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静脉注射甲硝唑联合口服万古霉素可改善艰难梭菌感染的危重症患者的死亡率。

The Addition of Intravenous Metronidazole to Oral Vancomycin is Associated With Improved Mortality in Critically Ill Patients With Clostridium difficile Infection.

机构信息

Department of Pharmacy, Wake Forest Baptist Medical Center.

Wake Forest University School of Medicine, Winston-Salem, North Carolina.

出版信息

Clin Infect Dis. 2015 Sep 15;61(6):934-41. doi: 10.1093/cid/civ409. Epub 2015 May 29.

Abstract

BACKGROUND

The optimal therapy for critically ill patients with Clostridium difficile infection (CDI) is not known. We aimed to evaluate mortality among critically ill patients with CDI who received oral vancomycin (monotherapy) vs oral vancomycin with intravenous (IV) metronidazole (combination therapy).

METHODS

A single-center, retrospective, observational, comparative study was performed. Patients with a positive C. difficile assay who received oral vancomycin while bedded in an intensive care unit (ICU) between June 2007 and September 2012 were evaluated. Patients meeting ≥3 of the following criteria were included: albumin <2.5 g/dL, heart rate >90 bpm, mean arterial pressure <60 mmHg, white blood cell count ≥15 000 cells/mL, age >60 years, serum creatinine ≥1.5 times baseline, or temperature ≥100.4°F. Patients in the combination therapy group received IV metronidazole within 48 hours after initiating vancomycin. Patients <18 years or with unrelated gastrointestinal disease were excluded. The primary outcome was in-hospital mortality. Patients were matched using Acute Physiology and Chronic Health Evaluation II scores.

RESULTS

Eighty-eight patients were included, 44 in each group. Patient characteristics were similar although more patients in the combination group had renal disease. Mortality was 36.4% and 15.9% in the monotherapy and combination therapy groups, respectively (P = .03). Secondary outcomes of clinical success, length of stay, and length of ICU stay did not differ between groups.

CONCLUSIONS

Our data are supportive of the use of combination therapy with oral vancomycin and IV metronidazole in critically ill patients with CDI. However, prospective, randomized studies are required to define optimal treatment regimens in this limited population of CDI patients.

摘要

背景

目前尚不清楚危重症艰难梭菌感染(CDI)患者的最佳治疗方法。我们旨在评估接受口服万古霉素(单药治疗)与口服万古霉素联合静脉(IV)甲硝唑(联合治疗)的危重症 CDI 患者的死亡率。

方法

进行了一项单中心、回顾性、观察性、比较研究。评估了 2007 年 6 月至 2012 年 9 月期间入住重症监护病房(ICU)时接受口服万古霉素治疗且艰难梭菌检测呈阳性的患者。符合以下≥3 项标准的患者包括:白蛋白<2.5 g/dL、心率>90 bpm、平均动脉压<60 mmHg、白细胞计数≥15 000 个细胞/mL、年龄>60 岁、血清肌酐≥基础值的 1.5 倍或体温≥100.4°F。在开始使用万古霉素后 48 小时内,联合治疗组患者接受 IV 甲硝唑治疗。排除年龄<18 岁或患有无关胃肠道疾病的患者。主要结局为院内死亡率。使用急性生理学和慢性健康评估 II 评分对患者进行匹配。

结果

共纳入 88 例患者,每组 44 例。虽然联合组中更多的患者患有肾脏疾病,但患者特征相似。单药治疗组和联合治疗组的死亡率分别为 36.4%和 15.9%(P=.03)。两组之间的临床成功率、住院时间和 ICU 住院时间等次要结局无差异。

结论

我们的数据支持在危重症 CDI 患者中使用口服万古霉素联合 IV 甲硝唑的联合治疗。然而,需要前瞻性、随机研究来确定该有限 CDI 患者人群的最佳治疗方案。

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