Evidence map›Paper›PMID 40155551›Full record

Observational studyVirchows Archiv : an international journal of pathology2025

Clinicopathologic correlation and interdependence of basic patterns of placental injury.

Jerzy Stanek, Dustin Funk

Abstract readObservational Study
In one paragraph

Observational study in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Jerzy StanekDivision of Pathology, Cincinnati Children's Medical Center, 3333 Burnet Avenue, Cincinnati, OH, 45229-3025, USA. stanekjw@gmail.com.ORCID http://orcid.org/0000-0002-6602-2638
Dustin FunkDivision of Pathology, Cincinnati Children's Medical Center, 3333 Burnet Avenue, Cincinnati, OH, 45229-3025, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Placental lesions rarely occur in isolation and placental lesion multiplicity is associated with poorer pregnancy outcome than that of isolated lesions. As little is known about mutual relations of various patterns of placental injury simultaneously occurring in the same placentas, particularly in relation to gestational age, this retrospective observational analysis was undertaken to study those in a population of 2486 cases of the second half high-risk pregnancy dominated by fetal congenital anomalies. To this end, 23 independent clinical and 48 placental phenotypes were statistically compared among 6 basic patterns of placental injury: Group 1: acute inflammation, Group 2: chronic inflammation, Group 3: maternal vascular malperfusion, Group 4: fetal vascular malperfusion, large vessel, Group 5: fetal vascular malperfusion, distal villous, and Group 6: shallow placental implantation. All cases had E cadherin/CD34 immunostaining performed for the diagnosis of recent fetal vascular malperfusion. There was a significant overlap among the studied patterns and lesions of placental injury. Placental distal villous fetal vascular malperfusion and acute inflammation was most frequently statistically significantly associated with abnormal clinical conditions, while lesions of distal villous fetal vascular malperfusion and maternal vascular malperfusion with other placental lesions/patterns of injury. The double immunostaining was responsible for the fetal vascular malperfusion being the most common type of placental injury in this population of placentas. The acute inflammation best correlated with clinical condition in preterm pregnancy and distal villous fetal vascular malperfusion at term. Maternal vascular malperfusion plus the above two patterns of placental injury correlated best with other placental phenotypes in mid third trimester.

Indexed as

PlacentaPlacenta DiseasesAdultFemaleHumansInflammationPregnancyRetrospective StudiesFetal vascular malperfusionHigh-risk pregnancyInflammationMaternal vascular malperfusionPlacenta

Identifiers

PMID40155551
PMCPMC12748087

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.