Evidence map›Paper›PMID 35021888›Full record

ArticleNucleic acid therapeutics2022

Combining Heparin and a FX/Xa Aptamer to Reduce Thrombin Generation in Cardiopulmonary Bypass and COVID-19.

Charlene V Chabata, James W Frederiksen, Lyra B Olson, Ibtehaj A Naqvi, Sharon E Hall, Ruwan Gunaratne, Bryan D Kraft, Loretta G Que, Lingye Chen, Bruce A Sullenger

Open access · greenAbstract read
In one paragraph

Article in Nucleic acid therapeutics, 2022. 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 22% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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 2 institutions in 1 country.

Charlene V ChabataDepartment of Surgery, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.ORCID 0000-0001-5626-6906
James W FrederiksenDepartment of Surgery, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.
Lyra B OlsonDepartment of Surgery, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.
Ibtehaj A NaqviDepartment of Surgery, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.
Sharon E HallDivision of Hematology, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.
Ruwan GunaratneDepartment of Medicine, Stanford University Medical Center, Stanford, California, USA.
Bryan D KraftDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Loretta G QueDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Lingye ChenDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Bruce A SullengerDepartment of Surgery, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA.
Duke University · USStanford Medicine · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Translating Mechanistic Insights into Intrinsic Xase FunctionP01HL139420 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Sriram Krishnaswamy · 2018 to 2026
$22.4M
Structural Correlates of Protease and Cofactor FunctionP01HL074124 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI KRISHNASWAMY, SRIRAM · 2003 to 2013
$17.6M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
NHLBI NIH HHS P01 HL074124NHLBI NIH HHS P01 HL139420NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Known limitations of unfractionated heparin (UFH) have encouraged the evaluation of anticoagulant aptamers as alternatives to UFH in highly procoagulant settings such as cardiopulmonary bypass (CPB). Despite progress, these efforts have not been totally successful. We take a different approach and explore whether properties of an anticoagulant aptamer can complement UFH, rather than replace it, to address shortcomings with UFH use. Combining RNA aptamer 11F7t, which targets factor X/Xa, with UFH (or low molecular weight heparin) yields a significantly enhanced anticoagulant cocktail effective in normal and COVID-19 patient blood. This aptamer-UFH combination (1) supports continuous circulation of human blood through an

Indexed as

Aptamers, NucleotideCOVID-19AnticoagulantsCardiopulmonary BypassFactor XHeparinHumansThrombinAnticoagulantsAptamers, NucleotideFactor XHeparinThrombinanticoagulationaptamercardiopulmonary bypassCOVID-19heparinthrombin generation

Identifiers

PMID35021888
PMCPMC9221171
OpenAlexW4205443023

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.