Evidence map›Paper›PMID 35829775›Full record

ReviewActa neurochirurgica2022

Prognostic factors for surgically managed intramedullary spinal cord tumours: a single-centre case series.

Asfand Baig Mirza, Axumawi Gebreyohanes, James Knight, James Bartram, Amisha Vastani, Dimitrios Kalaitzoglou, Jose Pedro Lavrador, Ahilan Kailaya-Vasan, Eleni Maratos, David Bell and 4 more

Abstract readReview
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In one paragraph

Review in Acta neurochirurgica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Asfand Baig MirzaDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK. asfand.mirza@nhs.net.ORCID 0000-0003-4177-9615
Axumawi GebreyohanesVictor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
James KnightDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
James BartramDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Amisha VastaniDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Dimitrios KalaitzoglouDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Jose Pedro LavradorDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Ahilan Kailaya-VasanDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Eleni MaratosDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
David BellDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Nick ThomasDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Richard GullanDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Irfan MalikDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.
Gordan GrahovacDepartment of Neurosurgery, King's College Hospital NHS Foundation Trust, London, SE5 9RS, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIntramedullary spinal cord tumours (IMSCTs) are comparatively rare neoplasms. We present a single-centre clinical case series of adult patients with surgically managed IMSCTs.

methodsWe performed a retrospective analysis of electronic patient records in the time period spanning July 2010 to July 2021. All adult patients that had undergone surgical management for IMSCTs were eligible for inclusion. Baseline and post-operative clinical and radiological characteristics, along with follow-up data, were assessed. We also performed a literature review with a focus on surgical outcomes for IMSCTs.

resultsSixty-six patients matched our selection criteria, with a median age of 42 years (range 23-85). Thirty-four ependymomas, 17 haemangioblastomas, 12 astrocytomas, 2 lymphomas and 1 teratoma were included. Statistical analysis yielded several significant findings: IMSCTs spanning a greater number of vertebral levels are significantly associated with poor McCormick outcomes (p = 0.03), presence of gait disturbance before surgery is significantly associated with poor outcome for both post-operative McCormick and Nurick scores (p = 0.007), and radicular pain present pre-operatively is significantly associated with a good post-operative McCormick score (p = 0.045). Haemangioblastomas are significantly more likely to have a clear intra-operative dissection plane compared to ependymomas and astrocytomas (p = 0.009). However, astrocytomas have a significantly higher prevalence of good McCormick outcomes compared to ependymomas and haemangioblastomas (p = 0.03).

conclusionHistological diagnosis, cranio-caudal extent of the tumour and the presence or absence of baseline deficits-such as gait impairment and radicular pain-are significant in determining neurological outcomes after surgery for IMSCTs.

Indexed as

AstrocytomaEpendymomaHemangioblastomaSpinal Cord NeoplasmsAdultAgedAged, 80 and overHumansMiddle AgedPainPrognosisRetrospective StudiesTreatment OutcomeYoung AdultIntramedullary spinal cord tumoursSpinal astrocytomasSpinal ependymomasSpinal oncologySurgical outcomes

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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.