Evidence map›Paper›PMID 31009343›Full record

Observational studyStroke2019

Arteriopathy Influences Pediatric Ischemic Stroke Presentation, but Sickle Cell Disease Influences Stroke Management.

Kristin P Guilliams, Fenella J Kirkham, Susanne Holzhauer, Steven Pavlakis, Bryan Philbrook, Catherine Amlie-Lefond, Michael J Noetzel, Nomazulu Dlamini, Mukta Sharma, Jessica L Carpenter and 5 more

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in Stroke, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Timely surgical intervention in sickle cell-related hemorrhagic stroke: a pediatric success story and literature review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Review
  2. Observational
  3. Neurological management of ischemic stroke in sickle cell disease- a case report with an updated review of the literature.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Review
  4. Article
  5. Article
  6. Aspirin use and platelet aggregation in ischemic onset-type pediatric moyamoya patients with intractable headaches (moya-ache).Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  7. 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

15 authors at 13 institutions in 4 countries.

Kristin P GuilliamsFrom the Departments of Neurology and Pediatrics, Washington University School of Medicine, St Louis, MO (K.P.G., M.J.N.).
Fenella J KirkhamDevelopmental Neurosciences and Biomedical Research Unit, UCL Great Ormond Street Institute of Child Health, London and Clinical and Experimental Sciences, University of Southampton, United Kingdom (F.J.K.).
Susanne HolzhauerDepartment of Pediatric Hematology and Oncology Charité University Medicine, Berlin, Germany (S.H.).
Steven PavlakisDepartment of Pediatrics and Neurology, The Brooklyn Hospital Center, Icahn School of Medicine at Mount Sinai, Brooklyn, NY (S.P.).
Bryan PhilbrookDepartment of Pediatrics, Pediatric Neurology, Emory University, Children's Healthcare of Atlanta, GA (B.P.).
Catherine Amlie-LefondDepartment of Neurology, Seattle Children's Hospital, University of Washington, Seattle (C.A.-L.).
Michael J NoetzelFrom the Departments of Neurology and Pediatrics, Washington University School of Medicine, St Louis, MO (K.P.G., M.J.N.).
Nomazulu DlaminiDepartment of Neurology, The Hospital for Sick Children, Toronto, Canada (N.D.).
Mukta SharmaDepartment of Pediatric Hematology Oncology, Children's Mercy Hospital, University of Missouri Kansas City School of Medicine (M.S.).
Jessica L CarpenterDepartment of Pediatrics, Neurology, and Neuroscience, George Washington University, Children's National Medical Center, Washington DC (J.L.C.).
Christine K FoxDepartments of Neurology and Pediatrics, University of California San Francisco (C.K.F.).
Marcela TorresDepartment of Pediatric Hematology Oncology, Cook Children's Medical Center, Fort Worth, TX (M.T.).
Rebecca N IchordDepartments of Neurology and Pediatrics, Perlman School of Medicine at the University of Pennsylvania, Philadelphia (R.N.I.).
Lori C JordanDepartment of Pediatrics, Division of Pediatric Neurology, Vanderbilt University Medical Center, Nashville, TN (L.C.J.).
Michael M DowlingDepartments of Pediatrics, Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center at Dallas and Children's Health Dallas (M.M.D.).
Washington University in St. Louis · USCharité - Universitätsmedizin Berlin · DEChildren's Mercy Hospital · USCook Children's Medical Center · USEmory University · USGeorge Washington University · USHospital for Sick Children · CAIcahn School of Medicine at Mount Sinai · USSeattle Children's Hospital · USUniversity College London · GBUniversity of California, San Francisco · USUniversity of Pennsylvania · USVanderbilt University Medical Center · US

Funding

Clinical and Transtional Science InstituteKL2TR000143 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$11.9M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
MRI-based quantitative brain oxygen metabolism identifying high risk of infarct recurrence in sickle cell anemiaR01NS096127 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JORDAN, LORI CHAFFIN · 2016 to 2020
$1.7M
Age-Dependence of Cerebral Oxygen Metabolism and Stroke Risk in Pediatric Sickle Cell DiseaseK23NS099472 · NINDS · WASHINGTON UNIVERSITY · PI GUILLIAMS, KRISTIN · 2017 to 2021
$951k
NCATS NIH HHS KL2 TR000143NICHD NIH HHS U54 HD083211NINDS NIH HHS K23 NS099472NINDS NIH HHS R01 NS096127
6 · The paper itself

Abstract

Background and Purpose- Sickle cell disease (SCD) and arteriopathy are pediatric stroke risk factors that are not mutually exclusive. The relative contributions of sickled red blood cells and arteriopathy to stroke risk are unknown, resulting in unclear guidelines for primary and secondary stroke prevention when both risk factors are present. We hypothesized that despite similarities in clinical presentation and radiographic appearance of arteriopathies, stroke evaluation and management differ in children with SCD compared with those without SCD. Methods- We compared presentation and management of children with and without SCD enrolled in the IPSS (International Pediatric Stroke Study) with acute arterial ischemic stroke, according to SCD and arteriopathy status. Regression modeling determined relative contribution of SCD and arteriopathy in variables with significant frequency differences. Results- Among 930 childhood arterial ischemic strokes, there were 98 children with SCD, 67 of whom had arteriopathy, and 466 without SCD, 392 of whom had arteriopathy. Arteriopathy, regardless of SCD status, increased likelihood of hemiparesis (odds ratio [OR], 1.94; 95% CI, 1.46-2.56) and speech abnormalities (OR, 1.67; 95% CI, 1.29-2.19). Arteriopathy also increased likelihood of headache but only among those without SCD (OR, 1.89; 95% CI, 1.40-2.55). Echocardiograms were less frequently obtained in children with SCD (OR, 0.58; 95% CI, 0.37-0.93), but the frequency of identified cardiac abnormalities was similar in both groups ( P=0.57). Children with SCD were less likely to receive antithrombotic therapy, even in the presence of arteriopathy (OR, 0.14; 95% CI, 0.08-0.22). Arteriopathy was associated with a significantly higher likelihood of antithrombotic therapy in children without SCD (OR, 5.36; 95% CI, 3.55-8.09). Conclusions- Arteriopathy, and not SCD status, was most influential of stroke presentation. However, SCD status influenced stroke management because children with SCD were less likely to have echocardiograms or receive antithrombotic therapy. Further work is needed to determine whether management differences are warranted.

Indexed as

Disease ManagementAdolescentAnemia, Sickle CellBrain IschemiaChildChild, PreschoolFemaleHumansMaleProspective StudiesRegistriesStrokeaspirinchildheadacheheparinrisk factor

Identifiers

PMID31009343
PMCPMC6481313
OpenAlexW2936686340

What OpenQuestion holds

Textmetadata
LicenceTDM
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.