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Model-based meta-analysis of the time to first acute urinary retention or benign prostatic hyperplasia-related surgery in patients with moderate or severe symptoms

机译:基于模型的META分析了第一急性尿尿潴留或良性前列腺增生相关手术的时间中度或严重症状

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Aims Combination therapy of 5α-reductase inhibitor and α-blocker is a guideline-endorsed therapeutic approach for patients with moderate-to-severe lower urinary tract symptoms or benign prostatic hyperplasia (LUTS/BPH) who are at risk of disease progression. We aimed to disentangle the contribution of clinical and demographic baseline characteristics affecting the risk of acute urinary retention or BPH-related surgery (AUR/S) from the effect of treatment with drugs showing symptomatic and disease-modifying properties. Methods A time-to-event model was developed using pooled data from patients (n?=?10?238) enrolled into six clinical studies receiving placebo, tamsulosin, dutasteride or tamsulosin-dutasteride combination therapy. A parametric hazard function was used to describe the time to first AUR/S. Covariate model building included the assessment of relevant clinical and demographic factors on baseline hazard. Predictive performance was evaluated by graphical and statistical methods. Results An exponential hazard model best described the time to first AUR/S in this group of patients. Baseline International Prostate Symptom Score, prostate-specific antigen, prostate volume and maximum urine flow were identified as covariates with hazard ratio estimates of 1.04, 1.08, 1.01 and 0.91, respectively. Dutasteride monotherapy and tamsulosin-dutasteride combination therapy resulted in a significant reduction in the baseline hazard (56.8% and 66.4%, respectively). By contrast, the effect of tamsulosin did not differ from placebo. Conclusions Our analysis showed the implications of disease-modifying properties of dutasteride and tamsulosin-dutasteride combination therapy for the risk of AUR/S. It also elucidated the contribution of different baseline characteristics to the risk of these events. The use of tamsulosin monotherapy (symptomatic treatment) has no impact on individual long-term risk. Abstract Visual predictive checks. The line shows observed survival over time, whereas the shaded area describes the model predicted 95% CI for the survival. The different slopes of the survival curves for dutasteride monotherapy and combination therapy (relative to placebo) reflect the disease-modifying properties of the intervention.
机译:5α-还原酶抑制剂和α-ressers的AIMS联合治疗是针对中度至严重的低尿路症状或患有疾病进展风险的患者的指南备受治疗方法。我们旨在解散影响急性尿潴留或BPH相关手术(AUR / S)的风险的临床和人口基线特征的贡献免于治疗症状和疾病修饰性能的药物。方法使用来自患者的池数据(N?= 10'238)开发了时间 - 事件模型,纳入六项临床研究,接受安慰剂,Tamsulosin,Colasteride或Tamsulosin-Colasteride联合治疗。参数危险功能用于描述第一AUR / s的时间。协变量模型建设包括对基线危害的相关临床和人口因子的评估。通过图形和统计方法评估预测性能。结果指数危险模型最好地描述了该组患者的第一AUR的时间。基线国际前列腺症状得分,前列腺特异性抗原,前列腺体积和最大尿液流量被鉴定为具有1.04,1.08,1.01和0.91的危险比估计的协变量。荷兰啶虫单疗法和杜鹃花瓶组合疗法导致基线危害的显着降低(分别为56.8%和66.4%)。相比之下,Tamsulosin的作用与安慰剂没有不同。结论我们的分析表明,荷兰甾醇和杜鹃花瓶组合治疗对Aur / s风险的影响。它还阐明了不同基线特征对这些事件的风险的贡献。使用Tamsulosin单药治疗(对症治疗)对个体长期风险没有影响。摘要视觉预测检查。该线显示随着时间的推移观察到的存活率,而阴影区域描述了用于存活率的95%CI的模型。荷兰甾醇单疗法和联合治疗(相对于安慰剂)的不同倾斜曲线反映了干预的疾病修饰性质。

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