Hong Jung Ae, Kim Min-Seok, Cho Min-Su, Choi Hyo In, Kang Duk-Hyun, Lee Sang-Eun, Lee Ga-Yeon, Jeon Eun-Seok, Cho Jae-Yeong, Kim Kye-Hun, Yoo Byung-Su, Lee Jong-Young, Kim Won-Jang, Kim Kyung-Hee, Chung Wook-Jin, Lee Ju-Hee, Cho Myeong-Chan, Kim Jae-Joong
Department of Cardiology, Asan Medical Center, University of Ulsan College of Medicine Department of Internal Medicine, Seoul National University Hospital Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul Department of Cardiology, Translational Research Center on Aging, Chonnam National University Hospital, Gwangju Department of Internal Medicine, Wonju College of Medicine,Yonsei University, Wonju Department of Internal Medicine, Kangbuk Samsung Hospital, Seoul Department of Internal Medicine, CHA Bundang Medical Center, CHA University school of Medicine, Bundang Department of Cardiology, Sejong General Hospital Department of Cardiovascular Medicine, Gachon University Gil Medical Center, Incheon Department of Internal Medicine, Chungbuk National University School of Medicine, Cheongju, Korea.
Medicine (Baltimore). 2017 Sep;96(36):e7886. doi: 10.1097/MD.0000000000007886.
Idiopathic restrictive cardiomyopathy (RCMP) has not been fully understood because this disease is difficult to diagnose. The present study aimed to assess the clinical profile and outcome of idiopathic RCMP from a multicenter cohort.This investigation is a retrospective study of consecutive patients with idiopathic RCMP at 10 centers in Korea between 1990 and 2010. We evaluated the clinical characteristics of the patients and prognostic factors associated with mortality using multivariate Cox proportional hazards regression analyses.The study included 53 patients (26 men, 49.1%). During a median follow-up of 1.7 years, 17 patients (32.1%) died and 5 patients (9.4%) received a heart transplant. The 5-year survival rate of the overall patients was 64.4% ± 7.8%. In multivariable analyses, the predictors of mortality were tricuspid regurgitation (TR) ≥ moderate (hazard ratio [HR] 32.55, P < .001) and left ventricular end-diastolic diameter (LVEDD) (HR 0.85, P < .001).Idiopathic RCMP showed unfavorable prognosis. Advanced TR and lower LVEDD are independent adverse predictors of mortality in patients with idiopathic RCMP.
特发性限制型心肌病(RCMP)尚未被完全理解,因为这种疾病难以诊断。本研究旨在评估来自多中心队列的特发性RCMP的临床特征和预后。这项调查是对1990年至2010年期间韩国10个中心连续的特发性RCMP患者进行的回顾性研究。我们使用多变量Cox比例风险回归分析评估了患者的临床特征以及与死亡率相关的预后因素。该研究纳入了53例患者(26例男性,占49.1%)。在中位随访1.7年期间,17例患者(32.1%)死亡,5例患者(9.4%)接受了心脏移植。所有患者的5年生存率为64.4%±7.8%。在多变量分析中,死亡率的预测因素是中度及以上三尖瓣反流(TR)(风险比[HR] 32.55,P<0.001)和左心室舒张末期直径(LVEDD)(HR 0.85,P<0.001)。特发性RCMP显示出不良预后。严重TR和较低的LVEDD是特发性RCMP患者死亡率的独立不良预测因素。