Evidence map›Paper›PMID 36186107›Full record

ArticleResearch and practice in thrombosis and haemostasis2022

Desmopressin testing in von Willebrand disease: Lowering the burden.

Jessica M Heijdra, Ferdows Atiq, Wala Al Arashi, Quincy Kieboom, Esmee Wuijster, Karina Meijer, Marieke J H A Kruip, Frank W G Leebeek, Marjon H Cnossen, OPTI‐CLOT Study Group

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Desmopressin testing in von Willebrand disease: Lowering the burden.Research and practice in thrombosis and haemostasis · 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

10 authors at 3 institutions in 1 country.

Jessica M HeijdraDepartment of Pediatric Hematology Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam Rotterdam The Netherlands.ORCID https://orcid.org/0000-0003-1069-8097
Ferdows AtiqDepartment of Hematology Erasmus MC, University Medical Center Rotterdam Rotterdam The Netherlands.ORCID https://orcid.org/0000-0002-3769-9148
Wala Al ArashiDepartment of Pediatric Hematology Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam Rotterdam The Netherlands.
Quincy KieboomDepartment of Pediatric Hematology Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam Rotterdam The Netherlands.
Esmee WuijsterDepartment of Hematology Erasmus MC, University Medical Center Rotterdam Rotterdam The Netherlands.
Karina MeijerDepartment of Hematology University of Groningen and University Medical Center Groningen Groningen The Netherlands.ORCID https://orcid.org/0000-0001-9447-0465
Marieke J H A KruipDepartment of Hematology Erasmus MC, University Medical Center Rotterdam Rotterdam The Netherlands.ORCID https://orcid.org/0000-0002-0265-4871
Frank W G LeebeekDepartment of Hematology Erasmus MC, University Medical Center Rotterdam Rotterdam The Netherlands.ORCID https://orcid.org/0000-0001-5677-1371
Marjon H CnossenDepartment of Pediatric Hematology Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam Rotterdam The Netherlands.ORCID https://orcid.org/0000-0003-1557-2995
OPTI‐CLOT Study Group
Erasmus MC - Sophia Children’s Hospital · NLErasmus MC · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Individuals with von Willebrand disease (VWD) require desmopressin testing because of interindividual response differences. However, testing is burdensome, while not all patients may need extensive testing. Objectives: To provide von Willebrand factor (VWF) cutoffs that predict desmopressin nonresponse and thereby identify individuals who do not need extensive testing in a retrospective cohort. We validated these cutoffs in a prospective cohort. Patients and Methods: We included 376 patients (Type 1 VWD with VWF activity [VWF:Act] <0.30 IU/ml: Results: All individuals with Type 1 VWD and Type 2 VWD, respectively, with baseline VWF:Act 0.34 IU/ml or greater or 0.28 IU/ml or greater were responders. In individuals with T1 VWF:Act ≥0.89 IU/ml (Type 1 VWD) or T1 VWF:Act 1.10 IU/ml or greater (Type 2 VWD), response remained at T4. Conclusion: Desmopressin testing is not needed when lowest historical VWF:Act is 0.30 IU/ml or greater. In patients with Type 1 VWD who require testing, measurements after T1 are often not needed. In patients with Type 2 VWD who require testing, we advise performing T1 and T4 measurements.

Indexed as

desmopressinfactor VIIIhumansvon Willebrand diseasevon Willebrand factor

Identifiers

PMID36186107
PMCPMC9512764
OpenAlexW4297360932

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.