Suppr超能文献

α1 受体阻滞剂坦索罗辛治疗良性前列腺增生患者:一项前瞻性多中心研究的 5 年结果分析。

α1-blocker tamsulosin as initial treatment for patients with benign prostatic hyperplasia: 5-year outcome analysis of a prospective multicenter study.

机构信息

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

Int J Urol. 2013 Apr;20(4):421-8. doi: 10.1111/j.1442-2042.2012.03165.x. Epub 2012 Sep 19.

Abstract

OBJECTIVE

To comprehensively analyze the 5-year outcomes of tamsulosin treatment for patients with benign prostatic hyperplasia.

METHODS

Tamsulosin (0.2 mg/day) was given to 112 patients who had International Prostate Symptom Scores ≥8. They were prospectively followed for 5 years with periodic evaluation. If tamsulosin had to be discontinued, the reason was determined. Treatment failure was considered in the case of disease progression (postvoid residual urine volume ≥200 mL, acute urinary retention, febrile urinary tract infection or hydronephrosis as a result of bladder outlet obstruction), conversion to other α1-blockers or need for surgery. An intention-to-treat analysis was carried out.

RESULTS

A total of 34 patients (30.4%) continued the same medication for the overall study period, whereas 78 patients (69.6%) discontinued the medication. International Prostate Symptom Scores, Benign Prostatic Hyperplasia Problem Index and Quality of Life Index were significantly improved over the 5-year period. Treatment failure was observed in 21 patients (18.8%). Baseline prostate volume and postvoid residual urine volume were independent factors to predicting treatment failure. A total of 21 patients (18.8%) discontinued tamsulosin because of an improvement of symptoms. They were younger and had lower prostate-specific antigen levels than the remaining 91 patients. Their symptoms were stable even 1 year after termination of therapy.

CONCLUSIONS

Long-term efficacy of tamsulosin was observed, although only a small portion of patients continued the treatment. α1-blocker monotherapy might be not appropriate for achieving a good long-term outcome in patients with a large prostate volume and a large amount of postvoid residual urine volume. Persistent improvement of symptoms, even after termination of tamsulosin, was observed in young patients with low prostate-specific antigen levels.

摘要

目的

全面分析坦索罗辛治疗良性前列腺增生患者的 5 年疗效。

方法

112 例国际前列腺症状评分≥8 分的患者接受坦索罗辛(0.2mg/天)治疗。前瞻性随访 5 年,定期评估。如果需要停用坦索罗辛,确定原因。如果出现疾病进展(残余尿量≥200ml、急性尿潴留、发热性尿路感染或膀胱出口梗阻导致肾积水)、转为其他α1 受体阻滞剂或需要手术,则认为治疗失败。采用意向治疗分析。

结果

共有 34 例(30.4%)患者在整个研究期间继续使用相同的药物,78 例(69.6%)患者停止用药。5 年内国际前列腺症状评分、良性前列腺增生问题指数和生活质量指数均显著改善。21 例(18.8%)患者出现治疗失败。基线前列腺体积和残余尿量是预测治疗失败的独立因素。共有 21 例(18.8%)患者因症状改善而停止使用坦索罗辛。他们比其余 91 例患者更年轻,前列腺特异性抗原水平更低。停药 1 年后,他们的症状仍然稳定。

结论

尽管只有一小部分患者继续治疗,但仍观察到坦索罗辛的长期疗效。α1 受体阻滞剂单药治疗可能不适合治疗前列腺体积大、残余尿量多的患者,获得良好的长期疗效。对于前列腺特异性抗原水平低、症状持续改善的年轻患者,即使停药后也可观察到症状改善。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验