4.5 Article

Cardiac sarcoidosis outcome differences: A comparison of patients with de novo cardiac versus known extracardiac sarcoidosis at presentation

期刊

RESPIRATORY MEDICINE
卷 198, 期 -, 页码 -

出版社

W B SAUNDERS CO LTD
DOI: 10.1016/j.rmed.2022.106864

关键词

Cardiomyopathy; Arrhythmia; Cardiac sarcoidosis; Pulmonary sarcoidosis; Immunosuppression

资金

  1. Foundation for Sarcoidosis Research Small Grant Program
  2. Johns Hopkins Specialized Center for Research Excellence in Sex Differences
  3. Foundation for Gender-Specific Medicine [U54AG062333]
  4. Johns Hopkins University School of Medicine Magic that Matters Fund for Cardiovascular Research

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This study compares the clinical characteristics and outcomes of patients with cardiac sarcoidosis (CS) as their first recognized organ manifestation and those with a prior history of sarcoidosis. The results show that patients with de novo CS have more advanced cardiac presentation, worse outcomes, and increased risk of adverse cardiac events compared to patients with prior extracardiac sarcoidosis (ECS).
Background: Sarcoidosis is a systemic disease characterized by granulomatous inflammation. Cardiac involvement is associated with increased morbidity. However, differences in clinical characteristics and outcomes based on initial sarcoidosis organ manifestation in patients with cardiac sarcoidosis (CS) have not been described. Methods: A retrospective cohort of 252 patients with CS at an urban, quaternary medical center was studied. Presentation, treatment and outcomes of de novo CS and prior ECS groups were compared. Survival free of primary composite outcome (left ventricular assist device implantation, orthotopic heart transplantation (OHT), or death) was assessed. Results: There were 124 de novo CS patients and 128 with prior ECS at time of CS diagnosis. De novo CS patients were younger at CS diagnosis (p = 0.020). De novo CS patients had a more advanced cardiac presentation: lower left ventricular ejection fraction (LVEF) (p < 0.001), more frequent sustained ventricular arrhythmias (VA) (p = 0.001), and complete heart block (p = 0.001). During follow-up, new VA (p < 0.001), ventricular tachycardia ablation (p < 0.001), and OHT (p = 0.003) were more common in the de novo CS group. Outcome free survival was significantly shorter for de novo CS patients (p = 0.005), with increased hazard of primary composite outcome (p = 0.034) and development of new VA (p = 0.027) when compared to ECS patients. Overall mortality was similar between groups. Conclusion: Patients presenting with CS as their first recognized organ manifestation of sarcoidosis have an increased risk of adverse cardiac outcomes as compared to those with a prior history of ECS. Improved awareness and diagnosis of CS is warranted for earlier recognition.

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