ReviewBreathe (Sheffield, England)2025
Pulmonary veno-occlusive disease: a clinical review.
Review in Breathe (Sheffield, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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
3 citing papers in PubMed.
- Survival Improvement With Steroid Use for Pulmonary Veno-Occlusive Disease With the Aid of Pulmonary Vasodilators and Tyrosine-Kinase Inhibitor, a Retrospective Study.Clinical cardiology · 2026Article
- One Health Insights into Pulmonary Hypertension: Bridging Human and Canine Medicine.Veterinary sciences · 2026Review
- Induced pluripotent stem cells from sporadic pulmonary veno-occlusive disease exhibit altered endothelial commitment and stress-related transcriptional programs.Frontiers in cell and developmental biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pulmonary vasculopathy presents as a spectrum of diseases affecting the precapillary pulmonary arterioles, the capillaries and the venules. Pulmonary veno-occlusive disease (PVOD) is classified under group 1 pulmonary arterial hypertension (PAH) as subgroup 1.5 (PAH with features of capillary/venous involvement), and represents a progressive and fatal spectrum of pulmonary vascular disorders. PVOD and pulmonary capillary haemangiomatosis (PCH) can be clinically indistinguishable and often coexist, along with the same risk factors and genetic alterations; they are referred to together as PVOD/PCH in the literature. For brevity, we use the clinical term PVOD in this article. PVOD cannot be distinguished from other forms of PAH based on symptoms and haemodynamics. Risk factors include exposure to toxins/chemotherapeutic drugs and genetic mutation in the
Identifiers
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.