Evidence map›Paper›PMID 18575870›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2008

Abnormal venous drainage in syndromic craniosynostosis and the role of CT venography.

Dhruve Satish Jeevan, Phillip Anlsow, Jayaratnam Jayamohan

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. A Unique Case of Pure Bilateral Lambdoid Craniosynostosis and Progression to Mercedes-Benz Syndrome Following Spring Cranioplasty.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Venous anomalies in hypoplastic posterior fossa: unsolved questions.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Review
  7. Sinus pericranii-unusual anatomic obstacle to posterior decompression on an amniotic band sequence.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  8. Article
  9. Article
  10. Review
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  12. Chiari 1 malformation and untreated sagittal synostosis: a new subset of complex Chiari?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Article
  13. Article
  14. Clinical Significance of Venous Anomalies in Syndromic Craniosynostosis.Plastic and reconstructive surgery. Global open · 2018
    Article
  15. Article
  16. Mechanics of the brain: perspectives, challenges, and opportunities.Biomechanics and modeling in mechanobiology · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. Cephalometric Features of Moyamoya Disease: A case control study.Journal of vascular and interventional neurology · 2014
    Article
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

3 authors.

Dhruve Satish JeevanDepartment of Paediatric Neurosurgery, John Radcliffe Hospital, West Wing Level 3, Headley Way, Oxford, OX3 9DU, UK.
Phillip Anlsow
Jayaratnam Jayamohan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveVenous hypertension is emerging as a significant contributor to intracranial pressure in children with syndromic craniosysnostosis. This is associated with jugular foramen stenosis or atresia and with the development of collateral emissary veins. We demonstrate how computed tomography venography can document the prevalence of these emissary veins and how their visualisation plays an important role in operative planning. MATERIALS AND

methodsPatients with known syndromic craniosynostosis underwent computed tomography venography as part of their routine pre-operative evaluation. The venous drainage pattern was examined in these patients, with a special note of the presence of abnormal venous pathways.

resultsEleven patients were recruited into the study from ages 3 months to 22 years. All had a diagnosis of syndromic craniosynostosis with six Crouzon's, four Pfeiffer's and one patient with Crouzon's and acanthosis nigricans. Nine of 11 patients had demonstrable evidences of transosseous venous drainage through an identifiable abnormal emissary vein. Four of 11 had a transosseous route as the main mechanism of drainage for the cerebral venous system.

conclusionsPatients with syndromic craniosynostosis often demonstrate abnormal venous anatomy, which can have serious consequences on craniofacial surgery, especially when a posterior decompression is being considered. Based on these findings, the authors assert that those children with some syndromic craniosynostosis being considered for surgery should undergo venographic studies as part of their pre-operative evaluation.

Indexed as

AdolescentCerebral VeinsCerebrovascular CirculationChildChild, PreschoolCranial SinusesCraniosynostosesFemaleHumansInfantInfant, NewbornJugular VeinsMalePhlebographyReproducibility of ResultsSyndrome

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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.