ArticleAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2014
Developing a CKD registry in primary care: provider attitudes and input.
Article in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 4 of them syntheses that pooled it.
What it found
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Who cites it
19 citing papers in PubMed, 4 syntheses or guidelines pooled it, 33 citations in OpenAlex.
- Challenges and strategies for managing early-to-moderate chronic kidney disease in primary care: A systematic integrative review in high-income countries.The European journal of general practice · 2026Pooled it
- Using an Integrated Framework to Investigate the Facilitators and Barriers of Health Information Technology Implementation in Noncommunicable Disease Management: Systematic Review.Journal of medical Internet research · 2022Pooled it
- Barriers and facilitators for the implementation of health condition and outcome registry systems: a systematic literature review.Journal of the American Medical Informatics Association : JAMIA · 2022Pooled it
- Barriers and enablers to detection and management of chronic kidney disease in primary healthcare: a systematic review.BMC nephrology · 2020Pooled it
- Pragmatic Trial of Hospitalization Rate in Chronic Kidney Disease.The New England journal of medicine · 2024Trial
- Impact of a Primary Care CKD Registry in a US Public Safety-Net Health Care Delivery System: A Pragmatic Randomized Trial.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2018Trial
- The Kidney Awareness Registry and Education (KARE) study: protocol of a randomized controlled trial to enhance provider and patient engagement with chronic kidney disease.BMC nephrology · 2015Trial
- Examining the Role of a Comprehensive eConsult System to Enhance Access to Nephrology Care.Kidney medicine · 2026Article
- Barriers and Facilitators of Family Meetings in Primary Palliative Care: Insights From Slovenia.Zdravstveno varstvo · 2025Article
- Primary care clinician perspectives on automated nephrology e-consults for diabetic kidney disease: a pre-implementation qualitative study.BMC primary care · 2024Article
- Improving hypertension surveillance from a data management prospective: Data requirements for implementation of population-based registry.Journal of education and health promotion · 2020Article
- Development of an electronic health record-based chronic kidney disease registry to promote population health management.BMC nephrology · 2019Article
- Putting patients at the center of kidney care transitions: PREPARE NOW, a cluster randomized controlled trial.Contemporary clinical trials · 2018Article
- Acceptability of a multilevel intervention to improve blood pressure control among patients with chronic kidney disease in a public health care delivery system.Clinical kidney journal · 2018Article
- A national surveillance project on chronic kidney disease management in Canadian primary care: a study protocol.BMJ open · 2017Observational
- Specialist and primary care physicians' views on barriers to adequate preparation of patients for renal replacement therapy: a qualitative study.BMC nephrology · 2015Article
- Reducing CKD risks among vulnerable populations in primary care.Advances in chronic kidney disease · 2015Review
- Chronic kidney disease care in the US safety net.Advances in chronic kidney disease · 2015Review
- Integrated Digital Health System Tools to Support Decision Making and Treatment Preparation in CKD: The PREPARE NOW Study.Kidney medicineArticle
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
Abstract
backgroundChronic disease registries have been successful at promoting the delivery of guideline-concordant primary care for patients with diabetes and hypertension, but not for chronic kidney disease (CKD). To understand whether a registry could be designed to improve CKD management in primary care, we explored primary care provider attitudes about the benefits (or lack thereof) of a CKD registry compared with other chronic diseases and the key facilitators of successfully implementing a CKD registry in safety-net primary care. STUDY
designQualitative, using semistructured interviews. SETTING &
participantsWe conducted and recorded semistructured 1-hour interviews with medical directors and quality improvement champions from safety-net adult primary care clinics in San Francisco. ANALYTIC APPROACH: Recordings were transcribed and analyzed using a grounded theory approach until thematic saturation was achieved.
results20 primary care providers were interviewed. 4 themes relevant to the development of a successful CKD registry for safety-net primary care were identified: (1) provider beliefs that a CKD registry could aid in the delivery of team-based high-quality CKD care; (2) clinic workflow redesign and staffing are key facilitators to successful implementation of a CKD registry; (3) unique complexities of CKD, such as varying etiologies, may limit the use of a CKD registry by nonphysicians; and (4) a CKD registry is aligned with current primary care priorities and health care delivery strategies. LIMITATIONS: Small sample size and reliance on clinician leaders within one health care delivery system.
conclusionsA CKD registry directed at the entire health care team, with the functionality to track, standardize, and enhance CKD care through decision support, has the potential to improve the management of CKD in safety-net primary care settings. These data directly informed the development of a CKD registry in these settings in San Francisco.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.