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戊聚糖多硫酸钠治疗间质性膀胱炎。一项双盲安慰剂对照临床研究。

Pentosan polysulfate sodium for therapy of interstitial cystitis. A double-blind placebo-controlled clinical study.

作者信息

Mulholland S G, Hanno P, Parsons C L, Sant G R, Staskin D R

机构信息

Department of Urology, Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

出版信息

Urology. 1990 Jun;35(6):552-8. doi: 10.1016/0090-4295(90)80116-5.

Abstract

Pentosan polysulfate sodium (PPS) was compared with placebo for the symptomatic therapy of interstitial cystitis in a double-blind, multicenter study. A total of 110 patients were enrolled and treated for three months. In this study, overall improvement of greater than 25 percent was reported by 28 percent of the PPS-treated patients and by 13 percent of the placebo-treated patients (p = 0.03). The investigators' overall evaluation provided similar results, 26 percent vs 11 percent in favor of PPS (p = 0.04). Improvement in pain and pressure to urinate also favored PPS over placebo and approached statistical significance (p = 0.07 and 0.08). The incidence of adverse reactions was 6 percent in the PPS-treated group and 13 percent in the placebo-treated group. All adverse reactions were minor, and treatment was discontinued by 1 patient in the PPS group and 2 in the placebo group. In this study, PPS was found to be significantly more effective than, and equally as safe as, placebo.

摘要

在一项双盲、多中心研究中,对戊聚糖多硫酸钠(PPS)与安慰剂治疗间质性膀胱炎的症状进行了比较。共有110名患者入组并接受了为期三个月的治疗。在这项研究中,28%接受PPS治疗的患者报告总体改善超过25%,而接受安慰剂治疗的患者为13%(p = 0.03)。研究者的总体评估提供了类似结果,支持PPS的比例分别为26%和11%(p = 0.04)。疼痛和排尿压力的改善也有利于PPS而非安慰剂,且接近统计学显著性(p = 0.07和0.08)。PPS治疗组的不良反应发生率为6%,安慰剂治疗组为13%。所有不良反应均较轻微,PPS组有1名患者、安慰剂组有2名患者停止治疗。在这项研究中,发现PPS比安慰剂显著更有效,且安全性相当。

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