Myocarditis and Chronic Inflammatory Cardiomyopathy, from Acute Inflammation to Chronic Inflammatory Damage: An Update on Pathophysiology and Diagnosis.

endomyocardial biopsy eosinophilic granulomatosis with polyangiitis inflammatory cardiomyopathy myocarditis sarcoidosis systemic lupus erythematosus systemic sclerosis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
27 Dec 2023
Historique:
received: 03 12 2023
revised: 18 12 2023
accepted: 20 12 2023
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 11 1 2024
Statut: epublish

Résumé

Acute myocarditis covers a wide spectrum of clinical presentations, from uncomplicated myocarditis to severe forms complicated by hemodynamic instability and ventricular arrhythmias; however, all these forms are characterized by acute myocardial inflammation. The term "chronic inflammatory cardiomyopathy" describes a persistent/chronic inflammatory condition with a clinical phenotype of dilated and/or hypokinetic cardiomyopathy associated with symptoms of heart failure and increased risk for arrhythmias. A continuum can be identified between these two conditions. The importance of early diagnosis has grown markedly in the contemporary era with various diagnostic tools available. While cardiac magnetic resonance (CMR) is valid for diagnosis and follow-up, endomyocardial biopsy (EMB) should be considered as a first-line diagnostic modality in all unexplained acute cardiomyopathies complicated by hemodynamic instability and ventricular arrhythmias, considering the local expertise. Genetic counseling should be recommended in those cases where a genotype-phenotype association is suspected, as this has significant implications for patients' and their family members' prognoses. Recognition of the pathophysiological pathway and clinical "red flags" and an early diagnosis may help us understand mechanisms of progression, tailor long-term preventive and therapeutic strategies for this complex disease, and ultimately improve clinical outcomes.

Identifiants

pubmed: 38202158
pii: jcm13010150
doi: 10.3390/jcm13010150
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Auteurs

Giuseppe Uccello (G)

Division of Cardiology, Alessandro Manzoni Hospital-ASST Lecco, 23900 Lecco, Italy.

Giacomo Bonacchi (G)

Division of Cardiology, Tor Vergata University Hospital, 00133 Rome, Italy.

Valentina Alice Rossi (VA)

Department of Cardiology, University Hospital of Zurich, 8091 Zurich, Switzerland.

Giulia Montrasio (G)

Inherited Cardiovascular Diseases Unit, Barts Heart Centre, St. Bartholomew's Hospital, London EC1A 7BS, UK.

Matteo Beltrami (M)

Cardiomyopathy Unit, Careggi University Hospital, 50134 Florence, Italy.
Arrhythmia and Electrophysiology Unit, Careggi University Hospital, 50134 Florence, Italy.

Classifications MeSH