Hanno P M
Division of Urology, Temple University School of Medicine, Philadephia, Pennsylvania 19140, USA.
Urology. 1997 May;49(5A Suppl):93-9. doi: 10.1016/s0090-4295(97)00179-9.
The long-term efficacy and safety of Elmiron (oral pentosan polysulfate sodium) in relieving recurring symptoms of interstitial cystitis (IC) were investigated in a long-term, open-label physician's usage study.
Patients with diagnosed interstitial cystitis who met the study entry criteria received shipments of Elmiron for 3 months at a dose of 100 mg 3 times a day and for the consecutive 3-month periods, provided they completed and returned questionnaires about their disease symptoms, reported any adverse events, and had laboratory data collected before each new shipment. Patients were required to purchase the medication. Responses to questionnaires provided the data reported here. Several symptomatic parameters of the disease (overall improvement, overall improvement in pain and urgency, urinary frequency, and nocturia) were recorded in this way and used to evaluate efficacy.
Elmiron usage was correlated with improvements in some symptoms, and these improvements increased with duration of treatment. Some symptoms were improved within 5 months, although most continued to show improvements in both severity rating and in percentage of positive responders over 1 to 2 years. Populations of patients receiving extended treatment, some for > 90 months, showed no further improvement or worsening in symptom values. Forty-six percent of patients dropped out of the study within the first 3 months of Elmiron treatment. The frequency of adverse events was < 4%. The most notable adverse events were reversible alopecia, diarrhea, nausea, headache, and rash.
Elmiron appears to be an efficacious long-term treatment for reducing a constellation of debilitating symptoms associated with interstitial cystitis in some patients. Patients with a positive response to Elmiron appear to maintain this response over time.
在一项长期、开放标签的医生使用研究中,调查了爱若明(口服戊聚糖多硫酸酯钠)缓解间质性膀胱炎(IC)复发症状的长期疗效和安全性。
符合研究入选标准的已确诊间质性膀胱炎患者接受爱若明治疗,剂量为每日3次,每次100毫克,为期3个月,并在随后连续的3个月期间持续用药,前提是他们完成并返回有关疾病症状的问卷,报告任何不良事件,并在每次新的药物配送前收集实验室数据。患者需自行购买药物。对问卷的回答提供了此处报告的数据。通过这种方式记录了该疾病的几个症状参数(总体改善情况、疼痛和尿急的总体改善情况、尿频和夜尿),并用于评估疗效。
使用爱若明显然与某些症状的改善相关,并且这些改善随着治疗时间的延长而增加。一些症状在5个月内有所改善,尽管大多数症状在1至2年的时间里在严重程度评分和阳性反应者百分比方面持续改善。接受延长治疗的患者群体,有些治疗时间超过90个月,症状值没有进一步改善或恶化。46%的患者在爱若明治疗的前3个月内退出了研究。不良事件的发生率低于4%。最显著的不良事件是可逆性脱发、腹泻、恶心、头痛和皮疹。
爱若明似乎是一种有效的长期治疗方法,可减轻一些患者与间质性膀胱炎相关的一系列使人衰弱的症状。对爱若明有阳性反应的患者似乎能长期维持这种反应。