物均有显著且相当的反应。舍曲林和丙咪嗪治疗后,MADRS评分改善分别为11.1±10.8和11.2±10.4,临床总体印象改善量表(CGI-I)评分分别为2.1±1.3和2.4±1.6。在完成研究的患者中,舍曲林的CGI-I有效率为88%,丙咪嗪为91%。约70%患者的两种诊断治疗结果一致,约30%不一致。总体而言,舍曲林耐受性显著更好,因不良事件停药的患者明显更少(11%对22%;χ² = 4.39,自由度 = 1,p = 0.04)。
舍曲林和丙咪嗪对重度抑郁症和惊恐障碍均为高效治疗药物,且舍曲林在长期治疗中的耐受性和依从性显著优于丙咪嗪。