Skip Navigation



NDT Advance Access published online on March 15, 2005

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfh771
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
20/6/1110    most recent
gfh771v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Bailie, G. R.
Right arrow Articles by Saran, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bailie, G. R.
Right arrow Articles by Saran, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org
Received September 23, 2004
Accepted February 11, 2005


Original Articles

Patterns of medication use in the RRI-CKD study: focus on medications with cardiovascular effects

George R. Bailie 1*, George Eisele 2, Lei Liu 3, Erik Roys 3, Margaret Kiser 4, Frederick Finkelstein 5, Robert Wolfe 6, Friedrich Port 6, Sally Burrows-Hudson 7, and Rajiv Saran 8

1 Albany Nephrology Pharmacy (ANephRx) Group, Albany College of Pharmacy, Albany, NY, USA
2 Albany College of Medicine, Albany, NY, USA
3 Kidney Epidemiology and Cost Center, University of Michigan, Ann Arbor, MI, USA
4 University of North Carolina-Chapel Hill, NC, USA
5 Metabolism Associates, New Haven, CT, USA
6 University Renal Research and Education Association, University of Michigan, Ann Arbor, MI, USA
7 Nephrology Management Group, Sunnyvale, CA, USA
8 Division of Nephrology, University of Michigan, Ann Arbor, MI, USA

* To whom correspondence should be addressed.
George R. Bailie, E-mail: bailieg{at}acp.edu



  Abstract

Background. Patients with chronic kidney disease (CKD) stages 2-5 are known to suffer numerous complications and co-morbidities associated with kidney disease. The medication prescription patterns in this population are not well understood. We report on prescription data collected as part of a multicentre longitudinal study in patients with CKD, with a focus on medications with cardiovascular or cardioprotective effects.

Methods. Patients were recruited from four academic nephrology centres in the USA, with patient recruitment from June 2000 to March 2002. Medication data were captured at the time of first enrolment into the study. Individual medications were classified into medication groups, and those with predominant cardioprotective effects or for prevention of progression of kidney disease (e.g. medications for treatment of anaemia, lipid-lowering agents, antihypertensives, statins, etc.) were recorded for analysis. Descriptive statistics were used for medication prescription according to baseline demographics and co-morbidities. Predictors of epoetin and iron use were determined by logistic regression adjusting for age, race, sex, diabetes, glomerular filtration rate (GFR), haemoglobin and serum albumin.

Results. Medication data were available for 619 patients with stages 2-5 CKD. Patients were 60.6±16.0 years of age, and were prescribed 8±4 (range 1-28) medications. Overall, the proportion of patients prescribed different classes of medications included epoetin (20%), intravenous iron (13%), HMG-CoA reductase inhibitors (16%), angiotensin-converting enzyme (ACE) inhibitors (44%), angiotensin receptor blockers (13%), {beta}-blockers (46%), calcium channel blockers (52%) and aspirin (37%). There was a low use of epoetin (45%) and iron (20%) in patients with anaemia. Only 24% of patients with coronary artery disease were prescribed statins, and ACE inhibitors and angiotensin receptor blockers were used in only 58 and 23% of diabetic patients with proteinuria. Positive predictors of epoetin and iron therapy included white race and diabetes. Higher GFR and higher serum albumin were associated with lower odds of being prescribed epoetin. White race and diabetics were more likely to be prescribed iron.

Conclusions. This study provides an overview of prescription practices in a cohort of CKD patients. Substantial underutilization of certain classes of cardioprotective medications is apparent, and systematic educational efforts in this direction may well prove worthwhile to impact outcomes.

Keywords: chronic kidney disease; medication use; prescription patterns; RRI-CKD study.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
N. Thilly, S. Boini, M. Kessler, S. Briancon, and L. Frimat
Management and control of hypertension and proteinuria in patients with advanced chronic kidney disease under nephrologist care or not: data from the AVENIR study (AVantagE de la Nephroprotection dans l'Insuffisance Renale)
Nephrol. Dial. Transplant., March 1, 2009; 24(3): 934 - 939.
[Abstract] [Full Text] [PDF]


Home page
CJASNHome page
R. Minutolo, P. Chiodini, B. Cianciaruso, A. Pota, V. Bellizzi, D. Avino, S. Mascia, S. Laurino, V. Bertino, G. Conte, et al.
Epoetin Therapy and Hemoglobin Level Variability in Nondialysis Patients with Chronic Kidney Disease
Clin. J. Am. Soc. Nephrol., March 1, 2009; 4(3): 552 - 559.
[Abstract] [Full Text] [PDF]


Home page
CJASNHome page
P. Ruggenenti and G. Remuzzi
Kidney Failure Stabilizes after a Two-Decade Increase: Impact on Global (Renal and Cardiovascular) Health
Clin. J. Am. Soc. Nephrol., January 1, 2007; 2(1): 146 - 150.
[Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
C. Jones-Burton, S. L. Seliger, J. Brown, L. Stackiewicz, V. Doren Hsu, and J. C. Fink
Racial variations in erythropoietic response to epoetin alfa in chronic kidney disease and the impact of smoking
Nephrol. Dial. Transplant., December 1, 2005; 20(12): 2739 - 2745.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.