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与皮质类固醇治疗相比,康瑞保局部应用于增生性瘢痕的安全性和有效性。德国一项多中心、比较性流行病学队列研究的结果

Safety and efficacy of local administration of contractubex to hypertrophic scars in comparison to corticosteroid treatment. Results of a multicenter, comparative epidemiological cohort study in Germany.

作者信息

Beuth J, Hunzelmann N, Van Leendert R, Basten R, Noehle M, Schneider B

机构信息

Institut zur wissenschaflichen Evaluation naturheilkundlicher Verfahren an der Universitaet zu Koeln, 50331 Koeln, Germany.

出版信息

In Vivo. 2006 Mar-Apr;20(2):277-83.

Abstract

OBJECTIVES

To investigate the safety and efficacy of Contractubex administration to hypertrophic scars in routine out-patient practice and to compare it to corticosteroid treatment.

PATIENTS AND METHODS

This was a multicenter, retrospective cohort study, based on 38 randomly selected practices representatively distributed in Germany, including dermatologists and general practitioners. Data from 859 patients fulfilling the inclusion criteria were assessed and analyzed. Of these, 771 patients were eligible for the per protocol treatment with Contractubex (n=555) and corticosteroid (n=216). The safety and efficacy of local administration of Contractubex to hypertrophic scars was compared to corticosteroid treatment.

RESULTS

At the end of defined treatment periods (minimum 28 days for local therapy with 1 intralesional corticosteroid application), normalization of the pre-treatment pathological parameters (erythema, pruritus, consistency) of hypertrophic scars was more frequent (42.5%) after Contractubex per protocol treatment as compared to corticosteroid per protocol treatment (22.2%). After adjusting imbalances of baseline characterisics between the treatment groups by the propensity score, the odds ratio was 2.274, demonstrating a significant superiority (p<0.001) of Contractubex treatment as compared to corticosteroid treatment. The time to normalization of erythema, pruritus and consistency was significantly (p=0.034) shorter with Contractubex treatment (median 344 days) than with corticosteroids (median 507 days). No unexpected or severe adverse events occurred in the Contractubex-treated patients. Apart from moderate pruritus (10% Contractubex vs. 1% corticosteroids), adverse events were significantly (p<0.001) more frequent in corticosteroid-treated patients (teleangiectasias 15% vs. 7% Contractubex; cutaneous atrophy of scars 10% vs. 2% Contractubex; cutaneous atrophy of scar surrounding skin tissue 11% vs. 1% Contractubex).

CONCLUSION

For the primary aim of this study (assessment of normalization of erythema, pruritus, and consistency of hypertrophic scars) and for time to normalization, local administration of Contractubex was significantly more effective than corticosteroid treatment. Concerning safety, Contractubex treatment was associated with significantly less adverse events (e.g. teleangiectasias, cutaneous atrophy of scars and surrounding skin tissue) than topical corticosteroid application.

摘要

目的

在常规门诊实践中研究康瑞保(Contractubex)治疗增生性瘢痕的安全性和有效性,并与皮质类固醇治疗进行比较。

患者与方法

这是一项多中心回顾性队列研究,基于在德国随机选取的38家具有代表性分布的医疗机构,包括皮肤科医生和全科医生。对符合纳入标准的859例患者的数据进行了评估和分析。其中,771例患者符合按方案接受康瑞保(n = 555)和皮质类固醇(n = 216)治疗的条件。比较了康瑞保局部治疗增生性瘢痕的安全性和有效性与皮质类固醇治疗的情况。

结果

在规定的治疗期结束时(局部治疗至少28天,病灶内注射1次皮质类固醇),按方案接受康瑞保治疗的增生性瘢痕治疗前病理参数(红斑、瘙痒、质地)恢复正常的频率(42.5%)高于按方案接受皮质类固醇治疗的频率(22.2%)。通过倾向评分调整治疗组之间基线特征的不平衡后,优势比为2.274,表明康瑞保治疗与皮质类固醇治疗相比具有显著优势(p < 0.001)。康瑞保治疗使红斑、瘙痒和质地恢复正常的时间(中位数344天)明显短于皮质类固醇治疗(中位数507天)(p = 0.034)。接受康瑞保治疗的患者未发生意外或严重不良事件。除了中度瘙痒(康瑞保组为10%,皮质类固醇组为1%)外,皮质类固醇治疗的患者不良事件明显更频繁(p < 0.001)(毛细血管扩张:皮质类固醇组为15%,康瑞保组为7%;瘢痕皮肤萎缩:皮质类固醇组为10%,康瑞保组为2%;瘢痕周围皮肤组织皮肤萎缩:皮质类固醇组为11%,康瑞保组为1%)。

结论

对于本研究的主要目的(评估增生性瘢痕红斑、瘙痒和质地的恢复正常情况)以及恢复正常的时间,康瑞保局部给药明显比皮质类固醇治疗更有效。在安全性方面,与局部应用皮质类固醇相比,康瑞保治疗相关的不良事件(如毛细血管扩张、瘢痕和周围皮肤组织的皮肤萎缩)明显更少。

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