Assessing Intrauterine Retention according to Microscopic Stillbirth Features: A Cluster Analysis Approach.

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2023-12-01 Epub Date: 2023-08-12 DOI:10.1080/15513815.2023.2246571
Tess E K Cersonsky, George R Saade, Robert M Silver, Uma M Reddy, Donald J Dudley, Halit Pinar
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Abstract

Background: Previous studies identified microscopic changes associated with intrauterine retention of stillbirths based on clinical time of death. The objective of this study was to utilize unsupervised machine learning (not reliant on subjective measures) to identify features associated with time from death to delivery. Methods: Data were derived from the Stillbirth Collaborative Research Network. Features were chosen a priori for entry into hierarchical cluster analysis, including fetal and placental changes. Results: A four-cluster solution (coefficient = 0.983) correlated with relative time periods of "no retention," "mild retention," "moderate retention," and "severe retention." Loss of nuclear basophilia within fetal organs were found at varying rates among these clusters. Conclusions: Hierarchical cluster analysis is able to classify stillbirths based on histopathological changes, roughly correlating to length of intrauterine retention. Such clusters, which rely solely on objective fetal and placental findings, can help clinicians more accurately assess the interval from death to delivery.

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根据显微死产特征评估宫内保留:聚类分析方法。
背景:先前的研究确定了基于临床死亡时间的死胎宫内潴留的显微变化。本研究的目的是利用无监督机器学习(不依赖于主观测量)来识别与死亡到分娩时间相关的特征。方法:数据来源于死产合作研究网络。特征被先验地选择进入层次聚类分析,包括胎儿和胎盘的变化。结果:四聚类溶液与“无滞留”、“轻度滞留”、“中度滞留”和“严重滞留”的相对时间相关(系数= 0.983)。在这些群集中,发现胎儿器官内嗜碱性核细胞的丧失率不同。结论:分层聚类分析能够根据组织病理学变化对死产进行分类,与宫内保留时间的长短大致相关。这种仅依靠客观胎儿和胎盘检查结果的聚类可以帮助临床医生更准确地评估从死亡到分娩的时间间隔。
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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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