新生儿感染性肺炎危险因素分析与预防措施

Risk factors for infectious pneumonia in neonates and prevention measures

  • 摘要: 目的 探讨雾化吸入布地奈德混悬液治疗急性感染性喉炎的临床效果,为临床选择有效药物提供依据。方法 选取2014年10月-2015年9月在医院儿科诊断为急性感染性喉炎的患儿120例为研究对象,随机将患儿分为观察组60例与对照组60例,两组患者均给予常规的支持治疗和对症治疗; 观察组给予布地奈德混悬液雾化吸入治疗,对照组给予地塞米松进行治疗。结果 观察组患者呼吸困难、喉鸣音、咳嗽及声嘶消失时间均短于对照组患者,差异均有统计学意义(P<0.05); 患者治疗总有效率观察组为98.33%、对照组为86.67%,观察组明显高于对照组,差异有统计学意义(P<0.05); 观察组患者不良反应发生率为6.67%、对照组为8.33%,差异无统计学意义。结论 雾化吸入布地奈德混悬液治疗急性感染性喉炎的临床效果显著,不良反应率低,临床症状消失时间短。

     

    Abstract: OBJECTIVE To observe the clinical effect of nebulized inhalation of budesonide suspension on treatment of children with acute infectious laryngitis so as to provide guidance for reasonable clinical use of antibiotics. METHODS A total of 120 children with conformed acute infectious laryngitis who were treated in the pediatrics department from Oct 2014 to Sep 2015 were recruited as the study objects and randomly divided into the observation group with 60 cases and the control group with 60 cases.Both groups were given the conventional supportive treatment and symptomatic treatment.The observation group was treated with nebulized inhalation of budesonide suspension, and the control group was treated with dexamethasone. RESULTS The time of disappearance of dyspnea, throat sound, cough, or hoarseness was significantly shorter in the observation group than in the control group (P<0.05).The total effective rate of treatment of the observation group was 98.33%, significantly higher than 86.67% of the control group (P<0.05).The incidence rate of adverse reactions was 6.67% in the observation group, 8.33% in the control group, and there was no significant difference. CONCLUSION The nebulized inhalation of budesonide suspension can achieve significant clinical effect on treatment of the acute infectious laryngitis, with incidence of adverse reactions low, the time of disappearance of clinical symptoms short.

     

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