α -1肾上腺素受体阻滞剂对勃起功能的影响:一项系统综述。

IF 2.5 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Ahmed M Bakr, Ahmed I El-Sakka
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引用次数: 0

摘要

α -1肾上腺素能受体拮抗剂(α1-ARA)是治疗良性前列腺增生(BPH)相关下尿路症状(LUTS)的有效方法。由于BPH和勃起功能障碍(ED)通常是并发疾病,因此研究α1-ARA在ED患者中的潜在作用的重要性正在上升。方法:我们系统地回顾了评估勃起功能(EF)指数与α1-ARA使用相关的研究文献。所有类型的比较都包括在内。结果:在1915条记录中,有21篇文章被纳入。所有的文章都存在高偏倚风险。与基线和安慰剂相比,α1-ARA在EF方面有显著改善。一些α1-ARA比其他的更容易勃起。联合磷酸二酯酶-5抑制剂治疗比单独治疗更能改善EF。相关的下尿症状、剂量、治疗时间等因素可改变α1-ARA对EF的影响。结论:Αlpha1-ARAs在主观和客观量表上都有潜在的改善EF的作用。然而,现有的证据是从α1-ARAs的其他适应症患者的研究中提取的,特别是bph相关的LUTS。进一步的研究应针对ED患者,以准确地确定其临床用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of alpha-1 adrenergic receptor blockers on erectile function: a systematic review.

Introduction: Alpha-1 adrenergic receptor antagonist (α1-ARA) are well established treatment for benign prostatic hyperplasia (BPH)-associated lower urinary tract symptoms (LUTS). Since BPH and erectile dysfunction (ED) are commonly concomitant conditions, the importance of addressing the potential role of α1-ARA in patients with ED is rising.

Methods: We systemically reviewed literature for studies that assessed erectile function (EF) indices in relation to α1-ARA use. All types of comparisons were included.

Results: Out of 1915 records, 21 articles have been included. All articles suffered high risk of bias. α1-ARA showed a significant improvement in EF in comparison to baseline and placebo. Some α1-ARA are more erectogenic than others. Combined therapy with phosphodiesterase-5 inhibitors improved EF better than either alone. Factors like associated lower urinary symptoms, dose, duration of therapy modify α1-ARA effects on EF.

Conclusion: Αlpha1-ARAs have a potential role in improving EF in subjective and objective scales. However, the available evidence is extracted from studies on patients with other indications for α1-ARAs, particularly BPH-related LUTS. Further investigations should target patients with ED only to precisely identify their clinical utility.

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来源期刊
CiteScore
5.60
自引率
3.10%
发文量
163
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Pharmacotherapy is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on newly approved/near to launch compounds mainly of chemical/synthetic origin, providing expert opinion on the likely impact of these new agents on existing pharmacotherapy of specific diseases.
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