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Real-world Experiences in the Transplantation of Hepatitis C-NAAT-positive Organs.
Steinbrink, Julie M; Byrns, Jennifer; Berg, Carl; Kappus, Matthew; King, Lindsay; Ellis, Matthew J; Sanoff, Scott; Agarwal, Richa; DeVore, Adam D; Reynolds, John M; Hartwig, Matthew G; Milano, Carmelo; Sudan, Debra; Maziarz, Eileen K; Saullo, Jennifer; Alexander, Barbara D; Wolfe, Cameron R.
  • Steinbrink JM; Division of Infectious Diseases, Duke University School of Medicine, Durham, NC.
  • Byrns J; Department of Pharmacy, Duke University Hospital, Durham, NC.
  • Berg C; Division of Gastroenterology, Duke University School of Medicine, Durham, NC.
  • Kappus M; Division of Gastroenterology, Duke University School of Medicine, Durham, NC.
  • King L; Division of Gastroenterology, Duke University School of Medicine, Durham, NC.
  • Ellis MJ; Division of Nephrology, Duke University School of Medicine, Durham, NC.
  • Sanoff S; Division of Nephrology, Duke University School of Medicine, Durham, NC.
  • Agarwal R; Division of Cardiology, Duke University School of Medicine, Durham, NC.
  • DeVore AD; Division of Cardiology, Duke University School of Medicine, Durham, NC.
  • Reynolds JM; Division of Pulmonary, Allergy and Critical Care, Duke University School of Medicine, Durham, NC.
  • Hartwig MG; Division of Cardiovascular and Thoracic Surgery, Duke University School of Medicine, Durham, NC.
  • Milano C; Division of Cardiovascular and Thoracic Surgery, Duke University School of Medicine, Durham, NC.
  • Sudan D; Division of Abdominal Transplant Surgery, Duke University School of Medicine, Durham, NC.
  • Maziarz EK; Division of Infectious Diseases, Duke University School of Medicine, Durham, NC.
  • Saullo J; Division of Infectious Diseases, Duke University School of Medicine, Durham, NC.
  • Alexander BD; Division of Infectious Diseases, Duke University School of Medicine, Durham, NC.
  • Wolfe CR; Division of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Transplant Direct ; 9(11): e1539, 2023 Nov.
Article en En | MEDLINE | ID: mdl-37829247
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.