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肾脏认知登记与教育(KARE)研究:一项提高医疗服务提供者和患者对慢性肾脏病参与度的随机对照试验方案

The Kidney Awareness Registry and Education (KARE) study: protocol of a randomized controlled trial to enhance provider and patient engagement with chronic kidney disease.

作者信息

Tuot Delphine S, Velasquez Alexandra, McCulloch Charles E, Banerjee Tanushree, Zhu Yunnuo, Hsu Chi-yuan, Handley Margaret, Schillinger Dean, Powe Neil R

机构信息

Division of Nephrology, University of California, San Francisco, San Francisco, CA, 94143, USA.

Center for Vulnerable Populations at San Francisco General Hospital, San Francisco, CA, USA.

出版信息

BMC Nephrol. 2015 Oct 22;16:166. doi: 10.1186/s12882-015-0168-4.

Abstract

BACKGROUND

Chronic kidney disease (CKD) is common and is associated with excess mortality and morbidity. Better management could slow progression of disease, prevent metabolic complications, and reduce cardiovascular outcomes. Low patient awareness of CKD and ineffective patient-provider communication can impede such efforts. We developed provider and patient-directed interventions that harness health information technology to enhance provider recognition of CKD and delivery of guideline concordant care and augment patient understanding and engagement in CKD care.

METHODS/DESIGN: We report the design and protocol of the Kidney Awareness Registry and Education (KARE) Study, a 2x2 factorial randomized controlled trial that examines the impact of a multi-level intervention on health outcomes among low-income English, Spanish and Cantonese-speaking patients with CKD in a safety net system. The intervention includes: (1) implementation of a primary care electronic CKD registry that notifies practice teams of patients' CKD status and employs a patient profile and quarterly feedback to encourage provision of guideline-concordant care at point-of-care and via outreach; and (2) a language-concordant, culturally-sensitive self-management support program that consists of automated telephone modules, provision of low-literacy written patient-educational materials and telephone health coaching. The primary outcomes of the trial are changes in systolic blood pressure (BP) and the proportion of patients with BP control (≤ 140/90 mmHg) after one year. Secondary outcomes include patient understanding of CKD, participation in healthy behaviors, and practice team delivery of guideline-concordant CKD care.

DISCUSSION

Results from the KARE study will provide data on the feasibility, effectiveness, and acceptability of technology-based interventions that support primary care efforts at improving health outcomes among vulnerable patients with CKD.

TRIAL REGISTRATION

ClinicalTrials.gov, number: NCT01530958.

摘要

背景

慢性肾脏病(CKD)很常见,与过高的死亡率和发病率相关。更好的管理可以减缓疾病进展,预防代谢并发症,并改善心血管结局。患者对CKD的认知度低以及医患沟通无效会阻碍这些努力。我们开发了针对医护人员和患者的干预措施,利用健康信息技术来提高医护人员对CKD的识别能力以及提供符合指南的治疗,并增强患者对CKD护理的理解和参与度。

方法/设计:我们报告了肾脏认知登记与教育(KARE)研究的设计和方案,这是一项2×2析因随机对照试验,旨在研究在安全网系统中,针对低收入的讲英语、西班牙语和粤语的CKD患者,多层次干预对健康结局的影响。干预措施包括:(1)实施初级保健电子CKD登记系统,该系统会通知医疗团队患者的CKD状态,并使用患者档案和季度反馈来鼓励在医疗点并通过外展服务提供符合指南的治疗;(2)一个语言一致、文化敏感的自我管理支持项目,该项目包括自动电话模块、提供低识字水平的书面患者教育材料以及电话健康指导。该试验的主要结局是一年后收缩压(BP)的变化以及血压得到控制(≤140/90 mmHg)的患者比例。次要结局包括患者对CKD的理解、参与健康行为的情况以及医疗团队提供符合指南的CKD护理的情况。

讨论

KARE研究的结果将提供基于技术的干预措施的可行性、有效性和可接受性的数据,这些干预措施支持初级保健改善弱势CKD患者健康结局的努力。

试验注册

ClinicalTrials.gov,编号:NCT01530958。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15cb/4618520/f3c656629775/12882_2015_168_Fig1_HTML.jpg

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