Madersbacher S, Rieken M, Reuber K, Kostev K
Abteilung für Urologie und Andrologie, Klinik Favoriten, Vienna, Austria.
Alta uro AG, Basel, Switzerland.
Postgrad Med. 2023 Mar;135(2):149-154. doi: 10.1080/00325481.2022.2149156. Epub 2022 Nov 21.
The present study aims to analyze the impact of prescriptions on the incidence of urinary incontinence, polyuria (including nocturia), urinary retention, and erectile dysfunction in a real-world setting in Germany and to compare these data with data for the 5-ARIs finasteride and dutasteride, and the α1-adrenoceptor antagonists tamsulosin and tamsulosin/dutasteride fixed-dose combination. This retrospective study was based on the IQVIA Disease Analyzer database and included male patients with an initial prescription of , finasteride, dutasteride, tamsulosin, or tamsulosin/dutasteride fixed-dose combination between January 2010 and September 2020. Multivariable logistic regression analyses adjusted for age, health insurance, specialty, and relevant co-diagnoses were performed to estimate the association between prescriptions and incidence of pre-defined outcomes. A total of 77,923 patients were included in the study, 3,035 of whom received was significantly associated with reduced incidence of urinary incontinence (OR: 1.48; 95% CI: 1.10-1.98) and urinary retention compared to tamsulosin (OR: 3.39; 95% CI: 1.75-6.57 and tamsulosin/dutasteride (OR: 2.81; 95% CI: 1.35-5.82). Furthermore, significantly reduced the incidence of erectile dysfunction compared to dutasteride (OR: 2.79; 95% CI: 1.49-5.25). At the same time, patients receiving showed the same incidence of the remaining complications as those taking the reference substances. In conclusion, we observed a significant association between prescription and reduced incidence of urinary incontinence and urinary retention compared to tamsulosin and tamsulosin/dutasteride, as well as reduced incidence of erectile dysfunction compared to dutasteride.
本研究旨在分析在德国的实际临床环境中,[某种药物]处方对尿失禁、多尿(包括夜尿症)、尿潴留和勃起功能障碍发生率的影响,并将这些数据与5α-还原酶抑制剂非那雄胺和度他雄胺,以及α1-肾上腺素能受体拮抗剂坦索罗辛和坦索罗辛/度他雄胺固定剂量组合的数据进行比较。这项回顾性研究基于艾昆纬疾病分析器数据库,纳入了2010年1月至2020年9月期间首次处方非那雄胺、度他雄胺、坦索罗辛或坦索罗辛/度他雄胺固定剂量组合的男性患者。进行了多变量逻辑回归分析,对年龄、医疗保险、专科和相关合并诊断进行了调整,以估计[某种药物]处方与预定义结局发生率之间的关联。该研究共纳入77,923例患者,其中3,035例接受了[某种药物]治疗。与坦索罗辛相比,[某种药物]与尿失禁发生率降低显著相关(比值比:1.48;95%置信区间:1.10 - 1.98),与尿潴留发生率降低显著相关(比值比:3.39;95%置信区间:1.75 - 6.57),与坦索罗辛/度他雄胺相比也显著相关(比值比:2.81;95%置信区间:1.35 - 5.82)。此外,与度他雄胺相比,[某种药物]显著降低了勃起功能障碍的发生率(比值比:2.79;95%置信区间:1.49 - 5.25)。同时,接受[某种药物]治疗的患者与服用对照药物的患者相比,其余并发症的发生率相同。总之,我们观察到,与坦索罗辛和坦索罗辛/度他雄胺相比,[某种药物]处方与尿失禁和尿潴留发生率降低显著相关,与度他雄胺相比,勃起功能障碍发生率也降低。