Suppr超能文献

贝卡普勒明(重组人血小板衍生生长因子-BB)治疗下肢糖尿病溃疡不愈合患者的疗效与安全性:四项随机研究的综合分析

Efficacy and safety of becaplermin (recombinant human platelet-derived growth factor-BB) in patients with nonhealing, lower extremity diabetic ulcers: a combined analysis of four randomized studies.

作者信息

Smiell J M, Wieman T J, Steed D L, Perry B H, Sampson A R, Schwab B H

机构信息

R.W. Johnson Pharmaceutical Research Institute, Raritan, NJ 08869, USA.

出版信息

Wound Repair Regen. 1999 Sep-Oct;7(5):335-46. doi: 10.1046/j.1524-475x.1999.00335.x.

Abstract

The results of a combined analysis and separate analyses of four multicenter, randomized, parallel group studies that evaluated the effects of once-daily topical administration of becaplermin gel for the treatment of chronic, full thickness, lower extremity diabetic ulcers are presented. The four studies included a total of 922 patients with nonhealing lower extremity diabetic ulcers of at least 8 weeks' duration. Following initial complete sharp debridement of the ulcer, patients were randomized to receive a standardized regimen of good ulcer care alone, good ulcer care plus placebo gel, or good ulcer care plus becaplermin gel-30 microg/g, or good ulcer care plus becaplermin gel-100 microg/g, with various combinations of regimens used in the four studies. Safety was assessed by monitoring adverse events and by clinical laboratory evaluations. Meta-analytic statistical techniques were used in the combined analysis to establish homogeneity of treatment comparisons across studies. Based on an analysis of patients with baseline ulcer area common to all trials (</= 10 cm2), representing 95% of all patients, becaplermin gel-100 microg/g significantly increased (p = 0.007) the probability of complete healing compared with placebo gel. It was determined that for the median ulcer area of these patients, which was 1.5 cm2, the becaplermin gel-100 microg/g treatment group showed a 39% increase in complete healing compared with that of the placebo gel treatment group (50% vs. 36%, respectively, p = 0.007). Becaplermin gel-100 microg/g significantly decreased (p = 0.01) the time to complete healing compared with placebo gel, with the 35th percentile of time to complete healing being reduced by 30% (14.1 weeks vs. 20. 1 weeks, respectively). In patients with ulcers </= 5 cm2 at baseline (a more homogeneous group), becaplermin gel-100 microg/g also significantly increased the incidence of complete healing with a similar decrease in the time to healing. Adverse events reported during treatment or during a 3-month follow-up period were not unexpected for this patient population and were similar in nature and incidence across all treatment groups. We therefore conclude that treatment with becaplermin gel at a dose of 100 microg/g once daily, in conjunction with good ulcer care, is effective and well tolerated in patients with full thickness lower extremity diabetic ulcers.

摘要

本文呈现了四项多中心、随机、平行组研究的联合分析及单独分析结果,这些研究评估了每日一次局部应用贝卡普勒明凝胶治疗慢性、全层、下肢糖尿病溃疡的效果。这四项研究共纳入922例下肢糖尿病溃疡不愈合且病程至少8周的患者。在对溃疡进行初始完全锐性清创后,患者被随机分为四组,分别接受单纯标准溃疡护理方案、标准溃疡护理加安慰剂凝胶、标准溃疡护理加30μg/g贝卡普勒明凝胶或标准溃疡护理加100μg/g贝卡普勒明凝胶,四项研究采用了不同的方案组合。通过监测不良事件和临床实验室评估来评估安全性。联合分析中使用了荟萃分析统计技术,以确定各研究中治疗比较的同质性。基于对所有试验中基线溃疡面积≤10 cm²的患者(占所有患者的95%)的分析,与安慰剂凝胶相比,100μg/g贝卡普勒明凝胶显著提高了(p = 0.007)完全愈合的概率。经测定,这些患者的中位溃疡面积为1.5 cm²,与安慰剂凝胶治疗组相比,100μg/g贝卡普勒明凝胶治疗组的完全愈合率提高了39%(分别为50%和36%,p = 0.007)。与安慰剂凝胶相比,100μg/g贝卡普勒明凝胶显著缩短了(p = 0.01)完全愈合时间,完全愈合时间的第35百分位数减少了30%(分别为14.1周和20.1周)。在基线溃疡面积≤5 cm²的患者中(这是一个更具同质性的组),100μg/g贝卡普勒明凝胶也显著提高了完全愈合的发生率,愈合时间也有类似程度的缩短。治疗期间或3个月随访期内报告的不良事件在该患者群体中并非意外,且在所有治疗组中的性质和发生率相似。因此,我们得出结论,对于全层下肢糖尿病溃疡患者,每日一次应用100μg/g贝卡普勒明凝胶并结合良好的溃疡护理,是有效且耐受性良好的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验