Affective disorders in general practice. Treatment of 6000 patients with fluvoxamine.

Pharmatherapeutica Pub Date : 1987-01-01
A J Martin, V M Tebbs, J J Ashford
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Abstract

A total of 6258 patients seen in general practice complaining of low mood with or without associated somatic symptoms was studied. The mean patient entry score on the Montgomery-Asberg Depression Rating Scale (MADRS) was 29.69 (moderately severe depressive disorder). Three-quarters (73%) of the patients were female, average age was 46.1 years, and a reactive element was considered to be present in 43%. Patients received fluvoxamine, a novel anti-depressant, over a treatment period of 6 weeks, dosage starting at either 50 or 100 mg at night increasing after the first week, if necessary, to a maximum of 300 mg per day. Results were analyzed for 5625 patients. Efficacy of treatment was assessed using the MADRS, Psychosomatic Symptom Scale and Clinical Global Impression scales. During treatment, there was a marked improvement in mood and a parallel improvement in somatic symptoms; there was no difference in overall response between those with or without somatic symptoms. By Week 6, patients had improved by approximately 65%, with suicidal ideation being most marked at 81%. Patient compliance was good, the most commonly reported unwanted effect being nausea. In overdoses up to 2 g fluvoxamine no lasting toxic effects were observed. In an 'elderly' sub-group of 1096 patients aged 60 years and over, efficacy and the incidence of unwanted effects were similar, but the drop-out rate due to intolerance was greater than in the younger age sub-group.

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一般实践中的情感性障碍。氟伏沙明治疗6000例患者。
共6258例患者在一般实践中看到的低情绪,有或没有相关的躯体症状进行研究。患者在Montgomery-Asberg抑郁评定量表(MADRS)上的平均入组得分为29.69分(中度重度抑郁障碍)。四分之三(73%)的患者为女性,平均年龄为46.1岁,43%的患者被认为存在反应性因素。患者接受氟伏沙明(一种新型抗抑郁药)治疗6周,剂量从每晚50或100毫克开始,在第一周后增加,如有必要,最多可达每天300毫克。结果分析了5625例患者。采用MADRS、心身症状量表和临床总体印象量表评估治疗效果。在治疗期间,患者情绪有明显改善,身体症状也有相应改善;有或没有躯体症状的患者在总体反应上没有差异。到第6周,患者的病情改善了约65%,其中自杀意念最为明显,达到81%。患者的依从性良好,最常见的不良反应是恶心。过量服用氟伏沙明达2g时,未观察到持久的毒性作用。在一个由1096名60岁及以上患者组成的“老年”亚组中,疗效和不良反应的发生率相似,但由于不耐受导致的退出率高于年轻亚组。
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