胎盘病理学及其在早产儿中的重要性。

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2023-10-01 Epub Date: 2023-06-21 DOI:10.1080/15513815.2023.2223297
Duygu Tugrul Ersak, Hakkı Şerbetçi, Bergen Laleli Koç, Özgür Kara, Şeyma Bütün Türk, Gülsüm Kadıoğlu Şimşek, Fuat Emre Canpolat, Özlem Moraloğlu Tekin, Dilek Şahin
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引用次数: 1

摘要

目的:我们评估了哪些胎盘病理与不良早产相关。材料和方法:根据阿姆斯特丹标准分类的胎盘检查结果与婴儿结局相关。排除胎儿血管病变、组织学绒毛膜羊膜炎(HCA)以外的炎症反应,以及合并母体血管灌注不良(MVM)和HCA的胎盘。结果:共对772个胎盘进行了评估。394例胎盘存在MVM,378例存在HCA。仅MVM组的早期新生儿败血症、早产儿视网膜病变、坏死性小肠结肠炎和新生儿死亡发生率高于仅HCA组。仅HCA组的支气管肺发育不良(BPD)发生率为38.6%,仅MVM组为20.3%(p 结论:胎盘炎症影响胎儿和新生儿的预后。HCA是BPD的一个独立风险因素。
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Placental Pathology and Its Importance in Preterm Infants.

Objective: We evaluated what placental pathologies were associated with adverse preterm births.

Materials and methods: Placental findings, classified according to the Amsterdam criteria, were correlated with infant outcomes. The fetal vascular lesions, inflammatory responses other than histological chorioamnionitis (HCA), and placentas with combined maternal vascular malperfusion (MVM) and HCA were excluded.

Results: A total of 772 placentas were evaluated. MVM was present in 394 placentas, HCA in 378. Early neonatal sepsis, retinopathy of prematurity, necrotizing enterocolitis, and neonatal death occurred more often in the MVM-only group than HCA-only group. The frequency of bronchopulmonary dysplasia (BPD) was 38.6% in the HCA-only group, and it was 20.3% in the MVM-only group (p < 0.001). HCA was the most important independent risk factor for BPD (OR 3.877, 95% CI 2.831-5.312).

Conclusion: Inflammation in the placenta influences fetal and neonatal outcomes. HCA is an independent risk factor for BPD.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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