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find Keyword "无创正压通气" 38 results
  • Risk factors associated with failure of noninvasive positive pressure ventilation in acute respiratory failure due to acute exacerbation of chronic obstructive pulmonary disease

    Objective To analyze the risk factors of treatment failure by noninvasive positive pressure ventilation (NPPV) in patients with acute respiratory failure (ARF) due to acute exacerbation of chronic obstructive pulmonary disease (AECOPD), and explore the best time that NPPV be replaced by invasive ventilation when NPPV failure occurs. Methods The data of patients with ARF due to AECOPD who were treated with NPPV from January 2013 to December 2015 were retrospectively collected. The patients were divided into two groups: the NPPV success group and the NPPV failure group (individuals who required endotracheal intubation or tracheotomy at any time). The Acute Physiology and Chronic Health Evaluation (APACHE) Ⅱ score was analyzed; the Glasgow Coma Scale score, respiratory rate (RR), pH value, partial pressure of oxygen (PaO2), PaO2/fraction of inspired oxygen (FiO2) ratio, and partial pressure of carbon dioxide were also analyzed at admission, after 2 hours of NPPV, and after 24 hours of NPPV. Results A total of 185 patients with ARF due to AECOPD were included. NPPV failed in 35.1% of the patients (65/185). Multivariate analysis identified the following factors to be independently associated with NPPV failure: APACHEⅡscore≥30 [odds ratio (OR)=20.603, 95% confidence interval (CI) (5.309, 80.525), P<0.001], RR at admission≥35 per minute [OR=3.723, 95%CI (1.197, 11.037), P=0.020], pH value after 2 hours of NPPV<7.25 [OR=2.517, 95%CI (0.905, 7.028), P=0.070], PaO2 after 2 hours of NPPV<60 mm Hg (1 mm Hg=0.133 kPa) [OR=3.915, 95%CI (1.374, 11.508), P=0.010], and PaO2/FiO2 after 2 hours of NPPV<200 mm Hg [OR=4.024, 95%CI (1.542, 11.004), P=0.010]. Conclusion When patients with ARF due to AECOPD have a higher severity score, have a rapid RR at admission, or fail to improve in terms of pH and oxygenation after 2 hours of NPPV, the risk of NPPV failure is higher.

    Release date:2017-11-24 10:58 Export PDF Favorites Scan
  • 重症加强治疗病房无创正压通气患者应用镇静治疗的安全性探讨

    目的探讨丙泊酚在无创正压通气镇静中应用的疗效及安全性。 方法回顾分析南方医科大学附属中山市小榄人民医院重症加强治疗病房(ICU)对133例呼吸衰竭患者在各种原因导致不配合无创通气的情况下,静脉泵入丙泊酚进行无创通气的临床资料。首先给予丙泊酚静脉注射进行镇静诱导,然后改用微量注射泵持续注射丙泊酚,根据Ramsay氏分级标准调整用量,观察镇静后患者无创通气的效果及生命体征的变化、无创通气的并发症等。 结果133例患者中,112例无创通气效果良好,生命体征逐渐稳定;21例失败,改用气管插管机械通气治疗。失败原因分别为:镇静效果差,患者仍烦躁不安、通气效果差;缺氧及二氧化碳潴留无改善;腹胀、呕吐、误吸、呼吸疲劳等。 结论适度镇静可提高无创通气成功率和通气效果,避免有创机械通气带来的不良作用,在ICU严密监测下使用具有良好的安全性,值得临床应用。

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  • 无创正压通气治疗慢性阻塞性肺疾病合并呼吸衰竭的护理

    【摘要】 目的 探讨无创正压通气治疗慢性阻塞性肺疾病合并呼吸衰竭的护理措施。 方法 回顾性分析2006年1月-2008年12月使用无创正压通气治疗合并呼吸衰竭的慢性阻塞性肺疾病患者的临床资料,比较其使用呼吸机前后的症状、舒适性、体温、心率及血气分析的变化。 结果 使用无创正压通气治疗后患者症状改善,无明显不适感,体温、心率趋于平稳,缺氧、高碳酸血症得到明显改善。 结论 无创正压通气治疗慢性阻塞性肺疾病合并呼吸衰竭易于护理,效果显著。

    Release date:2016-09-08 09:50 Export PDF Favorites Scan
  • The value of application noninvasive positive pressure ventilation in patients with high risk of weaning induced pulmonary oedema

