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多中心评估一种机械通气并发症监测新方案。

Multicenter evaluation of a novel surveillance paradigm for complications of mechanical ventilation.

机构信息

Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2011 Mar 22;6(3):e18062. doi: 10.1371/journal.pone.0018062.

Abstract

BACKGROUND

Ventilator-associated pneumonia (VAP) surveillance is time consuming, subjective, inaccurate, and inconsistently predicts outcomes. Shifting surveillance from pneumonia in particular to complications in general might circumvent the VAP definition's subjectivity and inaccuracy, facilitate electronic assessment, make interfacility comparisons more meaningful, and encourage broader prevention strategies. We therefore evaluated a novel surveillance paradigm for ventilator-associated complications (VAC) defined by sustained increases in patients' ventilator settings after a period of stable or decreasing support.

METHODS

We assessed 600 mechanically ventilated medical and surgical patients from three hospitals. Each hospital contributed 100 randomly selected patients ventilated 2-7 days and 100 patients ventilated >7 days. All patients were independently assessed for VAP and for VAC. We compared incidence-density, duration of mechanical ventilation, intensive care and hospital lengths of stay, hospital mortality, and time required for surveillance for VAP and for VAC. A subset of patients with VAP and VAC were independently reviewed by a physician to determine possible etiology.

RESULTS

Of 597 evaluable patients, 9.3% had VAP (8.8 per 1,000 ventilator days) and 23% had VAC (21.2 per 1,000 ventilator days). Compared to matched controls, both VAP and VAC prolonged days to extubation (5.8, 95% CI 4.2-8.0 and 6.0, 95% CI 5.1-7.1 respectively), days to intensive care discharge (5.7, 95% CI 4.2-7.7 and 5.0, 95% CI 4.1-5.9), and days to hospital discharge (4.7, 95% CI 2.6-7.5 and 3.0, 95% CI 2.1-4.0). VAC was associated with increased mortality (OR 2.0, 95% CI 1.3-3.2) but VAP was not (OR 1.1, 95% CI 0.5-2.4). VAC assessment was faster (mean 1.8 versus 39 minutes per patient). Both VAP and VAC events were predominantly attributable to pneumonia, pulmonary edema, ARDS, and atelectasis.

CONCLUSIONS

Screening ventilator settings for VAC captures a similar set of complications to traditional VAP surveillance but is faster, more objective, and a superior predictor of outcomes.

摘要

背景

呼吸机相关性肺炎(VAP)监测既耗时,又具有主观性,不够准确,且无法始终如一地预测结果。将监测重点从肺炎转移到一般并发症上,可能会规避 VAP 定义的主观性和不准确性,便于电子评估,使院内间比较更有意义,并鼓励更广泛的预防策略。因此,我们评估了一种新的呼吸机相关性并发症(VAC)监测模式,该模式定义为在一段时间的稳定或降低支持后,患者呼吸机设置持续升高。

方法

我们评估了来自 3 家医院的 600 例机械通气的内科和外科患者。每家医院各贡献了 100 例随机选择的机械通气 2-7 天的患者和 100 例机械通气>7 天的患者。所有患者均独立评估 VAP 和 VAC。我们比较了 VAP 和 VAC 的发生率密度、机械通气时间、重症监护和住院时间、住院死亡率以及 VAP 和 VAC 监测所需的时间。将 VAP 和 VAC 的部分患者随机分配给医生进行独立评估,以确定可能的病因。

结果

在 597 例可评估患者中,9.3%患有 VAP(每 1000 个机械通气日 8.8 例),23%患有 VAC(每 1000 个机械通气日 21.2 例)。与匹配的对照组相比,VAP 和 VAC 均延长了拔管时间(5.8,95%CI 4.2-8.0 和 6.0,95%CI 5.1-7.1)、入住重症监护病房的时间(5.7,95%CI 4.2-7.7 和 5.0,95%CI 4.1-5.9)和出院时间(4.7,95%CI 2.6-7.5 和 3.0,95%CI 2.1-4.0)。VAC 与死亡率增加相关(比值比 2.0,95%CI 1.3-3.2),但 VAP 不相关(比值比 1.1,95%CI 0.5-2.4)。VAC 评估速度更快(平均每位患者 1.8 分钟,而不是 39 分钟)。VAP 和 VAC 事件主要归因于肺炎、肺水肿、ARDS 和肺不张。

结论

筛查呼吸机设置的 VAC 可捕获到与传统 VAP 监测相似的并发症集,但速度更快、更客观,且是预后的更好预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8003/3062570/4dd1a8e70c44/pone.0018062.g001.jpg

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