Evidence map›Paper›PMID 37829247›Full record

ArticleTransplantation direct2023

Real-world Experiences in the Transplantation of Hepatitis C-NAAT-positive Organs.

Julie M Steinbrink, Jennifer Byrns, Carl Berg, Matthew Kappus, Lindsay King, Matthew J Ellis, Scott Sanoff, Richa Agarwal, Adam D DeVore, John M Reynolds and 7 more

Open access · goldAbstract read
In one paragraph

Article in Transplantation direct, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

17 authors at 2 institutions in 1 country.

Julie M SteinbrinkDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.ORCID https://orcid.org/0000-0003-0771-3647
Jennifer ByrnsDepartment of Pharmacy, Duke University Hospital, Durham, NC.
Carl BergDivision of Gastroenterology, Duke University School of Medicine, Durham, NC.
Matthew KappusDivision of Gastroenterology, Duke University School of Medicine, Durham, NC.
Lindsay KingDivision of Gastroenterology, Duke University School of Medicine, Durham, NC.
Matthew J EllisDivision of Nephrology, Duke University School of Medicine, Durham, NC.
Scott SanoffDivision of Nephrology, Duke University School of Medicine, Durham, NC.
Richa AgarwalDivision of Cardiology, Duke University School of Medicine, Durham, NC.
Adam D DeVoreDivision of Cardiology, Duke University School of Medicine, Durham, NC.
John M ReynoldsDivision of Pulmonary, Allergy and Critical Care, Duke University School of Medicine, Durham, NC.
Matthew G HartwigDivision of Cardiovascular and Thoracic Surgery, Duke University School of Medicine, Durham, NC.
Carmelo MilanoDivision of Cardiovascular and Thoracic Surgery, Duke University School of Medicine, Durham, NC.
Debra SudanDivision of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, NC.
Eileen K MaziarzDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Jennifer SaulloDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Barbara D AlexanderDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Cameron R WolfeDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Duke University · USDuke University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatitis C virus (HCV) nucleic acid amplification test (NAAT)-positive donors have increased the organ pool. Direct-acting antivirals (DAAs) have led to high rates of treatment success and sustained virologic response (SVR) in recipients with donor-derived HCV infection without significant adverse effects, although variability remains in the timing and duration of antivirals. Methods: This retrospective study analyzed all adult HCV-NAAT-negative transplant recipients who received an organ from HCV-NAAT-positive donors from November 24, 2018, to March 31, 2022, at Duke University Medical Center with protocolized delay of DAA initiation until after hospital discharge, with at least 180-d follow-up on all patients. Transplant and HCV-related outcomes were analyzed. Results: Two hundred eleven transplants (111 kidneys, 41 livers, 34 hearts, and 25 lungs) were performed from HCV-NAAT-positive donors to HCV-NAAT-negative recipients. Ninety percent of recipients became viremic within 7 d posttransplant. Ninety-nine percent of recipients were initiated on pangenotypic DAAs in the outpatient setting a median of 52 d posttransplant, most commonly with 12-wk courses of sofosbuvir-velpatasvir (lungs) and glecaprevir-pibrentasvir (heart, kidney, and liver). Ninety-seven percent of recipients had SVR after a first-line DAA; all ultimately achieved SVR at 12 wk after subsequent treatment courses. The median peak HCV RNA for all organ systems was 2 436 512 IU/mL; the median time from antiviral to undetectable RNA was 48 d, although differences were noted between organ groups. No patient deaths or graft losses were directly attributable to HCV infection. Conclusions: One hundred percent of transplant recipients of HCV-NAAT-positive organs ultimately developed SVR without significant adverse effects when HCV antivirals were initiated in the outpatient setting after transplant hospitalization, suggesting that this real-world treatment pathway is a viable option.

Identifiers

PMID37829247
PMCPMC10567032
OpenAlexW4387475249

What OpenQuestion holds

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Registered trials

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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.