Haeringer E, Graml W, Rangoonwala B, Roessner M
Pharmatherapeutica. 1982;3(4):233-42.
In an open multi-centre study, 51 patients with mild to moderate hypertension were treated with either a single dose of 40 mg penbutolol per day for 8 weeks or changed over at 4 weeks due to inadequate response with penbutolol alone to a single dose (1 tablet) of a fixed combination of 40 mg penbutolol and 20 mg furosemide per day for a further 4 weeks. Thirty-six (70%) of the patients showed an adequate reduction in diastolic blood pressure to 95 mmHg or less on penbutolol alone. Of the 15 patients who did not show the desired response to penbutolol alone, 13 (86.7%) showed a satisfactory reduction in blood pressure after 4 weeks on the combination product; 2 of these patients had received 1 tablet twice daily from Week 6 of treatment. Two other patients received 1 tablet of the combination twice daily from Week 8 onwards for 2 weeks. Only 1 of them did not respond to this therapy. Blood pressure reduction and weight loss were significantly greater on the combination product than on penbutolol alone. No clinically significant changes were noted in serum potassium, glucose, creatinine or uric acid levels, and mild gastric side-effects at the beginning of treatment were reported in only 3 patients, 1 of whom was also receiving indomethacin.
在一项开放性多中心研究中,51例轻度至中度高血压患者接受了以下治疗:要么每天单次服用40毫克喷布洛尔,持续8周;要么由于仅使用喷布洛尔效果不佳,在4周时换用每天单次服用(1片)含40毫克喷布洛尔和20毫克呋塞米的固定复方制剂,再持续4周。36例(70%)患者仅使用喷布洛尔时舒张压充分降低至95毫米汞柱或更低。在15例仅使用喷布洛尔未出现预期反应的患者中,13例(86.7%)在使用复方制剂4周后血压得到满意降低;其中2例患者从治疗第6周起每天服用2片。另外2例患者从第8周起每天服用2片复方制剂,持续2周。其中只有1例对此治疗无反应。复方制剂使血压降低和体重减轻的幅度明显大于仅使用喷布洛尔。血清钾、葡萄糖、肌酐或尿酸水平未出现临床显著变化,仅3例患者在治疗开始时报告有轻度胃部副作用,其中1例还同时服用吲哚美辛。