中国当代医药
中國噹代醫藥
중국당대의약
PERSON
2009年
13期
7-8
,共2页
咳嗽变异性哮喘%肺炎支原体%儿童%感染
咳嗽變異性哮喘%肺炎支原體%兒童%感染
해수변이성효천%폐염지원체%인동%감염
Cough variant asthma%Mycoplasma pnenumonia%Children%Infection
目的:探讨肺炎支原体(MP)感染与儿童咳嗽变异性哮喘(CVA)发病的关系.方法:人选86例CVA患儿作为观察组,98例上呼吸道感染患儿作为对照组,采用明胶颗粒凝集试验检测两组患儿血清肺炎支原体IgM(MP-IgM)抗体,同时采用同位素放射免疫法和血球分析仅常规法测定CVA患儿血清总IgE水平和外周血嗜酸粒细胞计数.结果:CVA组MP-IgE阳性率为3721%,对照组MP-IgE阳性率为20.41%,两组比较,差异有统计学意义(P(0.01).MP-IgE阳性的CVA患儿血清总IgE水平及嗜酸粒细胞计数(EOS)均高于MP-IgE阴性的CVA患儿(P<0.01).结论:肺炎支原体感染与儿童咳嗽变异性哮喘有密切相关性.
目的:探討肺炎支原體(MP)感染與兒童咳嗽變異性哮喘(CVA)髮病的關繫.方法:人選86例CVA患兒作為觀察組,98例上呼吸道感染患兒作為對照組,採用明膠顆粒凝集試驗檢測兩組患兒血清肺炎支原體IgM(MP-IgM)抗體,同時採用同位素放射免疫法和血毬分析僅常規法測定CVA患兒血清總IgE水平和外週血嗜痠粒細胞計數.結果:CVA組MP-IgE暘性率為3721%,對照組MP-IgE暘性率為20.41%,兩組比較,差異有統計學意義(P(0.01).MP-IgE暘性的CVA患兒血清總IgE水平及嗜痠粒細胞計數(EOS)均高于MP-IgE陰性的CVA患兒(P<0.01).結論:肺炎支原體感染與兒童咳嗽變異性哮喘有密切相關性.
목적:탐토폐염지원체(MP)감염여인동해수변이성효천(CVA)발병적관계.방법:인선86례CVA환인작위관찰조,98례상호흡도감염환인작위대조조,채용명효과립응집시험검측량조환인혈청폐염지원체IgM(MP-IgM)항체,동시채용동위소방사면역법화혈구분석부상규법측정CVA환인혈청총IgE수평화외주혈기산립세포계수.결과:CVA조MP-IgE양성솔위3721%,대조조MP-IgE양성솔위20.41%,량조비교,차이유통계학의의(P(0.01).MP-IgE양성적CVA환인혈청총IgE수평급기산립세포계수(EOS)균고우MP-IgE음성적CVA환인(P<0.01).결론:폐염지원체감염여인동해수변이성효천유밀절상관성.
Objective: To determine the relationship between mycoplasma pnenumonia (MP) infection and cough variant asthma (CVA)in children. Methods: 86 children with CVA were selected as the experiment group and 98 children with a-cute upper respiratory infection as the control group.The MP-IgM antibody level was determined by particle agglutination method in both groups and total serum IgE level determined by isotope radioimmunoassay in the CVA group.The count of eosinophils(EOS) was detected by blood cell analyzer in the CVA group. Results: The positive rate of MP-IgM was 37.21% in experiment group and 20.41% in control group with significant difference (P<0.01), The total MP-IgE was markedly higher in MP-IgM positive CVA children than in the MP-IgM negative CVA children (P<0.01). The count of Eosinophies in MP-IgM positive CVA children was more than in MP-IgM negative CVA children (P<0.01). Conclusion:There was close relationship between mycoplasma pnenumonia (MP) infection and cough variant asthma (CVA).