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NDT Advance Access originally published online on June 8, 2007
Nephrology Dialysis Transplantation 2007 22(9):2455-2457; doi:10.1093/ndt/gfm268
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©Royal College of Physicians of Edinburgh, 2007.

UK Consensus Conference on Early Chronic Kidney Disease—6 and 7 February 2007

G. Archibald, W. Bartlett, A. Brown, B. Christie, A. Elliott, K. Griffith, S. Pound, I. Rappaport, D. Robertson, Y. Semple, P. Slane, C. Whitworth and B. Williams

Head of Communications and Publishing, Royal College of Physicians of Edinburgh, Edinburgh, EH21JQ, UK

Correspondence and offprint requests to: Prof. Bryan Williams, Prof. of Medicine, Department of Cardiovascular Sciences, Clinical Sciences Building, Leicester Royal Infirmary, PO Box 65, Leicester LE2 7LX. Email: bw17@le.ac.uk

The first 10% of the full text of this article appears below.

Detection of adults with early chronic kidney disease (CKD) is important because some will progress to end-stage kidney disease and most are at higher risk of premature cardiovascular disease. Early identification provides the greatest opportunity to modify the course of disease and the associated cardiovascular risk.



   What is early CKD?
 
An international classification of CKD has identified five stages. Early CKD is described as stages 1–3. Stages 1 and 2 are characterized by structural abnormalities, presence of persistent proteinuria or albuminuria or haematuria. Stage 3 is characterized by impaired kidney function, as defined by estimated glomerular filtration rate (eGFR) of between 30 and 59 ml/min/1.73 m2 on at least two occasions at a minimal interval of 3 months.

Using this definition, it is estimated . . . [Full Text of this Article]



   Improving detection of early CKD
 
Estimating GFR


   Improving classification of early CKD
 


   Improving organization of care
 


   Clinical recommendations
 
Lifestyle
Blood pressure
Cardiovascular risk management
Bone mineral disorders
Anaemia
Medicines management
Research

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