文章摘要
陈诚,肖政祥,张丹,等.早产儿解脲脲原体菌血症和白细胞介素-6、白细胞介素-8浓度测定的临床意义[J].安徽医药,2017,21(2):306-308.
早产儿解脲脲原体菌血症和白细胞介素-6、白细胞介素-8浓度测定的临床意义
Clinical significance of the measurements of plasma Uu-DNA copies and IL-6,IL-8 concentration in very premature infants
投稿时间:2016-07-11  
DOI:
中文关键词: 解脲脲原体菌血症  白细胞介素-6  白细胞介素-8  血浆  极不成熟儿
英文关键词: Uu-DNA copies  IL-6 levels  IL-8 levels  Plasma  Very premature infants
基金项目:深圳市科技研发资金项目(JCYJ20140415133340848)(SIRS)、支气管肺发育不良(BPD)及脑室内出血(IVH)发生率也明显增高[1-2],但国内未见类似相关性研究的报道。本研究报道75例极不成熟婴儿(胎龄<32周)血浆Uu菌血症(Uu-DNA阳性)拷贝数和IL-6、IL-8浓度与宫内感染性肺炎、BPD、IVH的相关性,探讨Uu在新生儿临床中的意义,现报道如下。
作者单位
陈诚 深圳市龙岗区妇幼保健院新生儿科,广东 深圳 518172 
肖政祥 深圳市龙岗区妇幼保健院新生儿科,广东 深圳 518172 
张丹 深圳市龙岗区妇幼保健院新生儿科,广东 深圳 518172 
吕晓丹 深圳市龙岗区妇幼保健院新生儿科,广东 深圳 518172 
廖婷婷 深圳市龙岗区妇幼保健院新生儿科,广东 深圳 518172 
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中文摘要:
      目的 探讨早产儿血浆解脲脲原体菌血症(Uu-DNA阳性)和白细胞介素-6(IL-6)、白细胞介素-8(IL-8)浓度检测的意义。 方法 对75例胎龄<32周的极不成熟婴儿于生后不同时间分别采静脉血标本,测定血浆Uu-DNA拷贝数和IL-6、IL-8浓度,记录婴儿住院期间的病情变化。 结果 9例(12%)在出生后1 h内血浆标本中检出Uu-DNA,其中7例Uu-DNA出现在宫内感染性肺炎患儿,以后时间所采标本均未检出Uu-DNA;Uu-DNA阳性患儿出生后1 h内血浆IL-6、IL-8浓度明显增高(P<0.05);Uu-DNA阳性患儿支气管肺发育不良发生率显著增高。 结论 极不成熟儿Uu-DNA阳性率占12%;Uu-DNA阳性患儿血浆炎性因子明显增高,支气管肺发育不良(BPD)发生也明显升高。
英文摘要:
      Objective To explore clinical significance of the measurements of plasma Ureaplasma urealyticum (Uu)-DNA copies and interleukin(IL-6),IL-8 concentration in very premature infants. Methods Venous blood samples were collected during 1h,3d,7d,14d,21d of life from 75 consecutive singleton deliveries of very premature infants (gestational age<32 weeks),and plasma Uu-DNA copies and IL-6,IL-8 concentration were measured. Results 9 cases were detected plasma Uu-DNA copies from samples within 1 h,prevalence of Uu bacteremia was 12%(9/75).Uu-DNA copies in all cases were undetected.Plasma IL-6 and IL-8 concentration of Uu bacteremic infants were significant higher compared with others from samples within 1 h(P<0.05).The incidence of bronchopulmonary dysplasia (BPD) were significant higher in Uu bacteremic infants. Conclusions Prevalence of Uu bacteremia in very premature infants was 12 %.Uu bacteremic infants had significant higher plasma proinflammatory cytokines level and the higher incidence of BPD(p<0.05).
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