Evidence map›Paper›PMID 37770682›Full record

ReviewAdvances and technical standards in neurosurgery2023

Chiari Type 1 Malformation and Syringomyelia in Children: Classification and Treatment Options.

Jehuda Soleman, Jonathan Roth, Shlomi Constantini

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances and technical standards in neurosurgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Jehuda SolemanDepartment of Pediatric Neurosurgery, Tel Aviv Medical Center, Tel Aviv, Israel.
Jonathan RothDepartment of Pediatric Neurosurgery, Tel Aviv Medical Center, Tel Aviv, Israel.
Shlomi ConstantiniDepartment of Pediatric Neurosurgery, Tel Aviv Medical Center, Tel Aviv, Israel. sconsts@netvision.net.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chiari type 1 malformation (CIM) is defined as tonsillar ectopia of >5 mm, while syringomyelia (SM) is defined as a cerebrospinal fluid (CSF)-filled cavity larger than 3 mm dissecting the spinal cord. Over the last decades, our understanding of these pathologies has grown; however, many controversies still exist almost in every aspect of CIM and SM, including etiology, indication for treatment, timing of treatment, surgical technique, follow-up regime, and outcome. This chapter provides a comprehensive overview on different aspects of CIM and SM and on the still existing controversies, based on the evidence presently available. Future directions for clinical research concerning CIM and SM treatment and outcome are elaborated and discussed as well.

Indexed as

Arnold-Chiari MalformationNeurosurgical ProceduresSyringomyeliaChildHumansTreatment OutcomeBasilar invaginationChiari malformationForamen magnum decompressionHydrocephalusPediatric neurosurgeryScoliosisSyringomyeliaSyrinxTethered cord

Identifiers

PMID37770682

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.