首页> 外文期刊>Jundishapur Journal of Natural Pharmaceutical Products >Efficacy Evaluation of Nebulized Magnesium, as an Additional Complementary Treatment, in Clinical and Peak Flow Metric Improvements of Acute Asthma Attack: A Randomized Double-Blinded Clinical Trial
【24h】

Efficacy Evaluation of Nebulized Magnesium, as an Additional Complementary Treatment, in Clinical and Peak Flow Metric Improvements of Acute Asthma Attack: A Randomized Double-Blinded Clinical Trial

机译:雾化镁作为一种补充治疗,在急性哮喘发作的临床和峰值流量指标改善中的疗效评估:一项随机双盲临床试验

获取原文
       

摘要

Background: Exacerbation of acute asthma attacks is a medical challenging problem that a?ects health systems all around the world.Accordingtothereports,acuteasthmahasallocatedabout1to12% ofadults’ referraltotheemergencydepartmentsbyitself. Thisstudyaimedtoinvestigatethee?ectof additionalnebulizedmagnesiumsulfate,asanadditionalcomplementarytreatment, on the management of acute asthma attack. Due to controversies and the fact that previous research has been unable to con?rm thebene?tsof routineuseof magnesiuminthecourseof treatmentof asthmaacutephase,thistrialwasconducted. Methods: Patients with a possible clinically suggested acute asthma attack, aged 18 to 65, were divided into two groups of interventionandcontrol. Aninitialpeak?owmeterevaluationatarrivalidenti?edtheseverityof patients’ asthmaattack. 148patients withmoderatetosevereattackswereincludedinthestudyintwogroups. Patientsof thecontrolgroupreceivedstandardasthma treatmentconsistingofnebulizedalbuterol2.5mgandnebulizedipratropiumbromide0.5mg,bothinminutes0,20,and40after arrival and oral single-dose prednisolone 50 mg at arrival. Patients of the case group received additional doses of nebulized magnesium sulfate 0.3 g in minutes 0, 20, and 40 after arrival in addition to the standard treatment performed on the control group. Theclinicalsettingof dyspneaBorgscaleinboththecaseandcontrolgroups,aswellastheirPEFRandFEV1values,wererecorded duringthetrialinminutes0,20,40,and60afterarrival. Chi-square,T-test,andMannWhitneytestwereappliedfordataanalysis. Results:Thestudywasconductedon148subjectswhoweredividedintotwogroupsof75and73ascaseandcontrolgroups,respectively. PEFRvaluesinminutes40and60afterarrivalwere295.04and336.2inthecasegroupand249.64and282.86inthecontrol group, andtherewasasigni?cantdi?erenceinthePEFRimprovementsbetweenthecaseandcontrolgroups(P< 0.001). Inaddition,FEV1inminutes40and60afterarrivalwasrespectively2.26and2.66inthecasegroupand1.88and2.23inthecontrolgroup. Thereweresigni?cantdi?erencesinFEV1improvementsbetweenthecaseandcontrolgroups(P< 0.001). Conclusions: Accordingtotheresultsof thisstudy,itcanbeconcludedthatadministrationof nebulizedmagnesiumsulfateasan adjunctivemedicationtothestandardtreatmentisbene?cialinthemanagementof moderatetosevereacuteasthmaattacksand signi?cantlyleadstobettercontrolof acuteattackinshortterm
机译:背景:急性哮喘发作的加剧是一个医疗挑战性问题,影响着整个世界的卫生系统。据报告,急性哮喘患者自行分配了约1-12%的成年人转诊至急诊科。该研究旨在调查其他雾化硫酸镁的影响,作为辅助补充治疗,以治疗急性哮喘发作。由于存在争议,并且先前的研究未能证实在哮喘急性期的治疗过程中常规使用镁的益处,因此进行了该试验。方法:将18到65岁有可能在临床上建议的急性哮喘发作的患者分为干预和控制两组。初始峰值压力表评估可有效评估患者哮喘发作的严重程度。 148名重度中度发作的患者被分为两组。对照组患者在到达后接受标准的哮喘治疗,包括雾化的沙丁胺2.5mg和溴化的异丙托溴铵0.5mg,分别在0、20和40分钟,到达时口服口服单剂量泼尼松龙50 mg。除对照组的标准治疗外,病例组的患者在到达后的0、20和40分钟内分别接受0.3 g雾化的硫酸镁雾化剂。在到达后的0、20、40和60分钟内,记录病例和对照组的呼吸困难Borgscale的临床背景以及PEFR和FEV1值。应用卡方检验,T检验和曼惠特尼检验进行数据分析。结果:研究分别针对148个受试者,分别分为两组,分别为75组和73组。案例组中,到达后40分钟和60分钟内的PEFR值分别为295.04和336.2,对照组为249.64和282.86,案例与对照组之间的PEFR改善存在显着差异(P <0.001)。此外,到达案例后40分钟和60分钟内的FEV1分别为2.26和2.66(对照组)和1.88(2.23)。病例组和对照组之间FEV1的改善存在显着差异(P <0.001)。结论:根据本研究的结果,可以得出结论,将雾化硫酸镁作为标准治疗的辅助药物在中度至重度东部急性发作的管理中是有益的,并能在短期内有效地控制急性发作。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号