Janez Babnik, Irena Stucin-Gantar, Lilijana Kornhauser-Cerar, Jasna Sinkovec, Branka Wraber, Metka Derganc
{"title":"宫内炎症与早产儿脑室周围出血的发生。","authors":"Janez Babnik, Irena Stucin-Gantar, Lilijana Kornhauser-Cerar, Jasna Sinkovec, Branka Wraber, Metka Derganc","doi":"10.1159/000092070","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Peri-intraventricular hemorrhage (P/IVH) is a common neonatal morbidity among premature infants. The aim of the study was to examine the association between placental and/or fetal inflammation and the onset of P/IVH in premature infants.</p><p><strong>Methods: </strong>A prospective study included 125 infants with gestational age 23-29 weeks. Placentas were examined for the presence of chorioamnionitis and funisitis, cord blood was sampled for the measurement of cytokines (IL-6 and IL-8). Fetal inflammation was defined as levels of IL-6 higher than 7.6 pg/ml. P/IVH was defined as early if diagnosed within the 1st day after birth; thereafter P/IVH was defined as late.</p><p><strong>Results: </strong>Adjusted for the influence of gestational age, early-onset sepsis (OR 3.2, p = 0.045) and no or incomplete antenatal steroid course (OR 6.0, p = 0.001) significantly predicted early P/IVH. Funisitis (OR 1.6, p = 0.06) and fetal inflammation (OR 2.6, p = 0.06) were only partially associated with early hemorrhage. Contrary to that, respiratory distress syndrome (OR 3.4, p = 0.04), mechanical ventilation (OR 5.9, p = 0.008), low blood pressure (OR 3.5, p = 0.02), and vasopressors (OR 5.7, p = 0.002) were associated with late P/IVH. In multivariate analysis no or incomplete steroid course remained independent predictors for early and use of vasopressors for late P/IVH. The interaction of fetal inflammation and vaginal delivery with no or incomplete steroid course increased the risk of early P/IVH.</p><p><strong>Conclusions: </strong>These results indicate different risk factors for early and late P/IVH. Neither funisitis nor fetal inflammation independently predicts the onset of P/IVH. However, the interaction of fetal inflammation and vaginal delivery with no or incomplete antenatal steroid course increase the risk of early but not also late P/IVH.</p>","PeriodicalId":9091,"journal":{"name":"Biology of the neonate","volume":"90 2","pages":"113-21"},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000092070","citationCount":"40","resultStr":"{\"title\":\"Intrauterine inflammation and the onset of peri-intraventricular hemorrhage in premature infants.\",\"authors\":\"Janez Babnik, Irena Stucin-Gantar, Lilijana Kornhauser-Cerar, Jasna Sinkovec, Branka Wraber, Metka Derganc\",\"doi\":\"10.1159/000092070\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Peri-intraventricular hemorrhage (P/IVH) is a common neonatal morbidity among premature infants. The aim of the study was to examine the association between placental and/or fetal inflammation and the onset of P/IVH in premature infants.</p><p><strong>Methods: </strong>A prospective study included 125 infants with gestational age 23-29 weeks. Placentas were examined for the presence of chorioamnionitis and funisitis, cord blood was sampled for the measurement of cytokines (IL-6 and IL-8). Fetal inflammation was defined as levels of IL-6 higher than 7.6 pg/ml. P/IVH was defined as early if diagnosed within the 1st day after birth; thereafter P/IVH was defined as late.</p><p><strong>Results: </strong>Adjusted for the influence of gestational age, early-onset sepsis (OR 3.2, p = 0.045) and no or incomplete antenatal steroid course (OR 6.0, p = 0.001) significantly predicted early P/IVH. Funisitis (OR 1.6, p = 0.06) and fetal inflammation (OR 2.6, p = 0.06) were only partially associated with early hemorrhage. Contrary to that, respiratory distress syndrome (OR 3.4, p = 0.04), mechanical ventilation (OR 5.9, p = 0.008), low blood pressure (OR 3.5, p = 0.02), and vasopressors (OR 5.7, p = 0.002) were associated with late P/IVH. In multivariate analysis no or incomplete steroid course remained independent predictors for early and use of vasopressors for late P/IVH. The interaction of fetal inflammation and vaginal delivery with no or incomplete steroid course increased the risk of early P/IVH.