Evidence map›Paper›PMID 37140647›Full record

ArticleActa neurochirurgica2023

Recurrence of brain arteriovenous malformations in pediatric patients: a long-term follow-up study.

Elias Oulasvirta, Päivi Koroknay-Pál, Jussi Numminen, Ahmad Hafez, Rahul Raj, Behnam Rezai Jahromi, Mika Niemelä, Aki Laakso

Open access · hybridAbstract read
In one paragraph

Article in Acta neurochirurgica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Perioperative outcomes and risk stratification following pediatric arteriovenous malformation resection: an ACS NSQIP-P database analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  3. Article
  4. Review
  5. Cure or coincidence? The need for long-term rigor in pediatric arteriovenous malformation radiosurgery.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
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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

8 authors at 2 institutions in 1 country.

Elias OulasvirtaDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland. elias.oulasvirta@hus.fi.
Päivi Koroknay-PálDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Jussi NumminenDepartment of Radiology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Ahmad HafezDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Rahul RajDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Behnam Rezai JahromiDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Mika NiemeläDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Aki LaaksoDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
University of Helsinki · FIHelsinki University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreviously thought to be congenital, AVMs have shown evidence of de-novo formation and continued growth, thus shifting thoughts on their pathophysiology. Pediatric AVM patients have been reported to be more prone to develop AVM recurrence after a seemingly complete cure. Therefore, we assessed the risk of AVM treated in childhood to recur in adulthood after a long-term follow-up in our own cohort.

methodsControl DS-angiography was arranged during 2021-2022 as part of a new protocol for all AVM patients who were under 21 years of age at the time of their treatment and in whom the treatment had occurred at least five years earlier. Angiography was offered only to patients under 50 years of age at the time of the new protocol. The complete eradication of AVM after the primary treatment had been originally confirmed with DSA in every patient.

resultsA total of 42 patients participated in the late DSA control, and 41 of them were included in this analysis after excluding the patient diagnosed with HHT. The median age at the time of admission for AVM treatment was 14.6 (IQR 12-19, range 7-21 years) years. The median age at the time of the late follow-up DSA was 33.8 years (IQR 29.8-38.6, range 19.4-47.9 years). Two recurrent sporadic AVMs and one recurrent AVM in a patient with hereditary hemorrhagic telangiectasia (HHT) were detected. The recurrence rate was 4.9% for sporadic AVMs and 7.1% if HHT-AVM was included. All the recurrent AVMs had originally bled and been treated microsurgically. The patients with sporadic AVM recurrence had been smoking their whole adult lives.

conclusionsPediatric and adolescent patients are prone to develop recurrent AVMs, even after complete AVM obliteration verified by angiography. Therefore, imaging follow-up is recommended.

Indexed as

Intracranial Arteriovenous MalformationsRadiosurgeryTelangiectasia, Hereditary HemorrhagicAdolescentAdultAngiographyBrainChildFollow-Up StudiesHumansMiddle AgedRetrospective StudiesTreatment OutcomeYoung AdultArteriovenous malformationAVMDe-novoLong-term follow-upPediatricRecurrence

Identifiers

PMID37140647
PMCPMC10227118
OpenAlexW4368357171

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Registered trials

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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.