Anti-inflammatory therapies for pericardial diseases in the COVID-19 pandemic: safety and potentiality.


Journal

Journal of cardiovascular medicine (Hagerstown, Md.)
ISSN: 1558-2035
Titre abrégé: J Cardiovasc Med (Hagerstown)
Pays: United States
ID NLM: 101259752

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 14 7 2020
medline: 13 8 2020
entrez: 14 7 2020
Statut: ppublish

Résumé

: The COVID-19 pandemic is challenging our cardiovascular care of patients with heart diseases. In the setting of pericardial diseases, there are two possible different scenarios to consider: the patient being treated for pericarditis who subsequently becomes infected with SARS-CoV-2, and the patient with COVID-19 who develops pericarditis or pericardial effusion. In both conditions, clinicians may be doubtful regarding the safety of nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, colchicine, and biological agents, such as anti-IL1 agents (e.g. anakinra), that are the mainstay of therapy for pericarditis.For NSAIDs, there is no clear scientific evidence linking ibuprofen and other NSAIDs to worsening of COVID-19; however, it seems prudent to continue them, if necessary to control pericarditis, and on the other hand, to prefer paracetamol for fever and systemic symptoms related to COVID-19. Treatments with corticosteroids, colchicine, and anakinra appear well tolerated in the context of COVID-19 infection and are currently actively evaluated as potential therapeutic options for COVID infection at different stages of the disease. On this basis, currently most treatments for pericarditis do not appear contraindicated also in the presence of possible COVID-19 infection and should not be discontinued, and some (corticosteroids, colchicine, and anakinra) can be considered to treat both conditions.

Identifiants

pubmed: 32658005
doi: 10.2459/JCM.0000000000001059
pii: 01244665-202009000-00001
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Glucocorticoids 0
Interleukin 1 Receptor Antagonist Protein 0
Receptors, Interleukin-1 0
Colchicine SML2Y3J35T

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

625-629

Références

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Auteurs

Massimo Imazio (M)

University Cardiology, A.O.U. Città della Salute e della Scienza di Torino, Turin.

Antonio Brucato (A)

Dipartimento Scienze Biomediche e Cliniche Luigi Sacco, ASST Fatebenefratelli-Sacco, Università degli Studi di Milano, Milan, Italy.

George Lazaros (G)

First Cardiology Department, Hippokration General Hospital, National and Kapodistrian University of Athens, Greece.

Alessandro Andreis (A)

University Cardiology, A.O.U. Città della Salute e della Scienza di Torino, Turin.

Mirko Scarsi (M)

Internal Medicine Department, ASST Valcamonica, Brescia, Italy.

Allan Klein (A)

Center for the Diagnosis and Treatment for Pericardial Diseases, Cleveland Clinic, USA.

Gaetano Maria De Ferrari (GM)

University Cardiology, A.O.U. Città della Salute e della Scienza di Torino, Turin.

Yehuda Adler (Y)

College of Law and Business, Ramat Gan, Israel, Sackler Faculty of Medicine, Tel Aviv University, Mayanei Hayeshua Medical Center, Bnei Brak, Israel.

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