Division of Infectious Diseases, Jewish General Hospital, Montreal, Quebec, H3T 1E2 Canada.
Expert Opin Pharmacother. 2010 Jun;11(9):1569-78. doi: 10.1517/14656566.2010.485614.
Clostridium difficile infection (CDI) has become an increasingly important healthcare-associated complication in many countries. CDI outbreaks, a new 'hypervirulent' form and increased worldwide rates have underscored four urgent unmet needs for this disease: i) effective prevention of CDI; ii) therapies to produce faster resolution of CDI symptoms; iii) therapies to treat severe CDI more effectively and reduce its mortality; and iv) therapies to reduce the CDI recurrence rate following treatment.
Fidaxomicin, a new macrocyclic antibiotic, has demonstrated potent in vitro activity against C. difficile with limited or no activity against normal fecal flora. It is minimally absorbed from the intestinal tract, even in the presence of intestinal inflammation. When tested against oral vancomycin in clinical studies of CDI therapy, it has equivalent efficacy for curing CDI at end of treatment and a comparable safety profile to that agent. However, fidaxomicin therapy of CDI is associated with significantly fewer CDI recurrences in the 28 days following treatment. Symptom resolution is also slightly quicker in some CDI patients. Additional fecal flora analysis in the CDI trials showed that fewer individuals developed intestinal colonization with vancomycin-resistant enterococci (VRE) among the fidaxomicin-treated group. This new molecule, which has just completed two large Phase III multicenter studies, successfully addresses two of the four urgent and unmet needs for dealing with CDI.
Fidaxomicin is as effective and as safe as vancomycin therapy for treating CDI but is associated with far fewer recurrences post-treatment and a decreased risk of VRE acquisition.
Fidaxomicin is a potential new therapy for CDI which has the capacity to substantially decrease post-treatment recurrences and is as safe and well-tolerated as standard vancomycin treatment.
艰难梭菌感染(CDI)已成为许多国家日益重要的医疗保健相关并发症。CDI 爆发、一种新的“超毒力”形式以及全球范围内发病率的增加,突显了该疾病未满足的四个迫切需求:i)有效预防 CDI;ii)更快缓解 CDI 症状的治疗方法;iii)更有效地治疗严重 CDI 并降低其死亡率的治疗方法;iv)减少治疗后 CDI 复发率的治疗方法。
非达霉素,一种新型大环内酯类抗生素,对艰难梭菌具有强大的体外活性,对正常肠道菌群的活性有限或没有。即使在肠道炎症存在的情况下,它也很少从肠道吸收。在 CDI 治疗的临床研究中,与口服万古霉素相比,它在治疗结束时治疗 CDI 的疗效相当,与该药物的安全性相似。然而,非达霉素治疗 CDI 与治疗后 28 天内 CDI 复发率显著降低相关。在一些 CDI 患者中,症状缓解也稍快。在 CDI 试验中的额外粪便菌群分析显示,在非达霉素治疗组中,较少的个体出现万古霉素耐药肠球菌(VRE)肠道定植。这个新分子刚刚完成了两项大型 III 期多中心研究,成功解决了应对 CDI 的四个紧急和未满足需求中的两个。
非达霉素治疗 CDI 与万古霉素治疗一样有效且安全,但与治疗后复发率低得多且 VRE 获得风险降低相关。
非达霉素是一种治疗 CDI 的潜在新疗法,它有可能显著降低治疗后的复发率,并且与标准万古霉素治疗一样安全且耐受良好。