心源性休克登记处
的
美国心脏协会 has created the 心源性休克登记处 powered by Get With 的 Guidelines to improve the quality of care and better understand the 临床 manifestations, 管理模式, and outcomes in patients presenting with cardiogenic shock to hospitals across the nation. 的 registry focuses on real-time data from acute care hospitals to help clinicians and 研究人员 understand and provide feedback to healthcare organizations on how to best treat cardiogenic shock patients.
的 心源性休克登记处 builds upon over 20 years of quality improvement and registry experience rooted in the AHA's Get With 的 Guidelines® platform. 这方面的数据 免费 registry will help inform the larger medical community on how to best treat cardiogenic shock.
该登记处的核心科学目标包括:
- 研究心源性休克, 包括诊断, 治疗, and outcomes among patients in real-world acute care 临床 settings throughout the U.S.
- Provide high-quality evidence that helps inform clinicians, 研究人员, 联邦机构, industry and other healthcare stakeholders on best practices for treating cardiogenic shock patients.
- Develop streamlined longitudinal research infrastructure for pragmatic 临床 trials and other translational, 临床, 实施科学.
- Create and pilot evidence-based performance metrics for national benchmarking.
- Promote systems-of-care metrics for cardiogenic shock patients that strive for health equity.
全国合计, deidentified data will be available to 研究人员 through the 美国心脏协会’s 精准医疗平台, a secure cloud-computing platform to facilitate the research. 精准医疗平台, 由亚马逊网络服务提供支持, is a central hub for the cardiovascular and stroke research community to access vast and diverse datasets and cloud-based workspaces that enable state-of-the-art, 高性能计算, analytics and collaboration to accelerate scientific discovery.
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参与的好处
的 registry platform is a robust web-based tool for tracking all patients hospitalized with cardiogenic shock. 该工具的一些功能包括:
- On-demand reporting that includes national and regional benchmarks
- Customized downloadable reports for ad-hoc analyses
- Performance dashboards for responsive quality improvement
- 首先获得创新增强功能
数据收集
Data are reported in the 美国心脏协会's online registry platform, IRP. 的 心源性休克登记处 supports bulk upload of data and interoperability solutions to reduce abstraction burden.
研究的机会
Complete the 网上的建议 completely with details and suggested tables and charts for the proposed study.