裁定注册数据:好处和缺点- ACTION经验。

David M Kwiatkowski, Scott Auerbach, Robert A Niebler
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引用次数: 0

摘要

高级心脏治疗改善结果网络(ACTION)注册收集数据并判定参与中心接受机械循环支持的儿科患者的不良事件。迄今为止,该登记处包括来自48个中心的1500多名患者。收集的数据已用于研究出版物、质量改进项目和几种心室辅助装置的监管支持。虽然这个数据集很大,而且经过审核,但该注册表确实存在局限性,可能会限制对研究结果的解释。充分了解潜在的偏见和局限性,使研究人员和临床医生能够从患者群体中得出有意义的结论。本报告回顾了ACTION注册的优势和局限性,以确保在接受机械循环支持的儿科患者中获得最佳效用。它还提出了潜在的改进领域,以促进对这一弱势群体的最佳照顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adjudicating Registry Data: Benefits and Pitfalls-The ACTION Experience.

The Advanced Cardiac Therapies Improving Outcomes Network (ACTION) registry collects data and adjudicates adverse events on pediatric patients receiving mechanical circulatory support at participating centers. To date, the registry includes over 1500 patients from 48 centers. Data collected has been used for research publications, quality improvement projects, and the regulatory support of several ventricular assist devices. While this dataset is large and adjudicated, the registry has real limitations that may limit the interpretation of findings. A full understanding of potential biases and limitations allows researchers and clinicians to make meaningful conclusions from the patient population. This report reviews the strengths and limitations of the ACTION registry to ensure optimal utility among pediatric patients receiving mechanical circulatory support. It also suggests potential areas for improvement to facilitate best care of this vulnerable population.

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