Evidence map›Paper›PMID 20651014›Full record

ReviewAJNR. American journal of neuroradiology2010

Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous association.

A I Alomari, D B Orbach, J B Mulliken, A Bisdorff, S J Fishman, A Norbash, R Alokaili, D J Lord, P E Burrows

Open access · hybridAbstract readReview
In one paragraph

Review in AJNR. American journal of neuroradiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. A Review on Cutaneous and Musculoskeletal Manifestations of CLOVES Syndrome.Clinical, cosmetic and investigational dermatology · 2022
    Review
  5. Article
  6. Article
  7. Parkes Weber syndrome and spinal arteriovenous malformations.AJNR. American journal of neuroradiology · 2013
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 4 countries.

A I AlomariDivision of Interventional Radiology,Children’s Hospital Boston, 300 Longwood Ave., Boston, MA 02115, USA. ahmad.alomari@childrens.harvard.edu
D B Orbach
J B Mulliken
A Bisdorff
S J Fishman
A Norbash
R Alokaili
D J Lord
P E Burrows
Boston Children's Hospital · USHôpital Lariboisière · FRBoston Medical Center · USBoston University · USChildren's Hospital at Westmead · AUKing Abdulaziz Medical City · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeKTS is a rare limb overgrowth disorder with slow-flow vascular anomalies. This study examines the presumed association between KTS and spinal AVMs. MATERIALS AND

methodsWe performed a MEDLINE search of articles and reviewed textbooks of spinal diseases to study the association between KTS and spinal AVM. Our goal was to ascertain the basis on which the diagnosis of KTS was established and to evaluate the evidence of its association with spinal AVMs. In addition, the data base of the Vascular Anomalies Center at Children's Hospital Boston was queried for patients with KTS, and the association with spinal AVM was investigated.

resultsTwenty-four published reports on spinal AVMs in 31 patients with KTS were reviewed. None of these references provided solid evidence of the diagnosis of KTS in any patient. Clinical data were either incompatible with the diagnosis of KTS or were inadequate to establish the diagnosis. Alternative possible diagnoses (CLOVES syndrome and CM-AVM) were suggested by the first author for 9 of the patients reported in these articles. The medical records of 208 patients with the diagnosis of KTS were analyzed; not a single patient had clinical or radiologic evidence of a spinal AVM.

conclusionsAn association between KTS and spinal AVM, as posited in numerous references, is most likely erroneous. The association has neither been reliably proved in the limited published literature nor encountered in a large cohort.

Indexed as

Arteriovenous MalformationsChildChild, PreschoolComorbidityFemaleHumansIncidenceInfant, NewbornKlippel-Trenaunay-Weber SyndromeMaleRadiographyRisk AssessmentRisk FactorsSpinal Cord

Identifiers

PMID20651014
PMCPMC7964980
OpenAlexW2035733408

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.