Evidence map›Paper›PMID 33372698›Full record

ArticleClinical cardiology2021

Acquired von Willebrand syndrome and factor VIII in patients with moderate to severe mitral regurgitation undergoing transcatheter mitral valve repair.

Christine Meindl, Michael Paulus, Theresia Koller, Dominik Rogalski, Michael Hamerle, Christian Schach, Stefan Buchner, Florian Zeman, Lars S Maier, Kurt Debl and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Bleeding in valvular heart disease: is von Willebrand factor the culprit?Research and practice in thrombosis and haemostasis · 2024
    Article
  4. Article
  5. Article
  6. 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

12 authors at 2 institutions in 1 country.

Christine MeindlDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.ORCID https://orcid.org/0000-0001-7086-0469
Michael PaulusDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Theresia KollerDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Dominik RogalskiDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Michael HamerleDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Christian SchachDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Stefan BuchnerDepartment of Internal Medicine II, Sana Hospital Cham, Cham, Germany.
Florian ZemanCenter for Clinical Studies, University Hospital Regensburg, Regensburg, Germany.
Lars S MaierDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Kurt DeblDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Bernhard UnsöldDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Christoph BirnerDepartment of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
University Hospital Regensburg · DESana Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesisThe acquired von Willebrand syndrome (AvWS), which predisposes to bleeding events, is often related to valvular heart diseases. We investigated possible implications of AvWS and factor VIII levels in patients with moderate to severe mitral regurgitation (MR) undergoing transcatheter mitral valve repair (TMVR). METHODS AND

results123 patients with moderate to severe MR were prospectively enrolled. Complete measurements of von Willebrand Factor activity (vWFAct), von Willebrand Factor antigen (vWFAg), and factor VIII expression before and 4 weeks after TMVR were available in 85 patients. At baseline, seven patients had a history of gastrointestinal bleeding, two patients suffered bleeding events during their hospital stay, and one patient had a bleeding 4 weeks after TMVR. Even though vWFAct, vWFAct/vWFAg ratio and vWFAg values did not change after TMVR, we observed a significantly lower vWFAct/vWFAg ratio in patients with primary MR as compared to patients with secondary MR both at baseline (p = 0.022) and 4 weeks following the TMVR procedure (p = 0.003). Additionally, patients with a mean mitral valve gradient ≥4 mmHg after TMVR had significantly lower vWFAct/vWFAg ratios as compared to patients with a mean mitral valve gradient <4 mmHg (p = 0.001).

conclusionsMR of primary etiology was associated with lower vWFAct/vWFAg ratio, hinting toward HMWM loss due to shear stress caused by eccentric regurgitation jets. In addition, morphological changes leading to postprocedural transmitral gradients ≥4 mmHg were related to lower vWFAct/vWFAg ratio 4 weeks after the procedure. Alterations of the vWFAct/vWFAg ratio in turn did not translate into a greater risk for bleeding events.

Indexed as

Cardiac Surgical ProceduresHeart Valve Prosthesis ImplantationMitral Valve Insufficiencyvon Willebrand DiseasesCardiac CatheterizationFactor VIIIHumansMitral ValveFactor VIIIMitraClipmitral valve repairPASCALvon Willebrand factor

Identifiers

PMID33372698
PMCPMC7852171
OpenAlexW3115459954

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.