Tamsulosin and Dutasteride Combination Therapy for Asian Men With Moderate-to-Severe Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia: A Systematic Review of Clinical Considerations That Influence the Prescription.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Journal of clinical medicine research Pub Date : 2024-09-01 Epub Date: 2024-09-12 DOI:10.14740/jocmr5255
Fan Yang, Rahab Hashim, Julia Philippou
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Abstract

The goal of combination therapy for moderate-to-severe lower urinary tract symptoms secondary to benign prostatic hyperplasia (LUTS/BPH) is to ease both the dynamic and static symptoms by using agents that have complementary mechanisms of action. Similar to prescribing other drugs, LUTS/BPH combination therapy has been affected by multiple factors. Previous qualitative research discussed the individual perspectives that influenced combination therapy administration. Yet, until recently, there has been limited interest in clinical reasons that physicians have to consider before prescribing LUTS/BPH combination treatment. This systematic review aimed to identify the clinical considerations that influence the decision to prescribe combination therapy of tamsulosin 0.4 mg + dutasteride 0.5 mg for Asian men with LUTS/BPH. This review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A systematic search was performed in databases Medline, CINAHL, the Cochrane Library, and Embase from inception until January 2024 using Medical Subject Headings (MeSH) terms and keywords with truncation for alternative acronyms. A citation search was performed to gather works of literature on LUTS/BPH combination treatment in addition to the "PICO" framework for search terms. Five English-language primary randomized controlled trials (RCTs) were included in the narrative analysis using the Critical Appraisal Skills Program (CASP) checklist after critical appraisal. Several dosages of tamsulosin (0.2 mg and 0.4 mg) have been administered in LUTS/BPH combination treatment over the last few decades despite 0.2 mg tamsulosin being standardized as an effective regime in Asian countries. A remarkable correlation between prostate volume (PV) and prostate-specific antigen (PSA) was found in Asian men, which requires higher PSA secretion to enlarge each prostate unit and causes an increased risk of moderate-to-severe LUTS. Additionally, BPH baseline variables may lead to a different response to combination therapy, especially the PV and PSA differences. In conclusion, compared with Caucasian men, a significantly higher risk of moderate-to-severe LUTS was found in Asian men. Initiation of combination therapy, especially dutasteride, depends on a larger PV (≥ 30 mL); it is possible, therefore, that earlier PV and PSA examinations and baseline variables assessments ought to be performed by physicians before the combination therapy prescription. Alternative treatment options may be considered for a patient who prefers an active pattern of sexual activity during their BPH combined pharmacotherapy. These clinical considerations may influence the prescription of tamsulosin 0.4 mg + dutasteride 0.5 mg combination therapy for Asian men with moderate-to-severe LUTS/BPH. This study was registered on PROSPERO (CRD42024575528).

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坦索罗辛和度他雄胺联合疗法治疗因良性前列腺增生症而出现中度至重度下尿路症状的亚洲男性:影响处方的临床考虑因素的系统性综述。
对于继发于良性前列腺增生症(LUTS/BPH)的中重度下尿路症状,联合疗法的目标是通过使用具有互补作用机制的药物来缓解动态和静态症状。与处方其他药物类似,LUTS/BPH 综合疗法也受到多种因素的影响。之前的定性研究讨论了影响综合疗法用药的个人观点。然而,直到最近,人们对医生在开具 LUTS/BPH 联合疗法处方前必须考虑的临床原因的兴趣仍然有限。本系统性综述旨在确定影响亚洲男性 LUTS/BPH 患者处方坦索罗辛 0.4 毫克+度他雄胺 0.5 毫克联合疗法决定的临床考虑因素。本综述遵循了系统综述和荟萃分析首选报告项目(PRISMA)指南。我们使用医学主题词表(MeSH)术语和关键词对 Medline、CINAHL、Cochrane 图书馆和 Embase 等数据库进行了系统检索,检索期从开始到 2024 年 1 月。除了 "PICO "检索词框架外,还进行了引文检索,以收集有关 LUTS/BPH 联合治疗的文献作品。经过批判性评估后,使用批判性评估技能计划(CASP)核对表对五项英文主要随机对照试验(RCT)进行了叙述性分析。尽管在亚洲国家,0.2 毫克坦索罗辛已被标准化为一种有效的治疗方案,但在过去的几十年中,坦索罗辛的多种剂量(0.2 毫克和 0.4 毫克)已被用于 LUTS/BPH 联合治疗。在亚洲男性中,前列腺体积(PV)与前列腺特异性抗原(PSA)之间存在明显的相关性,前列腺特异性抗原需要更高的 PSA 分泌来增大每个前列腺单位,从而导致中重度 LUTS 风险增加。此外,良性前列腺增生症的基线变量可能会导致对联合疗法的不同反应,尤其是PV和PSA的差异。总之,与白种男性相比,亚洲男性患中重度 LUTS 的风险明显更高。联合疗法的启动,尤其是度他雄胺的启动,有赖于较大的PV(≥ 30 mL);因此,医生在开具联合疗法处方之前,有可能需要进行更早的PV和PSA检查以及基线变量评估。如果患者在接受良性前列腺增生症联合药物治疗期间喜欢积极的性活动模式,则可以考虑其他治疗方案。这些临床考虑因素可能会影响对患有中度至重度LUTS/BPH的亚洲男性患者处方坦索罗辛0.4毫克+度他雄胺0.5毫克联合疗法。本研究已在 PROSPERO(CRD42024575528)上注册。
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