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Cardiac sarcoidosis: Diagnosis, therapeutic management and prognostic factors
Catherine Chapelon-Abric1, Damien Sene2, David Saadoun1
1Département de Médecine Interne et d'Immunologie Clinique, CHU Pitié-Salpétrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France.
Insights
Cardiac sarcoidosis (CS) treatment with steroids, alone or combined with immunosuppressants, shows a good prognosis. Most patients recovered, with a 5-year survival rate of 92%.
Area of Science:
- Cardiology
- Immunology
- Pulmonology
Background:
- Cardiac sarcoidosis (CS) is a severe manifestation of sarcoidosis, often presenting in cardiology settings.
- Despite treatment, CS poses a significant mortality risk, contributing to a substantial portion of sarcoidosis-related deaths.
Purpose of the Study:
- To provide an overview of CS in a non-cardiac unit.
- To analyze the impact of initial immunosuppressive therapy on CS outcomes and survival.
- To identify factors associated with disease relapse in CS patients.
Main Methods:
- Retrospective analysis of 59 CS patients selected from 534 sarcoidosis cases using 2006 international criteria.
- Detailed review of symptoms, physical findings, and cardiac investigations.
- Median follow-up duration of 60 months.
Main Results:
- Eighty-one percent of patients had echocardiography abnormalities, 84% showed isotopic defects, and 92% had abnormal MRI findings.
- First-line treatment involved steroids alone (24 patients) or steroids plus immunosuppressants (35 patients).
- Overall recovery was 80%, with 5-year survival at 92%. No significant difference in recovery rates between treatment groups.
Conclusions:
- Patients with CS treated with steroids or combined immunosuppressive therapy exhibit a favorable prognosis.
- A 5-year survival rate of 92% and an 85% recovery rate were observed.
- Treatment approach (steroids alone vs. combined) did not significantly impact recovery rates.
Background:
Cardiac sarcoidosis (CS) is a severe localization, observed mostly in cardiology departments. Despite appropriate cardiological treatment, CS is a potentially life-threatening condition, and accounts for 13-85% of sarcoidosis-related deaths.
Aims:
This retrospective study aimed to give an overview of CS in a non-cardiac unit, to analyse the effect of first-line immunosuppressive treatment on outcome and survival and to evaluate factors associated with relapses.
Methods:
From 534 cases of sarcoidosis, we selected 59 patients with CS according to "2006 international criteria". We performed an in-depth analysis regarding symptoms, physical signs and cardiac investigation results. Patients were followed for a median period of 60 months.
Results:
The median age at cardiac signs was 42 years. Echocardiography abnormalities, isotopic defects and abnormal magnetic resonance imaging findings were observed in 81%, 84% and 92% of patients, respectively. First-line treatment included steroids alone in 24 patients and steroids plus immunosuppressive therapy in 35 patients. Forty-seven (80%) patients recovered; 12 stabilized or worsened. The recovery rate was 75% in the steroids alone group versus 83% in the steroids plus immunosuppressive therapy group. Five (9%) patients died during follow-up, with two deaths attributed to CS. The overall 1- and 5-year survival rates were 98% and 92%, respectively.
Conclusion:
Our series of patients with CS who received steroids alone or combined with immunosuppressive therapy had a good prognosis, with an overall 5-year survival rate of 92%. The recovery rate was 85%, with no significant difference between patients treated with steroids alone or plus immunosuppressive therapy.
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