Developing a CKD registry in primary care: Provider attitudes and input

American Journal of Kidney Diseases

Volumn 63, Issue 4, 2014, Pages 577-583

  McBride, Dannielle ^a   Dohan, Daniel ^b   Handley, Margaret A ^b,c   Powe, Neil R ^b,c   Tuot, Delphine S ^b,c  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c SAN FRANCISCO GENERAL HOSPITAL   (United States)

Author keywords

chronic disease management; chronic kidney disease (CKD) awareness; Chronic kidney disease (CKD) registry; decision support; guideline implementation; health information technology (IT); primary care; safety net

Indexed keywords

ADMINISTRATIVE PERSONNEL; ARTICLE; CHRONIC KIDNEY DISEASE; DECISION SUPPORT SYSTEM; FEMALE; GROUNDED THEORY; HEALTH CARE DELIVERY; HUMAN; MALE; PHYSICIAN ATTITUDE; PRIMARY MEDICAL CARE; REGISTER; SAMPLE SIZE; SEMI STRUCTURED INTERVIEW; TOTAL QUALITY MANAGEMENT; UNITED STATES; WORKFLOW;

CHRONIC DISEASE MANAGEMENT; CHRONIC KIDNEY DISEASE (CKD) AWARENESS; CHRONIC KIDNEY DISEASE (CKD) REGISTRY; DECISION SUPPORT; GUIDELINE IMPLEMENTATION; HEALTH INFORMATION TECHNOLOGY (IT); PRIMARY CARE; SAFETY NET;

ATTITUDE OF HEALTH PERSONNEL; DECISION SUPPORT TECHNIQUES; DISEASE MANAGEMENT; FEMALE; HEALTH PRIORITIES; HUMANS; MALE; PRIMARY HEALTH CARE; PROGRAM DEVELOPMENT; REGISTRIES; RENAL INSUFFICIENCY, CHRONIC;

EID: 84897116460     PISSN: 02726386     EISSN: 15236838     Source Type: Journal    
DOI: 10.1053/j.ajkd.2013.10.012     Document Type: Article

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