Fortes Precious Ann, Janzen Carla, Lei Margarida Y Y, Vangala Sitaram, Sung Kyunghyun, Devaskar Sherin U, Sullivan Peggy S
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, US.
Department of Obstetrics & Gynecology, David Geffen School of Medicine at UCLA, Los Angeles, CA, US.
Am J Clin Pathol. 2025 May 17;163(5):688-695. doi: 10.1093/ajcp/aqae174.
Before the Amsterdam Placental Workshop Group Consensus Statement, standardization in placental pathology assessment did not exist. This study evaluated the Amsterdam criteria's utility in correlating ischemic placental disease (IPD) with placental pathologic lesions in a cohort of largely unsubmitted term placentas with favorable outcomes.
In this prospective case-controlled study at a single institution, all placentas were examined using Amsterdam protocols for gross sampling and microscopic review by 2 reviewers who were blinded to clinical history. Pathologic findings including hypoxic and chronic villitis of unknown etiology (VUE) scores were correlated with IPD status and whether the placenta was submitted to pathology using either a χ² test or Fisher exact test, as appropriate.
A total of 172 placentas collected between 2017 and 2020 were included. Approximately 18.6% (n = 32) were in the IPD group, and 81.4% (n = 140) were in the non-IPD group. No statistically significant differences in microscopic findings were seen in ascending infection, maternal vascular malperfusion, fetal vascular malperfusion, or VUE between groups or by submission status. When tabulated as a hypoxic score, placentas from the IPD group were associated with greater hypoxic scores compared to non-IPD placentas (P = .011). A positive association was observed between greater VUE scores and hypoxic scores (P = .007).
In largely unsubmitted term placentas, the microscopic findings per Amsterdam criteria may be nonspecific. When tabulated as hypoxic or VUE scores, however, some clinicopathologic correlation may be seen in the setting of IPD. Further work is needed to refine the thresholds of meaningful reporting of placental pathology using the Amsterdam criteria.
在阿姆斯特丹胎盘研讨会小组共识声明发布之前,胎盘病理学评估尚无标准化方法。本研究评估了阿姆斯特丹标准在一组结局良好的足月未送检胎盘队列中,将缺血性胎盘疾病(IPD)与胎盘病理病变相关联的效用。
在一家机构进行的这项前瞻性病例对照研究中,所有胎盘均按照阿姆斯特丹方案进行大体标本采集和显微镜检查,由2名对临床病史不知情的审阅者进行。病理结果包括缺氧和病因不明的慢性绒毛炎(VUE)评分,通过χ²检验或Fisher精确检验(视情况而定)与IPD状态以及胎盘是否送检病理相关联。
纳入了2017年至2020年间收集的172个胎盘。约18.6%(n = 32)属于IPD组,81.4%(n = 140)属于非IPD组。在各组之间或按送检状态来看,在上行感染、母体血管灌注不良、胎儿血管灌注不良或VUE方面,显微镜检查结果未见统计学显著差异。当列为缺氧评分时,与非IPD胎盘相比,IPD组胎盘的缺氧评分更高(P = .0\(11\))。观察到VUE评分越高与缺氧评分之间存在正相关(P = .0\(07\))。
在大量未送检的足月胎盘中,按照阿姆斯特丹标准的显微镜检查结果可能不具有特异性。然而,当列为缺氧或VUE评分时,在IPD情况下可能会观察到一些临床病理相关性。需要进一步开展工作,以完善使用阿姆斯特丹标准进行胎盘病理学有意义报告的阈值。