دورية أكاديمية

Early use of PCSK9 inhibitor therapy after heart transplantation from a hepatitis C virus positive donor.

التفاصيل البيبلوغرافية
العنوان: Early use of PCSK9 inhibitor therapy after heart transplantation from a hepatitis C virus positive donor.
المؤلفون: Fanous, Matthew M., Gianos, Eugenia, Sperling, Laurence S., Mintz, Guy L., Majure, David T., Hirsh, Benjamin J.
المصدر: Journal of Clinical Lipidology; Jul2021, Vol. 15 Issue 4, p579-583, 5p
مصطلحات موضوعية: HEART transplantation, CARDIOMYOPATHIES, HEPATITIS C, ANTIVIRAL agents, DRUG interactions
مستخلص: • Statins in HCV heart transplant recipients may be avoided due to drug interactions. • Nonstatin therapy for prevention of CAV has not been well studied. • PCSK9 inhibitors appear safe among recipients of hepatitis C virus positive donors. • Early PCSK9 inhibition may be beneficial for recipients of hepatitis C virus donors. Although statin therapy is a primary treatment to prevent cardiac allograft vasculopathy (CAV), its use may be delayed due to pharmacologic interactions in the early post-transplant period among heart transplant (HT) recipients with hepatitis C virus positive (HCV+) donors. Further examination of the possible benefits of early, nonstatin lipid-lowering therapies (LLT), such as PCSK9 inhibitors (PCSK9i), among this specific subset of transplant recipients is therefore becoming increasingly important. We report a 60-year-old man who received a HT from a HCV+ donor for end-stage ischemic cardiomyopathy. In the early post-transplant period, there was concern for drug-drug interactions between statin, immunosuppressant, and direct acting antiviral (DAA) therapy. In addition, prior to transplant, he reported statin-associated muscle symptoms in response to multiple statins, which persisted despite attempts to re-challenge and use an every-other-day dosing strategy. Therefore, the patient was started on PCSK9i therapy after transplantation and while receiving curative DAA therapy for HCV. As the number of HT recipients of HCV+ donors continue to rise, investigation into the safety and benefits of early use of PCSK9i for the reduction of CAV and improved cardiovascular and mortality outcomes should be pursued. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Supplemental Index
الوصف
تدمد:19332874
DOI:10.1016/j.jacl.2021.05.003