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两种软膏和栓剂制剂(“尤尼罗伊德”和“安纳素栓”)在普通医疗中治疗二度痔疮的疗效和耐受性比较

Comparative efficacy and tolerability of two ointment and suppository preparations ('Uniroid' and 'Proctosedyl') in the treatment of second degree haemorrhoids in general practice.

作者信息

Smith R B, Moodie J

机构信息

Medical Department, Pharmakopius Ltd., Goring-on-Thames, England.

出版信息

Curr Med Res Opin. 1988;11(1):34-40. doi: 10.1185/03007998809111128.

DOI:10.1185/03007998809111128
PMID:2838221
Abstract

A multi-centre general practice, open study was carried out in 89 patients with second degree haemorrhoids to compare the efficacy and tolerability of two antibiotic-corticosteroid combinations ('Uniroid' and 'Proctosedyl') in ointment and suppository formulations. Patients were allocated at random into 4 groups and received treatment with one of the trial preparations for 1, 2 or 3 weeks, as required, with weekly assessments of response. There were no significant differences between the various groups at the start of treatment. Significant improvement occurred in all groups during treatment. Both suppository and ointment formulations were broadly comparable and control of symptoms was achieved from Week 2 onwards, building up to levels in excess of 90% after 3 weeks of therapy. With regard to the symptoms of pain and itching, suppositories gave marginally greater relief in the early stages of treatment, while both ointment and suppositories were associated with similar reduction in bleeding from haemorrhoids. Whereas both suppository formulations were about equal in reducing anal discharge, 'Uniroid' ointment was clinically superior to 'Proctosedyl' ointment in controlling this symptom over the 3-week trial period. No unwanted effects were experienced attributable to treatment. No statistically significant differences between the two ointment and the two suppository formulations were identified in this study and all four preparations were found to be efficacious in the majority of patients studied.

摘要

对89例二度痔疮患者进行了一项多中心全科开放研究,以比较两种抗生素 - 皮质类固醇组合(“尤尼罗伊德”和“痔根断”)的软膏剂和栓剂剂型的疗效和耐受性。患者被随机分为4组,并根据需要接受其中一种试验制剂治疗1、2或3周,每周评估反应情况。治疗开始时各小组之间无显著差异。治疗期间所有组均有显著改善。栓剂和软膏剂剂型大致相当,从第2周起症状得到控制,治疗3周后症状控制水平超过90%。关于疼痛和瘙痒症状,栓剂在治疗早期缓解程度略大,而软膏剂和栓剂在减少痔疮出血方面效果相似。两种栓剂剂型在减少肛门分泌物方面大致相同,在为期3周的试验期内,“尤尼罗伊德”软膏在控制该症状方面临床上优于“痔根断”软膏。未发现因治疗引起的不良反应。本研究未发现两种软膏剂和两种栓剂剂型之间有统计学显著差异,且发现所有四种制剂对大多数研究患者均有效。

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