University of Houston College of Pharmacy, Houston, TX 77030, USA.
J Antimicrob Chemother. 2011 Dec;66(12):2850-5. doi: 10.1093/jac/dkr377. Epub 2011 Sep 21.
Uncontrolled case series have demonstrated decreased Clostridium difficile infection (CDI) recurrence in patients given rifaximin after standard antibiotic therapy. However, clinical trials assessing whether rifaximin decreases recurrent diarrhoea in patients with CDI have not been performed. The purpose of this study was to assess rates of recurrent diarrhoea in patients with CDI given rifaximin versus placebo immediately after standard therapy.
This was a randomized, double-blind, placebo-controlled pilot study. Patients with CDI and a Horn's index ≥1 were randomized to receive rifaximin 400 mg three times daily or placebo for 20 days given immediately after finishing standard anti-CDI antibiotics. Patients were followed for 3 months and assessed for recurrent diarrhoea that included CDI recurrence (return of diarrhoea with a positive toxin test) and patient self-reported return of non-CDI diarrhoea after a period of wellness.
Sixty-eight patients aged 61 ± 18 years (50% male) were given rifaximin (n = 33) or placebo (n = 35). Twenty-four of 68 (35%) patients had recurrent diarrhoea either due to recurrent CDI (23.5%) or self-reported diarrhoea (11.5%). Recurrent diarrhoea occurred in 17 of 35 (49%) patients given placebo and 7 of 33 (21%) given rifaximin (P = 0.018). CDI recurrence occurred in 11 of 35 (31%) patients given placebo and 5 of 33 (15%) patients given rifaximin (P = 0.11). Self-reported diarrhoea occurred in 6 of 35 (17%) of patients given placebo and 2 of 33 (6%) given rifaximin (P = 0.15).
Patients with CDI given a rifaximin chaser regimen experienced a decreased incidence of recurrent diarrhoea compared with placebo.
非对照病例系列研究表明,在接受标准抗生素治疗后给予利福昔明的患者中,艰难梭菌感染(CDI)的复发率降低。然而,尚未进行评估利福昔明是否降低 CDI 患者复发性腹泻的临床试验。本研究的目的是评估在接受标准治疗后立即给予利福昔明与安慰剂的 CDI 患者中复发性腹泻的发生率。
这是一项随机、双盲、安慰剂对照的初步研究。CDI 患者 Horn 指数≥1 ,随机分为接受利福昔明 400mg 每日 3 次或安慰剂治疗 20 天,在完成标准抗 CDI 抗生素治疗后立即给予。患者随访 3 个月,并评估复发性腹泻,包括 CDI 复发(腹泻恢复且毒素检测阳性)和患者在一段时间的健康期后自我报告的非 CDI 腹泻恢复。
68 名年龄 61±18 岁(50%为男性)的患者接受了利福昔明(n=33)或安慰剂(n=35)治疗。68 例患者中有 24 例(35%)出现复发性腹泻,原因是 CDI 复发(23.5%)或自我报告腹泻(11.5%)。在给予安慰剂的 35 例患者中有 17 例(49%)发生复发性腹泻,给予利福昔明的 33 例患者中有 7 例(21%)发生复发性腹泻(P=0.018)。在给予安慰剂的 35 例患者中有 11 例(31%)发生 CDI 复发,给予利福昔明的 33 例患者中有 5 例(15%)发生 CDI 复发(P=0.11)。在给予安慰剂的 35 例患者中有 6 例(17%)报告出现腹泻,给予利福昔明的 33 例患者中有 2 例(6%)报告出现腹泻(P=0.15)。
与安慰剂相比,接受利福昔明追赶治疗的 CDI 患者腹泻复发发生率降低。