ReviewFrontiers in pediatrics2018
Takayasu Arteritis.
Review in Frontiers in pediatrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled 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.
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
62 citing papers in PubMed, 1 synthesis or guideline pooled it, 114 citations in OpenAlex.
- Therapeutic Management of Ocular Ischemia in Takayasu's Arteritis: A Case-Based Systematic Review.Frontiers in immunology · 2021Pooled it
- Home-Based Exercise Training in Childhood-Onset Takayasu Arteritis: A Multicenter, Randomized, Controlled Trial.Frontiers in immunology · 2021Trial
- How Organ Manifestations Beyond the Bone May Guide Risk Stratification and Treatment Decisions in Chronic Nonbacterial Osteomyelitis.Paediatric drugs · 2026Review
- Neurological Complications in Pediatric Takayasu Arteritis: Insights from a Single-Center Experience.Journal of clinical medicine · 2026Article
- Syncope as the Initial Presentation of Takayasu Arteritis in a 57-Year-Old Female: A Case Report and Literature Review.Clinical case reports · 2026Article
- Phenotypic Heterogeneity in Familial Takayasu Arteritis Across Two Families: A Case-Based Review.Mediterranean journal of rheumatology · 2026Article
- Prognostic Value of the Hata Angiographic Classification for Long-Term Outcomes in Takayasu Arteritis: A Single-Center, Retrospective Study.Arquivos brasileiros de cardiologia · 2026Article
- Ischemic Stroke as the First Manifestation of Takayasu Arteritis: A Case Report.Neurology international · 2026Article
- FDG-PET/MR in paediatric pyrexia of unknown origin: early detection of Takayasu arteritis-a single-centre experience.Frontiers in pediatrics · 2026Article
- Type V Takayasu arteritis with multivessel involvement: diagnostic challenges and imaging insights in a young female: A case report.Radiology case reports · 2025Article
- CT Angiography of the Upper Extremities: Review of Acute Arterial Entities.Radiographics : a review publication of the Radiological Society of North America, Inc · 2025Review
- Functional and Practical Insights Into the Genetic Basis of Takayasu Arteritis.ACR open rheumatology · 2025Review
- Therapeutic plasma exchange in autoimmune diseases: a retrospective study in a tertiary pediatric hospital in Mexico.Frontiers in pediatrics · 2025Article
- Renal artery angioplasty in Takayasu disease: Difficult anatomy addressed with a novel technique.Medical journal, Armed Forces India · 2024Article
- Hybrid PET/MRI of large vessel vasculitis : Radiation dose compared to PET/CT with view on cumulative effective dose.Wiener klinische Wochenschrift · 2024Article
- An uncommon cause of a common disease: a case report of a rare cause of hypertension.European heart journal. Case reports · 2024Article
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- Unusual manifestations of Takayasu arteritis: A diagnostic challenge.Clinical case reports · 2024Article
- Sudden onset of symptoms in concurrent Takayasu arteritis and Ulcerative colitis: A case report with neurological complications.Clinical case reports · 2024Article
2 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Takayasu arteritis is an idiopathic granulomatous vasculitis of the aorta and its main branches and it constitutes one of the more common vasculitides in children. Inflammation and intimal proliferation lead to wall thickening, stenotic or occlusive lesions, and thrombosis, while destruction of the elastica and muscularis layers originates aneurysms and dissection. Carotid artery tenderness, claudication, ocular disturbances, central nervous system abnormalities, and weakening of pulses are the most frequent clinical features. The diagnosis is usually confirmed by the observation of large vessel wall abnormalities: stenosis, aneurysms, occlusion, and evidence of increased collateral circulation in angiography, MRA or CTA imaging. The purpose of this revision is to address the current knowledge on pathogenesis, investigations, classification, outcome measures and management, and to emphasize the need for timely diagnosis, effective therapeutic intervention, and close monitoring of this severe condition.
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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.