Sari Freedman

University of Maryland Medical Center
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Articles (6)

Year:

2024

Year:

2023

Introduction Advanced liver disease or cirrhosis is associated with an increased risk of infections; however, the impact of high pretransplant model for end‐stage liver disease (MELD) score on cytomegalovirus (CMV) viremia after liver transplantation is unknown. Methods This single‐center, retrospective, cohort study evaluated CMV high‐risk (CMV immunoglobulin G D+/R−) liver transplant recipients who received valganciclovir prophylaxis for 3 months between 2009 and 2019. Patients were stratified by pretransplant MELD score of <35 (low MELD) and ≥35 (high MELD). The primary outcome was 12‐month CMV viremia, and secondary outcomes included CMV resistance and tissue invasive disease, mortality, biopsy‐proven acute rejection (BPAR), leukopenia, and thrombocytopenia. Multivariable Cox proportional‐hazards modeling was used to assess the association of MELD score with the time to CMV viremia. Results There were 162 and 79 patients in the low and high MELD groups, respectively. Pretransplant MELD score ≥35 was associated with an increased risk of CMV viremia (hazard ratio [HR] 1.73; confidence interval 1.06–2.82, p = .03). CMV viremia occurred at 162 ± 61 days in the low MELD group and 139 ± 62 days in the high MELD group. Although BPAR occurred early at 30 days (13–59) in the low‐MELD group and at 18 days (11–66) in the high‐MELD group ( p = .56), BPAR was not associated with an increased risk of CMV viremia (HR 1.55 [0.93–2.60], p = .1). Discussion MELD scores ≥35 were associated with an increased hazards of CMV viremia. In liver transplant recipients with MELD scores ≥35 who are CMV high‐risk, additional CMV intervention may be warranted. image

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Collaborators (3)

J. David Gatz

Assistant Professor

University of Maryland School of Medicine

UNITED STATES
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Rolf Barth

Professor of Surgery

University of Chicago

UNITED STATES
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Tracy Sparkes

-

UNITED STATES
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