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    Self-reported Medication Adherence and CKD Progression

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    Author
    Cedillo-Couvert, Esteban A.
    Ricardo, Ana C.
    Chen, Jinsong
    Cohan, Janet
    Fischer, Michael J.
    Krousel-Wood, Marie
    Kusek, John W.
    Lederer, Swati
    Lustigova, Eva
    Ojo, Akinlolu
    Porter, Anna C.
    Sharp, Lisa K.
    Sondheimer, James
    Diamantidis, Clarissa
    Wang, Xue
    Roy, Jason
    Lash, James P.
    Appel, Lawrence J.
    Feldman, Harold I.
    Go, Alan S.
    He, Jiang
    Kusek, John W.
    Lash, James P.
    Rahman, Mahboob
    Rao, Panduranga S.
    Townsend, Raymond R.
    Show allShow less
    Affiliation
    Univ Arizona, Dept Med
    Issue Date
    2018-05
    Keywords
    CKD
    death
    medication adherence
    
    Metadata
    Show full item record
    Publisher
    ELSEVIER SCIENCE INC
    Citation
    Cedillo-Couvert, E. A., Ricardo, A. C., Chen, J., Cohan, J., Fischer, M. J., Krousel-Wood, M., ... & Porter, A. C. (2018). Self-reported Medication Adherence and CKD Progression. Kidney international reports, 3(3), 645-651. https://doi.org/10.1016/j.ekir.2018.01.007
    Journal
    KIDNEY INTERNATIONAL REPORTS
    Rights
    © 2018 International Society of Nephrology. Published by Elsevier Inc.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Introduction: In the general population, medication nonadherence contributes to poorer outcomes. However, little is known about medication adherence among adults with chronic kidney disease (CKD). We evaluated the association of self-reported medication adherence with CKD progression and all-cause death in patients with CKD. Methods: In this prospective observational study of 3305 adults with mild-to-moderate CKD enrolled in the Chronic Renal Insufficiency Cohort (CRIC) Study, the baseline self-reported medication adherence was assessed by responses to 3 questions and categorized as high, medium, and low. CKD progression (50% decline in eGFR or incident end-stage renal disease) and all-cause death were measured using multivariable Cox proportional hazards. Results: Of the patients, 68% were categorized as high adherence, 17% medium adherence, and 15% low adherence. Over a median follow-up of 6 years, there were 969 CKD progression events and 675 deaths. Compared with the high-adherence group, the low-adherence group experienced increased risk for CKD progression (hazard ratio = 1.27, 95% confidence interval = 1.05, 1.54) after adjustment for sociodemographic and clinical factors, cardiovascular medications, number of medication types, and depressive symptoms. A similar association existed between low adherence and all-cause death, but did not reach standard statistical significance (hazard ratio - 1.14 95% confidence interval - 0.88, 1.47). Conclusion: Baseline self-reported low medication adherence was associated with an increased risk for CKD progression. Future work is needed to better understand the mechanisms underlying this association and to develop interventions to improve adherence.
    Note
    Open access journal.
    ISSN
    24680249
    PubMed ID
    29854972
    DOI
    10.1016/j.ekir.2018.01.007
    Version
    Final published version
    Sponsors
    U.S. National Institute of Diabetes and Digestive and Kidney Diseases [U01DK060990, U01DK060984, U01DK061022, U01DK061021, U01DK061028, U01DK060980, U01DK060963, U01DK060902]; Perelman School of Medicine at the University of Pennsylvania Clinical and Translational Science Award [NIH/NCATS UL1TR000003]; Johns Hopkins University [UL1 TR-000424]; University of Maryland [GCRC M01 RR-16500]; Clinical and Translational Science Collaborative of Cleveland from the National Center for Advancing Translational Sciences (NCATS) component of the National Institutes of Health [UL1TR000439]; Michigan Institute for Clinical and Health Research (MICHR) [UL1TR000433]; University of Illinois at Chicago [CTSA UL1RR029879]; Tulane University Translational Research in Hypertension and Renal Biology [P30GM103337]; Kaiser Permanente Northern California [NIH/NCRR UCSF-CTSI UL1 RR-024131]; NIDDK [K24DK092290, K23DK094829]; Research Supplement to Promote Diversity in Health-Related Research [U01-DK060980]; NIH roadmap for Medical Research
    Additional Links
    http://linkinghub.elsevier.com/retrieve/pii/S2468024918300147
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.ekir.2018.01.007
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