Evidence map›Paper›PMID 27766637›Full record

ArticleBritish journal of haematology2017

Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and stroke.

Michael M Dowling, Charles T Quinn, Claudio Ramaciotti, Julie Kanter, Ifeyinwa Osunkwo, Baba Inusa, Rathi Iyer, Janet L Kwiatkowski, Clarissa Johnson, Melissa Rhodes and 10 more

Open access · greenAbstract read
In one paragraph

Article in British journal of haematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Stroke and presence of patent foramen ovale in sickle cell disease.Journal of thrombosis and thrombolysis · 2021
    Review
  10. Epidemiology of Stroke in Sickle Cell Disease.Journal of clinical medicine · 2021
    Review
  11. Article
  12. Article
  13. Patent Foramen Ovale in Fetal Life, Infancy and Childhood.Medical sciences (Basel, Switzerland) · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Observational
  18. Article
  19. Review
  20. 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

20 authors at 17 institutions in 2 countries.

Michael M DowlingDepartments of Pediatrics and Neurology & Neurotherapeutics, UT Southwestern Medical Center, Dallas, TX, USA.
Charles T QuinnDivision of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Claudio RamaciottiDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, TX, USA.
Julie KanterDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Ifeyinwa OsunkwoThe Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
Baba InusaHaematology, Evelina Children's Hospital, Guy's and St. Thomas NHS Trust, London, UK.
Rathi IyerUniversity of Mississippi Medical Center, Jackson, MS, USA.
Janet L KwiatkowskiDivision of Hematology, Children's Hospital of Philadelphia and Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Clarissa JohnsonCook Children's Health Care System, Ft. Worth, TX, USA.
Melissa RhodesPediatric Hematology/Oncology, University of Mississippi Medical Center, Jackson, MS, USA.
William OwenChildren's Cancer and Blood Disorders Center, Children's Hospital of the King's Daughters, Norfolk, VA, USA.
John J StrouseThe Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Julie A PanepintoDepartment of Pediatrics, Hematology/Oncology, Medical College of Wisconsin/Children's Hospital of Wisconsin, Milwaukee, WI, USA.
Lynne NeumayrDepartment of Hematology Oncology, UCSF Benioff Children's Hospital, Oakland, CA, USA.
Sharada SarnaikDepartment of Pediatrics, Division of Hematology & Oncology, Wayne State University, Detroit, MI, USA.
Patricia A PlumbDepartment of Neurology & Neurotherapeutics, UT Southwestern Medical Center, Dallas, TX, USA.
Nomazulu DlaminiDepartment of Paediatric Neurology, Evelina Children's Hospital, London, UK.
Fenella KirkhamDevelopmental Neurosciences, UCL Institute of Child Health, London, UK.
Linda S HynanDepartments of Clinical Science (Biostatistics) and Psychiatry, UT Southwestern Medical Center, Dallas, TX, USA.
PFAST Investigators
Southwestern Medical Center · USCarolinas Healthcare System · USChildren's Hospital of Philadelphia · USChildren's Hospital of The King's Daughters · USCincinnati Children's Hospital Medical Center · USCook Children's Health Care System · USEvelina London Children's Healthcare · GBGuy's and St Thomas' NHS Foundation Trust · GBJackson Memorial Hospital · USJohns Hopkins Medicine · USMedical College of Wisconsin · USMedical University of South Carolina · USSouthwestern Medical CenterUCSF Benioff Children's Hospital · USUniversity College London · GBUniversity of Mississippi Medical Center · USWayne State University · US

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
NCATS NIH HHS UL1 TR000003NCATS NIH HHS UL1 TR001878
6 · The paper itself

Abstract

'Paradoxical' embolization via intracardiac or intrapulmonary right-to-left shunts (RLS) is an established cause of stroke. Hypercoagulable states and increased right heart pressure, which both occur in sickle cell anaemia (SCA), predispose to paradoxical embolization. We hypothesized that children with SCA and overt stroke (SCA + stroke) have an increased prevalence of potential RLS. We performed contrasted transthoracic echocardiograms on 147 children (aged 2-19 years) with SCA + stroke) mean age 12·7 ± 4·8 years, 54·4% male) and a control group without SCA or stroke (n = 123; mean age 12·1 ± 4·9 years, 53·3% male). RLS was defined as any potential RLS detected by any method, including intrapulmonary shunting. Echocardiograms were masked and adjudicated centrally. The prevalence of potential RLS was significantly higher in the SCA+stroke group than controls (45·6% vs. 23·6%, P < 0·001). The odds ratio for potential RLS in the SCA + stroke group was 2·7 (95% confidence interval: 1·6-4·6) vs controls. In post hoc analyses, the SCA + stroke group had a higher prevalence of intrapulmonary (23·8% vs. 5·7%, P < 0·001) but not intracardiac shunting (21·8% vs. 18·7%, P = 0·533). SCA patients with potential RLS were more likely to report headache at stroke onset than those without. Intrapulmonary and intracardiac shunting may be an overlooked, independent and potentially modifiable risk factor for stroke in SCA.

Indexed as

AdolescentAnemia, Sickle CellChildChild, PreschoolEchocardiographyEmbolism, ParadoxicalFemaleHeadacheHeart Septal DefectsHumansMalePrevalenceRisk FactorsStrokeYoung Adultcardiologyclinical researchsickle cell anaemiastroke

Identifiers

PMID27766637
PMCPMC5239723
OpenAlexW2535166404

What OpenQuestion holds

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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.