Evidence map›Paper›PMID 35352362›Full record

ArticleTransfusion2022

How do I implement an outpatient program for the administration of convalescent plasma for COVID-19?

Evan M Bloch, Aaron A R Tobian, Shmuel Shoham, Daniel F Hanley, Thomas J Gniadek, Edward R Cachay, Barry R Meisenberg, Kimberly Kafka, Christi Marshall, Sonya L Heath and 27 more

Open access · greenAbstract read
In one paragraph

Article in Transfusion, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Estimates of actual and potential lives saved in the United States from the use of COVID-19 convalescent plasma.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Coronavirus Disease 2019 Convalescent Plasma Utilization in the United States: Data From the National Inpatient Sample.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  8. Article
  9. Guidance on the Use of Convalescent Plasma to Treat Immunocompromised Patients With Coronavirus Disease 2019.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. 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

37 authors at 20 institutions in 1 country.

Evan M BlochDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0001-8181-9517
Aaron A R TobianDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-0517-3766
Shmuel ShohamDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Daniel F HanleyDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Thomas J GniadekDepartment of Pathology, Northshore University Health System, Evanston, Illinois, USA.
Edward R CachayDepartment of Medicine, Division of Infectious Diseases, University of California, San Diego, California, United States.
Barry R MeisenbergLuminis Health, Annapolis, Maryland, USA.
Kimberly KafkaDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Christi MarshallDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sonya L HeathDepartment of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Aarthi ShenoyDepartment of Medicine, Division of Hematology and Oncology, Medstar Washington Hospital Center, Washington, District of Columbia, USA.
James H PaxtonDepartment of Emergency Medicine, Wayne State University, Detroit, Michigan, USA.
Adam LevineDepartment of Emergency Medicine, Rhode Island Hospital/Brown University, Providence, Rhode Island, USA.
Donald ForthalDepartment of Medicine, Division of Infectious Diseases, University of California, Irvine, California, United States.
Yuriko FukutaDepartment of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, Texas, USA.
Moises A HuamanDepartment of Medicine, Division of Infectious Diseases, University of Cincinnati, Cincinnati, Ohio, USA.
Alyssa ZimanDepartment of Pathology, University of California, Los Angeles, California, USA.ORCID 0000-0002-1814-9319
Jill AdamskiDepartment of Laboratory Medicine, Mayo Clinic Hospital, Phoenix, Arizona, USA.ORCID 0000-0002-8862-4808
Jonathan GerberDepartment of Medicine, Division of Hematology and Oncology, University of Massachusetts, Worchester, Massachusetts, USA.
Daniel CruserNuvance Health Vassar Brothers Medical Center, Poughkeepsie, New York, USA.
Seble G KassayeDepartment of Medicine, Division of Infectious Diseases, Medstar Georgetown University Hospital, Washington, District of Columbia, USA.
Giselle S MosnaimDivision of Allergy and Immunology, Department of Medicine, Northshore University Health System, Evanston, Illinois, USA.
Bela PatelDepartment of Medicine, Divisions of Pulmonary and Critical Care Medicine, University of Texas Health Science Center, Houston, Texas, USA.
Ryan A MetcalfDepartment of Medicine, Division of Infectious Diseases, University of Utah, Salt Lake City, Utah, USA.
Shweta AnjanDepartment of Medicine, Division of Infectious Diseases, University of Miami, Miller School of Medicine, Miami, Florida, USA.
Ronald B ReislerDavis Defense Group, Stafford, Virginia, USA.
Anusha YaravaDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Karen LaneDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Nichol McBeeDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Amy GawadDepartment of Neurology, Brain Injury Outcomes Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jay S RavalDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, USA.ORCID 0000-0001-9835-957X
Martin ZandDepartment of Medicine, University of Rochester, Rochester, New York, USA.
Matthew AbinanteAscada Research, Fullerton, California, USA.
Patrick B BroderickNuvance Health Danbury Hospital, Danbury, Connecticut, USA.
Arturo CasadevallDepartments of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
David SullivanDepartments of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Kelly A GeboDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USNorthShore University HealthSystem · USAnne Arundel Medical Center · USBaylor College of Medicine · USBrown University · USDanbury Hospital · USDefense Systems (United States) · USFullerton College · USGeorgetown University · USMayo Clinic Hospital · USMedStar Washington Hospital Center · USThe University of Texas Health Science Center at Houston · USUniversity of Alabama at Birmingham · USUniversity of California, Irvine · USUniversity of California, Los Angeles · USUniversity of California System · USUniversity of Cincinnati · USUniversity of Massachusetts Chan Medical School · USUniversity of Miami · USUniversity of New Mexico · US

Funding

Maternal Morbidity and Mortality: Risk Factors, Early Detection and Personalized InterventionUL1TR001409 · NCATS · GEORGETOWN UNIVERSITY · PI GONDRE-LEWIS, MARJORIE C, MELLMAN, THOMAS A · 2015 to 2024
$37.8M
Johns Hopkins-Tufts Trial Innovation Center HEAL Pain ERN SupplementU24TR001609 · NCATS · JOHNS HOPKINS UNIVERSITY · PI HANLEY, DANIEL F · 2016 to 2022
$36.3M
University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
Conjugate vaccines for prevention and treatment of cryptococcosis - COVID-19 Revision SupplementR01AI152078 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CASADEVALL, ARTURO · 2020 to 2024
$5.1M
The Malaria Transfusion Risk (MATRix) StudyK23HL151826 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BLOCH, EVAN MARTIN · 2020 to 2024
$882k
Intramural NIH HHSNCATS NIH HHS U24 TR001609NCATS NIH HHS U24TR001609-S3NCATS NIH HHS UL1 TR001409NCATS NIH HHS UL1 TR001414NHLBI NIH HHS 1K23HL151826NHLBI NIH HHS K23 HL151826NIAID NIH HHS 3R01AI152078-01S1NIAID NIH HHS R01 AI152078
6 · The paper itself

Abstract

Convalescent plasma, collected from donors who have recovered from a pathogen of interest, has been used to treat infectious diseases, particularly in times of outbreak, when alternative therapies were unavailable. The COVID-19 pandemic revived interest in the use of convalescent plasma. Large observational studies and clinical trials that were executed during the pandemic provided insight into how to use convalescent plasma, whereby high levels of antibodies against the pathogen of interest and administration early within the time course of the disease are critical for optimal therapeutic effect. Several studies have shown outpatient administration of COVID-19 convalescent plasma (CCP) to be both safe and effective, preventing clinical progression in patients when administered within the first week of COVID-19. The United States Food and Drug Administration expanded its emergency use authorization (EUA) to allow for the administration of CCP in an outpatient setting in December 2021, at least for immunocompromised patients or those on immunosuppressive therapy. Outpatient transfusion of CCP and infusion of monoclonal antibody therapies for a highly transmissible infectious disease introduces nuanced challenges related to infection prevention. Drawing on our experiences with the clinical and research use of CCP, we describe the logistical considerations and workflow spanning procurement of qualified products, infrastructure, staffing, transfusion, and associated management of adverse events. The purpose of this description is to facilitate the efforts of others intent on establishing outpatient transfusion programs for CCP and other antibody-based therapies.

Indexed as

COVID-19COVID-19 SerotherapyHumansImmunization, PassiveOutpatientsPandemicsSARS-CoV-2United Statesambulatory careantibodiesblood transfusionCOVID-19COVID-19 serotherapymonoclonalplasma

Identifiers

PMID35352362
PMCPMC9086144
OpenAlexW4220783189

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.