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孕妇生殖道支原体感染的临床干预试验
引用本文:叶元康,涂少华,李怀芳,汪宁,庄桂霞. 孕妇生殖道支原体感染的临床干预试验[J]. 中华流行病学杂志, 2001, 22(4): 293-295
作者姓名:叶元康  涂少华  李怀芳  汪宁  庄桂霞
作者单位:1. 同济大学附属同济医院性医学实验室
2. 东南大学公共卫生学院
3. 上海国际妇幼保健院
基金项目:国家自然科学基金资助项目(39670646)
摘    要:目的:探索孕妇生殖道支原体感染与异常围产结局的病因学关系。方法:经产前检查支原体阳性妇488例,随要分成红霉素干预组和非干预组,比较两组间孕妇支原体感染阴转率,母婴传播率和异常围产结局的发生率,结果:红霉素干预组解脲支原体(Uu)的阴转率为67.3%(128/190),明显高于非干预组的25.6%(50/195),P<0.05,非干预组Uu的母婴传播率为46.2%(90/195),干预组降至25.2%(48/190),P<0.05,结论;红霉素干预措施能有效地降低孕妇解脲支原体感染,阻断其母传播,降低与支原体感染有关的异常围产结局。

关 键 词:孕妇 支原体感染 临床干预试验 异常围产结局 生殖道感染
收稿时间:2000-12-17
修稿时间:2000-12-17

Clinic intervention study on urogenital mycoplasma infection of pregnant women
Ye Yuankang,Tu Shaohu,Li Huaifang. Clinic intervention study on urogenital mycoplasma infection of pregnant women[J]. Chinese Journal of Epidemiology, 2001, 22(4): 293-295
Authors:Ye Yuankang  Tu Shaohu  Li Huaifang
Affiliation:Tongji Hospital, Tongji University, Shanghai, 200065, China.
Abstract:Objective To explore the hypothesis of pathogenic relationship between urogenital mycoplasma infection and adverse perinatal outcomes. Methods Four hundred and eighty eight mycoplasma positive pregnant women detected by culture method were randomly divided into erythromycine intervention group and non intervention group. Comparison was made on rate of reverse sero conversion, of vertical transmission to mycoplasma and adverse perinatal outcomes incidence between groups. Results Ureaplasma urealyticum sero conversion rate and rate of vertical transmission in intervention group were significantly lower than in non intervention group ( P < 0.05 ). The incidences rates of preturm labor,post partum fever,puerperal infection and neonate pneumonia in intervention group were significantly lower than in non intervention group ( P < 0.05 ). Conclusion Erythromycin is effective in control of ureaplasma urealyticum infection among pregnant women through cutting off vertical transmission passway and lowering adverse perinatal outcomes against ureaplasma urealyticum.
Keywords:Pregnant woman  Mycoplasma infection  Clinic intervention trial  Adverse perinatal outcome
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