University of Chicago Medical Center, Chicago, IL 60637, USA.
Gastroenterol Res Pract. 2011;2011:106978. doi: 10.1155/2011/106978. Epub 2011 Nov 9.
Objectives. This open-label trial assessed the efficacy and safety of rifaximin as first-line therapy in hospitalized patients with Clostridium difficile-associated diarrhea (CDAD). Methods. We enrolled thirteen patients who had a confirmed diagnosis of CDAD characterized by ≥3 unformed stools/day and positive C. difficile toxin assay. Those patients received rifaximin 400 mg three times daily for 10 days. Resolution of symptoms, repeat assay 10 days after treatment, and followup for recurrence were assessed. Results. Eight patients completed the study, and all reported symptom resolution during treatment. Mean time to last unformed stool was 132 h ± 42.5 h. Seven patients had no relapse by week 2 and in longer followup (median 162 days). One patient had recurrent CDAD during a repeat hospitalization. Conclusions. Rifaximin was effective and safe as first-line treatment for CDAD and did not result in recurrence in most patients.
本开放性试验评估了利福昔明作为住院伴有艰难梭菌相关性腹泻(CDAD)患者一线治疗的疗效和安全性。
我们纳入了 13 名确诊 CDAD 的患者,其特征为每天排 ≥3 次不成形便,且 C. difficile 毒素检测阳性。这些患者接受利福昔明 400mg,每日 3 次,治疗 10 天。评估症状缓解、治疗后 10 天重复检测和随访复发情况。
8 名患者完成了研究,所有患者均报告在治疗期间症状缓解。最后一次排不成形便的平均时间为 132±42.5 小时。7 名患者在第 2 周及更长时间的随访(中位时间 162 天)内无复发。1 名患者在再次住院期间复发 CDAD。
利福昔明作为 CDAD 的一线治疗是有效且安全的,大多数患者未复发。