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多西环素 40mg 与米诺环素 100mg 治疗酒渣鼻的随机、单盲、非劣效性试验:比较疗效和安全性。

DOMINO, doxycycline 40 mg vs. minocycline 100 mg in the treatment of rosacea: a randomized, single-blinded, noninferiority trial, comparing efficacy and safety.

机构信息

Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.

出版信息

Br J Dermatol. 2017 Jun;176(6):1465-1474. doi: 10.1111/bjd.15155. Epub 2017 May 8.

Abstract

BACKGROUND

There is a lack of evidence for minocycline in the treatment of rosacea.

OBJECTIVES

To compare the efficacy and safety of doxycycline 40 mg vs. minocycline 100 mg in papulopustular rosacea.

METHODS

In this randomized, single-centre, 1 : 1 allocation, assessor-blinded, noninferiority trial, patients with mild-to-severe papulopustular rosacea were randomly allocated to either oral doxycycline 40 mg or minocycline 100 mg for a 16-week period with 12 weeks of follow-up. Our primary outcomes were the change in lesion count and change in patient's health-related quality of life (using RosaQoL). Intention-to-treat and per protocol analyses were performed.

RESULTS

Of the 80 patients randomized (40 minocycline, 40 doxycycline), 71 were treated for 16 weeks. Sixty-eight patients completed the study. At week 16, the median change in lesion count was comparable in both groups: doxycycline vs. minocycline, respectively 13 vs. 14 fewer lesions. The RosaQoL scores were decreased for both doxycycline and minocycline, respectively by 0·62 and 0·86. Secondary outcomes were comparable except for Investigator's Global Assessment success, which was seen significantly more often in the minocycline group than in the doxycycline group (60% vs. 18%, P < 0·001). At week 28, outcomes were comparable, except for RosaQoL scores and PaGA, which were significantly different in favour of minocycline (P = 0·005 and P = 0·043, respectively), and fewer relapses were recorded in the minocycline group than in the doxycycline group (7% and 48%, respectively; P < 0·001). No serious adverse reactions were reported.

CONCLUSIONS

Minocycline 100 mg is noninferior to doxycycline 40 mg in efficacy over a 16- week treatment period. At follow-up, RosaQoL and PaGA were statistically significantly more improved in the minocycline group than in the doxycycline group, and minocycline 100 mg gives longer remission. In this study there was no significant difference in safety between these treatments; however, based on previous literature minocycline has a lower risk-to-benefit ratio than doxycycline. Minocycline 100 mg may be a good alternative treatment for those patients who, for any reason, are unable or unwilling to take doxycycline 40 mg.

摘要

背景

米诺环素在酒渣鼻治疗中的证据不足。

目的

比较多西环素 40mg 与米诺环素 100mg 治疗丘疹脓疱性酒渣鼻的疗效和安全性。

方法

这是一项随机、单中心、1:1 分配、评估者设盲、非劣效性试验,纳入轻至重度丘疹脓疱性酒渣鼻患者,随机分配至口服多西环素 40mg 或米诺环素 100mg 治疗 16 周,随访 12 周。主要结局为皮损计数的变化和患者健康相关生活质量的变化(使用 RosaQoL 评估)。进行意向治疗和方案分析。

结果

80 例患者随机分组(米诺环素 40 例,多西环素 40 例),71 例完成 16 周治疗。68 例患者完成研究。16 周时,两组皮损计数的变化中位数相当:多西环素组比米诺环素组分别少 13 个和 14 个皮损。多西环素组和米诺环素组的 RosaQoL 评分分别降低了 0.62 和 0.86。除了研究者总体评估成功率外,其他次要结局相当,米诺环素组明显高于多西环素组(60%比 18%,P<0.001)。28 周时,除了米诺环素组的 RosaQoL 评分和 PaGA 显著更优(P=0.005 和 P=0.043)以及米诺环素组的复发率更低(7%比 48%,P<0.001)外,其他结局相当。未报告严重不良反应。

结论

在 16 周治疗期间,米诺环素 100mg 的疗效与多西环素 40mg 相当。随访时,米诺环素组的 RosaQoL 和 PaGA 改善情况显著优于多西环素组,米诺环素组的缓解期更长。在这项研究中,这两种治疗方法的安全性没有显著差异;然而,基于既往文献,米诺环素的风险-效益比低于多西环素。对于那些因任何原因不能或不愿服用多西环素 40mg 的患者,米诺环素 100mg 可能是一种较好的替代治疗方法。

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