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广谱β-内酰胺单药治疗与联合氨基糖苷类药物治疗严重弥漫性腹膜炎的疗效相当:一项多中心随机对照试验。严重弥漫性腹膜炎研究组

Monotherapy with a broad-spectrum beta-lactam is as effective as its combination with an aminoglycoside in treatment of severe generalized peritonitis: a multicenter randomized controlled trial. The Severe Generalized Peritonitis Study Group.

作者信息

Dupont H, Carbon C, Carlet J

机构信息

Department of Surgical ICU, University Hospital Bichat, Paris, France.

出版信息

Antimicrob Agents Chemother. 2000 Aug;44(8):2028-33. doi: 10.1128/AAC.44.8.2028-2033.2000.

Abstract

In a randomized trial conducted in 35 centers, we compared the clinical efficacy and safety of piperacillin plus tazobactam (TAZ) alone (monotherapy [MT]) versus those of TAZ combined with amikacin (AMK) (combined therapy [CT]) for the treatment of severe generalized peritonitis (SGP). Primary analysis consisted of blind assessment by an independent committee of the failure rate 30 days after the end of treatment in the modified intent-to-treat (ITT) analysis (mITT) population. Of the 241 patients with suspected SGP randomized into the study, 227 were eligible for ITT analysis, including 204 (99 in the MT group and 105 in the CT group) with confirmed SGP (mITT population). A total of 159 patients were eligible for per-protocol (PP) analysis. The clinical failure rates were equivalent in the mITT and PP populations (MT versus CT): 56 versus 52%, (odds ratio [OR] 0.87, 90% confidence interval [CI] = 0. 6 to 1.27) for mITT and 49 versus 49% (OR = 1.03, 90% CI = 0.67 to 1. 59) for PP analysis. Mortality rates (ITT population, 19%; PP population, 21%) and overall adverse event rates (ITT population, 55%; PP population, 54%) were also similar. Six patients (three in MT group and three in the CT group) developed acute renal failure. In conclusion, the addition of AMK to TAZ does not seem to be necessary for the treatment of SGP, even after adjustment for the simplified acute physiology score (SAPS II) and type of SGP.

摘要

在一项由35个中心开展的随机试验中,我们比较了哌拉西林加他唑巴坦(TAZ)单药治疗(单药疗法[MT])与TAZ联合阿米卡星(AMK)(联合疗法[CT])治疗严重弥漫性腹膜炎(SGP)的临床疗效和安全性。主要分析包括由独立委员会在改良意向性治疗(ITT)分析(mITT)人群中对治疗结束后30天的失败率进行盲法评估。在随机纳入该研究的241例疑似SGP患者中,227例符合ITT分析条件,其中204例(MT组99例,CT组105例)确诊为SGP(mITT人群)。共有159例患者符合符合方案(PP)分析条件。mITT和PP人群中的临床失败率相当(MT组与CT组):mITT分析中分别为56%和52%(优势比[OR]0.87,90%置信区间[CI]=0.6至1.27),PP分析中分别为49%和49%(OR=1.03,90%CI=0.67至1.59)。死亡率(ITT人群为19%;PP人群为21%)和总体不良事件发生率(ITT人群为55%;PP人群为54%)也相似。6例患者(MT组3例,CT组3例)发生急性肾衰竭。总之,即使在对简化急性生理学评分(SAPS II)和SGP类型进行校正后,TAZ联合AMK治疗SGP似乎也无必要。

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