Evidence map›Paper›PMID 32393196›Full record

ArticleBMC neurology2020

The Filum disease and the Neuro-Cranio-vertebral syndrome: definition, clinical picture and imaging features.

Miguel B Royo-Salvador, Marco V Fiallos-Rivera, Horia C Salca, Gabriel Ollé-Fortuny

Open access · goldAbstract read
In one paragraph

Article in BMC neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. The management of Chiari malformation type 1 and syringomyelia in children: a review of the literature.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Pooled it
  2. Article
  3. Article
  4. Review
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

4 authors at 1 institution in 1 country.

Miguel B Royo-SalvadorInstitut Chiari & Siringomielia & Escoliosis de Barcelona, Passeig Manuel Girona 16, 08034, Barcelona, Spain. mroyo@institutchiaribcn.com.
Marco V Fiallos-RiveraInstitut Chiari & Siringomielia & Escoliosis de Barcelona, Passeig Manuel Girona 16, 08034, Barcelona, Spain.
Horia C SalcaInstitut Chiari & Siringomielia & Escoliosis de Barcelona, Passeig Manuel Girona 16, 08034, Barcelona, Spain.
Gabriel Ollé-FortunyAnesthesia Department, CIMA Hospital, Barcelona, Spain.
Institut Català de Traumatologia i Medicina de l'Esport · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe propose two new concepts, the Filum Disease (FD) and the Neuro-cranio-vertebral syndrome (NCVS), that group together conditions thus far considered idiopathic, such as Arnold-Chiari Syndrome Type I (ACSI), Idiopathic Syringomyelia (ISM), Idiopathic Scoliosis (IS), Basilar Impression (BI), Platybasia (PTB) Retroflexed Odontoid (RO) and Brainstem Kinking (BSK).

methodWe describe the symptomatology, the clinical course and the neurological signs of the new nosological entities as well as the changes visible on imaging studies in a series of 373 patients.

resultsOur series included 72% women with a mean age of 33.66 years; 48% of the patients had an interval from onset to diagnosis longer than 10 years and 64% had a progressive clinical course. The commonest symptoms were: headache 84%, lumbosacral pain 72%, cervical pain 72%, balance alteration 72% and paresthesias 70%. The commonest neurological signs were: altered deep tendon reflexes in upper extremities 86%, altered deep tendon reflexes in lower extremities 82%, altered plantar reflexes 73%, decreased grip strength 70%, altered sensibility to temperature 69%, altered abdominal reflexes 68%, positive Mingazzini's test 66%, altered sensibility to touch 65% and deviation of the uvula and/or tongue 64%. The imaging features most often seen were: altered position of cerebellar tonsils 93%, low-lying Conus medullaris below the T12L1 disc 88%, idiopathic scoliosis 76%, multiple disc disease 72% and syringomyelic cavities 52%.

conclusionsThis is a paradigm shift that opens up new paths for research and broadens the range of therapeutics available to these patients.

Indexed as

AdolescentAdultAgedArnold-Chiari MalformationBrain StemChildChild, PreschoolFemaleHeadacheHumansMagnetic Resonance ImagingMaleMiddle AgedPlatybasiaScoliosisSyringomyeliaArnold-Chiari syndromeFilum terminaleScoliosisSyringomyelia

Identifiers

PMID32393196
PMCPMC7212596
OpenAlexW3027594191

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.