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首页> 外文期刊>Liver transplantation: official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society >Systematic Review on Preventing Bacterial Sepsis and Wound Complications in Liver Transplant Patients Methods of preventing bacterial sepsis and wound complications for liver transplantation.
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Systematic Review on Preventing Bacterial Sepsis and Wound Complications in Liver Transplant Patients Methods of preventing bacterial sepsis and wound complications for liver transplantation.

机译:预防肝移植患者细菌性败血症和伤口并发症的系统评价预防肝移植的细菌性败血症和伤口并发症的方法。

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Background: Bacterial sepsis and wound complications after liver transplantation increase mortality, morbidity, hospital stay, and overall transplant costs. Objectives: To assess the benefits and harms of different methods aimed at preventing bacterial sepsis and wound complications In patients undergoing liver transplantation. Search Strategy: We searched The Cochrane Hepato-Biliary Group Controlled Trials Register, the Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library, MEDLINE, EMBASE, and Science Citation Index Expanded until June 2007. Selection Criteria: We included only randomised clinical trials irrespective of language or publication status. Data Collection and Analysis: We collected the data on infections, adverse effects of intervention, ITU (intensive therapy unit) stay, and hospital stay. We analysed the data with both the fixed-effect and the random-effects models using RevMan Analysis and risk ratio (RR) or weighted mean difference (WMD) with 95% confidence intervals (CI) based on intention-to-treat analysis. Main Results: We identified seven trials for inclusion including 614 patients. Four trials compared selective bowel decontamination versus placebo or no treatment. In one trial, patients were randomised to selective bowel decontamination, active lactobacillus with fibres (probiotic with prebiotic), or to inactivated lactobacillus with fibres (preblotic). In another trial, different doses of granulocyte-colony stimulating factor and placebo were compared. The remaining two trials compared lactobacillus with fibres versus fibres alone and early enteral feeding versus no intervention. Only one trial was of low bias-risk. There was no statistically significant difference in any outcome between the selective bowel decontamination and the control groups. Selective bowel decontamination increased incidence of cholangitis (RR 4.84, 95% CI 1.15 to 20.35), incidence of bacterial infection (RR 3.63, 95% CI 1.36 to 9.74), and hospital stay (WMD 4.00, 95% CI 3.14 to 4.86) than the participants in the combined pre- and probiotic group. Hospital stay was prolonged in the selective bowel decontamination group compared to the prebiotic group. There was a statistically significant lower occurrence of urinary infection in the pre- and probiotic group than in the prebiotic group. The number of people experiencing gram negative bacterial infection was not significantly lower in the probiotic group (RR 0.18, 95% CI 0.03 to 1.17). The ITU stay was lower in the probiotic group (WMD -1.41 days, 95% CI -2.09 to -0.73). There were no differences in any outcomes in the other comparisons.
机译:背景:肝移植后细菌性败血症和伤口并发症会增加死亡率,发病率,住院时间和总体移植费用。目的:评估旨在预防细菌性败血症和伤口并发症的不同方法对肝移植患者的利弊。搜索策略:我们在Cochrane图书馆,MEDLINE,EMBASE和《科学引文索引》中搜索了Cochrane肝胆胆道疾病组对照试验注册资料库,Cochrane对照试验中央注册资料库(CENTRAL),直到2007年6月为止。选择标准:我们仅包括随机临床试验,无论语言或出版状态如何。数据收集和分析:我们收集了有关感染,干预措施的不良反应,ITU(重症监护病房)住院时间和住院时间的数据。我们使用RevMan分析和风险比(RR)或具有95%置信区间(CI)的加权均数差(WMD),基于意向性治疗分析,使用固定效应和随机效应模型对数据进行了分析。主要结果:我们确定了包括614例患者在内的7项纳入试验。四个试验比较了选择性肠道去污与安慰剂或不治疗的比较。在一项试验中,患者被随机分为选择性肠净化,纤维活性乳杆菌(益生元和益生元)或纤维失活乳酸菌(前血)。在另一项试验中,比较了不同剂量的粒细胞集落刺激因子和安慰剂。其余两项试验比较了乳酸菌与纤维与单独的纤维以及早期肠内喂养与无干预的比较。只有一项试验的偏倚风险低。选择性肠净化与对照组之间的任何结果之间均无统计学意义的差异。选择性肠净化增加了胆管炎的发生率(RR 4.84,95%CI 1.15至20.35),细菌感染的发生率(RR 3.63,95%CI 1.36至9.74)和住院时间(WMD 4.00,95%CI 3.14至4.86)益生菌和益生菌联合治疗组的参与者。与益生元组相比,选择性肠净化组的住院时间延长了。益生菌和益生菌组的尿道感染发生率在统计学上显着低于益生菌组。益生菌组发生革兰氏阴性细菌感染的人数没有显着降低(RR 0.18,95%CI 0.03至1.17)。益生菌组的ITU停留时间较低(WMD -1.41天,95%CI -2.09至-0.73)。在其他比较中,任何结果均无差异。

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