ReviewHematology. American Society of Hematology. Education Program2025
What's new in hereditary hemorrhagic telangiectasia?
Review in Hematology. American Society of Hematology. Education Program, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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
4 citing papers in PubMed.
- Safety of antithrombotic therapy in hereditary hemorrhagic telangiectasia: results from a prospective cohort study.Research and practice in thrombosis and haemostasis · 2026Observational
- Article
- Genotype-driven cerebrovascular risk across age and sex in hereditary hemorrhagic telangiectasia.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Article
- Bronchial Dieulafoy disease: A case report and literature review.Respiratory medicine case reports · 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
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hereditary hemorrhagic telangiectasia (HHT) is an inherited vasculopathy that results in dysregulated angiogenesis leading to the development of mucocutaneous telangiectasias and visceral organ arteriovenous malformations. HHT is the second most common inherited bleeding disorder. Recurrent, spontaneous epistaxis occurs in over 90% of affected individuals and is the hallmark of this disorder. Epistaxis and gastrointestinal bleeding result in the development of iron deficiency anemia in nearly half of all affected individuals. Considerable advances have been made in the understanding of the pathobiology, manifestations, and treatment of HHT in the last decade. International consensus treatment guidelines have been developed. Medical therapeutics have become the primary approach for treating HHT-related bleeding. The initial clinical studies evaluating medications for the treatment of HHT have involved repurposing drugs that were previously approved for other indications. In the wake of these efforts, several therapies specifically for HHT are currently being developed and are in preclinical studies and early phase human trials or may soon start pivotal phase III trials. The landscape of HHT is changing fast with increased awareness and diagnosis and the development of new and novel therapies, all of which will decrease morbidity and improve the quality of life of affected individuals.
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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.