Evidence map›Paper›PMID 25982122›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2015

Utility of a Paediatric Bleeding Questionnaire as a screening tool for von Willebrand disease in apparently healthy children.

N Mittal, R Naridze, P James, S Shott, L A Valentino

Abstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
–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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Sixth Åland Island Conference on von Willebrand disease.Haemophilia : the official journal of the World Federation of Hemophilia · 2022
    Article
  9. Epistaxis in a Pediatric Outpatient Clinic: Could It be an Alarming Sign?International archives of otorhinolaryngology · 2022
    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

5 authors.

N MittalDepartment of Pediatric Hematology Oncology, Rush University Medical Center, Chicago, IL, USA.
R NaridzeDepartment of Pediatric Hematology Oncology, Rush University Medical Center, Chicago, IL, USA.
P JamesDepartment of Medicine, Queens University, Kingston, ON, Canada.
S ShottDepartment of Medicine, Rush University Medical Center, Chicago, IL, USA.
L A ValentinoDepartment of Pediatric Hematology Oncology, Rush University Medical Center, Chicago, IL, USA.

Funding

Zimmerman Program for the Molecular and Clinical Biology of VWDP01HL081588 · NHLBI · VERSITI WISCONSIN, INC. · PI MONTGOMERY, ROBERT R · 2005 to 2016
$19.3M
NHLBI NIH HHS P01 HL081588
6 · The paper itself

Abstract

unlabelledvon Willebrand disease (VWD), an inherited bleeding disorder caused by deficiency or dysfunction of von Willebrand factor (VWF) is diagnosed when a personal and often a family history of excessive mucocutaneous bleeding is present along with abnormal laboratory studies. An accurate assessment of haemorrhagic symptoms is key in suspecting VWD but presents a challenge especially in children due to overlap between normal and abnormal bleeding. Bleeding questionnaire (BQ) scores have been validated in adults and have recently been validated in children with VWD for assessing bleeding severity. However, there are limited data supporting their use prospectively in healthy children with bleeding complaints.

aimThe objectives of this study were to obtain normative data from children and validate a paediatric BQ (PBQ) to determine the discriminative ability of its total score and its individual components for identifying children likely to have VWD.

methodsThe PBQ was administered to 1281 multiethnic, healthy children between 30 days and 18 years of age presenting to a general paediatric office and to 35 children with VWD based on VWF antigen, activity and multimer pattern.

resultsWhen children with total BQ scores of 3 or more were predicted to have VWD, the sensitivity was 97.2%, the specificity was 97.1%, the positive predictive value was 48.6% and the negative predictive value was 99.9%.

conclusionsThe PBQ may help discriminate a significant bleeding history from trivial bleeding, may be integrated into the primary care algorithm for evaluating children suspected with VWD.

Indexed as

Healthy VolunteersAdolescentAdultChildChild, PreschoolFemaleHemorrhageHumansInfantMaleMass ScreeningReproducibility of ResultsSurveys and Questionnairesvon Willebrand Diseasesbleeding scoresbleeding symptomsPaediatric Bleeding Questionnairescreening toolvon Willebrand disease

Identifiers

PMID25982122
PMCPMC4673659

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Registered trials

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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.