Multicenter study of universal prophylaxis versus pre‐emptive therapy for patients at intermediate risk (R+) for CMV following heart transplantation

Author:

Lerman Joseph B.12ORCID,Green Cynthia L.23ORCID,Molina Maria R.4,Maharaj Valmiki5ORCID,Ortega‐Legaspi Juan M.4ORCID,Sen Sounok6ORCID,Flattery Maureen7,Maziarz Eileen K.8ORCID,Shah Keyur B.7ORCID,Martin Cindy M.9,Alexy Tamas5,Shah Palak10ORCID,Morris Alanna A.11ORCID,DeVore Adam D.12ORCID,Cole Robert T.12ORCID

Affiliation:

1. Division of Cardiology Duke University School of Medicine Durham North Carolina USA

2. Duke Clinical Research Institute Durham North Carolina USA

3. Department of Biostatistics and Bioinformatics Duke University School of Medicine Durham North Carolina USA

4. Department of Medicine Division of Cardiovascular Medicine University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA

5. Division of Cardiology University of Minnesota Minneapolis Minnesota USA

6. Section of Cardiovascular Medicine Yale University School of Medicine New Haven Connecticut USA

7. VCU Pauley Heart Center Virginia Commonwealth University Richmond Virginia USA

8. Division of Infectious Diseases Duke University School of Medicine Durham North Carolina USA

9. Department of Cardiovascular Medicine Houston Methodist Hospital Houston Texas USA

10. Heart Failure, MCS and Transplant Inova Heart and Vascular Institute Falls Church Virginia USA

11. Division of Cardiology Emory University School of Medicine Atlanta Georgia USA

12. Samsky Advanced Heart Failure Center Piedmont Heart Institute Atlanta Georgia USA

Abstract

AbstractIntroductionHeart transplant (HT) recipients with prior exposure to cytomegalovirus (CMV R+) are considered intermediate risk for CMV‐related complications. Consensus guidelines allow for either universal prophylaxis (UP) or preemptive therapy (PET) (serial CMV testing) approaches to CMV prevention in such patients. Whether an optimal approach to mitigate CMV related risks exists in this setting remains uncertain. We therefore assessed the utility of PET as compared to UP in CMV R+ HT recipients.MethodsRetrospective analysis of all CMV R+ HT recipients from 6 U.S. centers between 2010 and 2018 was performed. The primary outcome was the development of CMV DNAemia or end‐organ disease resulting in the initiation/escalation of anti‐CMV therapy. The secondary outcome was CMV‐related hospitalization. Additional outcomes included incidence of acute cellular rejection (ACR) ≥ grade 2R, death, cardiac allograft vasculopathy (CAV), and leukopenia.ResultsOf 563 CMV R+ HT recipients, 344 (61.1%) received UP. PET was associated with increased risk for the primary (adjusted HR 3.95, 95% CI: 2.65–5.88, p < .001) and secondary (adjusted HR 3.19, 95% CI: 1.47–6.94, p = .004) outcomes, and with increased ACR ≥ grade 2R (PET 59.4% vs. UP 34.4%, p < .001). Incidence of detectable CAV was similar at 1 year (PET 8.2% vs. UP 9.5%, p = .698). UP was associated with increased incidence of leukopenia within 6 months post‐HT (PET 34.7% vs. UP 43.6%, p = .036).ConclusionThe use of a PET CMV prophylaxis strategy in intermediate risk HT recipients associated with increased risk of CMV infection and CMV‐related hospitalization, and may associate with worse post‐HT graft outcomes.

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Transplantation

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