ReviewCureus2026
Placental Histopathologic Lesions Associated With Stillbirth: A Systematic Review.
Review in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Stillbirth is a major contributor to perinatal mortality. Placental examination is central to stillbirth evaluation. Published evidence is heterogeneous in lesion taxonomy, sampling approaches, comparator selection, and confounder control. We conducted a systematic review following PRISMA guidelines. We searched PubMed, Embase, and Scopus and screened reference lists to identify comparative observational studies. These studies evaluated placental histopathology in stillbirth compared with live birth or other clearly defined nonstillbirth comparator groups. We included studies that estimated stillbirth associations and those providing comparative insights into lesion reporting. Data were extracted on study design, stillbirth definition, comparator characteristics, placental sampling and reporting methods, lesion definitions, and reported association measures. Risk of bias was assessed using the Newcastle-Ottawa Scale. Due to substantial clinical and methodological heterogeneity, findings were synthesized narratively with structured tabulation. Across included studies, stillbirth was consistently associated with multidomain placental pathology. This was most prominent for vascular malperfusion and obstructive or hemorrhagic injury. Recurrent signals were also observed for villous maturation and hypoxia pattern abnormalities. Inflammatory lesions frequently co-occurred with vascular findings. These results support placental vascular pathology, villous developmental abnormalities, and inflammation as recurring domains linked to stillbirth. The findings underscore the need for more standardized definitions, sampling, and reporting. Standardization is needed to improve comparability and clinical interpretability.
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What OpenQuestion holds
Registered trials
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.