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多中心、阶梯式、整群随机对照试验的方案:停用口服氯己定预防和实施机械通气危重症患者口腔护理包:CHORAL 研究。

Protocol for a multi-centered, stepped wedge, cluster randomized controlled trial of the de-adoption of oral chlorhexidine prophylaxis and implementation of an oral care bundle for mechanically ventilated critically ill patients: the CHORAL study.

机构信息

Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, Canada.

Trauma, Emergency and Critical Care, Sunnybrook Health Sciences Centre, Toronto, Canada.

出版信息

Trials. 2019 Oct 24;20(1):603. doi: 10.1186/s13063-019-3673-0.

Abstract

BACKGROUND

Routine application of chlorhexidine oral rinse is recommended to reduce risk of ventilator-associated pneumonia (VAP) in mechanically ventilated patients. Recent reappraisal of the evidence from two meta-analyses suggests chlorhexidine may cause excess mortality in non-cardiac surgery patients and does not reduce VAP. Mechanisms for possible excess mortality are unclear. The CHORAL study will evaluate the impact of de-adopting chlorhexidine and implementing an oral care bundle (excluding chlorhexidine) on mortality, infection-related ventilator-associated complications (IVACs), and oral health status.

METHODS

The CHORAL study is a stepped wedge, cluster randomized controlled trial in six academic intensive care units (ICUs) in Toronto, Canada. Clusters (ICU) will be randomly allocated to six sequential steps over a 14-month period to de-adopt oral chlorhexidine and implement a standardized oral care bundle (oral assessment, tooth brushing, moisturization, and secretion removal). On study commencement, all clusters begin with a control period in which the standard of care is oral chlorhexidine. Clusters then begin crossover from control to intervention every 2 months according to the randomization schedule. Participants include all mechanically ventilated adults eligible to receive the standardized oral care bundle. The primary outcome is ICU mortality; secondary outcomes are IVACs and oral health status. We will determine demographics, antibiotic usage, mortality, and IVAC rates from a validated local ICU clinical registry. With six clusters and 50 ventilated patients on average each month per cluster, we estimate that 4200 patients provide 80% power after accounting for intracluster correlation to detect an absolute reduction in mortality of 5.5%. We will analyze our primary outcome of mortality using a generalized linear mixed model adjusting for time to account for secular trends. We will conduct a process evaluation to determine intervention fidelity and to inform interpretation of the trial results.

DISCUSSION

The CHORAL study will inform understanding of the effectiveness of de-adoption of oral chlorhexidine and implementation of a standardized oral care bundle for decreasing ICU mortality and IVAC rates while improving oral health status. Our process evaluation will inform clinicians and decision makers about intervention delivery to support future de-adoption if justified by trial results.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT03382730 . Registered on December 26, 2017.

摘要

背景

常规应用洗必泰口腔冲洗液可降低机械通气患者呼吸机相关性肺炎(VAP)的风险。最近对两项荟萃分析的重新评估表明,洗必泰可能导致非心脏手术患者的死亡率增加,并且不能降低 VAP。可能导致死亡率增加的机制尚不清楚。CHORAL 研究将评估停用洗必泰和实施不包括洗必泰的口腔护理包(excluding chlorhexidine)对死亡率、与感染相关的呼吸机相关性并发症(IVACs)和口腔健康状况的影响。

方法

CHORAL 研究是一项在加拿大多伦多的六家学术性重症监护病房(ICUs)进行的阶梯式楔形、集群随机对照试验。集群(ICU)将在 14 个月的时间内被随机分配到六个连续的步骤中,以停用口腔洗必泰和实施标准化的口腔护理包(口腔评估、刷牙、保湿和分泌物清除)。在研究开始时,所有集群都开始了一个对照期,在这个对照期内,标准护理是口腔洗必泰。根据随机分组方案,每两个月集群将开始从对照期向干预期交叉。参与者包括所有有资格接受标准化口腔护理包的机械通气成人。主要结局是 ICU 死亡率;次要结局是 IVACs 和口腔健康状况。我们将从一个经过验证的当地 ICU 临床登记处确定人口统计学数据、抗生素使用、死亡率和 IVAC 率。在每个集群平均每月有 50 名通气患者的情况下,我们估计在考虑到组内相关性以检测死亡率绝对降低 5.5%的情况下,4200 名患者将提供 80%的效力。我们将使用广义线性混合模型分析死亡率这一主要结局,该模型调整时间以考虑到时间趋势。我们将进行一个过程评估,以确定干预的一致性,并为解释试验结果提供信息。

讨论

CHORAL 研究将为理解停用口腔洗必泰和实施标准化口腔护理包以降低 ICU 死亡率和 IVAC 率、同时改善口腔健康状况的有效性提供信息。我们的过程评估将为临床医生和决策者提供关于干预措施实施的信息,以支持未来的停用,如果试验结果证明是合理的。

试验注册

ClinicalTrials.gov,NCT03382730。于 2017 年 12 月 26 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cedd/6814100/04945bb95c91/13063_2019_3673_Fig1_HTML.jpg

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