Program for Infection Prevention & Healthcare Epidemiology, Duke University Medical Center, Durham, NC 27710, USA.
Future Microbiol. 2012 Jun;7(6):677-83. doi: 10.2217/fmb.12.44.
Clostridium difficile is emerging as one of the most important and devastating pathogens affecting hospitalized populations around the world. The incidence of C. difficile infection is increasing and disease severity is worsening. Thus, an effective alternative to metronidazole and oral vancomycin is urgently needed. Two Phase III trials, OPT-80-003 and OPT-80-004, showed that oral fidaxomicin for 10 days was noninferior compared with treatment with oral vancomycin among adult patients with toxin-positive C. difficile-associated diarrhea (CDAD). Furthermore, fidaxomicin was associated with a lower rate of recurrence of CDAD within 4 weeks of completion of therapy. The safety and tolerability of fidaxomicin was consistent with earlier studies and established that fidaxomicin is an efficacious and well-tolerated treatment option for CDAD. Despite these potential advantages, the cost-effectiveness of this expensive agent remains poorly understood.
艰难梭菌正成为全球住院人群中最重要和最具破坏性的病原体之一。艰难梭菌感染的发病率正在上升,疾病的严重程度也在恶化。因此,迫切需要一种有效的替代甲硝唑和口服万古霉素的药物。两项 III 期试验 OPT-80-003 和 OPT-80-004 表明,口服菲达霉素 10 天与口服万古霉素治疗毒素阳性艰难梭菌相关性腹泻(CDAD)的成人患者相比非劣效。此外,菲达霉素治疗后 4 周内 CDAD 的复发率较低。菲达霉素的安全性和耐受性与早期研究一致,证实菲达霉素是 CDAD 一种有效且耐受性良好的治疗选择。尽管有这些潜在的优势,但这种昂贵药物的成本效益仍知之甚少。