Versiani M, Mehilane L, Gaszner P, Arnaud-Castiglioni R
Institute of Psychiatry, Federal University, Rio de Janeiro, Brazil.
J Clin Psychiatry. 1999 Jun;60(6):400-6. doi: 10.4088/jcp.v60n0610.
The long-term efficacy and tolerability of the antidepressant reboxetine, a unique selective norepinephrine reuptake inhibitor (selective NRI), were assessed in an international study.
Two hundred eighty-three patients with recurrent DSM-III-R major depression who responded to 6 weeks of reboxetine treatment (> or =50% decrease in Hamilton Rating Scale for Depression [HAM-D] total score) were randomly assigned to receive reboxetine or placebo for 46 weeks in a double-blind phase. Relapse (> or =50% increase in HAM-D total score and/or a HAM-D total score > or =18) rate was the principal assessment criterion and included patients who experienced relapse or recurrence. Only patients who remained relapse-free at the end of the first 6-month treatment period were included in the relapse rate assessment at the end of the second 6-month treatment period.
Reboxetine was associated with a markedly lower relapse rate than placebo (22% vs. 56%; p<.001) and a greater cumulative probability of a maintained response (p = .0001) during long-term treatment. Patients in remission (HAM-D total score < or =10) at the time of random assignment were less likely to relapse (16% reboxetine, 48% placebo; p<.001). The proportion of patients who were relapse-free and therefore remained in the study was significantly (p< or =.001) higher among those on reboxetine treatment than on placebo at the end of the first (61% vs. 40%) and second (88% vs. 59%) 6 months of treatment. Additional efficacy measures supported these findings. The incidence of adverse events with reboxetine was low and comparable with that for placebo. Discontinuation due to adverse events occurred infrequently.
Reboxetine treatment over 1 year is more effective than placebo in the prevention of relapse in patients with recurrent depression. The low relapse rates at the end of the second 6 months of treatment further suggest that reboxetine effectively prevents recurrence of depressive symptoms following episode resolution. Reboxetine is well tolerated in long-term treatment of depression, a finding that bodes well for long-term patient compliance.
在一项国际研究中评估了抗抑郁药瑞波西汀(一种独特的选择性去甲肾上腺素再摄取抑制剂,即选择性NRI)的长期疗效和耐受性。
283例对瑞波西汀治疗6周有反应(汉密尔顿抑郁量表[HAM-D]总分降低≥50%)的复发性DSM-III-R重度抑郁症患者,在双盲阶段被随机分配接受瑞波西汀或安慰剂治疗46周。复发率(HAM-D总分增加≥50%和/或HAM-D总分≥18)是主要评估标准,包括经历复发或再发的患者。仅在第一个6个月治疗期结束时无复发的患者才纳入第二个6个月治疗期结束时的复发率评估。
在长期治疗期间,瑞波西汀的复发率明显低于安慰剂(22%对56%;p<0.001),维持反应的累积概率更高(p = 0.0001)。随机分组时病情缓解(HAM-D总分≤10)的患者复发可能性较小(瑞波西汀组为16%,安慰剂组为48%;p<0.001)。在治疗的第一个6个月(61%对40%)和第二个6个月(88%对59%)结束时,接受瑞波西汀治疗的患者中无复发并因此留在研究中的比例显著高于接受安慰剂治疗的患者(p≤0.001)。其他疗效指标也支持这些发现。瑞波西汀不良事件的发生率较低,与安慰剂相当。因不良事件停药的情况很少发生。
在预防复发性抑郁症患者复发方面,超过1年的瑞波西汀治疗比安慰剂更有效。治疗第二个6个月结束时的低复发率进一步表明,瑞波西汀能有效预防抑郁症状在发作缓解后的复发。瑞波西汀在抑郁症的长期治疗中耐受性良好,这一发现对患者长期依从性而言是个好兆头。