阿姆斯特丹共识后的死胎胎盘病变:系统回顾和荟萃分析。

IF 3 2区 医学 Q2 DEVELOPMENTAL BIOLOGY
Brenda F. Narice , Victoria Byrne , Mariam Labib , Marta C. Cohen , Dilly O. Anumba
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引用次数: 0

摘要

胎盘疾病仍是死胎的主要原因之一。然而,由于缺乏标准化的命名方法,胎盘组织学的临床应用受到很大限制。阿姆斯特丹共识分类法允许对全球的胎盘组织学进行适当的比较,根据该分类法,我们进行了首次系统回顾和荟萃分析(Prospero CRD42023410469),以评估全球最常见的死胎相关胎盘病变。18项研究共纳入了3082个胎盘。母体血管灌注不良和胎儿血管灌注不良是死胎中最常见的胎盘病变,且死胎的发生率明显高于活胎[OR 3.0 (95 % CI 2.0-4.5), p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Placental lesions in stillbirth following the Amsterdam consensus: A systematic review and meta-analysis
Placental disorders remain one of the main causes of stillbirth. However, the lack of standardised nomenclature has significantly limited the clinical utility of placental histology. Following the Amsterdam consensus classification, which now allows proper comparisons of placenta histology across the world, we conducted the first systematic review and meta-analysis (Prospero CRD42023410469) to assess the commonest stillbirth-associated placental lesions worldwide. Eighteen studies with 3082 placentas were included. Maternal vascular malperfusion and fetal vascular malperfusion were the most prevalent placental lesions in stillbirth, and significantly more frequent in stillbirths than livebirths [OR 3.0 (95 % CI 2.0–4.5), p < 0.001 and OR 5.12 (95 % CI 3.09–8.47), p < 0.001, respectively]. However, when adjusting for gestational age, only maternal vascular malperfusion remained significant at term. Better understanding of the pathophysiology underlying placental lesions is needed to inform timely risk assessment and therapeutic interventions capable of reducing placental-related stillbirths.
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来源期刊
Placenta
Placenta 医学-发育生物学
CiteScore
6.30
自引率
10.50%
发文量
391
审稿时长
78 days
期刊介绍: Placenta publishes high-quality original articles and invited topical reviews on all aspects of human and animal placentation, and the interactions between the mother, the placenta and fetal development. Topics covered include evolution, development, genetics and epigenetics, stem cells, metabolism, transport, immunology, pathology, pharmacology, cell and molecular biology, and developmental programming. The Editors welcome studies on implantation and the endometrium, comparative placentation, the uterine and umbilical circulations, the relationship between fetal and placental development, clinical aspects of altered placental development or function, the placental membranes, the influence of paternal factors on placental development or function, and the assessment of biomarkers of placental disorders.
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