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首页> 外文期刊>Pediatric critical care medicine: a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies >Treatment of acute hypoxemic respiratory failure with continuous positive airway pressure delivered by a new pediatric helmet in comparison with a standard full face mask: a prospective pilot study.
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Treatment of acute hypoxemic respiratory failure with continuous positive airway pressure delivered by a new pediatric helmet in comparison with a standard full face mask: a prospective pilot study.

机译:与标准的全口罩相比,新型儿童头盔提供的持续气道正压通气治疗急性低氧性呼吸衰竭:一项前瞻性研究。

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OBJECTIVES: To evaluate the feasibility and efficacy of continuous positive airway pressure delivered by a new pediatric helmet in comparison with a standard facial mask in infants with acute hypoxemic respiratory failure. DESIGN: A single-center prospective case-control study. SETTING: Pediatric intensive care unit in a tertiary children hospital. PATIENTS AND INTERVENTIONS: Twenty consecutive infants treated with continuous positive airway pressure by a helmet matched with a control patient treated with continuous positive airway pressure by facial mask and selected by age, weight, PaO2:Fio2, and PaCO2 on pediatric intensive care unit admission. MEASUREMENTS AND MAIN RESULTS: Feasibility was defined as the incidence of continuous positive airway pressure protocol failure secondary to 1) failure to administer continuous positive airway pressure because of intolerance to the interface; 2) deterioration in gas exchange soon after continuous positive airway pressure institution; and 3) major clinical adverse events such as pneumothorax or any hemodynamic instability related to the continuous positive airway pressure safety system device's failure. Evaluation of feasibility included also the total application time of respiratory treatment, the number of continuous positive airway pressure discontinuations/first 24 hrs. Interface-related complications included air leaks, cutaneous pressure sores, eye irritation, inhalation, and gastric distension. The 20 patients and control subjects had similar matching characteristics. Continuous positive airway pressure delivered by a helmet compared with a facial mask reduced continuous positive airway pressure trial failure rate (p = .02), increased application time (p = .001) with less discontinuations (p = .001), and was not associated with an increased rate of major adverse events, resulting in decreased air leaks (p = .04) and pressure sores (p = .002). Both continuous positive airway pressure systems resulted in early and sustained improvement in oxygenation. CONCLUSIONS: The helmet might be considered a viable and safe alternative to a standard facial mask to deliver continuous positive airway pressure in hypoxemic infants in the pediatric intensive care unit setting. In our study, the helmet allowed more prolonged application of continuous positive airway pressure compared with a facial mask, ensuring similar improvement in oxygenation without any adverse events and clinical intolerance.
机译:目的:评价与急性面部低氧血症性呼吸衰竭婴儿相比,新型儿童头盔与标准面罩持续提供持续气道正压的可行性和有效性。设计:单中心前瞻性病例对照研究。地点:三级儿童医院的儿科重症监护室。患者和干预措施:连续20例接受头盔持续气道正压通气治疗的婴儿,与对照患者接受面罩持续气道正压通气治疗,并根据年龄,体重,PaO2:Fio2和PaCO2在小儿重症监护病房入院时进​​行选择。测量和主要结果:可行性定义为继发于以下原因的持续气道正压通气协议失败的发生率:1)由于对接口的不耐受而无法给予持续气道正压通气; 2)持续的气道正压形成后不久,气体交换恶化; 3)主要临床不良事件,例如气胸或与持续气道正压通气安全系统装置故障有关的任何血液动力学不稳定性。可行性评估还包括呼吸治疗的总应用时间,连续气道正压中断/前24小时的次数。与界面有关的并发症包括漏气,皮肤压疮,眼睛刺激,吸入和胃胀。 20名患者和对照受试者具有相似的匹配特征。与面罩相比,头盔提供的持续气道正压降低了持续的气道正压试验失败率(p = .02),应用时间增加了(p = .001),停药次数较少(p = .001),并且没有与主要不良事件发生率增加相关,导致漏气(p = .04)和褥疮(p = .002)减少。两种持续的气道正压系统均导致早期和持续的氧合改善。结论:在小儿重症监护病房,低氧血症婴儿可以连续呼吸道正压通气,可以认为头盔是标准面罩的可行且安全的替代品。在我们的研究中,与面罩相比,头盔允许更长时间地施加持续的气道正压通气,确保在无任何不良事件和临床耐受性的情况下,氧合水平得到类似的改善。

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