Evidence map›Paper›PMID 22906074›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2012

von Willebrand's disease: a report from a meeting in the Åland islands.

E Berntorp, I Peake, U Budde, M Laffan, R Montgomery, J Windyga, A Goodeve, P Petrini, M von Depka, W Miesbach and 4 more

Abstract readConference Proceedings
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.5field-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

5 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. [Research progress of alloantibodies against von Willebrand factor].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2015
    Article
  4. Review
  5. Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report.Haemophilia : the official journal of the World Federation of Hemophilia · 2013
    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

14 authors at 12 institutions in 8 countries.

E BerntorpLund University, Department of Hematology and Coagulation Disorders Skåne University Hospital, Malmö, Sweden.
I Peake
U Budde
M Laffan
R Montgomery
J Windyga
A Goodeve
P Petrini
M von Depka
W Miesbach
D Lillicrap
A B Federici
R Lassila
G White
University of Sheffield · GBAsklepios Klinik Altona · DEChildren's Hospital of Wisconsin · USHelsinki University Hospital · FIImperial College London · GBInstytut Hematologii i Transfuzjologi · PLKarolinska University Hospital · SELund University · SEMedical College of Wisconsin · USQueen's University · CAUniversity of Milan · ITWerlhof Institute · DE

Funding

Transgenic/Knockout CoreP01HL044612 · NHLBI · VERSITI WISCONSIN, INC. · PI NEWMAN, PETER J · 1990 to 2015
$33.4M
Zimmerman Program for the Molecular and Clinical Biology of VWDP01HL081588 · NHLBI · VERSITI WISCONSIN, INC. · PI MONTGOMERY, ROBERT R · 2005 to 2016
$19.3M
British Heart Foundation PG/11/50/28984NHLBI NIH HHS P01 HL044612NHLBI NIH HHS P01 HL081588
6 · The paper itself

Abstract

von Willebrand's disease (VWD) is probably the most common bleeding disorder, with some studies indicating that up to 1% of the population may have the condition. Over recent years interest in VWD has fallen compared to that of haemophilia, partly the result of focus on blood-borne diseases such as HIV and hepatitis. Now the time has come to revisit VWD, and in view of this some 60 international physicians with clinical and scientific interest in VWD met over 4 days in 2010 in the Åland islands to discuss state-of-the-art issues in the disease. The Åland islands are where Erik von Willebrand had first observed a bleeding disorder in a number of members of a family from Föglö, and 2010 was also the 140th anniversary of his birth. This report summarizes the main papers presented at the symposium; topics ranged from genetics and biochemistry through to classification of VWD, pharmacokinetics and laboratory assays used in the diagnosis of the disease, inhibitors, treatment guidelines in different age groups including the elderly who often have comorbid conditions that present challenges, and prophylaxis. Other topics included managing surgeries in patients with VWD and the role of FVIII in VWF replacement, a controversial subject.

Indexed as

Factor VIIIGenetic TherapyHumansPractice Guidelines as TopicScandinavian and Nordic CountriesUnited KingdomUnited Statesvon Willebrand Diseasesvon Willebrand FactorFactor VIIIvon Willebrand Factor

Identifiers

PMID22906074
PMCPMC4170876
OpenAlexW2049169130

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.