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Doxazosin gastrointestinal therapeutic system: a review of its use in benign prostatic hyperplasia.

机译:多沙唑嗪胃肠道治疗系统:在良性前列腺增生中的应用综述。

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摘要

Doxazosin, a well established treatment in patients with bothersome lower urinary tract symptoms from benign prostatic hyperplasia (BPH), is available in a new controlled-release formulation, doxazosin gastrointestinal therapeutic system (GITS). Doxazosin GITS (Cardura XL, Cardular PP Uro, Diblocin PP Uro) has an altered pharmacokinetic profile, which allows a higher initial dosage to be used than with the standard formulation and less titration steps to reach a clinically effective dosage. In two large, double-blind, randomised studies (one was placebo-controlled) in patients with BPH, doxazosin GITS (4-8 mg once daily) was as effective as the standard formulation (2-8 mg once daily), and both were more effective than placebo, after 13 weeks' treatment in improving symptom scores, health-related quality of life (HR-QOL), and maximum urinary flow rate (Qmax). Doxazosin GITS was at least as well tolerated as the standard formulation of doxazosin in clinical studies in patients with BPH.
机译:新的控释制剂多沙唑嗪胃肠道治疗系统(GITS)中提供了多沙唑嗪,这是一种针对良性前列腺增生(BPH)引起的下尿路症状困扰的患者的完善治疗方法。多沙唑嗪GITS(Cardura XL,Cardular PP Uro,Diblocin PP Uro)的药代动力学特征有所改变,与标准制剂相比,可以使用更高的初始剂量,并且达到临床有效剂量的滴定步骤更少。在两项针对BPH患者的大型,双盲,随机研究(一项是安慰剂对照)中,多沙唑嗪GITS(每天4-8 mg一次)与标准制剂(每天2-8 mg一次)一样有效,并且两者在改善症状评分,健康相关生活质量(HR-QOL)和最大尿流率(Qmax)后,经过13周的治疗,比安慰剂更有效。在BPH患者的临床研究中,多沙唑嗪GITS的耐受性至少与多沙唑嗪的标准制剂相同。

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