Evidence map›Paper›PMID 42830897›Full record

ArticleBrain & spine2026

Permanent neurological morbidity after microsurgical resection of hereditary hemorrhagic telangiectasia-associated brain arteriovenous malformations: a systematic review and illustrative case.

Ján Buvala, Christopher S Ogilvy, Juraj Šteňo, Juraj Klepoch, Vladimír Javorka, Michaela Jezberová, Peter Jankovič, Parvez M Shaikh, Andrej Šteňo

Abstract read
In one paragraph

Article in Brain & spine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Ján BuvalaDepartment of Neurosurgery, Faculty of Medicine of Comenius University and University Hospital Bratislava, Limbová 5, Bratislava, 83305, Slovakia.
Christopher S OgilvyNeurosurgical Service, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis St., Boston, MA, 02215, United States.
Juraj ŠteňoClinical Neuroscience Research Unit, Department of Neurosurgery, Faculty of Medicine of Comenius University and University Hospital Bratislava, Limbová 5, Bratislava, 83305, Slovakia.
Juraj KlepochDepartment of Neurosurgery, Faculty of Medicine of Comenius University and University Hospital Bratislava, Limbová 5, Bratislava, 83305, Slovakia.
Vladimír JavorkaDepartment of Radiology, Faculty of Medicine of Comenius University and University Hospital Bratislava, Limbová 5, Bratislava, 83305, Slovakia.
Michaela JezberováDr. Magnet Kramáre, Dr. Magnet s.r.o., Limbová 5, Bratislava, 83305, Slovakia.
Peter JankovičDepartment of Neurosurgery, F.D. Roosevelt University Hospital with Policlinic, Nám. L. Svobodu 1, Banská Bystrica, 97517, Slovakia.
Parvez M ShaikhDepartment of Radiation Oncology, West Virginia University, PO Box 9234, 44 Medical Center Drive, Morgantown, WV, 26506-9234, United States.
Andrej ŠteňoDepartment of Neurosurgery, Faculty of Medicine of Comenius University and University Hospital Bratislava, Limbová 5, Bratislava, 83305, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The optimal management of brain arteriovenous malformations (AVMs) in patients with hereditary hemorrhagic telangiectasia (HHT) remains controversial. Some authors recommend conservative management based on the presumed lower rupture risk compared to sporadic AVMs, others advocate surgical treatment. No systematic review has focused on permanent neurological morbidity following resection of HHT-associated AVMs, leaving a significant gap in the literature. Research question: Do the unique genetic features and angio-architecture of HHT-associated AVMs result in a different profile of postoperative neurological morbidity compared to sporadic AVMs? Materials and methods: A systematic search of PubMed, Embase, and Cochrane databases (1947-April 2026) was conducted per PRISMA 2020 guidelines; 18 publications reporting surgically treated HHT-associated brain AVMs were identified, 12 were included in the comparative analysis. Study quality was assessed using the Joanna Briggs Institute Critical Appraisal Checklist. Permanent morbidity rates were compared with unselected sporadic AVM series using Fisher's exact test with sensitivity analyses. Results: Among 91 patients, pooled incidence of new permanent neurological deficits was 9.9% (95% CI: 4.6-18.0%). No significant difference was found compared to unselected sporadic AVM cohorts. One study contributed 78% of permanent deficit events; its exclusion reduced the rate to 2.9%. No postoperative mortality was reported. Discussion and conclusion: No significant difference in permanent neurological morbidity was demonstrated between HHT-associated and sporadic AVM resections. However, the small sample size precludes definitive conclusions. These hypothesis-generating findings may aid in individualized risk assessment and shared decision-making. An illustrative case is presented to demonstrate the clinical context motivating this review.

Indexed as

Brain arteriovenous malformationHereditary hemorrhagic telangiectasiaNeurological morbidityRendu-Osler-Weber diseaseSurgical outcomeSystematic review

Identifiers

PMID42830897
PMCPMC13634297

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.