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急性呼吸衰竭的无创通气:一项前瞻性随机安慰剂对照试验。

Noninvasive ventilation for acute respiratory failure: a prospective randomised placebo-controlled trial.

作者信息

Thys F, Roeseler J, Reynaert M, Liistro G, Rodenstein D O

机构信息

Dept of Emergency, Cliniques universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium.

出版信息

Eur Respir J. 2002 Sep;20(3):545-55. doi: 10.1183/09031936.02.00287402.

Abstract

The aim of the present study was to clarify whether the known effects of noninvasive positive-pressure ventilation (NPPV) in patients with respiratory failure are real or due to placebo effects and whether early application of NPPV in the emergency department leads to rapid improvement of the patients condition and outcome. A prospective randomised placebo-controlled study was conducted in 20 patients with severe acute respiratory failure (ARF) secondary to an acute exacerbation of chronic obstructive pulmonary disease (COPD) or acute pulmonary oedema, not improving under conventional medical therapy and on the edge of intubation. Patients received either conventional medical therapy plus two-level NPPV (hi-level NPPV) or conventional medical therapy plus "placebo" NPPV. The main outcome measures involved the need for endotracheal intubation in the bi-level NPPV arm and in the placebo arm after crossing over to active NPPV. Morbidity, length of stay, mortality and the effect of the ventilatory mode on clinical, arterial-blood gas parameters, and the sternocleidomastoid muscles electromyogram (EMG) activity were also measured. The 10 patients in the active NPPV group rapidly improved and none needed intubation. Placebo NPPV resulted in no change in the clinical condition of patients that continued to worsen and the 10 patients were crossed over to active NPPV. Three patients were intubated. No differences in terms of morbidity, length of stay or mortality between the two groups were observed. Active NPPV (but not placebo NPPV) led to a rapid and significant improvement in the clinical parameters, pH and the carbon dioxide tension in arterial blood and to a decrease in respiratory frequency and sternocleidomastoid EMG activity. Early application of bi-level noninvasive positive-pressure ventilation in patients with severe acute respiratory failure, due to chronic obstructive pulmonary disease and acute pulmonary oedema, leads to a rapid improvement in clinical status and blood gases. Noninvasive positive-pressure ventilation had no placebo effect.

摘要

本研究的目的是阐明无创正压通气(NPPV)对呼吸衰竭患者的已知疗效是真实的还是由安慰剂效应所致,以及在急诊科早期应用NPPV是否能使患者病情和预后迅速改善。对20例因慢性阻塞性肺疾病(COPD)急性加重或急性肺水肿继发严重急性呼吸衰竭(ARF)、在传统药物治疗下病情无改善且处于插管边缘的患者进行了一项前瞻性随机安慰剂对照研究。患者接受传统药物治疗加两级NPPV(高流量NPPV)或传统药物治疗加“安慰剂”NPPV。主要观察指标包括在交叉至活性NPPV后,双水平NPPV组和安慰剂组气管插管的需求。还测量了发病率、住院时间、死亡率以及通气模式对临床、动脉血气参数和胸锁乳突肌肌电图(EMG)活动的影响。活性NPPV组的10例患者病情迅速改善,无一例需要插管。安慰剂NPPV组患者的临床状况无变化,病情持续恶化,这10例患者交叉至活性NPPV组。3例患者进行了插管。两组在发病率、住院时间或死亡率方面未观察到差异。活性NPPV(而非安慰剂NPPV)使临床参数、pH值和动脉血二氧化碳分压迅速显著改善,呼吸频率和胸锁乳突肌EMG活动降低。对于因慢性阻塞性肺疾病和急性肺水肿导致的严重急性呼吸衰竭患者,早期应用双水平无创正压通气可使临床状况和血气迅速改善。无创正压通气无安慰剂效应。

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