Evidence map›Paper›PMID 37890145›Full record

ReviewBlood2024

Hemocompatibility and biophysical interface of left ventricular assist devices and total artificial hearts.

Angelo Nascimbene, David Bark, David M Smadja

Open access · greenAbstract readReview
In one paragraph

Review in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Observational
  9. The Total Artificial Heart: A Historical Perspective.Journal of clinical medicine · 2025
    Article
  10. Article
  11. 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

3 authors at 2 institutions in 2 countries.

Angelo NascimbeneAdvanced Cardiopulmonary Therapies and Transplantation, University of Texas, Houston, TX.
David BarkDivision of Hematology and Oncology, Department of Pediatrics, Washington University in St. Louis, St. Louis, MO.ORCID 0000-0002-9865-6176
David M SmadjaUniversité de Paris-Cité, Innovative Therapies in Haemostasis, INSERM, Paris, France.ORCID 0000-0001-7731-9202
Inserm · FRWashington University in St. Louis · US

Funding

Von Willebrand Factor Hyperactivity, Angiogenesis and LVAD-Induced BleedingR01HL163549 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Angelo Nascimbene · 2023 to 2026
$2.4M
Impact of turbulence on blood in mechanical circulatory supportR01HL164424 · NHLBI · WASHINGTON UNIVERSITY · PI Matthew Kipper · 2022 to 2026
$2.0M
Paper-based high shear hemostatic analytical deviceR21EB034579 · NIBIB · WASHINGTON UNIVERSITY · PI BARK, DAVID · 2023 to 2024
$431k
NHLBI NIH HHS R01 HL163549NHLBI NIH HHS R01 HL164424NIBIB NIH HHS R21 EB034579
6 · The paper itself

Abstract

abstractOver the past 2 decades, there has been a significant increase in the utilization of long-term mechanical circulatory support (MCS) for the treatment of cardiac failure. Left ventricular assist devices (LVADs) and total artificial hearts (TAHs) have been developed in parallel to serve as bridge-to-transplant and destination therapy solutions. Despite the distinct hemodynamic characteristics introduced by LVADs and TAHs, a comparative evaluation of these devices regarding potential complications in supported patients, has not been undertaken. Such a study could provide valuable insights into the complications associated with these devices. Although MCS has shown substantial clinical benefits, significant complications related to hemocompatibility persist, including thrombosis, recurrent bleeding, and cerebrovascular accidents. This review focuses on the current understanding of hemostasis, specifically thrombotic and bleeding complications, and explores the influence of different shear stress regimens in long-term MCS. Furthermore, the role of endothelial cells in protecting against hemocompatibility-related complications of MCS is discussed. We also compared the diverse mechanisms contributing to the occurrence of hemocompatibility-related complications in currently used LVADs and TAHs. By applying the existing knowledge, we present, for the first time, a comprehensive comparison between long-term MCS options.

Indexed as

Heart, ArtificialHeart-Assist DevicesHeart FailureThrombosisEndothelial CellsHemorrhageHumans

Identifiers

PMID37890145
PMCPMC10900168
OpenAlexW4387969030

What Socratic 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 Socratic graph.