    ObjectiveTo investigate the value of noninvasive positive pressure ventilation in patients with high risk of weaning induced pulmonary oedema.MethodsFrom June 2018 to June 2019, 63 patients with mechanical ventilation in the Department of Critical Care Medicine of the First Hospital of Lanzhou University were enrolled. Randomized digital table method was randomly divided into two groups and the resulting random number assignment was hidden in opaque envelopes, the experimental group received non-invasive positive pressure ventilation (n=32), and the control group received mask oxygen therapy ventilation (n=31). The heart rate, respiratory rate, means arterial pressure, hypoxemia, reintubation, blood gas analysis and other indicators were compared between the two groups after 2 hours of weaning. The length of hospital stay, mortality and complications were compared between the two groups.ResultsAfter 2 hours of weaning, the heart rate and respiratory rate were significantly lower in the non-invasive positive pressure ventilation group than in the mask group (P<0.05). There was no difference in mean arterial pressure between the two groups of patients, which was not statistically significant (P>0.05). The incidence of hypoxemia, laryngeal edema and reintubation in the noninvasive positive pressure ventilation group was significantly lower than that in the mask group, which was statistically significant (P<0.05), and the blood gas analysis index was better than the mask group (P<0.05). The non-invasive positive pressure ventilation group was significantly shorter than the mask group in the length of hospital stay and intensive care unit (P<0.05). The hospital mortality rate in 28 days was lower than that in the mask group (P<0.05), but there was no difference in tracheotomy, pneumothorax and subcutaneous emphysema between the two groups (P>0.05).ConclusionsNoninvasive positive pressure ventilation can effectively prevent hypoxemia, laryngeal edema, and re-intubation in patients at high risk of withdrawal related pulmonary edema. It can also shorten the length of hospital stay, which is worth clinical attention and promotion.

    Release date:2021-03-25 10:46 Export PDF Favorites Scan
  • Clinical Effect of Noninvasive Positive Pressure Ventilation on Severe Acute Pancreatitis Combined with Acute Lung Injury in Emergency

    ObjectiveTo analyze the effect of noninvasive positive pressure ventilation (NPPV) on the treatment of severe acute pancreatitis (SAP) combined with lung injury [acute lung injury (ALI)/acute respiratory distress syndrome (ARDS)] in emergency treatment. MethodsFifty-six patients with SAP combined with ALI/ARDS treated between January 2013 and March 2015 were included in our study. Twenty-eight patients who underwent NPPV were designated as the treatment group, while the other 28 patients who did not undergo NPPV were regarded as the control group. Then, we observed patients' blood gas indexes before and three days after treatment. The hospital stay and mortality rate of the two groups were also compared. ResultsBefore treatment, there were no significant differences between the two groups in terms of pH value and arterial partial pressure of oxygen (PaO2) (P>0.05). Three days after treatment, blood pH value of the treatment group and the control group was 7.41±0.07 and 7.34±0.04, respectively, with a significant difference (P<0.05); the PaO2 value was respectively (60.60±5.11) and (48.40±3.57) mm Hg (1 mm Hg=0.133 kPa), also with a significant difference (P<0.05). The hospital stay of the treatment group and the control group was (18.22±3.07) and (23.47±3.55) days with a significant difference (P<0.05); and the six-month mortality was 17% and 32% in the two groups without any significant difference (P>0.05). ConclusionIt is effective to treat patients with severe acute pancreatitis combined with acute lung injury in emergency by noninvasive positive pressure ventilation.

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  • 无创正压通气治疗慢性阻塞性肺疾病合并Ⅱ型呼吸衰竭

    【摘要】 目的 探讨无创正压通气在慢性阻塞性肺疾病(COPD)合并Ⅱ型呼吸衰竭的治疗作用。方法 2005年10月—2009年10月对COPD合并Ⅱ型呼吸衰竭患者40例,随机分为对照组和治疗组(各20例)。在行常规抗感染、对症治疗的同时,分别予以持续静脉滴注尼可刹米或无创正压通气治疗6 h,比较两组治疗前后生命体征及血气分析变化。结果 治疗6 h后,治疗组在收缩压、呼吸频率及心率方面改善均显著优于对照组(P<005)。pH值对照组无改善,治疗组显著改善,两组比较有统计学意义(P<005)。治疗后治疗组动脉血氧分压由(51.2±3.7) mm Hg上升至(82.3±5.7) mm Hg,对照组由(51.4±4.6) mm Hg上升至(66.7±8.3) mm Hg,治疗组动脉血二氧化碳分压由(78.9±10.0) mm Hg降低至(46.9±7.2) mm Hg,对照组由(78.6±6.5) mm Hg降低至(61.2±5.7) mm Hg,治疗组改善明显(P<0.01)。结论 无创正压通气治疗慢性阻塞性肺疾病合并Ⅱ型呼吸衰竭效果明显。

    Release date:2016-09-08 09:37 Export PDF Favorites Scan
  • 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。

    Release date:2021-11-18 04:57 Export PDF Favorites Scan
  • Effects of Enteral Tube Feeding on Moderate AECOPD Patients Received Noninvasive Positive Pressure Ventilation

