Grolman David Charles
Sandton and Fourways Hospitals, Chris Hani Baragwanath Academic Hospital, Department of Intensive Care, Johannesburg, South Africa.
Int J Infect Dis. 2007 May;11 Suppl 1:S7-15. doi: 10.1016/S1201-9712(07)60002-2.
Complicated skin and skin structure infections encompass a diverse range of diseases frequently caused by Gram-positive pathogens, and most commonly by Staphylococcus aureus and Streptococcus pyogenes. Treatment of these infections represents a growing clinical challenge as increases in multi-drug-resistant organisms and cross-resistance to antimicrobial therapy have made empiric therapeutic choices more difficult, particularly for patients with known risk factors or who are immunocompromised. Complicating this issue has been the relative lack of new agents with antimicrobial potency against prevalent resistant species such as meticillin resistant S. aureus (MRSA). Tigecycline, a novel glycylcycline, is a broad-spectrum antibiotic with potent microbiological activity against the wide variety of organisms implicated in the aetiology of complicated skin and skin structure infections. Recent phase III clinical data confirm previous observations on the safety and efficacy of tigecycline for the treatment of complicated skin and skin structure infections. Tigecycline was shown to be non-inferior to combination vancomycin-aztreonam regimens and exhibited high clinical success rates. MIC(90) values for tigecycline were uniformly low for both susceptible and resistant pathogens. Adverse events were similar in incidence for both patient populations, with nausea and vomiting reported more frequently with tigecycline treated patients while rash and elevated liver transaminases were most commonly observed in the vancomycin-aztreonam treatment group. Tigecycline helps to address the urgent need for new antimicrobial agents to combat the emergence of multi-drug-resistant Gram-positive pathogens. Current clinical, microbiological and safety data support the use of tigecycline as a valuable therapeutic option in the treatment of complicated skin and skin structure infections.
复杂皮肤及皮肤结构感染涵盖多种常由革兰氏阳性病原体引起的疾病,最常见的是金黄色葡萄球菌和化脓性链球菌。随着多重耐药菌的增加以及对抗菌治疗的交叉耐药性,这些感染的治疗面临着日益严峻的临床挑战,这使得经验性治疗选择更加困难,尤其是对于有已知风险因素或免疫功能低下的患者。使问题更加复杂的是,相对缺乏对常见耐药菌如耐甲氧西林金黄色葡萄球菌(MRSA)具有抗菌效力的新型药物。替加环素是一种新型甘氨酰环素,是一种广谱抗生素,对复杂皮肤及皮肤结构感染病因中涉及的多种微生物具有强大的微生物活性。最近的III期临床数据证实了之前关于替加环素治疗复杂皮肤及皮肤结构感染的安全性和有效性的观察结果。结果显示,替加环素不劣于万古霉素-氨曲南联合治疗方案,且临床成功率较高。替加环素对敏感和耐药病原体的MIC(90)值均普遍较低。两组患者的不良事件发生率相似,替加环素治疗的患者恶心和呕吐的报告更为频繁,而皮疹和肝转氨酶升高在万古霉素-氨曲南治疗组中最为常见。替加环素有助于满足对抗多重耐药革兰氏阳性病原体出现的新型抗菌药物的迫切需求。目前的临床、微生物学和安全性数据支持将替加环素作为治疗复杂皮肤及皮肤结构感染的一种有价值的治疗选择。