地方病通报
地方病通報
지방병통보
ENDEMIC DISEASES BULLETIN
2007年
4期
14-16,18
,共4页
麻疹%实验室监测%IgM抗体
痳疹%實驗室鑑測%IgM抗體
마진%실험실감측%IgM항체
Measles%Surveillance,laboratory%IgM antibody
目的 揭示娄底市麻疹IgM抗体的分布特征,探讨该市麻疹相对高发的主要原因.方法 采集麻疹疑似病例血清标本用ELISA法检测IgM抗体,全部数据录入MS Excel并用SPSS软件进行分析.结果 308份合格血清IgM总阳性率为50.99%,其中按要求完整填写相关信息的219份,标本总阳性率为49.32%;按有明确免疫史、无免疫史和免疫史不详分3组统计,其阳性率分别为38.46%,46.52%和52%,3组阳性率无统计学差异(χ2=1.793 0,P=0.408 0);按采样时间分组统计,出疹后5~10日采样检测阳性率显著高于其他组(χ2=16.967 0,P<0.000 1),对其中麻疹IgM阴性的34份血清做风疹IgM检测,结果仅有4份显示弱阳性.结论 麻疹IgM检测采样的最佳时间为出疹后5~10日;免疫空白人群和原始免疫失败为本市麻疹感染发病的主要影响因素.
目的 揭示婁底市痳疹IgM抗體的分佈特徵,探討該市痳疹相對高髮的主要原因.方法 採集痳疹疑似病例血清標本用ELISA法檢測IgM抗體,全部數據錄入MS Excel併用SPSS軟件進行分析.結果 308份閤格血清IgM總暘性率為50.99%,其中按要求完整填寫相關信息的219份,標本總暘性率為49.32%;按有明確免疫史、無免疫史和免疫史不詳分3組統計,其暘性率分彆為38.46%,46.52%和52%,3組暘性率無統計學差異(χ2=1.793 0,P=0.408 0);按採樣時間分組統計,齣疹後5~10日採樣檢測暘性率顯著高于其他組(χ2=16.967 0,P<0.000 1),對其中痳疹IgM陰性的34份血清做風疹IgM檢測,結果僅有4份顯示弱暘性.結論 痳疹IgM檢測採樣的最佳時間為齣疹後5~10日;免疫空白人群和原始免疫失敗為本市痳疹感染髮病的主要影響因素.
목적 게시루저시마진IgM항체적분포특정,탐토해시마진상대고발적주요원인.방법 채집마진의사병례혈청표본용ELISA법검측IgM항체,전부수거록입MS Excel병용SPSS연건진행분석.결과 308빈합격혈청IgM총양성솔위50.99%,기중안요구완정전사상관신식적219빈,표본총양성솔위49.32%;안유명학면역사、무면역사화면역사불상분3조통계,기양성솔분별위38.46%,46.52%화52%,3조양성솔무통계학차이(χ2=1.793 0,P=0.408 0);안채양시간분조통계,출진후5~10일채양검측양성솔현저고우기타조(χ2=16.967 0,P<0.000 1),대기중마진IgM음성적34빈혈청주풍진IgM검측,결과부유4빈현시약양성.결론 마진IgM검측채양적최가시간위출진후5~10일;면역공백인군화원시면역실패위본시마진감염발병적주요영향인소.
Objective To reveal the distribution characteristics of measles IgM and their implication for measles control in Loudi City. Methods Samples from suspected measles cases were tested by measles IgM-capture ELISA and results were analyzed using MS Excel and SPSS software package. Results Total IgM positive rate was 50.99% for the 308 adequate samples submitted to the city CDC laboratory and that for the 219 samples that met the information requests for detailed analysis was 49.32%.Of the 219 samples,positive rates were 38.46%,46.52% and 52% for the groups of cases: (1) vaccinated,(2 ) unvaccinated and (3) no documented vaccination,respectively,showing no statistical differences(χ2=1.793 0,P=0.408 0),and positive rates were significantly higher(χ2=16.967 0,P<0.000 1)for the group of samples taken between 5-10 days post rash onset.Only 4 showed weak positive results when 34 measles IgM-negative sera were tested for differential diagnosis from rubella.Conclusions The optimum sampling time for measles IgM detection was 5-10 days post rash onset.Gaps in population immunity and primary failures in immunization were principle factors leading to measles infection and epidemic in Loudi City.