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QJM Advance Access originally published online on February 23, 2006
QJM 2006 99(3):153-160; doi:10.1093/qjmed/hcl016
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© The Author 2006. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

The joint diabetic-renal clinic in clinical practice: 10 years of data from a District General Hospital

M.K. Jayapaul1,, R. Messersmith2, D.N. Bennett-Jones3, P.A. Mead3 and D.M. Large1

From the Departments of 1Diabetes and Endocrinology, 2Clinical Audit, and 3Renal Medicine, Cumberland Infirmary, Carlisle, UK

Address correspondence to Dr M. Jayapaul, Floor 4, William Leech Building, School of Clinical Medical Sciences, The Medical School, Framlington Place, Newcastle upon Tyne NE2 4HH. email: m.k.jayapaul{at}ncl.ac.uk

Received 23 September 2005 and in revised form 22 January 2006

Background: Diabetic nephropathy is the leading cause of end-stage renal failure. Untreated, it causes continuous decline in glomerular function, worsening hypertension and a marked increase in cardiovascular risk. Joint diabetic-renal clinics were established to address these factors and prepare patients for renal replacement therapy.

Aim: To determine whether our joint diabetic-renal clinic influenced progression of renal disease, and whether we were able to achieve targets from clinical trials and guidelines in routine practice.

Design: Retrospective review.

Methods: We collected data using clinical notes and electronic records for 130 patients attending the clinic over 10 years.

Results: Our patients had 62% type 2 and 38% type 1 diabetes. Mean duration of diabetes was 24 years for type 1 and 11 years for type 2 diabetes. At referral, 56% had evidence of vascular disease and 45%, proliferative retinopathy. Baseline median creatinine was 124 µmol/l. Significant improvements were made in systolic BP, diastolic BP and cholesterol (p < 0.001), compared to measurements at presentation. We analysed progression of renal disease by linear regression on 45 patients who had follow-up data for 3 years. Rate of decline of GFR was significantly reduced from 1.09 ml/min/month in the first year to 0.39 ml/min/month in the third year, (p < 0.004).

Discussion: Our findings suggest that the rate of deterioration of renal function can be reduced by aggressive management of risk factors. Joint diabetic-renal clinics appear to be useful in achieving targets in routine clinical practice.


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