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Epithelializing stent for benign prostatic hyperplasia: a systematic review of the literature.

机译:良性前列腺增生的上皮支架:文献综述。

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PURPOSE: We systematically reviewed the literature on the effectiveness, durability and safety of the UroLume stent for men with benign prostatic hyperplasia. MATERIALS AND METHODS: We searched the MEDLINE and EMBASE databases for 1989 to 2005. Reference lists of included studies and review articles were also searched. We contacted the UroLume manufacturer and key authors for additional information. Primary outcomes were treatment failure and urological symptom scores. Secondary outcomes were uroflow parameters and minor complications. Two reviewers independently assessed the methodological quality of the studies and extracted data. RESULTS: A total of 20 case series evaluated the UroLume stent in a total of 990 patients with benign prostatic hyperplasia. Of the patients 84% who were catheter dependent voided spontaneously after stent insertion. Ten studies assessed symptoms before stent insertion and at some point within 1 year after stent insertion. All reported decreases in symptom scores, includingMadsen-Iversen by 7.9 to 14.3 points and International Prostate Symptom Score by 10 to 12.4 points. Peak urine flow rates increased by 4.2 to 13.1 ml per second. A total of 104 stents (16%) failed in 606 patients who were evaluable at 1 year and migration was the commonest cause of failure (38 stents or 37%). Most patients initially experienced perineal pain or irritative voiding symptoms following stent placement. CONCLUSIONS: Of men who were catheter dependent 84% voided spontaneously after insertion of a UroLume stent and the improvement in symptoms was similar to that seen after transurethral prostate resection. However, 1 of 6 men needed the UroLume removed within a year because of complications. Inadequate followup prevented conclusions on stent durability beyond 1 year. This review supports the recommendation that stents should be considered only in patients at high risk.
机译:目的:我们系统地回顾了有关UroLume支架对前列腺增生男性患者的有效性,耐用性和安全性的文献。材料和方法:我们检索了1989年至2005年的MEDLINE和EMBASE数据库。还检索了包括研究和评价文章的参考文献清单。我们联系了UroLume制造商和主要作者,以获取更多信息。主要结局为治疗失败和泌尿科症状评分。次要结果是尿流参数和轻微并发症。两名评论者独立评估了研究的方法学质量并提取了数据。结果:总共20个病例系列对总共990例前列腺增生患者中的UroLume支架进行了评估。在支架插入后自发排空导管的患者中有84%。十项研究评估了支架置入前和支架置入后1年内某个时间点的症状。所有报告的症状评分均下降,包括Madsen-Iversen降低7.9至14.3分和国际前列腺症状评分降低10至12.4分。峰值尿流率增加了4.2至每秒13.1 ml。 606例在1年内可评估的患者中共有104个支架(占16%)失败,并且迁移是最常见的失败原因(38个支架或37%)。大多数患者最初在放置支架后会阴会痛或有刺激性的排尿症状。结论:在男性患者中,在插入UroLume支架后自发排尿的患者中有84%依赖导管,并且症状的改善与经尿道前列腺切除术后的症状相似。但是,由于并发症,一年之内需要将6名男性中的1名移除UroLume。随访不充分,无法得出关于支架耐用性超过1年的结论。该评价支持以下建议:仅在高风险患者中才应考虑使用支架。

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