The Complex Management of Atrial Fibrillation and Cancer in the COVID-19 Era: Drug Interactions, Thromboembolic Risk, and Proarrhythmia.
Antineoplastic Agents
/ adverse effects
Arrhythmias, Cardiac
/ chemically induced
Atrial Fibrillation
/ complications
COVID-19
/ complications
Cytochrome P-450 Enzyme Inhibitors
/ adverse effects
Cytochrome P-450 Enzyme System
Drug Interactions
Factor Xa Inhibitors
/ adverse effects
Hemorrhage
/ chemically induced
Humans
Long QT Syndrome
/ chemically induced
Neoplasms
/ complications
Thromboembolism
/ etiology
COVID-19 Drug Treatment
Anticancer agents
Atrial fibrillation
COVID-19
Direct oral anticoagulants
Drug-drug interactions
QT prolongation
Journal
Current heart failure reports
ISSN: 1546-9549
Titre abrégé: Curr Heart Fail Rep
Pays: United States
ID NLM: 101196487
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
pubmed:
8
10
2020
medline:
15
12
2020
entrez:
7
10
2020
Statut:
ppublish
Résumé
Cardiotoxicity by anticancer agents has emerged as a multifaceted issue and is expected to affect both mortality and morbidity. This review summarizes clinical challenges in the management of oncological patients requiring anticoagulants for atrial fibrillation (AF) also considering the current outbreak of the COVID-19 (coronavirus disease 2019) pandemic, since this infection can add challenges to the management of both conditions. Specifically, the aims are manyfold: (1) describe the evolving use of direct oral anticoagulants (DOACs) in AF patients with cancer; (2) critically appraise the risk of clinically important drug-drug interactions (DDIs) between DOACs and oral targeted anticancer agents; (3) address expected DDIs between DOACs and candidate anti-COVID drugs, with implications on management of the underlying thrombotic risk; and (4) characterize the proarrhythmic liability in cardio-oncology in the setting of COVID-19, focusing on QT prolongation. AF in cardio-oncology poses diagnostic and management challenges, also due to the number of anticancer drugs recently associated with AF onset/worsening. Oral targeted drugs can potentially interact with DOACs, with increased bleeding risk mainly due to pharmacokinetic DDIs. Moreover, the vast majority of oral anticancer agents cause QT prolongation with direct and indirect mechanisms, potentially resulting in the occurrence of torsade de pointes, especially in susceptible patients with COVID-19 receiving additional drugs with QT liability. Oncologists and cardiologists must be aware of the increased bleeding risk and arrhythmic susceptibility of patients with AF and cancer due to DDIs. High-risk individuals with COVID-19 should be prioritized to target preventive strategies, including optimal antithrombotic management, medication review, and stringent monitoring.
Identifiants
pubmed: 33025463
doi: 10.1007/s11897-020-00485-9
pii: 10.1007/s11897-020-00485-9
pmc: PMC7537958
doi:
Substances chimiques
Antineoplastic Agents
0
Cytochrome P-450 Enzyme Inhibitors
0
Factor Xa Inhibitors
0
Cytochrome P-450 Enzyme System
9035-51-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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