Friedman N Deborah, Athan Eugene, Walton Aaron L, O'Brien Daniel P
Department of Infectious Diseases, Barwon Health, Geelong, Victoria, Australia
Department of Infectious Diseases, Barwon Health, Geelong, Victoria, Australia.
Antimicrob Agents Chemother. 2016 Apr 22;60(5):2692-5. doi: 10.1128/AAC.02853-15. Print 2016 May.
Buruli ulcer (BU) is a necrotizing infection of subcutaneous tissue that is caused by Mycobacterium ulcerans and is responsible for disfiguring skin lesions. The disease is endemic to specific geographic regions in the state of Victoria in southeastern Australia. Growing evidence of the effectiveness of antibiotic therapy for M. ulcerans disease has evolved our practice to the use of primarily oral medical therapy. An observational cohort study was performed on all confirmed M. ulcerans cases treated with primary rifampin-based medical therapy at Barwon Health between October 2010 and December 2014 and receiving 12 months of follow-up. One hundred thirty-two patients were managed with primary medical therapy. The median age of patients was 49 years, and nearly 10% had diabetes mellitus. Lesions were ulcerative in 83.3% of patients and at WHO stage 1 in 78.8% of patients. The median duration of therapy was 56 days, with 22 patients (16.7%) completing fewer than 56 days of antimicrobial treatment. Antibiotic-associated complications requiring cessation of one or more antibiotics occurred in 21 (15.9%) patients. Limited surgical debridement was performed on 30 of these medically managed patients (22.7%). Cure was achieved, with healing within 12 months, in 131 of 132 patients (99.2%), and cosmetic outcomes were excellent. Primary rifampin-based oral medical therapy for M. ulcerans disease, combined with either clarithromycin or a fluoroquinolone, has an excellent rate of cure and an acceptable toxicity profile in Australian patients. We advocate for further research to determine the optimal and safest minimum duration of medical therapy for BU.
布鲁里溃疡(BU)是由溃疡分枝杆菌引起的皮下组织坏死性感染,可导致皮肤病变毁容。该疾病在澳大利亚东南部维多利亚州的特定地理区域呈地方性流行。越来越多的证据表明抗生素疗法对溃疡分枝杆菌病有效,这促使我们的治疗方法主要转向使用口服药物治疗。对2010年10月至2014年12月期间在巴旺健康中心接受以利福平为主的初始药物治疗并接受12个月随访的所有确诊溃疡分枝杆菌病例进行了一项观察性队列研究。132例患者接受了初始药物治疗。患者的中位年龄为49岁,近10%患有糖尿病。83.3%的患者病变为溃疡性,78.8%的患者处于世界卫生组织1期。治疗的中位持续时间为56天,22例患者(16.7%)完成的抗菌治疗少于56天。21例(15.9%)患者出现需要停用一种或多种抗生素的抗生素相关并发症。其中30例接受药物治疗的患者(22.7%)进行了有限的手术清创。132例患者中有131例(99.2%)在12个月内治愈并愈合,美容效果极佳。在澳大利亚患者中,以利福平为主的口服药物治疗溃疡分枝杆菌病,联合克拉霉素或氟喹诺酮,治愈率高且毒性可接受。我们主张进一步研究以确定布鲁里溃疡最佳和最安全的最短药物治疗持续时间。