Amar David, Zhang Hao, Pedoto Alessia, Desiderio Dawn P, Shi Weiji, Tan Kay See
From the Departments of *Anesthesiology and Critical Care Medicine and †Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Anesth Analg. 2017 Jul;125(1):190-199. doi: 10.1213/ANE.0000000000002151.
Protective lung ventilation (PLV) during one-lung ventilation (OLV) for thoracic surgery is frequently recommended to reduce pulmonary complications. However, limited outcome data exist on whether PLV use during OLV is associated with less clinically relevant pulmonary morbidity after lung resection.
Intraoperative data were prospectively collected in 1080 patients undergoing pulmonary resection with OLV, intentional crystalloid restriction, and mechanical ventilation to maintain inspiratory peak airway pressure <30 cm H2O. Other ventilator settings and all aspects of anesthetic management were at the discretion of the anesthesia care team. We defined PLV and non-PLV as <8 or ≥8 mL/kg (predicted body weight) mean tidal volume. The primary outcome was the occurrence of pneumonia and/or acute respiratory distress syndrome (ARDS). Propensity score matching was used to generate PLV and non-PLV groups with comparable characteristics. Associations between outcomes and PLV status were analyzed by exact logistic regression, with matching as cluster in the anatomic and nonanatomic lung resection cohorts.
In the propensity score-matched analysis, the incidence of pneumonia and/or ARDS among patients who had an anatomic lung resection was 9/172 (5.2%) in the non-PLV compared to the PLV group 7/172 (4.1%; odds ratio, 1.29; 95% confidence interval, 0.48-3.45, P= .62). The incidence of pneumonia and/or ARDS in patients who underwent nonanatomic resection was 3/118 (2.5%) in the non-PLV compared to the PLV group, 1/118 (0.9%; odds ratio, 3.00; 95% confidence interval, 0.31-28.84, P= .34).
In this prospective observational study, we found no differences in the incidence of pneumonia and/or ARDS between patients undergoing lung resection with tidal volumes <8 or ≥8 mL/kg. Our data suggest that when fluid restriction and peak airway pressures are limited, the clinical impact of PLV in this patient population is small. Future randomized trials are needed to better understand the benefits of a small tidal volume strategy during OLV on clinically important outcomes.
胸科手术单肺通气(OLV)期间,常推荐采用肺保护性通气(PLV)以减少肺部并发症。然而,关于OLV期间使用PLV是否与肺切除术后临床相关的肺部发病率降低相关的结局数据有限。
前瞻性收集1080例行OLV肺切除术、有意限制晶体液输入并采用机械通气以维持吸气峰压<30 cm H2O患者的术中数据。其他通气设置及麻醉管理的所有方面由麻醉护理团队自行决定。我们将PLV和非PLV定义为平均潮气量<8或≥8 mL/kg(预测体重)。主要结局为肺炎和/或急性呼吸窘迫综合征(ARDS)的发生。采用倾向评分匹配法生成具有可比特征的PLV组和非PLV组。通过精确逻辑回归分析结局与PLV状态之间的关联,在解剖性和非解剖性肺切除队列中以匹配作为聚类。
在倾向评分匹配分析中,解剖性肺切除患者中,非PLV组肺炎和/或ARDS的发生率为9/172(5.2%),而PLV组为7/172(4.1%);比值比为1.29;95%置信区间为0.48 - 3.45,P = 0.62。非解剖性切除患者中,非PLV组肺炎和/或ARDS的发生率为3/118(2.5%),而PLV组为1/118(0.9%);比值比为3.00;95%置信区间为0.31 - 28.84,P = 0.34。
在这项前瞻性观察性研究中,我们发现潮气量<8或≥8 mL/kg的肺切除患者在肺炎和/或ARDS发生率方面无差异。我们的数据表明,当液体限制和气道峰压受到限制时,PLV对该患者群体的临床影响较小。未来需要进行随机试验,以更好地了解OLV期间小潮气量策略对临床重要结局的益处。