β-受体阻滞剂对脓毒症早期急性低氧性呼吸衰竭患者的保护作用

易玲娴, 吴柳琳, 张慧, 等. β-受体阻滞剂对脓毒症早期急性低氧性呼吸衰竭患者的保护作用[J]. 临床急诊杂志, 2020, 21(10): 794-799. doi: 10.13201/j.issn.1009-5918.2020.10.006
引用本文: 易玲娴, 吴柳琳, 张慧, 等. β-受体阻滞剂对脓毒症早期急性低氧性呼吸衰竭患者的保护作用[J]. 临床急诊杂志, 2020, 21(10): 794-799. doi: 10.13201/j.issn.1009-5918.2020.10.006
YI Ling-xian, WU Liu-lin, ZHANG Hui, et al. Protective effects of β-blockers on patients with acute hypoxemic respiratory failure in the early sepsis[J]. J Clin Emerg, 2020, 21(10): 794-799. doi: 10.13201/j.issn.1009-5918.2020.10.006
Citation: YI Ling-xian, WU Liu-lin, ZHANG Hui, et al. Protective effects of β-blockers on patients with acute hypoxemic respiratory failure in the early sepsis[J]. J Clin Emerg, 2020, 21(10): 794-799. doi: 10.13201/j.issn.1009-5918.2020.10.006

β-受体阻滞剂对脓毒症早期急性低氧性呼吸衰竭患者的保护作用

详细信息
    通讯作者: 胡美,E-mail:clinical2019m@163.com
  • 中图分类号: R459.7

Protective effects of β-blockers on patients with acute hypoxemic respiratory failure in the early sepsis

More Information
  • 目的:探索β受体阻滞剂对脓毒症早期急性低氧性呼吸衰竭(AHRF)患者临床特征及结局的影响。方法:回顾性收集2015-01-01-2019-12-31期间所有入住中国人民解放军战略支援部队特色医学中心重症医学科的脓毒症患者数据,根据入院后有无使用β受体阻滞剂分为β受体阻滞剂组和non-β受体阻滞剂组,比较两组患者血气指标、生化指标、循环状态以及机械通气天数、ICU住院天数、28 d存活情况。结果:总共有105例脓毒症早期AHRF患者纳入研究,其中β受体阻滞剂组47例,non-β受体阻滞剂组58例。与non-β受体阻滞剂组相比,β受体阻滞剂可以改善PO2和氧合指数,降低乳酸水平,增加淋巴细胞数量,减少血管活性药物的使用(P<0.05)。并且β受体阻滞剂可明显减少脓毒症早期AHRF患者的机械通气天数,ICU住院天数和28 d病死率(P<0.05)。多因素COX回归分析显示,β受体阻滞剂可以降低脓毒症早期AHRF患者的死亡风险(OR=0.781,95%CI:0.726~0.841,P<0.05),而高乳酸(OR=1.198,95%CI:1.178~1.218,P<0.01)、高SOFA评分(OR=1.222,95%CI:1.207~1.238,P<0.01)以及男性(OR=1.676,95%CI:1.559~1.806,P<0.01)可增加28 d病死率。结论:β受体阻滞剂是脓毒症早期AHRF患者的保护因素,而高乳酸、高SOFA评分以及男性是危险因素。
  • 加载中
  • [1]

    Rudd KE,Johnson SC,Agesa KM,et al.Global,regional,and national sepsis incidence and mortality,1990-2017:analysis for the Global Burden of Disease Study[J].Lancet,2020,395(10219):200-211.

    [2]

    Levy MM,Evans LE,Rhodes A.The Surviving Sepsis Campaign Bundle:2018 Update[J].Crit Care Med,2018,46(6):997-1000.

    [3]

    Rhodes A,Evans LE,Alhazzani W,et al.Surviving Sepsis Campaign:International Guidelines for Management of Sepsis and Septic Shock:2016[J].Crit Care Med,2017,45(3):486-552.

    [4]

    Van der Jagt M,Miranda DR.Beta-blockers in intensive care medicine:potential benefit in acute brain injury and acute respiratory distress syndrome[J].Recent Pat Cardiovasc Drug Discov,2012,7(2):141-151.

    [5]

    Anoop UR,Kavita V.Pulmonary Edema in COVID19-A Neural Hypothesis[J].ACS Chem.Neurosci,2020,11,2048-2050.

