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Non-invasive ventilation: a safe and effective respiratory support method in hypoxemic acute respiratoryfailure due to pneumonia with or without acute respiratory distress syndrome

机译:非侵入性通风:由于肺炎缺氧急性呼吸缺乏症的安全有效呼吸呼吸促进方法,因肺炎有或没有急性呼吸窘迫综合征

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Introduction: The benefit of non-invasive ventilation (NIV) in cases of hypercapnic acute respiratory failure (ARF) has already been proven. Still, its safety and efficacy as a respiratory support method for patients with hypoxemic ARF hasn't been studied so well.Aim: The aim of our study was to examine the safety and efficacy of NIV in hypoxemic ARF of primary lung origin.Materials and methods: This was a prospective observational cohort study of patients with hypoxemic ARF due to communityacquired pneumonia with or without acute respiratory distress syndrome (ARDS) treated using NIV. They were divided into four groups: pneumonia without ARDS, mild, moderate, or severe ARDS. Their clinical and ABG parameters were recorded before initiation of NIV, at 1 hour and 24 hours after ventilation onset and at transition to non-intensive NIV or before endotracheal intubation in NIV failure cases.Results: A total of 63 patients were included. NIV trial was successful in 85.71% of them, while 14.29% experienced NIV failure. In the general population, we observed a significant difference in PaO2/FiO2 only before transition to non-intensive NIV in comparison to the value at admission. This trend was seen in the patients with pneumonia without ARDS and moderate ARDS, but not in those with mild and severe ARDS. The clinical parameters showed improvement early in the course of treatment both in the entire study population and all subgroups.Conclusions: NIV is an effective and safe option for respiratory support in patients with severe CAP only when an adequate etiological treatment has been applied.
机译:简介:已经证明了非侵入性通风(NIV)在过度急性呼吸衰竭(ARF)的益处。尽管如此,它仍然是对缺氧ARF患者的呼吸支持方法的安全性和有效性尚未得到那么好。我们的研究目的是探讨NIV在原发性肺源性缺氧ARF中NIV的安全性和功效。方法:这是由于使用NIV治疗的患有或不含急性呼吸窘迫综合征(ARDS),患有缺氧血症患者的前瞻性观察队列研究。它们分为四组:肺炎没有ARDS,轻度,中度或严重的ARDS。他们的临床和ABG参数在通风发病后1小时和24小时内并在核育失败病例中过渡到非强化NIV或气管插管前的1小时和24小时之前记录了它们的临床和ABG参数。结果:总共包括63名患者。核心审判在85.71%的85.71%中取得了成功,而14.29%经历过核育核育失败。在一般人群中,我们只观察到PAO2 / FIO2的显着差异,只有与入学价值相比过渡到非强化核育。在没有ARDS和中度ARDS的肺炎患者中,患有这种趋势,但不含温和和严重的ARDS的患者。在整个研究人群和所有亚组中,临床参数在治疗过程中显示出改善

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