Evidence map›Paper›PMID 27244102›Full record

ReviewAnnals of the New York Academy of Sciences2016

The emerging threat of superwarfarins: history, detection, mechanisms, and countermeasures.

Douglas L Feinstein, Belinda S Akpa, Manuela A Ayee, Anne I Boullerne, David Braun, Sergey V Brodsky, David Gidalevitz, Zane Hauck, Sergey Kalinin, Kathy Kowal and 8 more

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 68 citations in OpenAlex.

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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

18 authors at 5 institutions in 1 country.

Douglas L FeinsteinDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Belinda S AkpaDepartment of Molecular Biomedical Sciences, North Carolina State University, Raleigh, North Carolina.
Manuela A AyeeDepartment of Medicine, University of Illinois, Chicago, Illinois.
Anne I BoullerneDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
David BraunDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Sergey V BrodskyDepartment of Pathology, the Ohio State University, Columbus, Ohio.
David GidalevitzDepartment of Physics and the Center for the Molecular Study of Condensed Soft Matter, Illinois Institute of Technology, Chicago, Illinois.
Zane HauckDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago, Illinois.
Sergey KalininDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Kathy KowalDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Ivan KuzmenkoX-ray Science Division, Argonne National Laboratory, Lemont, Illinois.
Kinga LisDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Natalia MarangoniDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Michael W MartynowyczDepartment of Physics and the Center for the Molecular Study of Condensed Soft Matter, Illinois Institute of Technology, Chicago, Illinois.
Israel RubinsteinDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Richard van BreemenDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
Kyle WareDepartment of Pathology, the Ohio State University, Columbus, Ohio.
Guy WeinbergDepartment of Anesthesiology, University of Illinois, Chicago, Illinois.
University of Illinois Chicago · USIllinois Institute of Technology · USThe Ohio State University · USArgonne National Laboratory · USNorth Carolina State University · US

Funding

Intralipid: A novel frontline countermeasure for brodifacoum poisoningU01NS083457 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FEINSTEIN, DOUGLAS L. · 2013 to 2018
$3.6M
NINDS NIH HHS U01 NS083457
6 · The paper itself

Abstract

Superwarfarins were developed following the emergence of warfarin resistance in rodents. Compared to warfarin, superwarfarins have much longer half-lives and stronger affinity to vitamin K epoxide reductase and therefore can cause death in warfarin-resistant rodents. By the mid-1970s, the superwarfarins brodifacoum and difenacoum were the most widely used rodenticides throughout the world. Unfortunately, increased use was accompanied by a rise in accidental poisonings, reaching >16,000 per year in the United States. Risk of exposure has become a concern since large quantities, up to hundreds of kilograms of rodent bait, are applied by aerial dispersion over regions with rodent infestations. Reports of intentional use of superwarfarins in civilian and military scenarios raise the specter of larger incidents or mass casualties. Unlike warfarin overdose, for which 1-2 days of treatment with vitamin K is effective, treatment of superwarfarin poisoning with vitamin K is limited by extremely high cost and can require daily treatment for a year or longer. Furthermore, superwarfarins have actions that are independent of their anticoagulant effects, including both vitamin K-dependent and -independent effects, which are not mitigated by vitamin K therapy. In this review, we summarize superwarfarin development, biology and pathophysiology, their threat as weapons, and possible therapeutic approaches.

Indexed as

AnimalsAnticoagulantsBiomarkersEnvironmental ExposureHumansKidneyNervous SystemWarfarinAnticoagulantsBiomarkersWarfarinbrodifacoumHPLCintralipidlipid membranenephrotoxicityneuropathologysuperwarfarins

Identifiers

PMID27244102
PMCPMC4940222
OpenAlexW2413953473

What OpenQuestion holds

Textmetadata
LicenceTDM
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.