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耳鼻喉科手术中的流量控制通气:一项前瞻性观察研究。

Flow-controlled ventilation during ear, nose and throat surgery: A prospective observational study.

机构信息

From the Department of Anaesthesiology and Critical Care, Medical Centre - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg (JS, FG, JW, SW, SS), Department of Anaesthesiology, Emergency and Intensive Care Medicine, University Medical Centre Göttingen, Göttingen, Germany (IB), University of Greenwich, London, UK (TB), and Department of Anaesthesiology, Intensive Care and Pain Medicine, University Hospital Münster, Münster, Germany (AZ, DE).

出版信息

Eur J Anaesthesiol. 2019 May;36(5):327-334. doi: 10.1097/EJA.0000000000000967.

Abstract

BACKGROUND

Flow-controlled ventilation (FCV) is a new mechanical ventilation mode that maintains constant flow during inspiration and expiration with standard tidal volumes via cuffed narrow-bore endotracheal tubes. Originating in manually operated 'expiratory ventilation assistance', FCV extends this technique by automatic control of airway flow, monitoring of intratracheal pressure and control of peak inspiratory pressure and end-expiratory pressure. FCV has not yet been described in a clinical study.

OBJECTIVE

The aim of this study was to provide an initial assessment of FCV in mechanically ventilated patients undergoing ear, nose and throat surgery and evaluate its potential for future use.

DESIGN

An observational study.

SETTING

Two German academic medical centres from 24 November 2017 to 09 January 2018.

PATIENTS

Consecutive patients (≥ 18 years) scheduled for elective ear, nose and throat surgery. Exclusion criteria were planned laser surgery, intended fibreoptic awake intubation, emergency procedures, increased risk of aspiration, American Society of Anesthesiologists (ASA) physical status more than III and chronic obstructive pulmonary disease classified as GOLD stage more than II.

INTERVENTION

Peri-operative use of FCV provided by a new type of ventilator (Evone) via a narrow-bore endotracheal tube (Tritube).

MAIN OUTCOME MEASURES

Minute volume, respiratory rate, intratidal tracheal pressure amplitude (Δp) and end-tidal CO2 (PetCO2) were recorded every 5 min. All adverse events were noted. Data are presented as median [IQR].

RESULTS

Sixteen patients provided 15 evaluable data sets. A minute volume of 5.0 [4.4 to 6.4] l min and a respiratory rate of 9 [8 to 11] min generated a PetCO2 of 4.9 [4.8 to 5.0] kPa. Δp was 10 [9 to 12] cmH2O. Five adverse events were recorded: a tube obstruction due to airway secretions and four tube dislocations (two attributed to coughing, two not study-related).

CONCLUSION

FCV achieves adequate PetCO2 levels with minute volume and Δp in the normal range. Tritube's high flow resistance may increase the likelihood of tube dislocations if the patient coughs. Although further evaluation is necessary, FCV provides a new option for short-term mechanical ventilation. The successful operation of FCV with narrow-bore tubes contributes to the armamentarium for airway management.

TRIAL REGISTRATION

DRKS00013312.

摘要

背景

流量控制通气(FCV)是一种新的机械通气模式,通过带套的窄口径气管内导管在吸气和呼气期间保持恒定流量,并采用标准潮气量。它源自于手动操作的“呼气通气辅助”,通过自动控制气道流量、监测气管内压力以及控制峰吸气压和呼气末压力,FCV 扩展了该技术。目前还没有关于 FCV 的临床研究。

目的

本研究旨在初步评估 FCV 在接受耳鼻喉手术的机械通气患者中的应用,并评估其未来应用的潜力。

设计

观察性研究。

设置

2017 年 11 月 24 日至 2018 年 1 月 9 日,两家德国学术医学中心。

患者

连续入选的择期耳鼻喉手术患者(≥18 岁)。排除标准为计划激光手术、拟纤维光学清醒插管、急诊手术、有较高的误吸风险、美国麻醉医师协会(ASA)身体状况超过 III 级和慢性阻塞性肺疾病(COPD)分类为 GOLD 阶段超过 II 级。

干预措施

使用新型呼吸机(Evone)通过窄口径气管内导管(Tritube)进行围手术期 FCV。

主要观察指标

每 5 分钟记录一次分钟通气量、呼吸频率、潮气量内气管压力振幅(Δp)和呼气末 CO2(PetCO2)。记录所有不良事件。数据以中位数(四分位数间距)表示。

结果

16 名患者提供了 15 组可评估数据。分钟通气量为 5.0[4.4 至 6.4]L/min,呼吸频率为 9[8 至 11]min,PetCO2 为 4.9[4.8 至 5.0]kPa。Δp 为 10[9 至 12]cmH2O。记录到 5 起不良事件:由于气道分泌物引起的管腔阻塞和 4 起管腔脱位(2 起归因于咳嗽,2 起与研究无关)。

结论

FCV 以正常范围内的分钟通气量和 Δp 实现了足够的 PetCO2 水平。如果患者咳嗽,Tritube 的高流量阻力可能会增加管腔脱位的可能性。尽管还需要进一步评估,但 FCV 为短期机械通气提供了一种新的选择。FCV 与窄口径管一起成功操作有助于气道管理的手段。

试验注册

DRKS00013312。

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