Literature DB >> 24726628

Identification of incident CKD stage 3 in research studies.

Morgan E Grams1, Casey M Rebholz2, Blaithin McMahon3, Seamus Whelton3, Shoshana H Ballew2, Elizabeth Selvin2, Lisa Wruck4, Josef Coresh5.   

Abstract

BACKGROUND: In epidemiologic research, incident chronic kidney disease (CKD) commonly is determined by laboratory tests performed at planned study visits. Given the morbidity and mortality associated with CKD, persons with incident disease may be less likely to attend scheduled visits, affecting observed associations. The objective of this study was to quantify loss to follow-up by CKD status and determine whether supplementation with diagnostic code data improves capture of incident CKD. STUDY
DESIGN: Prospective cohort study. SETTING &amp; PARTICIPANTS: 11,560 participants in the Atherosclerosis Risk in Communities (ARIC) Study underwent continuous surveillance for hospitalizations and death from baseline visit (1996-1999) to follow-up visit (2011-2013). A subset of hospitalizations in Washington County, MD, was used in diagnostic code validation (n=2,540). PREDICTOR: Baseline demographics and comorbid conditions. OUTCOMES: Incident CKD stage 3 ascertained by follow-up visit (visit-based definition) or hospitalization surveillance (hospitalization-based definition). MEASUREMENTS: Visit-based definition: ≥25% decline from baseline estimated glomerular filtration rate to <60 mL/min/1.73 m2 at follow-up visit; hospitalization-based definition: hospitalization CKD diagnostic code.
RESULTS: Of 11,560 participants, 5,951 attended the follow-up visit and 9,264 were hospitalized. Never-hospitalized participants were younger, more often female, and had fewer comorbid conditions; 73.5% attended the follow-up visit. Incident CKD stage 3 occurred in 1,172 participants by the visit-based definition (251 were never hospitalized) and 1,078 participants by the hospitalization-based definition (237 attended the follow-up study visit). Sensitivity of the hospitalization-based CKD definition was 35.5% (95% CI, 31.6%-39.7%); specificity was 95.7% (95% CI, 94.2%-96.8%). Sensitivity was higher with later time period, older participant age, and baseline prevalent diabetes and CKD. LIMITATIONS: A subset of hospitalizations was used for validation; 15-year gap between study visits.
CONCLUSIONS: The sensitivity of diagnostic code-identified CKD is low and varies by certain factors; however, supplementing a visit-based definition with hospitalization information can increase disease identification during periods of follow-up without study visits.
Copyright © 2014 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CKD surveillance; Chronic kidney disease (CKD); administrative data; diagnostic codes; identification; incident; loss to follow-up; screening; validation

Mesh:

Year:  2014        PMID: 24726628      PMCID: PMC4112019          DOI: 10.1053/j.ajkd.2014.02.021

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


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3.  Performance and limitations of administrative data in the identification of AKI.

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8.  A new equation to estimate glomerular filtration rate.

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9.  A population-based study of the incidence and outcomes of diagnosed chronic kidney disease.

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Authors:  Carmen A Peralta; Ronit Katz; Mark J Sarnak; Joachim Ix; Linda F Fried; Ian De Boer; Walter Palmas; David Siscovick; Andrew S Levey; Michael G Shlipak
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  45 in total

1.  Obstructive Sleep Apnea, Other Sleep Characteristics, and Risk of CKD in the Atherosclerosis Risk in Communities Sleep Heart Health Study.

Authors:  Kelsie M Full; Chandra L Jackson; Casey M Rebholz; Kunihiro Matsushita; Pamela L Lutsey
Journal:  J Am Soc Nephrol       Date:  2020-06-26       Impact factor: 10.121

2.  Associations of 1,5-Anhydroglucitol and 2-Hour Glucose with Major Clinical Outcomes in the Atherosclerosis Risk in Communities (ARIC) Study.

Authors:  Bethany Warren; Alexandra K Lee; Christie M Ballantyne; Ron C Hoogeveen; James S Pankow; Morgan E Grams; Anna Köttgen; Elizabeth Selvin
Journal:  J Appl Lab Med       Date:  2020-11-01

3.  Competing Risks of Fracture and Death in Older Adults with Chronic Kidney Disease.

Authors:  Rasheeda K Hall; Richard Sloane; Carl Pieper; Courtney Van Houtven; Joanne LaFleur; Robert Adler; Cathleen Colón-Emeric
Journal:  J Am Geriatr Soc       Date:  2018-01-10       Impact factor: 5.562

4.  Serum fibroblast growth factor-23 is associated with incident kidney disease.

Authors:  Casey M Rebholz; Morgan E Grams; Josef Coresh; Elizabeth Selvin; Lesley A Inker; Andrew S Levey; Paul L Kimmel; Ramachandran S Vasan; John H Eckfeldt; Harold I Feldman; Chi-Yuan Hsu; Pamela L Lutsey
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5.  Risk prediction of major complications in individuals with diabetes: the Atherosclerosis Risk in Communities Study.

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6.  Proton Pump Inhibitor Use and the Risk of Chronic Kidney Disease.

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7.  Serum Potassium, Mortality, and Kidney Outcomes in the Atherosclerosis Risk in Communities Study.

Authors:  Yan Chen; Alex R Chang; Mara A McAdams DeMarco; Lesley A Inker; Kunihiro Matsushita; Shoshana H Ballew; Josef Coresh; Morgan E Grams
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8.  Dietary Protein Sources and Risk for Incident Chronic Kidney Disease: Results From the Atherosclerosis Risk in Communities (ARIC) Study.

Authors:  Bernhard Haring; Elizabeth Selvin; Menglu Liang; Josef Coresh; Morgan E Grams; Natalia Petruski-Ivleva; Lyn M Steffen; Casey M Rebholz
Journal:  J Ren Nutr       Date:  2017-01-05       Impact factor: 3.655

9.  The Loss of GSTM1 Associates with Kidney Failure and Heart Failure.

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10.  Plasma galectin-3 levels are associated with the risk of incident chronic kidney disease.

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