Evidence map›Paper›PMID 38881210›Full record

ArticleTransplant infectious disease : an official journal of the Transplantation Society2024

Hepatitis B transmission/reactivation associated with Hepatitis B core antibody and Hepatitis C nucleic acid testing positive organs: A report from the Organ Procurement and Transplantation Network Disease Transmission Advisory Committee.

Helen S Te, Dong Heun Lee, Ann E Woolley, Maheen Z Abidi, Cynthia Fisher, Marty T Sellers, Sarah Taimur, Taylor Livelli, Tamika Watkins, Dzhuliyana Handarova and 13 more

Abstract read
In one paragraph

Article in Transplant infectious disease : an official journal of the Transplantation Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

23 authors.

Helen S TeCenter for Liver Diseases, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-3172-6184
Dong Heun LeeDivision of Infectious Diseases, University of California San Francisco Medical Center, San Francisco, California, USA.
Ann E WoolleyDivision of Infectious Diseases, Boston, Massachusetts, USA.
Maheen Z AbidiDivision of Infectious Diseases, Denver, Colorado, USA.ORCID https://orcid.org/0000-0002-0783-6535
Cynthia FisherDivision of Allergy & Infectious Diseases, Seattle, Washington, USA.
Marty T SellersTennessee Donor Services, Nashville, Tennessee, USA.
Sarah TaimurDivision of Infectious Diseases, Mt. Sinai Medical Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-1776-7510
Taylor LivelliUnited Network for Organ Sharing, Richmond, Virginia, USA.
Tamika WatkinsUnited Network for Organ Sharing, Richmond, Virginia, USA.
Dzhuliyana HandarovaUnited Network for Organ Sharing, Richmond, Virginia, USA.
Gerald J BerryDepartment of Pathology, Stanford University Medical Center, Stanford, California, USA.ORCID https://orcid.org/0000-0002-6176-2629
Riki GravesSherrie and Alan Conover Center for Liver Disease & Transplantation, Houston Methodist Hospital, Houston, Texas, USA.
Chak-Sum HoGift of Hope Organ & Tissue Donor Network, Itasca, Illinois, USA.
Anna L HughartWilliam J. von Liebig Center for Transplantation and Clinical Regeneration, Mayo Clinic, Minnesota, Minnesota, USA.
Michelle KittlesonCardiology Department, Cedars Sinai Medical Center, Los Angeles, California, USA.
Charles C MarboeDepartment of Pathology and Cell Biology, New York Presbyterian Hospital/Columbia University Medical Center, New York, New York, USA.
Rachel A MillerDivision of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Tanvi S SharmaDivision of Infectious Diseases, Boston Children's Hospital, Boston, Massachusetts, USA.
Anil J TrindadeDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0003-1399-7228
R Patrick WoodLifeGift Organ Donation Center, Houston, Texas, USA.
Lorenzo N ZaffiriDivision of Pulmonary and Critical Care Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Stephanie M PouchDivision of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0002-5628-2444
Lara Danziger-IsakovDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0002-5691-5221

Funding

CMV and CMV-Immune Responses in Geriatric Conditions Post-Kidney Transplant (CMV-GeriKT)K23AG073534 · NIA · UNIVERSITY OF COLORADO DENVER · PI ABIDI, MAHEEN ZEHRA · 2021 to 2025
$944k
Division of Transplantation HHSH250201900001CHealth Systems BureauHRSA HHSNIA NIH HHS K23 AG073534United States Department of Health and Human Services
6 · The paper itself

Abstract

backgroundBetter access to direct-acting antiviral (DAA) therapy has broadened the utilization of hepatitis C virus (HCV) nucleic acid testing (NAT) positive organs with excellent outcomes. However, DAA therapy has been associated with hepatitis B virus (HBV) reactivation.

aimTo determine the risk of HBV transmission or reactivation with utilization of HBV core antibody positive (HBcAb+) and HCV NAT positive (HCV+) organs, which presumably required DAA therapy.

methodsThe number of HBcAb+ donors with delineated HCV NAT status was obtained from the Organ Procurement and Transplantation Network (OPTN) database. The number of unexpected HBV infections from transplanted organs adjudicated as "proven" or "probable" transmission was obtained from the OPTN Ad Hoc Disease Transmission Advisory Committee database. A chart review of the donors of "proven" or "probable" cases was conducted.

resultsFrom January 1, 2016, to December 31, 2021, 7735 organs were procured from 3767 HBcAb+ donors and transplanted into 7469 recipients; 545 (14.5%) donors were also HCV+. HBV transmission or reactivation occurred in seven recipients. The rate is not significantly different between recipients of HCV+ (0.18%, 2/1115) and the HCV NAT negative (HCV-) organs (0.08%, 5/6354) (p = 0.28) or between recipients of HCV+ and HCV- livers as well as non-liver organs. HBV transmission or reactivation occurred within a median of 319 (range, 41-1117) days post-transplant in the setting of missing, inadequate, or truncated prophylaxis.

conclusionHBV reactivation associated with DAA therapy for HBcAb+ HCV+ organs is less frequent than reported in the non-transplant population, possibly due to the common use of HBV prophylaxis in the at-risk transplant population.

Indexed as

Antiviral AgentsHepacivirusHepatitis BHepatitis B AntibodiesHepatitis B virusHepatitis COrgan TransplantationTissue and Organ ProcurementTissue DonorsVirus ActivationAdvisory CommitteesDNA, ViralFemaleHepatitis B Core AntigensHumansMaleAntiviral AgentsDNA, ViralHepatitis B AntibodiesHepatitis B Core AntigensRNA, Viraldirect‐acting antiviraldonorhepatitis Bhepatitis Creactivationtransmissiontransplant

Identifiers

PMID38881210
PMCPMC11578277

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.