Høstmaelingen H J, Asskilt O, Austad S G, Fjellheim J, Høstmaelingen E A, Kristiansen P H, Olsen T I, Skotte T, Ofsti E
Curr Med Res Opin. 1989;11(9):593-9. doi: 10.1185/03007998909112676.
A multi-centre general practice study was carried out to compare flupenthixol and a sustained-release preparation of amitriptyline in the primary care treatment of depression in the elderly. Fifty-one clinically depressed patients, aged 65 years or over, were allocated at random to one of the two treatment groups in this 4-week double-blind, double-dummy study. On entry, patients received either a 0.5 mg flupenthixol tablet in the morning and a placebo capsule at night (25 patients) or a 25 mg sustained-release amitriptyline capsule at night and a placebo tablet in the morning (26 patients), but at the end of the first or second weeks the dosage could be doubled according to the assessed clinical need. Fourteen patients in each treatment group had their dosages doubled. Patient assessment was undertaken on study entry and after 1, 2 and 4 weeks of treatment using a 0 to 3 scale global assessment and the Montgomery Asberg Depression Rating Scale; side-effects were recorded on the UKU Scale. After 4-weeks' treatment, over 80% of patients in each group had improved and in the flupenthixol group there was additionally a noticeable and highly significant reduction in symptom severity after only 1 week of treatment. Patients treated with flupenthixol had fewer and milder side-effects.
一项多中心全科医学研究开展,以比较氟哌噻吨与阿米替林缓释制剂在老年抑郁症初级保健治疗中的效果。在这项为期4周的双盲、双模拟研究中,51名年龄在65岁及以上的临床抑郁症患者被随机分配到两个治疗组之一。入组时,患者要么早上服用0.5毫克氟哌噻吨片,晚上服用安慰剂胶囊(25名患者),要么晚上服用25毫克阿米替林缓释胶囊,早上服用安慰剂片(26名患者),但在第一周或第二周结束时,可根据评估的临床需要将剂量加倍。每个治疗组有14名患者的剂量加倍。在研究入组时以及治疗1周、2周和4周后,使用0至3级整体评估和蒙哥马利-阿斯伯格抑郁评定量表对患者进行评估;使用UKU量表记录副作用。经过4周治疗后,每组超过80%的患者病情有所改善,并且在氟哌噻吨组中,仅治疗1周后症状严重程度就有明显且高度显著的降低。接受氟哌噻吨治疗的患者副作用更少、更轻微。