Evidence map›Paper›PMID 34269797›Full record

ArticleBlood advances2021

Continuous-infusion von Willebrand factor concentrate is effective for the management of acquired von Willebrand disease.

Kathryn E Dane, John P Lindsley, Thomas Kickler, Michael B Streiff, Alison Moliterno, Jennifer Yui, Rakhi Naik, Shruti Chaturvedi

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. von Willebrand disease: an illustrated review.Research and practice in thrombosis and haemostasis · 2026
    Review
  2. Article
  3. Article
  4. Review
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

8 authors at 1 institution in 1 country.

Kathryn E DaneDepartment of Pharmacy and.
John P LindsleyDepartment of Pharmacy and.
Thomas KicklerDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.
Michael B StreiffDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.ORCID 0000-0002-6429-3493
Alison MoliternoDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.ORCID 0000-0002-8673-4317
Jennifer YuiDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.
Rakhi NaikDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.
Shruti ChaturvediDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD.
Johns Hopkins Hospital · US

Funding

ADAMTS13 and Late Neurologic Morbidity after Thrombotic Thrombocytopenic PurpuraK99HL150594 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CHATURVEDI, SHRUTI · 2020 to 2023
$907k
NHLBI NIH HHS K99 HL150594
6 · The paper itself

Abstract

Acquired von Willebrand disease (aVWD) is a rare disorder associated with a reduction in von Willebrand factor (VWF) activity, leading to increased bleeding risk. Monoclonal gammopathy of undetermined significance (MGUS) is the most common cause of lymphoproliferative disorder-associated aVWD and is caused by accelerated clearance of circulating VWF. Standard VWF replacement protocols for congenital VWD based on intermittent bolus dosing are typically less effective for aVWD because of antibody-mediated clearance. Intermittent bolus dosing of VWF concentrates often leads to inadequate peak response and profoundly shortened VWF half-life in aVWD. Intravenous immune globulin (IVIG) has demonstrated efficacy in aVWD; however, treatment effect is delayed up to 4 days, limiting its efficacy in acutely bleeding patients. We report the successful use of continuous-infusion VWF concentrate (with or without concomitant IVIG) in 3 patients with MGUS-associated aVWD who had demonstrated an inadequate response to bolus dosing. VWF concentrate doses required in this cohort were higher than typical doses for bleeding treatment in congenital VWD. This report illustrates that continuous-infusion VWF concentrate administration with or without intravenous immunoglobulin rapidly achieves target ristocetin cofactor activity and provides adequate hemostasis in aVWD associated with immunoglobulin G MGUS.

Indexed as

von Willebrand Diseasesvon Willebrand FactorHemorrhageHemostasisHumansImmunoglobulins, IntravenousImmunoglobulins, Intravenousvon Willebrand Factor

Identifiers

PMID34269797
PMCPMC8341349
OpenAlexW3181074098

What OpenQuestion holds

Textmetadata
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.