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BACKGROUND Familial dilated cardiomyopathy(FDCM)account for 20%-30%of non-ischemic cardiomyopathies(NICM).Previous published data showed that some patients with FDCM tend to have rapidly progressive disease;however,five-year mortality was not significantly different in the familial and non-familial forms of NICM with optimal medical therapy.AIM To better define the characteristics and clinical outcomes of FDCM patients listed for heart transplantation(HT).METHODS We queried the United Network for Organ Sharing Registry to identify FDCM patients listed for HT between January 2008 and September 2015 and compared them to NICM and ischemic cardiomyopathy(ICM)patients.We included all patients≥18 years old and we separated patients to three groups:FDCM,NICM and ICM.Chi-square test was used to compare between categorical variables,the t-test was used to compare between continues variables,and Cox-proportional hazards model was used to perform time-dependent survival analyses.RESULTS Of the 24809 adults listed for HT,we identified 677 patients(2.7%)with the diagnosis of FDCM.Compared to patients with NICM and ICM,FDCM patients were younger(FDCM 43.9±13.5 vs NICM 50.9±12.3,P﹤0.001,vs ICM 58.5±8.1,P﹤0.001),more frequently listed as status 2(FDCM 35.2%vs NICM 26.5%,P﹤0.001),with significantly lower left ventricular assist device(LVAD)utilization(FDCM 18.4%vs NICM 25.1%,P﹤0.001;vs ICM 25.6%,P﹤0.001),but higher use of total artificial heart(FDCM 1.3%vs NICM 0.6%,P=0.039;vs ICM 0.4%,P=0.002).Additionally,patients with FDCM were less frequently delisted for clinical deterioration or death and more likely to be transplanted compared to those with NICM[hazard ratio(HR):0.617,95%confidence interval(CI):0.47-0.81;HR:1.25,95%CI:1.14-1.37,respectively],and ICM(HR:0.5,95%CI:0.38-0.66;HR:1.18,95%CI:1.08-1.3,respectively).There was more frequent rejection among patients with FDCM(FDCM 11.4%vs NICM 9.8%,P=0.28;vs ICM 8.4%,P=0.034).One,three,and five post-transplant survival of patients with FDCM(91%,88%and 80%)was similar
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篇名 Contemporary characteristics and outcomes of adults with familial dilated cardiomyopathy listed for heart transplantation
来源期刊 世界心脏病学杂志:英文版(电子版) 学科 医学
关键词 FAMILIAL DILATED CARDIOMYOPATHY END-STAGE heart failure Wait list TRANSPLANT OUTCOMES
年,卷(期) 2019,(1) 所属期刊栏目
研究方向 页码范围 38-46
页数 9页 分类号 R
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FAMILIAL
DILATED
CARDIOMYOPATHY
END-STAGE
heart
failure
Wait
list
TRANSPLANT
OUTCOMES
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研究分支
研究去脉
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世界心脏病学杂志:英文版(电子版)
月刊
1949-8462
北京市朝阳区东四环中路62号楼远洋国际中
出版文献量(篇)
78
总下载数(次)
1
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