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Long-term follow-up study to evaluate the efficacy and safety of the doxazosin gastrointestinal therapeutic system in patients with benign prostatic hyperplasia with or without concomitant hypertension.

机译:长期随访研究,评估多沙唑嗪胃肠治疗系统在良性前列腺增生伴或不伴伴有高血压的患者中的疗效和安全性。

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OBJECTIVE: To assess the long-term efficacy and safety of extended-release doxazosin gastrointestinal therapeutic system (GITS) under routine clinical care conditions over 12 months in Korean men with benign prostatic hyperplasia (BPH) with and without coexisting hypertension. PATIENTS AND METHODS: In this open-label, multicentre, uncontrolled, flexible-dose study, 475 men (> or =40 years old) with clinical evidence of BPH were enrolled from 40 centres. Patients were evaluated at baseline and at 1, 2, 6 and 12 months of treatment. The primary efficacy variable was the Clinicians Global Assessment of Change (CGAC; improved, no change, or worse). Secondary efficacy variables were International Prostate Symptom Score (IPSS), quality of life (QoL), maximum urinary flow rate (Q(max)), and postvoid residual (PVR) urine volume. Adverse events (AEs) and blood pressure (BP) were also recorded. RESULTS: In all, 186 patients completed the study; based on the CGAC, most patients (155, 83.8%) improved and 31 (16.2%) had no change in symptoms. The mean (sd) change in the IPSS and QoL from baseline were -9.0 (6.8) and -1.6 (1.4), respectively (both P < 0.05). The Q(max) and PVR urine volume were significantly better than at baseline, with means of 10.5 (4.3) vs 13.7 (6.3), and 39.1 (37.0) vs 23.2 (33.7); P < 0.05). The decrease in systolic BP (SBP) and diastolic BP (DBP) from baseline in 52 hypertensive patients was significantly greater than in 134 normotensive patients, at (SBP/DBP) -9.5 (18.4)/-13.4 (10.9) vs -3.3 (12.5)/-1.4 (9.5); P < 0.05). A total of 47 AEs were reported in 41 of 475 patients (8.6%); the most common were dizziness (2.7%), erectile dysfunction (1.1%), dry mouth (1.1%), prostatic disorder (0.6%), and postural hypotension (0.4%). CONCLUSIONS: After 12 months, treatment with doxazosin GITS resulted in an improvement in > 83% of patients based on the CGAC, with significant improvements in IPSS, QoL, Q(max,) and PVR urine volume. Doxazosin GITS was effective and well tolerated as long-term therapyfor Korean patients with BPH.
机译:目的:评估多沙唑嗪胃肠治疗系统(GITS)在12个月以内的良性前列腺增生(BPH)伴或不伴高血压的韩国男性中,在常规临床护理条件下的长期疗效和安全性。患者与方法:在这项开放性,多中心,不受控制的灵活剂量研究中,从40个中心招募了475名BPH临床证据的男性(≥40岁)。在基线以及治疗1、2、6和12个月时对患者进行评估。主要功效变量是临床医师全球变化评估(CGAC;改善,无变化或更差)。次要疗效变量是国际前列腺症状评分(IPSS),生活质量(QoL),最大尿流率(Q(max))和无尿残留(PVR)尿量。还记录了不良事件(AEs)和血压(BP)。结果:总共有186例患者完成了研究。根据CGAC,大多数患者(155,83.8%)有所改善,31例(16.2%)的症状没有变化。与基线相比,IPSS和QoL的平均(sd)变化分别为-9.0(6.8)和-1.6(1.4)(均P <0.05)。 Q(max)和PVR尿量明显好于基线,平均值分别为10.5(4.3)对13.7(6.3)和39.1(37.0)对23.2(33.7); P <0.05)。 52名高血压患者的收缩压(SBP)和舒张压(DBP)相对于基线的降低显着大于134名血压正常的患者,(SBP / DBP)-9.5(18.4)/-13.4(10.9)vs -3.3( 12.5)/-1.4(9.5); P <0.05)。在475名患者中的41名(8.6%)中报告了47种AE。最常见的是头晕(2.7%),勃起功能障碍(1.1%),口干(1.1%),前列腺疾病(0.6%)和体位性低血压(0.4%)。结论:在12个月后,多沙唑嗪GITS治疗使基于CGAC的患者改善了83%以上,IPSS,QoL,Q(max)和PVR尿量显着改善。多沙唑嗪GITS作为韩国BPH患者的长期治疗有效且耐受性良好。

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