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坦索罗辛,一种选择性α1c-肾上腺素能受体拮抗剂:一项针对良性前列腺“梗阻”(有症状的良性前列腺增生)患者的随机对照试验。欧洲坦索罗辛研究组。

Tamsulosin, a selective alpha 1c-adrenoceptor antagonist: a randomized, controlled trial in patients with benign prostatic 'obstruction' (symptomatic BPH). The European Tamsulosin Study Group.

作者信息

Abrams P, Schulman C C, Vaage S

机构信息

Southmead Hospital, Bristol, UK.

出版信息

Br J Urol. 1995 Sep;76(3):325-36. doi: 10.1111/j.1464-410x.1995.tb07709.x.

Abstract

OBJECTIVE

To evaluate the efficacy and safety of tamsulosin 0.4 mg once daily (as a modified-release formulation) compared with placebo in patients with benign prostatic enlargement, lower urinary tract symptoms and prostatic 'obstruction' (symptomatic benign prostatic hyperplasia [BPH]).

PATIENTS AND METHODS

Of 313 patients with symptomatic BPH enrolled in a 2-week placebo run-in period, 296 were subsequently randomized to receive either placebo (98 patients) or tamsulosin 0.4 mg once daily (198 patients) for 12 weeks. The primary variables assessed to determine efficacy were maximum urinary flow rate (Qmax) from free-flow measurements and the total Boyarsky symptom score.

RESULTS

Tamsulosin produced greater improvements in Qmax (1.4 mL/s, 13.1%) than did placebo (0.4 mL/s, 3.8%) (P = 0.028) and a greater decrease in total symptom score (3.4 points, 35.8% reduction) than did placebo (2.2 points, 23.7% reduction) (P = 0.002). Significantly more tamsulosin-treated patients (67%) than placebo-treated patients (44%) had a > or = 25% decrease in total symptom score after 12 weeks (P < 0.001). Treatment with tamsulosin for 12 weeks also produced significant improvements in average urinary flow rate (P = 0.040), irritative (P = 0.013) and obstructive (P = 0.014) symptom scores and symptoms of nocturia (P = 0.022) and hesitancy (P = 0.004). Tamsulosin was tolerated well by the patients. The incidence of adverse events emerging during treatment was comparable in the tamsulosin- and placebo-treated groups (34% and 24% respectively, P = 0.109), as was the incidence of cardiovascular-related adverse events (5% and 7% respectively; P = 0.596). There were no significant differences in changes in blood pressure or pulse rates between the tamsulosin- and placebo-treated groups.

CONCLUSION

Tamsulosin 0.4 mg once daily is safe, well tolerated and clinically effective in improving symptoms and urinary flow rate in patients with symptomatic BPH.

摘要

目的

评估每日一次服用0.4毫克坦索罗辛(缓释制剂)相较于安慰剂,对良性前列腺增生、下尿路症状及前列腺“梗阻”(有症状的良性前列腺增生[BPH])患者的疗效和安全性。

患者与方法

在313例有症状的BPH患者进入为期2周的安慰剂导入期后,296例患者随后被随机分为两组,分别接受安慰剂(98例患者)或每日一次服用0.4毫克坦索罗辛(198例患者),为期12周。评估疗效的主要变量为自由尿流测量中的最大尿流率(Qmax)和总博亚尔斯基症状评分。

结果

坦索罗辛使Qmax的改善程度(1.4毫升/秒,提高13.1%)大于安慰剂(0.4毫升/秒,提高3.8%)(P = 0.028),且使总症状评分的降低幅度(3.4分,降低35.8%)大于安慰剂(2.2分,降低23.7%)(P = 0.002)。12周后,接受坦索罗辛治疗的患者中总症状评分降低≥25%的比例(67%)显著高于接受安慰剂治疗的患者(44%)(P < 0.001)。坦索罗辛治疗12周还使平均尿流率(P = 0.040)、刺激性症状评分(P = 0.013)、梗阻性症状评分(P = 0.014)、夜尿症状(P = 0.022)和排尿犹豫症状(P = 0.004)有显著改善。患者对坦索罗辛耐受性良好。治疗期间出现不良事件的发生率在坦索罗辛治疗组和安慰剂治疗组中相当(分别为34%和24%,P = 0.109),心血管相关不良事件的发生率也相当(分别为5%和7%;P = 0.596)。坦索罗辛治疗组和安慰剂治疗组在血压和脉搏率变化方面无显著差异。

结论

每日一次服用0.4毫克坦索罗辛对有症状的BPH患者改善症状和尿流率是安全、耐受性良好且临床有效的。

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