    Objective To explore the effects of enteral tube feeding on moderate AECOPD patients who underwent noninvasive positive pressure ventilation ( NPPV) . Methods Sixty moderate AECOPD patients with NPPV admitted from January 2009 to April 2011 were recruited for the study. They were randomly divided into an enteral tube feeding group (n=30) received enteral tube feeding therapy, and an oral feeding group (n=30) received oral feeding therapy. Everyday nutrition intake and accumulative total nutrition intake in 7 days, plasma level of prealbumin and transferrin, success rate of weaning, duration of mechanical ventilation, length of ICU stay, rate of trachea cannula, and mortality rate in 28 days were compared between the two groups. Results Compared with the oral feeding group, the everyday nutrition intake and accumulative total nutrition intake in 7 days obviously increased (Plt;0.05) , while the plasma prealbumin [ ( 258.4 ±16.5) mg/L vs. (146.7±21.6) mg/L] and transferrin [ ( 2.8 ±0.6) g/L vs. ( 1.7 ±0.3) g/L] also increased significantly after 7 days in the enteral tube feeding group( Plt;0.05) . The success rate of weaning ( 83.3% vs. 70.0%) , the duration of mechanical ventilation [ 5. 6( 3. 2-8. 6) days vs. 8. 4( 4. 1-12. 3) days] , the length of ICU stay [ 9. 2( 7. 4-11. 8) days vs. 13. 6( 8.3-17. 2) days] , the rate of trachea cannula ( 16. 6% vs. 30. 0% ) , the mortality rate in 28 days ( 3. 3% vs. 10. 0% ) all had significant differences between the enteral tube feeding group and the oral feeding group. Conclusions For moderate AECOPD patients with NPPV, enteral tube feeding can obviously improve the condition of nutrition and increase the success rate of weaning, shorten the mechanical ventilation time and the mean stay in ICU, decrease the rate of trachea cannula and mortality rate in 28 days. Thus enteral tube feeding should be preferred for moderate AECOPD patients with NPPV.

    Release date:2016-09-13 04:00 Export PDF Favorites Scan
  • 无创正压通气治疗重度支气管哮喘疗效分析

    目的 观察无创双水平气道正压通气( BiPAP) 治疗重度支气管哮喘的疗效。方法 29 例重度支气管哮喘患者随机分为研究组( 15 例) 和对照组( 14 例) 。研究组在常规药物治疗基础上, 早期给予BiPAP 呼吸机治疗。比较两组患者治疗前和治疗4 h、治疗24 h 后动脉血气变化。结果研究组有14 例治疗4 h后临床症状和体征明显好转, 治疗有效率为93. 3% ; 1 例因呼吸衰竭加重, 改用气管插管机械通气治疗。对照组治疗4 h后有10 例临床症状和体征好转, 治疗有效率为71. 4% , 4 例无明显好转, 2 例改用BiPAP 呼吸机治疗。研究组未改变治疗方式的14 例经治疗4 h、治疗24 h 后血气分析的改善均优于未改变治疗方式的10 例对照组( P lt;0. 05) 。结论 早期应用BiPAP 呼吸机治疗重度支气管哮喘能迅速改善动脉血气分析指标, 使用安全有效。

    Release date:2016-09-14 11:24 Export PDF Favorites Scan
  • Clinical efficacy of sequential HFNC versus NIPPV after extubation in AECOPD patients: a meta-analysis of randomized controlled trials

    ObjectiveTo systematically evaluate the efficacy of high-flow nasal cannula oxygen therapy (HFNC) in Post-extubation acute exacerbation of chronic obstructive pulmonary disease (AECOPD) patients. MethodsThe Domestic and foreign databases were searched for all published available randomized controlled trials (RCTs) about HFNC therapy in post-extubation AECOPD patients. The experimental group was treated with HFNC, while the control group was treated with non-invasive positive pressure ventilation (NIPPV). The main outcome measurements included reintubation rate. The secondary outcomes measurements included oxygenation index after extubation, length of intensive care unit (ICU) stay, mortality, comfort score and adverse reaction rate. Meta-analysis was performed by Revman 5.3 software. ResultA total of 20 articles were enrolled. There were 1516 patients enrolled, with 754 patients in HFNC group, and 762 patients in control group. The results of Meta-analysis showed that there were no significant difference in reintubation rate [RR=1.41, 95%CI 0.97 - 2.07, P=0.08] and mortality [RR=0.91, 95%CI 0.58 - 1.44, P=0.69]. Compared with NIPPV, HFNC have advantages in 24 h oxygenation index after extubation [MD=4.66, 95%CI 0.26 - 9.05, P=0.04], length of ICU stay [High risk group: SMD –0.52, 95%CI –0.74 - –0.30; Medium and low risk group: MD –1.12, 95%CI –1.56- –0.67; P<0.00001], comfort score [MD=1.90, 95%CI 1.61 - 2.19, P<0.00001] and adverse reaction rate [RR=0.22, 95%CI 0.16 - 0.31, P<0.00001]. ConclusionsCompared with NIPPV, HFNC could improve oxygenation index after extubation, shorten the length of ICU stay, effectively improve Patient comfort, reduce the occurrence of adverse reactions and it did not increase the risk of reintubation and mortality. It is suggested that HFNC can be cautiously tried for sequential treatment of AECOPD patients after extubation, especially those who cannot tolerate NIPPV.

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