Diltiazem as a cyclosporine A-sparing agent in heart transplantation: Benefits beyond dose reduction

Diltiazem (DZ) is widely prescribed in transplant recipients because of its drug-drug interactions with calcineurin inhibitors (CNI). However, these interactions have been primarily investigated in renal transplantation, and data regarding the long-term efficacy and safety of DZ in orthotopic heart...

Verfasser: Alyaydin, Emyal
Reinecke, Holger
Tuleta, Izabela
Sindermann, Jürgen
FB/Einrichtung:FB 05: Medizinische Fakultät
Dokumenttypen:Artikel
Medientypen:Text
Erscheinungsdatum:2022
Publikation in MIAMI:31.05.2023
Datum der letzten Änderung:15.06.2023
Angaben zur Ausgabe:[Electronic ed.]
Quelle:Medicine 101 (2022) 41, e31166, 1-6
Schlagwörter:cyclosporin A; diltiazem; immunosuppression; orthotopic heart transplantation; survival
Fachgebiet (DDC):610: Medizin und Gesundheit
Lizenz:CC BY-NC 4.0
Sprache:Englisch
Förderung:Finanziert durch den Open-Access-Publikationsfonds der Westfälischen Wilhelms-Universität Münster (WWU Münster).
Format:PDF-Dokument
URN:urn:nbn:de:hbz:6-90019497166
Weitere Identifikatoren:DOI: 10.17879/70029679550
Permalink:https://nbn-resolving.de/urn:nbn:de:hbz:6-90019497166
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Onlinezugriff:10.1097_MD.0000000000031166.pdf

Diltiazem (DZ) is widely prescribed in transplant recipients because of its drug-drug interactions with calcineurin inhibitors (CNI). However, these interactions have been primarily investigated in renal transplantation, and data regarding the long-term efficacy and safety of DZ in orthotopic heart transplantation (OHT) are still sparse. Our study aimed to elucidate the extent to which the co-prescription of DZ reduces the dose required to maintain adequate blood levels of cyclosporine A (CsA) and the resulting effect on morbidity and mortality in OHT recipients. We performed a retrospective single-center analysis of OHT recipients on a long-term immunosuppressive regimen based on CsA and mycophenolate mofetil (MMF). The study population consisted of 95 adult OHT recipients with a mean follow-up of 15.8 ± 6.7 years. DZ was co-prescribed in 39 subjects (41.1%) and was associated with a 28.6% reduction of the mean CsA daily dose (P