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Many new ideas for the treatment of bladder pain syndrome are proposed every year and few ultimately pan out. The vast majority is accepted for publication prematurely and highlight case reports, anecdotal results, and nonrandomized, small, uncontrolled trials. I think this article should be a model for publication of new treatments. It reveals the results of a small, randomized, double-blind, placebo-controlled trial using low-dose sildenafil for the treatment of non—Hunner lesion bladder pain syndrome in women meeting National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) criteria. Although the numbers are small, the end point parameters are multiple and all but the visual analog pain scale shows a signal that further studies are worthwhile and should be pursued using phosphodiesterase type 5 (PDE5) inhibitors for bladder pain syndrome (BPS). I suspect that the reason that the visual analogue scale scores (VAS) does not suggest efficacy is that the benefits of pain reduction are reflected in the global response, improvements in nocturia and frequency, and urodynamic parameters. Patients modulate their pain by emptying their bladder, and as their pain improves, their voiding intervals would tend to increase, with the pain recurring at similar intensity at a longer interval, which drives micturition. This would not necessarily be judged by the patient as having less pain intensity.
机译:每年提出许多用于治疗膀胱疼痛综合征的新思路,但最终很少有人提出。绝大多数人都接受过早出版,并着重强调病例报告,传闻结果以及非随机,小型,无对照的试验。我认为本文应该成为发布新疗法的典范。它揭示了一项小剂量,随机,双盲,安慰剂对照试验的结果,该试验使用低剂量西地那非治疗符合美国国家糖尿病与消化与肾脏病研究所(NIDDK)标准的非亨氏病灶性膀胱疼痛综合征。尽管数量很少,但终点参数却很多,但视觉类似物疼痛量表显示的信号表明,进一步的研究是值得的,应使用5型磷酸二酯酶(PDE5)抑制剂治疗膀胱疼痛综合征(BPS)。我怀疑视觉模拟量表评分(VAS)不能表明疗效的原因是,缓解疼痛的益处反映在总体反应,夜尿症和频率的改善以及尿动力学参数上。患者通过排空膀胱来调节疼痛,并且随着疼痛的改善,排尿间隔会趋于增加,并且疼痛会在更长的间隔内以相似的强度反复发作,从而导致排尿困难。患者不必将其判断为疼痛强度较小。

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  • 来源
    《Urology》 |2014年第1期|共1页
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    HannoP.; ChenH.; WengZ.;

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