Cardiac involvement in the adult primary vasculitides
Giulia Pazzola1, Nicolò Pipitone1, Carlo Salvarani1
1Rheumatology Unit, Department of Internal Medicine, Azienda USL-IRCCS di Reggio Emilia e Università di Modena e Reggio Emilia , Reggio Emilia, Italy.
Insights
Heart involvement in vasculitis is rare but serious, necessitating a multidisciplinary approach for diagnosis and management. Early immunosuppressive treatment and surgery can improve outcomes for patients with cardiac disease in vasculitis.
Area of Science:
- Cardiology
- Rheumatology
- Vascular Medicine
Background:
- Heart involvement in vasculitis, though infrequent, poses significant risks.
- Diagnosing cardiac disease in vasculitis requires a comprehensive, multidisciplinary strategy.
Purpose of the Study:
- To review the literature on cardiac manifestations of vasculitis.
- To highlight the importance of a collaborative approach in managing heart disease in vasculitis.
Main Methods:
- A literature search was conducted using PubMed.
- Keywords included 'heart' and 'vasculitis'.
Main Results:
- Any form of vasculitis can impact the heart.
- Cardiac involvement is more prevalent in Takayasu arteritis, polyarteritis nodosa, and eosinophilic granulomatosis with polyangiitis.
- Treatment strategies include immunosuppression and surgical intervention.
Conclusions:
- Effective management of cardiac vasculitis relies on integrated care from Rheumatologists, Radiologists, Cardiologists, and Heart Surgeons.
- Timely immunosuppressive therapy and surgical options can enhance patient prognosis.
Introduction:
Heart involvement in vasculitis is rare, but potentially severe. The ascertainment of cardiac disease in vasculitis is complex and requires an integrated multidisciplinary approach involving the Rheumatologist, Radiologist, Cardiologist, and Heart surgeon.
Areas Covered:
the authors searched PubMed using the keywords 'heart'[Mesh] and vasculitis"[Mesh].
Expert Opinion:
Virtually any vasculitis can affect the heart, but cardiac involvement is more common in some vasculitides such as Takayasu arteritis, polyarteritis nodosa, and eosinophilic granulomatosis with polyangiitis. Immunosuppressive treatment and when indicated surgery can improve the prognosis.
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