    [6]

    Zhang L,Nie Y,Zheng Y,et al.Esmolol attenuates lung injury and inflammation in severe acute pancreatitis rats[J].Pancreatology,2016,16(5):726-32.

    [7]

    Auriemma CL,Zhuo H,Delucchi K,et al.Acute respiratory distress syndrome-attributable mortality in critically ill patients with sepsis[J].Intensive Care Med,2020,46(6):1222-1231.

    [8]

    Liu P,Wu Q,Tang Y,et al.The influence of esmolol on septic shock and sepsis:A meta-analysis of randomized controlled studies[J].Am J Emerg Med,2018,36(3):470-474.

    [9]

    Coppola S,Froio S,Chiumello D.beta-blockers in critically ill patients:from physiology to clinical evidence[J].Crit Care,2015,19:119.

    [10]

    Pemberton P,Veenith T,Snelson C,et al.Is It Time to Beta Block the Septic Patient?[J].Biomed Res Int,2015,2015:424308.

    [11]

    武冬,王顺达,符莹莹,等.艾司洛尔对脓毒症急性肺损伤大鼠肺泡炎症因子及氧化应激蛋白的调控研究[J].中南医学科学杂志,2019,47(4):363-366.

    [12]

    李霞,王姣.酒石酸美托洛尔对脂多糖致急性肺损伤小鼠的炎症及凋亡的影响[J].医学理论与实践,2020,33(4):638-639.

    [13]

    李杜鹏,赵妮,罗书航,等.艾司洛尔对脓毒症大鼠肺脏保护作用的实验研究[J].中华急诊医学杂志,2018,27(1):78-84.

    [14]

    Singer M,Deutschman CS,Seymour CW,et al.The Third International Consensus Definitions for Sepsis and Septic Shock(Sepsis-3)[J].JAMA,2016,315(8):801-810.

    [15]

    Dellinger RP,Levy MM,Rhodes A,et al.Surviving sepsis campaign:international guidelines for management of severe sepsis and septic shock:2012[J].Crit Care Med,2013,41(2):580-637.

    [16]

    Brown RM,Wang L,Coston TD,et al.Balanced Crystalloids versus Saline in Sepsis.A Secondary Analysis of the SMART Clinical Trial[J].Am J Respir Crit Care Med,2019,200(12):1487-1495.

    [17]

    Gennaro P,Graziamaria C,Nicola F.Adrenergic Nervous System and Hemostasis[J].J Hematol Thrombo Dis,2014,2:e108.

    [18]

    Chignalia AZ,Weinberg G,Dull RO,Norepinephrine Induces Lung Microvascular Endothelial Cell Death by NADPH Oxidase-Dependent Activation of Caspase-3[J].Oxid Med Cell Longev,2020,2020:2563764.

    [19]

    Richter T,Bergmann R,Pietzsch J,et al.Effects of pulmonary acid aspiration on the regional pulmonary blood flow within the first hour after injury:An observational study in rats[J].Clin Hemorheol Microcirc,2015,60(2):253-262.

    [20]

    Matsuishi Y,Jesmin S,Kawano S,et al.Landiolol hydrochloride ameliorates acute lung injury in a rat model of early sepsis through the suppression of elevated levels of pulmonary endothelin-1[J].Life Sci 2016,166:27-33.

    [21]

    Suzuki T,Inoue K,Igarashi T,et al.Beta-Blocker Therapy Preserves Normal Splenic T-Lymphocyte Numbers Reduced in Proportion to Sepsis Severity in a Sepsis Model[J].Crit Care Res Pract,2019,2019:8157482.

    [22]

    Asai N,Shiota A,Ohashi W,et al.The SOFA score could predict the severity and prognosis of infective endocarditis[J].J Infect Chemother 2019,25(12):965-971.

    [23]

    Wang Y,Wang D,Fu J,et al.Predictive value of SOFA,qSOFA score and traditional evaluation index on sepsis prognosis[J].Zhonghua Wei Zhong Bing Ji Jiu Yi Xue,2017,29(8):700-704.

    [24]

    Bösch F,Angele MK,Chaudry IH.Gender differences in trauma,shock and sepsis[J].Mil Med Res,2018,5(1):35.

  • 加载中
计量
  • 文章访问数:  96
  • PDF下载数:  89
  • 施引文献:  0
出版历程
收稿日期:  2020-08-02

目录