</p><p><strong>Conclusions: </strong>These results indicate different risk factors for early and late P/IVH. Neither funisitis nor fetal inflammation independently predicts the onset of P/IVH. However, the interaction of fetal inflammation and vaginal delivery with no or incomplete antenatal steroid course increase the risk of early but not also late P/IVH.</p>\",\"PeriodicalId\":9091,\"journal\":{\"name\":\"Biology of the neonate\",\"volume\":\"90 2\",\"pages\":\"113-21\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000092070\",\"citationCount\":\"40\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biology of the neonate\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000092070\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2006/3/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology of the neonate","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000092070","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2006/3/17 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 40
摘要
背景:脑室周围出血(P/IVH)是早产儿常见的新生儿疾病。该研究的目的是检查胎盘和/或胎儿炎症与早产儿P/IVH发病之间的关系。方法:前瞻性研究纳入125例胎龄23-29周的婴儿。检查胎盘是否存在绒毛膜羊膜炎和尿道炎,采集脐带血检测细胞因子(IL-6和IL-8)。胎儿炎症定义为IL-6水平高于7.6 pg/ml。如果在出生后第1天内诊断出P/IVH,则定义为早期;此后,P/IVH被定义为晚期。结果:调整胎龄的影响后,早发性脓毒症(OR 3.2, p = 0.045)和没有或不完全的产前类固醇疗程(OR 6.0, p = 0.001)可显著预测早期p /IVH。输卵管炎(OR 1.6, p = 0.06)和胎儿炎症(OR 2.6, p = 0.06)与早期出血仅部分相关。与此相反,呼吸窘迫综合征(OR 3.4, p = 0.04)、机械通气(OR 5.9, p = 0.008)、低血压(OR 3.5, p = 0.02)和血管加压药物(OR 5.7, p = 0.002)与晚期p /IVH相关。在多变量分析中,没有或不完全类固醇疗程仍然是晚期P/IVH早期和使用血管加压药物的独立预测因素。没有或不完全类固醇疗程的胎儿炎症和阴道分娩的相互作用增加了早期P/IVH的风险。结论:这些结果提示早期和晚期P/IVH的危险因素不同。输卵管炎和胎儿炎症都不能独立预测P/IVH的发生。然而,没有或不完整的产前类固醇疗程的胎儿炎症和阴道分娩的相互作用会增加早期但不会增加晚期P/IVH的风险。
Intrauterine inflammation and the onset of peri-intraventricular hemorrhage in premature infants.
Background: Peri-intraventricular hemorrhage (P/IVH) is a common neonatal morbidity among premature infants. The aim of the study was to examine the association between placental and/or fetal inflammation and the onset of P/IVH in premature infants.
Methods: A prospective study included 125 infants with gestational age 23-29 weeks. Placentas were examined for the presence of chorioamnionitis and funisitis, cord blood was sampled for the measurement of cytokines (IL-6 and IL-8). Fetal inflammation was defined as levels of IL-6 higher than 7.6 pg/ml. P/IVH was defined as early if diagnosed within the 1st day after birth; thereafter P/IVH was defined as late.
Results: Adjusted for the influence of gestational age, early-onset sepsis (OR 3.2, p = 0.045) and no or incomplete antenatal steroid course (OR 6.0, p = 0.001) significantly predicted early P/IVH. Funisitis (OR 1.6, p = 0.06) and fetal inflammation (OR 2.6, p = 0.06) were only partially associated with early hemorrhage. Contrary to that, respiratory distress syndrome (OR 3.4, p = 0.04), mechanical ventilation (OR 5.9, p = 0.008), low blood pressure (OR 3.5, p = 0.02), and vasopressors (OR 5.7, p = 0.002) were associated with late P/IVH. In multivariate analysis no or incomplete steroid course remained independent predictors for early and use of vasopressors for late P/IVH. The interaction of fetal inflammation and vaginal delivery with no or incomplete steroid course increased the risk of early P/IVH.
Conclusions: These results indicate different risk factors for early and late P/IVH. Neither funisitis nor fetal inflammation independently predicts the onset of P/IVH. However, the interaction of fetal inflammation and vaginal delivery with no or incomplete antenatal steroid course increase the risk of early but not also late P/IVH.