心力衰竭住院患者的全球健康和经济负担:从心力衰竭住院登记中吸取的经验教训。
The global health and economic burden of hospitalizations for heart failure: lessons learned from hospitalized heart failure registries.
机构信息
Department of Medicine, Stanford University School of Medicine, Palo Alto, California.
Ahmanson-UCLA Cardiomyopathy Center, Ronald Reagan-UCLA Medical Center, Los Angeles, California.
出版信息
J Am Coll Cardiol. 2014 Apr 1;63(12):1123-1133. doi: 10.1016/j.jacc.2013.11.053. Epub 2014 Feb 5.
Heart failure is a global pandemic affecting an estimated 26 million people worldwide and resulting in more than 1 million hospitalizations annually in both the United States and Europe. Although the outcomes for ambulatory HF patients with a reduced ejection fraction (EF) have improved with the discovery of multiple evidence-based drug and device therapies, hospitalized heart failure (HHF) patients continue to experience unacceptably high post-discharge mortality and readmission rates that have not changed in the last 2 decades. In addition, the proportion of HHF patients classified as having a preserved EF continues to grow and may overtake HF with a reduced EF in the near future. However, the prognosis for HF with a preserved EF is similar and there are currently no available disease-modifying therapies. HHF registries have significantly improved our understanding of this clinical entity and remain an important source of data shaping both public policy and research efforts. The authors review global HHF registries to describe the patient characteristics, management, outcomes and their predictors, quality improvement initiatives, regional differences, and limitations of the available data. Moreover, based on the lessons learned, they also propose a roadmap for the design and conduct of future HHF registries.
心力衰竭是一种全球性的流行疾病,影响着全球约 2600 万人,每年在美国和欧洲导致超过 100 万人住院。尽管发现了多种基于证据的药物和设备治疗方法,降低射血分数(EF)的门诊心力衰竭(HF)患者的预后有所改善,但住院心力衰竭(HHF)患者的出院后死亡率和再入院率仍然居高不下,近 20 年来没有变化。此外,被归类为射血分数保留的 HHF 患者的比例继续增加,在不久的将来可能超过射血分数降低的 HF。然而,射血分数保留的 HF 的预后相似,目前尚无可用的疾病修正治疗方法。HHF 登记处极大地提高了我们对这一临床实体的认识,仍然是制定公共政策和研究工作的重要数据来源。作者回顾了全球 HHF 登记处,以描述患者特征、管理、结果及其预测因素、质量改进举措、区域差异以及现有数据的局限性。此外,基于所吸取的经验教训,他们还为未来 HHF 登记处的设计和开展提出了路线图。