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氯己定口腔去污用于预防儿童呼吸机相关性肺炎的随机对照试验。

Oral mucosal decontamination with chlorhexidine for the prevention of ventilator-associated pneumonia in children - a randomized, controlled trial.

机构信息

From the Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

Pediatr Crit Care Med. 2012 Sep;13(5):e305-10. doi: 10.1097/PCC.0b013e31824ea119.

Abstract

OBJECTIVE

To study the efficacy of oral mucosal decontamination with chlorhexidine gel for the prevention of ventilator-associated pneumonia in children between 3 months and 15 yrs.

DESIGN

Double blind randomized placebo controlled trial.

SETTING

Pediatric intensive care unit of a tertiary care hospital in North India.

PATIENTS

Eligible participants were patients aged 3 months to 15 yrs who required orotracheal or nasotracheal intubation and mechanical ventilation. Two hundred eighty-three children admitted to the pediatric intensive care unit between November 2007 and April 2009 were screened. Eighty-six patients fulfilled the study requirements.

INTERVENTION

Either 1% chlorhexidine or placebo gel was applied on the buccal mucosa at 8-hr intervals for the entire duration of ventilation, subject to a maximum of 21 days. Patients were followed up for the development of ventilator-associated pneumonia, diagnosed using the Centers for Disease Control and Prevention criteria.

MAIN OUTCOME MEASURES

Incidence of ventilator-associated pneumonia, duration of hospital stay, duration of intensive care unit stay, mortality, and characteristics of organisms isolated.

RESULTS

Fourty-one children received 1% chlorhexidine, whereas 45 received placebo application. Patients of both groups were comparable with respect to baseline characteristics. Incidence of ventilator-associated pneumonia was 39.6/1,000 ventilator days with 1% chlorhexidine and 38.1/1,000 ventilator days with placebo (relative risk 1.03, confidence interval 0.44-2.42, p = .46). The duration of intensive care unit stay and hospital stay was a mean of 8.4 ± 5.8 vs. 9.6 ± 11.4 days (p = .58) and 16.1 ± 10.2 days vs. 15.1 ± 14.3 days (p = .19) with chlorhexidine and placebo, respectively. The mortality rates were similar in the two groups (p = .81). All but two isolates causing ventilator-associated pneumonia were gram-negative, with Acinetobacter species being the most common (14 of 26). No side effects of the applied gel were seen in either group.

CONCLUSION

Oral mucosal application on 1% chlorhexidine gel did not prevent the development of ventilator-associated pneumonia in children 3 months to 15 yrs age.

摘要

目的

研究口腔黏膜氯己定凝胶消毒对 3 个月至 15 岁儿童呼吸机相关性肺炎的预防效果。

设计

双盲随机安慰剂对照试验。

地点

印度北部一家三级医院的儿科重症监护病房。

患者

纳入标准为需要经口或经鼻插管和机械通气的 3 个月至 15 岁患儿。2007 年 11 月至 2009 年 4 月期间,共筛选了 283 名入住儿科重症监护病房的患儿,其中 86 名患儿符合研究要求。

干预措施

8 小时 1 次给予 1%氯己定凝胶或安慰剂凝胶涂擦口腔黏膜,持续使用至通气时间最长 21 天。观察患儿呼吸机相关性肺炎的发生情况,采用美国疾病预防控制中心的标准诊断。

主要观察指标

呼吸机相关性肺炎的发生率、住院时间、重症监护病房停留时间、病死率以及分离病原体的特征。

结果

41 名患儿使用 1%氯己定凝胶,45 名患儿使用安慰剂凝胶。两组患儿的基线特征无差异。使用 1%氯己定凝胶和安慰剂凝胶时,呼吸机相关性肺炎的发生率分别为 39.6/1000 机械通气日和 38.1/1000 机械通气日(相对危险度 1.03,95%置信区间 0.44~2.42,P =.46)。氯己定凝胶组和安慰剂组患儿的重症监护病房停留时间和住院时间分别为平均 8.4 ± 5.8 天和 9.6 ± 11.4 天(P =.58)和 16.1 ± 10.2 天和 15.1 ± 14.3 天(P =.19)。两组病死率相似(P =.81)。所有导致呼吸机相关性肺炎的病原体除 2 株外均为革兰阴性菌,以不动杆菌属最为常见(26 株中的 14 株)。两组患儿均未出现凝胶应用相关的不良反应。

结论

3 个月至 15 岁儿童口腔黏膜应用 1%氯己定凝胶并不能预防呼吸机相关性肺炎的发生。

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