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首页> 外文期刊>Circulation journal >Clinical characteristics and outcome of hospitalized patients with heart failure in Japan.
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Clinical characteristics and outcome of hospitalized patients with heart failure in Japan.

机译：日本住院心力衰竭患者的临床特征和结局。

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BACKGROUND: Heart failure (HF), defined as a complex clinical syndrome that can result from any structural or functional cardiac disorder that impairs the ability of the ventricle to fill with or eject blood, is a leading cause of mortality and hospitalization for adults older than 65 years in the industrialized countries. The characteristics and outcome of patients with HF have been described by several epidemiological studies and large scale clinical trials, performed mainly in the United States and Europe. Very little information is available on this issue in Japan. METHODS AND RESULTS: The Japanese Cardiac Registry of Heart Failure in Cardiology (JCARE-CARD) is designed to prospectively study the characteristics, treatment, and outcomes of a broad sample of patients hospitalized with HF at teaching hospitals throughout Japan between January 2004 to June 2005 and the outcomes, including death and hospital readmission, will be followed through 2006 (mean follow-up at least 1 year). Participating cardiologists identify patients admitted for worsening of HF symptoms. Demographics, medical history, severity, treatment, and outcome data are collected and entered into a database via secure web browser technology. As of June 2005, baseline data for 2,676 patients with HF have been registered from 164 participating hospitals. CONCLUSIONS: The JCARE-CARD will provide important insights into the management of patients with HF in routine clinical practice in Japan, thus providing the framework for improved management strategies for these patients.
机译：背景：心力衰竭（HF）被定义为一种复杂的临床综合征，可能由任何损害心室充血或排出血液能力的结构性或功能性心脏病引起，是导致19岁以上成年人死亡和住院的主要原因在工业化国家已有65年的历史。主要在美国和欧洲进行的几项流行病学研究和大规模临床试验已经描述了HF患者的特征和结局。在日本，有关此问题的信息很少。方法和结果：日本心脏病心力衰竭心脏登记系统（JCARE-CARD）旨在前瞻性研究2004年1月至2005年6月在日本各教学医院住院的大量HF患者的特征，治疗和结局包括死亡和住院再住院在内的结果将一直持续到2006年（平均随访至少1年）。参与的心脏病学家确定了因心衰症状恶化而入院的患者。收集人口统计信息，病史，严重程度，治疗和结果数据，然后通过安全的Web浏览器技术将其输入数据库。截至2005年6月，已经从164家参与医院登记了2676名HF患者的基线数据。结论：JCARE-CARD将为日本常规临床实践中的HF患者管理提供重要见识，从而为改善这些患者的管理策略提供框架。

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