慢性阻塞性肺疾病加重患者无创机械通气头盔:一项随机对照试验

F. Glumcher, Ye.Yu Dyomin
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引用次数: 0

摘要

目的:比较头盔无创机械通气(NIV)与全面罩无创机械通气(NIV)的并发症发生率和主要治疗结果。材料和方法。一项单中心随机开放标签对照临床试验。有呼吸衰竭症状的慢性阻塞性肺疾病(COPD)加重患者随机接受面罩或头盔的无创通气治疗。该研究纳入59例患者,随机分为两组:通过头盔(n = 29)或面罩(n = 30)进行NIV。患者平均年龄分别为(59.24±14.20)岁和(59.06±15.90)岁。在这两组中,男性占主导地位,分别为23人(79%)和27人(90%)。在压力支持(PS)模式下使用Draeger Carina器械进行通气。主要终点是NIV并发症的累积发生率。次要终点为PaO2/FiO2比率、治疗耐受性、插管次数、重症监护病房(ICU)住院时间和ICU死亡率。共有59名患者参与了这项研究。头盔组并发症发生率较低(10 % (n = 3)比43 % (n = 13), p = 0.004),在NIV第1小时和结束时PaO2/FiO2比值较高(253.14±64.74)mmHg比(216.06±43.86)mmHg,(277.07±84.89)mmHg比(225.81±63.64)mmHg, p = 0.013和p = 0.012)。在治疗第4小时,更多的患者表示头盔耐受性优于口罩(24(83%)对14 (47%),p = 0.004),在通气结束时(69%(20/29)对30% (9/30),p = 0.03)。1例患者因口罩不耐受而无法继续治疗。两组患者插管率、ICU住院时间、死亡率差异均无统计学意义(p = 0.612、p = 0.100、p = 1.000)。与面罩通气相比,面罩通气通气可降低COPD加重期患者并发症的发生率,增加PaO2/FiO2比值,提高耐受性。需要更大规模的研究来确定界面选择对ICU死亡率、ICU住院时间和插管频率的影响。
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Noninvasive mechanical ventilation with helmet in patients with exacerbation of chronic obstructive pulmonary disease: a randomized controlled trial
Objective ‒ to compare the incidence of complications and the main treatment outcomes of non-invasive mechanical ventilation (NIV) with a helmet versus NIV with a full face mask.Materials and methods. A monocentric randomized open-labeled controlled clinical trial. Patients with exacerbation of chronic obstructive pulmonary disease (COPD) with signs of respiratory failure were randomized to receive NIV through a mask or helmet. The study included 59 patients who were randomized into two groups: NIV through helmet (n = 29) or mask (n = 30). The average age of the patients was (59.24 ± 14.20) and (59.06 ± 15.90) years, respectively. In both groups men predominated ‒ 23 (79 %) and 27 (90 %) respectively. Ventilation was performed with a Draeger Carina apparatus in pressure support (PS) mode. The primary endpoint was the cumulative incidence of NIV complications. Secondary endpoints were PaO2/FiO2 ratio, tolerance to therapy, frequency of intubations, duration of stay in the intensive care unit (ICU), and ICU mortality. A total of 59 patients were involved in the study.Results. The complication rate was lower in the helmet group (10 % (n = 3) versus 43 % (n = 13), p = 0.004) and the PaO2/FiO2 ratio was higher at the first hour and at the end of NIV (253.14 ± 64.74) mm Hg versus (216.06 ± 43.86) mm Hg and (277.07 ± 84.89) mmHg versus (225.81 ± 63.64) mm Hg, p = 0.013 and p = 0.012) compared with NIV through a full face mask. More patients noted excellent helmet tolerance than masks at the 4th hour of therapy (24 (83 %) versus 14 (47 %), p = 0.004) and at the end of ventilation (69 % (20/29) versus 30 % (9/30), p = 0.03). One patient was unable to continue therapy due to mask intolerance. Differences in intubation rates, length of ICU stay, and mortality were statistically insignificant (p = 0.612, p = 0.100, p = 1.000 respectively).Conclusions. NIV through a helmet can reduce the incidence of complications and increase the PaO2/FiO2 ratio, as well as improve tolerance compared to NIV through a face mask in patients with exacerbation of COPD. A larger scale of study is needed to establish the effect of interface choice on ICU mortality, time spent in ICU, and frequency of intubation.
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