Anakinra for constrictive pericarditis associated with incessant or recurrent pericarditis.


Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
10 2020
Historique:
received: 14 03 2020
revised: 25 04 2020
accepted: 05 05 2020
pubmed: 2 9 2020
medline: 29 6 2021
entrez: 2 9 2020
Statut: ppublish

Résumé

Frequent flares of pericardial inflammation in recurrent or incessant pericarditis with corticosteroid dependence and colchicine resistance may represent a risk factor for constrictive pericarditis (CP). This study was aimed at the identification of CP in these patients, evaluating the efficacy and safety of anakinra, a third-line treatment based on interleukin-1 inhibition, to treat CP and prevent the need for pericardiectomy. Consecutive patients with recurrent or incessant pericarditis with corticosteroid dependence and colchicine resistance were included in a prospective cohort study from 2015 to 2018. Enrolled patients received anakinra 100 mg once daily subcutaneously. The primary end point was the occurrence of CP. A clinical and echocardiographic follow-up was performed at 1, 3, 6 months and then every 6 months. Thirty-nine patients (mean age 42 years, 67% females) were assessed, with a baseline recurrence rate of 2.76 flares/patient-year and a median disease duration of 12 months (IQR 9-20). During follow-up, CP was diagnosed in 8/39 (20%) patients. After anakinra dose of 100 mg/day, 5 patients (63%) had a complete resolution of pericardial constriction within a median of 1.2 months (IQR 1-4). In other three patients (37%), CP became chronic, requiring pericardiectomy within a median of 2.8 months (IQR 2-5). CP occurred in 11 patients (28%) with incessant course, which was associated with an increased risk of CP over time (HR for CP 30.6, 95% CI 3.69 to 253.09). In patients with recurrent or incessant pericarditis, anakinra may have a role in CP reversal. The risk of CP is associated with incessant rather than recurrent course.

Identifiants

pubmed: 32868281
pii: heartjnl-2020-316898
doi: 10.1136/heartjnl-2020-316898
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Interleukin 1 Receptor Antagonist Protein 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1561-1565

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Alessandro Andreis (A)

University Cardiology, Department of Medical Sciences, AOU Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.

Massimo Imazio (M)

University Cardiology, AOU Città della Salute e della Scienza di Torino, Torino, Italy massimo_imazio@yahoo.it.
Department of Public Health and Pediatrics, University of Torino, Torino, Italy.

Carla Giustetto (C)

University Cardiology, Department of Medical Sciences, AOU Città della Salute e della Scienza di Torino and University of Torino, Torino, Italy.

Antonio Brucato (A)

Department of Medicine, Azienda Socio Sanitaria Territoriale (ASST) Fatebenefratelli-Sacco and Department of Biomedical and Clinical Sciences Luigi Sacco, University of Milan, Milano, Italy.

Yehuda Adler (Y)

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

Gaetano Maria De Ferrari (GM)

University Cardiology, Department of Medical Sciences, AOU Città della Salute e della Scienza di Torino and University of Torino, Torino, Piemonte, Italy.

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Classifications MeSH