Relationship of Mild to Moderate Impairment of Left Ventricular Ejection Fraction With Fatal Ventricular Arrhythmic Events in Cardiac Sarcoidosis

Author:

Akama Yuka1ORCID,Fujimoto Yudai1ORCID,Matsue Yuya1ORCID,Maeda Daichi1ORCID,Yoshioka Kenji2,Dotare Taishi1ORCID,Sunayama Tsutomu1,Nabeta Takeru3ORCID,Naruse Yoshihisa4ORCID,Kitai Takeshi5ORCID,Taniguchi Tatsunori6ORCID,Sato Shuntaro7ORCID,Tanaka Hidekazu8ORCID,Okumura Takahiro9ORCID,Baba Yuichi10ORCID,Minamino Tohru111ORCID

Affiliation:

1. Department of Cardiovascular Biology and Medicine Juntendo University Graduate School of Medicine Tokyo Japan

2. Department of Cardiology Kameda Medical Center Chiba Japan

3. Department of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan

4. Division of Cardiology, Internal Medicine III Hamamatsu University School of Medicine Hamamatsu Japan

5. Department of Cardiovascular Medicine National Cerebral and Cardiovascular Center Osaka Japan

6. Department of Cardiovascular Medicine Osaka University Graduate School of Medicine Osaka Japan

7. Clinical Research Canter Nagasaki University Hospital Nagasaki Japan

8. Division of Cardiovascular Medicine, Department of Internal Medicine Kobe University Graduate School of Medicine Kobe Japan

9. Department of Cardiology Nagoya University Graduate School of Medicine Nagoya Japan

10. Department of Cardiology and Geriatrics, Kochi Medical School Kochi University Nankoku Japan

11. Japan Agency for Medical Research and Development‐Core Research for Evolutionary Medical Science and Technology (AMED‐CREST), Japan Agency for Medical Research and Development Tokyo Japan

Abstract

Background Current guidelines recommend placing an implantable cardiac defibrillator for patients with cardiac sarcoidosis and a severely impaired left ventricular ejection fraction (LVEF) of ≤35%. In this study, we determined the association between mild or moderate LVEF impairment and fatal ventricular arrhythmic event (FVAE). Methods and Results We retrospectively analyzed 401 patients with cardiac sarcoidosis without sustained ventricular arrhythmia at diagnosis. The primary end point was an FVAE, defined as the combined endpoint of documented ventricular tachycardia or ventricular fibrillation and sudden cardiac death. Two cutoff points for LVEF were used: a sex‐specific lower threshold of normal range of LVEF (52% for men and 54% for women) and an LVEF of 35%, which is used in the current guidelines. During a median follow‐up of 3.2 years, 58 FVAEs were observed, and the 5‐ and 10‐year estimated incidences of FVAEs were 16.8% and 23.0%, respectively. All patients were classified into 3 groups according to LVEF: impaired LVEF group, mild to moderate impairment of LVEF group, and maintained LVEF group. Multivariable competing risk analysis showed that both the impaired LVEF group (hazard ratio [HR], 3.24 [95% CI, 1.49–7.04]) and the mild to moderate impairment of LVEF group (HR, 2.16 [95% CI, 1.04–4.46]) were associated with a higher incidence of FVAEs than the maintained LVEF group after adjustment for covariates. Conclusions Patients with cardiac sarcoidosis are at a high risk of FVAEs, regardless of documented ventricular arrhythmia at the time of diagnosis. In patients with cardiac sarcoidosis, mild to moderate impairment of LVEF is associated with FVAEs.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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