Evidence map›Paper›PMID 29243830›Full record

ArticleTransfusion2018

Proceedings of the Food and Drug Administration's public workshop on new red blood cell product regulatory science 2016.

Jaroslav G Vostal, Paul W Buehler, Monique P Gelderman, Abdu I Alayash, Alan Doctor, James C Zimring, Simone A Glynn, John R Hess, Harvey Klein, Jason P Acker and 16 more

Abstract readConference Proceedings
In one paragraph

Article in Transfusion, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Superoxide measurement as a novel probe of red blood cell storage quality.Blood transfusion = Trasfusione del sangue · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Objective assessment of stored blood quality by deep learning.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

26 authors.

Jaroslav G VostalDivision of Blood Components and Devices, OBRR, CBER, Food and Drug Administration, Silver Spring, Maryland.
Paul W BuehlerDivision of Blood Components and Devices, OBRR, CBER, Food and Drug Administration, Silver Spring, Maryland.
Monique P GeldermanDivision of Blood Components and Devices, OBRR, CBER, Food and Drug Administration, Silver Spring, Maryland.
Abdu I AlayashDivision of Blood Components and Devices, OBRR, CBER, Food and Drug Administration, Silver Spring, Maryland.
Alan DoctorDepartment of Pediatric Critical Care, St Louis Children's Hospital, St Louis, Missouri.
James C ZimringPuget Sound Blood Center, Seattle, Washington.
Simone A GlynnDivision of Blood Diseases and Resources, NHLBI, NIH, Bethesda, Maryland.
John R HessDepartment of Laboratory Medicine and Hematology, University of Washington, School of Medicine, Seattle, Washington.ORCID 0000-0001-8596-4420
Harvey KleinDepartment of Transfusion Medicine, National Institutes of Health, Clinical Center, Bethesda, Maryland.
Jason P AckerDepartment of Research & Development, Canadian Blood Services, Edmonton, Alberta, Canada.
Philip C SpinellaDepartment of Pediatric Critical Care, Washington University School of Medicine, St Louis, Missouri.
Angelo D'AlessandroDepartment of Biochemistry and Molecular Genetics, University of Colorado-Anschutz Medical Campus, Denver, Colorado.
Bernhard PalssonCenter for Systems Biology, University of Iceland, Reykjavik, Iceland.
Thomas J RaifeDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
Michael P BuschBlood Systems Research Institute, San Francisco, California.
Timothy J McMahonDepartment of Medicine, Pulmonary, Allergy, & Critical Care Medicine, Duke University Medical Center, and the Durham VA Medical Center, Durham, North Carolina.
Marcos IntagliettaDepartment of Bioengineering, University of California at San Diego, San Diego, California.
Harold M SwartzDepartment of Radiology, Dartmouth College Geisel School of Medicine, Hanover, New Hampshire.
Michael A DubickUS Army Institute of Surgical Research, San Antonio, Texas.
Sylvain CardinNaval Medical Research Unit-San Antonio, San Antonio, Texas.
Rakesh P PatelCenter for Free Radical Biology and Translational and Molecular Sciences Certificate Program, University of Alabama, Birmingham, Alabama.
Charles NatansonCritical Care Medicine, NIH Clinical Center, Bethesda, Maryland.
John W WeiselCell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Jennifer A MuszynskiDivision of Critical Care Medicine, The Ohio State University College of Medicine, Columbus, Ohio.
Philip J NorrisBlood Systems Research Institute, Blood Systems, Inc., San Francisco, California.
Paul M NessDivision of Transfusion Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Funding

SEPSIS-INDUCED RED CELL DYSFUNCTION (SIRD)R01GM113838 · NIGMS · WASHINGTON UNIVERSITY · PI DOCTOR, ALLAN, MARSHALL, GARLAND ROSS · 2015 to 2019
$4.0M
SNO transport regulates endothelial adhesion of RBCsI01BX003478 · VA · DURHAM VA MEDICAL CENTER · PI TIMOTHY J MCMAHON · 2017 to 2026
–
BLRD VA I01 BX003478Intramural FDA HHS FD999999NIGMS NIH HHS R01 GM113838
6 · The paper itself

Abstract

The US Food and Drug Administration (FDA) held a workshop on red blood cell (RBC) product regulatory science on October 6 and 7, 2016, at the Natcher Conference Center on the National Institutes of Health (NIH) Campus in Bethesda, Maryland. The workshop was supported by the National Heart, Lung, and Blood Institute, NIH; the Department of Defense; the Office of the Assistant Secretary for Health, Department of Health and Human Services; and the Center for Biologics Evaluation and Research, FDA. The workshop reviewed the status and scientific basis of the current regulatory framework and the available scientific tools to expand it to evaluate innovative and future RBC transfusion products. A full record of the proceedings is available on the FDA website (http://www.fda.gov/BiologicsBloodVaccines/NewsEvents/WorkshopsMeetingsConferences/ucm507890.htm). The contents of the summary are the authors' opinions and do not represent agency policy.

Indexed as

ErythrocytesUnited States Food and Drug AdministrationAdultAnimalsBiological ProductsBlood PreservationBlood SafetyChildErythrocyte TransfusionHumansModels, AnimalRandomized Controlled Trials as TopicTransfusion ReactionUnited StatesBiological Products

Identifiers

PMID29243830
PMCPMC6258195

What OpenQuestion holds

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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.