Blot Stijn I, Poelaert Jan, Kollef Marin
Dept, of Internal Medicine, Faculty of Medicine & Health Sciences, Ghent University, De Pintelaan 185, 9000 Ghent, Belgium.
BMC Infect Dis. 2014 Nov 28;14:119. doi: 10.1186/1471-2334-14-119.
Microaspiration of subglottic secretions through channels formed by folds in high volume-low pressure poly-vinyl chloride cuffs of endotracheal tubes is considered a significant pathogenic mechanism of ventilator-associated pneumonia (VAP). Therefore a series of prevention measures target the avoidance of microaspiration. However, although some of these can minimize microaspiration, benefits in terms of VAP prevention are not always obvious. Polyurethane-cuffed endotracheal tubes successfully reduce microaspiration but high quality data demonstrating VAP rate reduction are lacking. An analogous conclusion can be made regarding taper-shaped cuffs compared with classic barrel-shaped cuffs. More clinical data regarding these endotracheal tube designs are needed to demonstrate clinical value in addition to in vitro-based evidence. The clinical usefulness of endotracheal tubes developed for subglottic secretions drainage is established in multiple studies and confirmed by meta-analysis. Any change in cuff design will fail to prevent microaspiration if the cuff is insufficiently inflated. At least one well-designed trial demonstrated that continuous cuff pressure monitoring and control decrease the risk of VAP. Gel lubrication of the cuff prior to intubation temporarily hampers microaspiration through sludging the channels formed by folds in high volume-low pressure cuffs. As the beneficial effect of gel lubrication is temporarily, its potential to reduce VAP risk is probably nonsignificant. A minimum positive end-expiratory pressure of at least 5 cmH2O can be recommended as it reduces the risk of microaspiration in vitro and in vivo. One randomized controlled study demonstrated a reduced risk of VAP in patients ventilated with PEEP (5-8 cmH2O). Regarding head-of-bed elevation, it can be recommended to avoid supine positioning. Whether a 45° head-of-bed elevation is to be preferred above 25-30° head-of-bed elevation remains unproven. Finally, the routine monitoring of gastric residual volumes in mechanically ventilated patients receiving enteral nutrition cannot be recommended.
经气管内导管大容量低压聚氯乙烯袖带褶皱形成的通道对声门下分泌物进行微误吸被认为是呼吸机相关性肺炎(VAP)的一个重要致病机制。因此,一系列预防措施旨在避免微误吸。然而,尽管其中一些措施可以将微误吸降至最低,但在预防VAP方面的益处并不总是明显的。聚氨酯袖带气管内导管成功减少了微误吸,但缺乏高质量数据证明其降低了VAP发生率。与经典桶形袖带相比,锥形袖带也有类似结论。除了基于体外的证据外,还需要更多关于这些气管内导管设计的临床数据来证明其临床价值。为声门下分泌物引流而开发的气管内导管的临床实用性已在多项研究中得到证实,并经荟萃分析确认。如果袖带充气不足,袖带设计的任何改变都无法预防微误吸。至少一项设计良好的试验表明,持续监测和控制袖带压力可降低VAP风险。插管前对袖带进行凝胶润滑会通过使大容量低压袖带褶皱形成的通道淤塞而暂时阻碍微误吸。由于凝胶润滑的有益效果是暂时的,其降低VAP风险的潜力可能不大。可以建议至少维持5 cmH2O的最小呼气末正压,因为它可降低体外和体内的微误吸风险。一项随机对照研究表明,接受PEEP(5 - 8 cmH2O)通气的患者VAP风险降低。关于床头抬高,建议避免仰卧位。床头抬高45°是否比床头抬高25 - 30°更可取仍未得到证实。最后,不建议对接受肠内营养的机械通气患者常规监测胃残余量。