Pépin Jacques, Valiquette Louis, Gagnon Sandra, Routhier Sophie, Brazeau Isabel
Department of Microbiology and Infectious Diseases, University of Sherbrooke, Sherbrooke, Quebec, Canada.
Am J Gastroenterol. 2007 Dec;102(12):2781-8. doi: 10.1111/j.1572-0241.2007.01539.x. Epub 2007 Sep 26.
To reassess the comparative efficacy of vancomycin versus metronidazole in the treatment of Clostridium difficile-associated disease (CDAD) after the emergence in 2003 of the hypervirulent NAP1/027 strain.
A retrospective cohort study was conducted in a tertiary-care Canadian hospital among 1,616 patients treated initially with metronidazole (N=1,360), vancomycin (N=219), or both (N=37), between 1991 and 2006, and followed for 60 days after diagnosis. Primary outcome was severe/complicated CDAD (SC-CDAD) defined as any of: (a) death within 30 days, (b) septic shock, (c) megacolon, (d) perforation, or (e) emergency colectomy. Adjusted odds ratios (AOR) and their 95% confidence intervals (CI) were calculated, stratifying into pre-epidemic (1991-2002) and epidemic (2003-2006) periods. Secondary outcome was recurrence within 60 days.
Risk factors for SC-CDAD were the same in both periods: age>or=65 yr, male sex, immunosuppression, hospital acquisition, tube feeding, short duration of diarrhea, fever, elevated leukocytosis, or creatinine. Adjusting for confounders and using metronidazole therapy as baseline, vancomycin therapy was associated with a lower probability of developing SC-CDAD in 1991-2002 (AOR 0.21, 95% CI 0.05-0.99, P=0.048) but not during 2003-2006 (AOR 0.90, 95% CI 0.53-1.55, P=0.71). For both metronidazole and vancomycin, risk of recurrence increased in 2003-2004 but decreased in 2005-2006.
Loss of superiority of vancomycin over metronidazole coincided with the emergence of NAP1/027. Toxin hyperproduction by NAP1/027 might be such that the disease follows its natural course. Novel therapeutic approaches are needed. The higher risk of recurrence in 2003-2004 probably reflected reinfections rather than relapses.
在2003年高毒力NAP1/027菌株出现后,重新评估万古霉素与甲硝唑治疗艰难梭菌相关性疾病(CDAD)的相对疗效。
在加拿大一家三级医疗医院进行了一项回顾性队列研究,研究对象为1991年至2006年间最初接受甲硝唑治疗(N = 1360)、万古霉素治疗(N = 219)或两者联合治疗(N = 37)的1616例患者,并在诊断后随访60天。主要结局为严重/复杂性CDAD(SC - CDAD),定义为以下任何一种情况:(a)30天内死亡,(b)感染性休克,(c)巨结肠,(d)穿孔,或(e)急诊结肠切除术。计算调整后的比值比(AOR)及其95%置信区间(CI),并分为流行前时期(早发性,1991 - 2002年)和流行时期(晚发性,2003 - 2006年)。次要结局为60天内复发。
两个时期SC - CDAD的危险因素相同:年龄≥65岁、男性、免疫抑制、医院获得性感染、管饲、腹泻持续时间短、发热、白细胞增多或肌酐升高。在调整混杂因素并以甲硝唑治疗作为基线后,1991 - 2002年万古霉素治疗与发生SC - CDAD的概率较低相关(AOR 0.21,95% CI 0.05 - 0.99,P = 0.048),但在2003 - 2006年期间并非如此(AOR 0.90,95% CI 0.53 - 1.55,P = 0.71)。对于甲硝唑和万古霉素,复发风险在2003 - 2004年增加,但在2005 - 2006年降低。
万古霉素相对于甲硝唑的优势丧失与NAP1/027的出现同时发生。NAP1/027产生的毒素过多可能导致疾病遵循其自然病程发展。需要新的治疗方法。2003 - 2004年较高复发风险可能反映再感染而非复发。