Prospective renal insufficiency cohort evaluation: PRICE

描述（由申请人提供）： 在2003-2007年期间，前瞻性慢性肾功能不全队列（CRIC）研究招募了3400多名患有慢性肾脏疾病的成年人，以解决确定肾脏疾病快速进展的预测因素并通过最初5年随访阐明肾功能不全与亚临床和临床心血管事件风险、死亡和资源利用之间的关系的总体目标。拟议的审评委第二届会议将后续行动延长至2013年，这提供了一个独特的机会，可以利用审评委第一届会议的现有努力和成功，建立一个慢性肾病参与者队列，对肾病进展和各种不同的结果进行长期前瞻性随访。这一无与伦比的资源也将扩展与慢性肾脏疾病自然史相关的科学，以及对心血管疾病和其他不良事件的影响。宾夕法尼亚大学临床中心要解决的具体目标是：1。将较高比例的审评委第一阶段参与者重新纳入审评委第二届会议第二阶段。按照审评委第1和第2阶段方案收集接触和结果数据3.保持高水平的保留在研究4.调查自我报告的临床事件，并获得支持性病历和文件。5.输入数据和处理/运输生物标本。6.实施当地的质量保证和质量控制程序，以获得标准化的高质量测量。监测数据收集、数据录入和随访率8.通过研究范围内的小组委员会和活动，参与审评委研究的管理和监督发表和介绍审评委第十次研究的结果。促进和支持CRIC辅助研究的开展，包括与更广泛的肾脏病学研究界的合作。在本申请中，我们将概述我们的研究中心如何履行其在第1阶段的义务，尤其是如何为CRIC的辅助研究做出贡献。

DESCRIPTION (provided by applicant): Between 2003-2007, the prospective Chronic Renal Insufficiency Cohort (CRIC) Study enrolled >3400 adults with chronic kidney disease to address overarching goals of identifying predictors of rapid progression of kidney disease and clarifying the relationship between kidney dysfunction and the risks of subclinical and clinical cardiovascular events, death, and resource utilization through an initial 5-year follow-up. The proposed CRIC-2 extended follow-up through 2013 offers a unique opportunity to leverage the existing effort and success of CRIC-1 to establish a cohort of participants with chronic kidney disease who have long-term prospective follow-up on progression of kidney disease and a variety of different outcomes. This unparalleled resource will also expand the science related to chronic kidney disease natural history as well as the impact on cardiovascular disease and other adverse events. Specific Aims to be addressed by the University of Pennsyvania Clinical Center are: 1. To re-enroll a high percentage of CRIC Phase 1 participants into Phase 2 of CRIC 2. To collect exposure and outcome data per the CRIC Phase 1 and 2 protocols 3. To maintain high levels of retention in the study 4. To investigate self-reported clinical events and obtain supporting medical records and documentation. 5. To enter data and process/ship biological specimens. 6. To implement local quality assurance and quality control procedures as a means to obtain standardized, high quality measurements 7. To monitor data collection, data entry, and follow-up rates 8. To participate in governance and oversight of the CRIC study through studywide subcommittees and activities 9. To publish and present findings from the CRIC Study 10. To promote and support the conduct of ancillary studies in CRIC, including collaboration with the broader nephrology research community. In this application we will outline how our site has fulfilled its obligation in phase 1, how it has contributed in particular to ancillary studies in CRIC.