The Use of High-Flow Nasal Oxygen Therapy in the Management of Severe Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Feasibility Study.

IF 0.8 Q4 RESPIRATORY SYSTEM
Pervin Hancı, Serpil Öcal, Esat Kıvanç Kaya, Arzu Topeli
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Abstract

Objective: This study investigated the efficacy of high-flow nasal oxygen therapy in patients with severe acute exacerbation of chronic obstructive pulmonary disease admitted to the intensive care unit.

Material and methods: Totally, 23 patients were enrolled in the study. High-flow nasal oxygen therapy was administered with a predefined protocol. Vital signs, Visual Analog Scale for dyspnea, and arterial blood gas parameters were recorded at the beginning under low-flow oxygen support therapy and the 1st, 6th, 12th, and 24th hours of high-flow nasal oxygen therapy. High-flow nasal oxygen therapy duration, intensive care unit length of stay, and intensive care unit, in-hospital, and 60-day mortality were recorded as outcomes and compared according to the presence of pneumonia upon admission.

Results: In 12 patients (52.2%), pneumonia was present. High-flow nasal oxygen therapy was applied for a median of 57 hours [49.2-104.5]. Overall decreases were detected in heart rate (P = .001), respiratory rate (P < .001), and Visual Analog Scale for dyspnea (P = .001) during the first 24 hours of the therapy. Although there was an increase in PaCO2 (P = .001), pH increased (P < .001) over time too. No change in partial arterial oxygen pressure (P = .63) and partial arterial oxygen pressure/fraction of inspired oxygen ratio (P = .22) was noted. Nineteen patients (77%) were successfully weaned from high-flow nasal oxygen therapy. While the high-flow nasal oxygen therapy failure rate was 23%, the in-hospital and 60-day mortality rates were 8.6%. Outcomes were not different between patients with and without pneumonia.

Conclusion: High-flow nasal oxygen therapy was efficient in relieving respiratory distress and well-tolerated with no adverse out- come in severe acute exacerbation of chronic obstructive pulmonary disease patients admitted to the intensive care unit.

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高流量鼻吸氧治疗慢性阻塞性肺疾病严重急性加重期的可行性研究
目的:探讨高流量鼻吸氧治疗慢性阻塞性肺疾病重症急性加重期入住重症监护病房的疗效。材料与方法:共纳入23例患者。高流量鼻氧治疗按照预先确定的方案进行。记录低流量氧支持治疗开始及高流量鼻氧治疗第1、6、12、24小时的生命体征、呼吸困难视觉模拟量表、动脉血气参数。记录高流量鼻氧治疗持续时间、重症监护病房住院时间、重症监护病房、住院和60天死亡率,并根据入院时是否存在肺炎进行比较。结果:12例(52.2%)患者出现肺炎。高流量鼻氧治疗的中位时间为57小时[49.2-104.5]。在治疗的前24小时内,心率(P = .001)、呼吸频率(P < .001)和呼吸困难视觉模拟量表(P = .001)的总体下降。随着时间的推移,PaCO2升高(P = 0.001), pH也升高(P < 0.001)。动脉血分氧压(P = 0.63)和动脉血分氧压/吸入氧比(P = 0.22)无变化。19例(77%)患者成功脱离高流量鼻氧治疗。高流量鼻氧治疗失败率为23%,住院死亡率和60天死亡率为8.6%。结果在肺炎患者和非肺炎患者之间没有差异。结论:高流量鼻吸氧治疗慢性阻塞性肺疾病重症急性加重期患者呼吸窘迫有效,耐受性好,无不良反应。
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来源期刊
Turkish Thoracic Journal
Turkish Thoracic Journal Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.40
自引率
11.10%
发文量
2
期刊介绍: Turkish Thoracic Journal (Turk Thorac J) is the double-blind, peer-reviewed, open access, international publication organ of Turkish Thoracic Society. The journal is a quarterly publication, published on January, April, July, and October and its publication language is English. Turkish Thoracic Journal started its publication life following the merger of two journals which were published under the titles “Turkish Respiratory Journal” and “Toraks Journal” until 2007. Archives of both journals were passed on to the Turkish Thoracic Journal. The aim of the journal is to convey scientific developments and to create a dynamic discussion platform about pulmonary diseases. With this intent, the journal accepts articles from all related scientific areas that address adult and pediatric pulmonary diseases, as well as thoracic imaging, environmental and occupational disorders, intensive care, sleep disorders and thoracic surgery. Clinical and research articles, reviews, statements of agreement or disagreement on controversial issues, national and international consensus reports, abstracts and comments of important international articles, interesting case reports, writings related to clinical and practical applications, letters to the editor, and editorials are accepted.
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