An update on chronic renal failure: follow-up and when to refer ? Assoc Prof Johan Rosman Renal Department Waitemata DHB johan.rosman@waitematadhb.govt.nz Apollo Health Centre, Albany www.bloodpressure.org.nz Chronic renal failure Diagnosis Presentations and stages of CRF in general Causes of CRF Monitoring CRF Consequences of CRF Progression of CRF Principles of treatment Differentiation acute-chronic renal failure Short History (ds-wks) Normal Hb Normal renal size No osteodystrophy Periph neuropathy Normal Ca and P Normal PTH Long history (mo-yrs) Low Hb Reduced renal size Often osteodystrophy Periph neuropathy + Low Ca / elevated P Increased PTH Acute on chronic renal failure Recrudescence of primary disease Complication of primary disease Accelerated hypertension Volume depletion Cardiac failure Sepsis Nephrotoxins (radiocontrast, drugs) Renal artery occlusion Urinary tract obstruction Dietary protein load Presentation of CRF Asymptomatic serum biochemical abnormality Asymptomatic proteinuria/haematuria Hypertension Symptomatic primary disease Symptomatic uraemia Complications of renal failure Commonest causes of ESRF (ANZData) Glomerulonephritis Diabetes Hypertension Polycystic kidney disease Vesicoureteral reflux Analgesic nephropathy Unknown Others 30% 25% 10% 5% 5% 5% 10% 10% GFR (glomerular filtration rate) equals creatinine clearance ?? The accurate assessment of GFR is desirable Planning for the treatment of end stage renal disease Referral to nephrology Trace the course of progression of chronic renal disease or response to therapy What is the best, most practical way to assess GFR? Creatinine: an imperfect marker Afferent arteriole Efferent arteriole Glomerulus Filtered Secreted Reabsorbed 20 40 60 80 100 120 GFR ml/min/1.73m2 BSA [Creatinine]s micromole/L 200 400 600 800 1000 “Normal” GFR by Age Age (years) Average eGFR 20 - 29 116 ml/min/1.73m2 BSA 30 - 39 107 ml/min/1.73m2 BSA 40 - 49 99 ml/min/1.73m2 BSA 50 - 59 93 ml/min/1.73m2 BSA 60 - 69 85 ml/min/1.73m2 BSA > 70 years 75 ml/min/1.73m2 BSA Measuring glom. filtration rate Many formulas have attempted to predict GFR from a serum creatinine measurement only, most factoring in age, weight/height, and gender, which are all independent of serum creatinine in influencing GFR. This would be the easiest approach clinically a serum creatinine of 130 umol/l is normal in an athlete, but can mean dialysis dependency in a 80 year old ! Aids in monitoring GFR (creat clearance) Use the Cockroft Gault equation Use the MDRD equation But: in the follow up of a patient stick to the same way of estimating GFR Formula’s for free available on the web (spreadsheet) or free for Palmtop (Medcalc) Use 1/creatinine in individual patients to see whether a rise in creatinine represent an acute on chronic event Renal Screen BP MSU RBC morphology; ACR; 24-hour proteinuria Serum urea, creatinine, Na+, K+ Ultrasound scan renal tract Albumin, calcium, phosphate PTH eGFR Why do 24-hour urine collection? Extremes of age / body size Malnutrition or obesity Catabolic states Amputees / paraplegia / mm. wasting Vegetarians / vegans Pregnancy Medication-dosing Rapidly changing renal function Problems of ESRD Cardiovascular disease Anaemia Renal Bone Disease Metabolic acidosis Malnutrition Sodium and water Potassium Bleeding Diathesis Dermatologic manifestations Neurologic manifestations Endocrine abnormalities Immunity Psychological manifestations Factors causing progression of CRF Cont activity of primary disease Systemic hypertension Intraglomerular hypertension Proteinuria Nephrocalcinosis (dystr and metast) Dyslipidaemia Imbalance renal energy demands and supply Cardiovascular Morbidity and Proteinuria Proteinuria Cumulative incidence (%) of CV morbidity 40 30 p < 0.001 20 No Proteinuria 10 0 0 1 2 3 4 5 Years Adapted from Samuelsson et al. J Hypertens 1985;3:72 6 7 8 9 RPLM Hoogma 10 Relationship between BP and progression of CRF MAP (mm Hg) GFR (mL/min per year) 98 100 102 104 106 108 110 0 –2 r = 0.66; P<0.05 –4 –6 –8 –10 Clinical trials of >3–years duration Adapted with permission from Bakris. Diabetes Res Clin Pract 1998;39:S35 RPLM Hoogma Principles of treatment of pat with CRF Differentiate from ARF on CRF Establish aetiology Establish severity Seek and treat reversible factors Seek and treat complications Lifestyle improvements Seek and treat factors that promote progression Planned and timely refer to nephrologist When to refer to renal physician? eGFR < 30 ml/min/1.73m2 BSA Proteinuria > 1G per 24 hours Glomerular haematuria Difficult to control hypertension Rapidly declining GFR <45 in diabetics; anaemia (Hb < 100g/L) >15% in 3 months (Australia) Electrolytes, vascular disease, etc. Early detection is paramount CKD Preventable Growing @ 6%pa Delayed progression Renal abnormality is prevalent! 16% of Australians (AusDIAB) 15% NZers (Simmonds) 20 x more likely to die than get RRT Asymptomatic Keith et al. Arch Int Med 164:659; 2004 The key to good care Communication Communication Communication 021- KIDNEY (021-543639)