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find Keyword "Ⅰ型呼吸衰竭" 2 results
  • 重症肺炎合并Ⅰ型呼吸衰竭经鼻高流量湿化氧疗临床效果评价

    目的 对比文丘里面罩吸氧及无创正压通气(NPPV),评价经鼻高流量湿化氧疗(HFNC)在重症肺炎Ⅰ型呼吸衰竭患者中应用效果。方法 选择 2017 年 3 月至 2019 年 12 月我院呼吸与危重症医学科重症肺炎合并Ⅰ型呼吸衰竭经文丘里面罩吸氧、HFNC 及 NPPV 治疗患者 142 例。随机数字表法分为文丘里面罩吸氧组为面罩组 46 例,HFNC 组 49 例,NPPV 组 47 例,分别比较治疗后 2 h 三组患者 SpO2、PaO2、PaO2/FiO2、PaCO2、pH、RR、HR、舒适度、耐受性程度、鼻腔干燥程度、咽喉干燥程度、咳痰难易程度、气管插管率。结果 HFNC 组与面罩组间 SpO2、PaO2、PaO2/FiO2 差异有统计学意义(均 P<0.05),HFNC 组与 NPPV 组间SpO2差异无统计学意义(P>0.05);HFNC 组与 NPPV 组间 PaO2、PaO2/FiO2 差异有统计学意义(均 P<0.05);三组间 PaCO2、pH、RR、HR 差异无统计学意义(P>0.05)。HFNC 组与 NPPV 组间舒适度、耐受性、鼻腔干燥程度、咽喉干燥程度、咳痰难易程差异有统计学意义(P<0.05);HFNC 组与面罩组鼻腔黏膜干燥程度、咳痰难易程度、气管插管差异有统计学意义(均 P<0.05),NPPV 组与面罩组间气管插管差异有统计学意义(P<0.05);HFNC 组与 NPPV 组间气管插管差异无统计学意义(P>0.05)。结论 HFNC 可应用于重症肺炎Ⅰ型呼吸衰竭早期呼吸支持治疗,患者依从性好,不良反应少,临床治疗效果肯定,值得在临床推广。

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  • Retrospective studies of volume-OXygeneration index in predicting the effect of early non-invasive positive pressure ventilation in patients with type I Respiratory failure

    ObjectiveTo observe the predictive value of Volume OXygeneration (VOX) index for early non-invasive positive pressure ventilation (NIPPV) treatment in patients with type I Respiratory failure. MethodsRetrospective analysis was made on the patients with type I Respiratory failure admitted to the intensive care medicine from September 2019 to September 2022, who received early NIPPV treatment. After screening according to the discharge standard, they were grouped according to the NIPPV 2-hour VOX index. The observation group was VOX Youden index >20.95 (n=69), and the control group was VOX index ≤20.95 (n=64). Collect patient baseline data and NIPPV 2-hour, 12-hour, and 24-hour arterial blood gas values, and calculate NIPPV outcomes, intubation status, NIPPV usage time, hospital stay, and mortality rate. ResultsThere was a statistically significant difference in respiratory rate (RR) between the baseline data onto the two groups of patients, but others not. After early NIPPV treatment, the 2-hour oxygenation index (P/F) [(182.5 ± 66.14) vs. (144.1 ± 63.6) mm Hg, P<0.05] of the observation group showed a more significant increase. The failure rate of NIPPV intubation within 12 hours was lower (4.35% vs. 32.81%, P<0.05), the success rate of NIPPV withdrawal from 24 hours was higher (40.58% vs. 0%, P<0.05), and the failure rate of NIPPV intubation was lower (4.35% vs. 46.88%, P<0.05). The comparison of treatment outcomes showed that the intubation rates in the observation group (4.35% vs. 67.19%, P<0.05) was lower. The threshold of NIPPV 2-hour VOX index 20.95 was used as a predictor of Tracheal intubation, with sensitivity of 74.7% and specificity of 93.5%. ConclusionIn the early NIPPV treatment of patients with type I Respiratory failure, the NIPPV 2-hour VOX index>20.91 is taken as the evaluation index, which can better to predict the improvement in hypoxia and the risk of NIPPV failure Tracheal intubation, and has clinical significance.

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