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驱动压力限制策略治疗急性呼吸窘迫综合征患者:一项初步随机临床试验。

Driving Pressure-limited Strategy for Patients with Acute Respiratory Distress Syndrome. A Pilot Randomized Clinical Trial.

机构信息

HCor Research Institute, São Paulo, Brazil.

Postgraduate Program of Anesthesiology, Surgical Sciences and Perioperative Medicine-Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

出版信息

Ann Am Thorac Soc. 2020 May;17(5):596-604. doi: 10.1513/AnnalsATS.201907-506OC.

Abstract

Evidence from observational studies suggests that driving pressure is strongly associated with pulmonary injury and mortality, regardless of positive end-expiratory pressure (PEEP) levels, tidal volume, or plateau pressure. Therefore, it is possible that targeting driving pressure may improve the safety of ventilation strategies for patients with acute respiratory distress syndrome (ARDS). However, the clinical effects of a driving pressure-limited strategy for ARDS has not been assessed in randomized controlled trials. To evaluate the feasibility of testing a driving pressure-limited strategy in comparison with a conventional lung-protective ventilation strategy in patients with ARDS and a baseline driving pressure of ≥13 cm HO. This was a randomized, controlled, nonblinded trial that included 31 patients with ARDS who were on invasive mechanical ventilation and had a driving pressure of ≥13 cm HO. Patients allocated to the driving pressure-limited strategy were ventilated with volume-controlled or pressure-support ventilation modes, with tidal volume titrated to 4-8 ml/kg of predicted body weight (PBW), aiming at a driving pressure of 10 cm HO, or the lowest possible. Patients in the control group were ventilated according to the ARDSNet (Acute Respiratory Distress Syndrome Network) protocol, using a tidal volume of 6 ml/kg PBW, which was allowed to be set down to 4 ml/kg PBW if the plateau pressure was >30 cm HO. The primary endpoint was the driving pressure on Days 1-3. Sixteen patients were randomized to the driving pressure-limited group and 15 were randomized to the conventional strategy group. All patients were considered in analyses. Most of the patients had mild ARDS with a mean arterial oxygen tension/fraction of inspired oxygen ratio of 215 (standard deviation [SD] = 95). The baseline driving pressure was 15.0 cm HO (SD = 2.6) in both groups. In comparison with the conventional strategy, driving pressure from the first hour to the third day was 4.6 cm HO lower in the driving pressure-limited group (95% confidence interval [CI], 6.5 to 2.8;  < 0.001). From the first hour up to the third day, tidal volume in the driving pressure-limited strategy group was kept lower than in the control group (mean difference [ml/kg of PBW], 1.3; 95% CI, 1.7 to 0.9;  < 0.001). We did not find statistically significant differences in the incidence of severe acidosis (pH < 7.10) within 7 days (absolute difference -12.1; 95% CI, -41.5 to -17.3) or any clinical secondary endpoint. In patients with ARDS, a trial assessing the effects of a driving pressure-limited strategy using very low tidal volumes versus a conventional ventilation strategy on clinical outcomes is feasible.Clinical trial registered with ClinicalTrials.gov (NCT02365038).

摘要

来自观察性研究的证据表明,无论呼气末正压(PEEP)水平、潮气量或平台压如何,驱动压与肺损伤和死亡率密切相关。因此,靶向驱动压可能会改善急性呼吸窘迫综合征(ARDS)患者的通气策略的安全性。然而,在随机对照试验中尚未评估 ARDS 的驱动压限制策略的临床效果。本研究旨在评估在基线驱动压≥13cmH2O 的 ARDS 患者中,与传统肺保护性通气策略相比,驱动压限制策略的可行性。这是一项随机、对照、非盲试验,纳入了 31 名接受有创机械通气且基线驱动压≥13cmH2O 的 ARDS 患者。将驱动压限制组的患者置于容量控制或压力支持通气模式下,潮气量滴定至 4-8ml/kg 预测体重(PBW),目标驱动压为 10cmH2O 或尽可能低。对照组患者根据 ARDSNet(急性呼吸窘迫综合征网络)方案进行通气,潮气量为 6ml/kg PBW,如果平台压>30cmH2O,则允许降至 4ml/kg PBW。主要终点是第 1-3 天的驱动压。16 名患者被随机分配至驱动压限制组,15 名患者被随机分配至常规策略组。所有患者均纳入分析。大多数患者为轻度 ARDS,平均动脉氧分压/吸入氧浓度比为 215(标准差 [SD] = 95)。两组的基线驱动压均为 15.0cmH2O(SD = 2.6)。与常规策略相比,驱动压限制组从第 1 小时到第 3 天的驱动压低 4.6cmH2O(95%置信区间 [CI],6.5 至 2.8; < 0.001)。从第 1 小时到第 3 天,驱动压限制组的潮气量保持低于对照组(每公斤预测体重的毫升差异,1.3;95%CI,1.7 至 0.9; < 0.001)。我们没有发现 7 天内严重酸中毒(pH<7.10)发生率有统计学显著差异(绝对差值-12.1;95%CI,-41.5 至-17.3)或任何临床次要终点。在 ARDS 患者中,评估使用极低潮气量的驱动压限制策略与传统通气策略对临床结局影响的试验是可行的。临床试验已在 ClinicalTrials.gov(NCT02365038)注册。

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