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合生元疗法对重症患者呼吸机相关性肺炎发病率的影响:一项随机、双盲、安慰剂对照试验。

Effect of synbiotic therapy on the incidence of ventilator associated pneumonia in critically ill patients: a randomised, double-blind, placebo-controlled trial.

作者信息

Knight David J W, Gardiner Dale, Banks Amanda, Snape Susan E, Weston Vivienne C, Bengmark Stig, Girling Keith J

机构信息

Department of Intensive Care, Christchurch Hospital, Christchurch, New Zealand.

出版信息

Intensive Care Med. 2009 May;35(5):854-61. doi: 10.1007/s00134-008-1368-1. Epub 2008 Dec 16.

DOI:10.1007/s00134-008-1368-1
PMID:19083199
Abstract

OBJECTIVE

To investigate the effect of enteral Synbiotic 2000 FORTE (a mixture of lactic acid bacteria and fibre) on the incidence of ventilator associated pneumonia (VAP) in critically ill patients.

DESIGN

Prospective, randomised, double blind, placebo controlled trial.

SETTING

Tertiary referral centre, general Adult Intensive Care Unit (ICU).

PATIENTS AND PARTICIPANTS

259 enterally fed patients requiring mechanical ventilation for 48 h or more were enrolled.

INTERVENTION

All patients were enterally fed as per a standard protocol and randomly assigned to receive either synbiotic 2000 FORTE (twice a day) or a cellulose-based placebo for a maximum of 28 days.

MEASUREMENTS AND RESULTS

Treatment group (n = 130) was well matched with placebo group (n = 129) for age (mean 49.5 and 50 years, respectively) and APACHE II score (median 17 for both). Oropharyngeal microbial flora and colonisation rates were unaffected by synbiotics. The overall incidence of VAP was lower than anticipated (11.2%) and no statistical difference was demonstrated between groups receiving synbiotic and placebo in the incidence of VAP (9 and 13%, P = 0.42), VAP rate per 1,000 ventilator days (13 and 14.6, P = 0.91) or hospital mortality (27 and 33%, P = 0.39), respectively.

CONCLUSIONS

Enteral administration of Synbiotic 2000 FORTE has no statistically significant impact on the incidence of VAP in critically ill patients.

摘要

目的

研究肠内合生元2000 FORTE(一种乳酸菌与纤维的混合物)对重症患者呼吸机相关性肺炎(VAP)发病率的影响。

设计

前瞻性、随机、双盲、安慰剂对照试验。

地点

三级转诊中心,综合性成人重症监护病房(ICU)。

患者和参与者

纳入259例需要机械通气48小时及以上的肠内喂养患者。

干预措施

所有患者均按照标准方案进行肠内喂养,并随机分配接受合生元2000 FORTE(每日两次)或纤维素基安慰剂,最长持续28天。

测量和结果

治疗组(n = 130)与安慰剂组(n = 129)在年龄(分别为49.5岁和50岁)和急性生理与慢性健康状况评分系统II(APACHE II)评分(两者中位数均为17)方面匹配良好。合生元对口咽微生物菌群和定植率无影响。VAP的总体发病率低于预期(11.2%),接受合生元和安慰剂的组在VAP发病率(9%和13%,P = 0.42)、每1000个呼吸机日的VAP发生率(13和14.6,P = 0.91)或医院死亡率(27%和33%,P = 0.39)方面均无统计学差异。

结论

肠内给予合生元2000 FORTE对重症患者VAP的发病率无统计学上的显著影响。

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