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Chronic Renal Failure (CRF)

See related article Chronic Kidney Disease and its Management.

Chronic renal failure is usually taken to be synonymous with stage 4 (severe impairment) chronic kidney disease (CKD) or stage 5 CKD (established renal failure) - see the Assessing Renal Function article for information about glomerular filtration rate (GFR).

The 5 stages of Chronic Kidney Disease (CKD)1

eGFR (estimated GFR)

STAGE

>90 ml/min/1.73m2 with another abnormality* Stage 1 CKD - without another abnormality, regard as normal
60-89 ml/min/1.73m2 with another abnormality* Stage 2 CKD - otherwise regard as normal
30-59 ml/min/1.73m2 (moderate impairment) Stage 3 CKD
15-29 ml/min/1.73m2 (severe impairment) Stage 4 CKD
<15 ml/min/1.73m2 (established renal failure) Stage 5 CKD
*e.g. already known to have proteinuria, haematuria (but no urological cause), microalbuminuria (in diabetes), polycystic disease or reflux nephropathy

Management

All stages of CKD2

  • Regular measurements of kidney function and other laboratory tests depending on the severity of kidney impairment.
  • General health advice: smoking cessation, weight loss, aerobic exercise, limiting alcohol intake, limiting sodium intake.
  • Avoidance of nephrotoxins, e.g. IV radiocontrast agents, NSAIDs, aminoglycosides.
  • Cardiovascular prophylaxis:
    • For patients with 10 year risk of cardiovascular disease of greater than 20%, consider aspirin treatment (if BP is below 150/90 mmHg) and lipid-lowering drug therapy.
    • Blood pressure monitoring: blood pressure should be measured at least annually.
    • Control of hypertension: hypertension should be tightly controlled. The threshold for initiation of anti-hypertensive medication:
      • If urine protein/creatinine ratio (PCR) is below 100 mg/mmol: threshold 140/90 mmHg, target 130/80 mmHg.
      • If urine PCR is above 100 mg/mmol: threshold 130/80 mmHg, target 125/75 mmHg.
  • ACE inhibitor or angiotensin receptor blocker to be started:
    • If urine PCR is above 100 mg/mmol.
    • In diabetic patients with micro-albuminuria.
    • Serum creatinine and potassium should be checked before starting medication, two weeks after starting, and after subsequent increases in dose. If creatinine increases by more than 20% or fall in GFR of more than 15%, repeat creatinine, check potassium and refer for specialist opinion on whether to stop treatment or to investigate for renal artery stenosis.
    • If hyperkalaemia is present (serum K above 6 mmol/l): stop relevant drugs, eg. NSAIDs and potassium-retaining diuretics; check diet and proprietary treatments, e.g. LoSalt. If hyperkalaemia persists the ACE or ARB should be stopped.

Additional management for CKD stage 3 includes2

  • Annual measurement of haemoglobin, potassium, calcium and phosphate.
  • If Hb below 11 g/dL and other causes excluded, treat with erythropoiesis stimulating agents to maintain Hb 11-12 g/dL depending on the patient's functional needs.
  • Request renal ultrasound in patients with lower urinary tract symptoms, refractory hypertension, unexpected progressive fall in GFR.
  • Immunise against influenza and pneumococcus.
  • Review all prescribed medication regularly to ensure appropriate doses.
  • Avoid nephrotoxic drugs including NSAIDs wherever possible.
  • Check parathyroid hormone concentration when Stage 3 is first diagnosed: if raised, check serum 25-hydroxyvitamin D and if low, treat with ergocalciferol or cholecalciferol with calcium supplement (not calcium phosphate). Repeat PTH after 3 months and refer if still raised.

Additional management for CKD Stages 4-5 includes2

  • Care of all patients with stage 4 or 5 CKD should be discussed formally with a nephrologist even if it is not anticipated that renal replacement therapy will be appropriate. Exceptions may include:
    • Patients with another terminal illness.
    • Patients with stable function in whom all the appropriate investigations and management interventions have been performed and who have an agreed and understood care pathway.
    • Patients in whom further investigation and management is clearly inappropriate.
  • 3-monthly tests: serum creatinine (for eGFR), Hb, calcium, phosphate, bicarbonate, parathyroid hormone.
  • Dietary assessment.
  • Immunisation against hepatitis B.
  • Investigation and treatment of phosphate retention and hyperparathyroidism.
  • Correction of acidosis.
  • Timely provision of dialysis access depending on treatment choice.

Renal replacement therapy

Indications for renal replacement therapy (haemodialysis, peritoneal dialysis, chronic ambulatory peritoneal dialysis or renal transplantation) include:

Complications
  • Anaemia: left ventricular hypertrophy, fatigue, impaired cognitive functioning
  • Coagulopathy
  • Hypertension: left ventricular hypertrophy, heart failure, stroke, cardiovascular disease
  • Calcium phosphate loading: cardiovascular and cerebrovascular disease, arthropathy, soft tissue calcification
  • Renal osteodystrophy: disorders of calcium, phosphorus and bone, most commonly osteitis fibrosa cystica
  • Bone changes of secondary hyperparathyroidism: bone pain and fractures
  • Neurological: uraemic encephalopathy, neuropathy including peripheral neuropathy
  • Dialysis amyloid: bone pain, arthropathy, carpal tunnel syndrome
  • Fluid overload: pulmonary oedema, hypertension
  • Malnutrition: increased morbidity and mortality, infections, poor wound healing
  • Glucose intolerance due to peripheral insulin resistance
Management of complications
  • Water and electrolyte balance:
    • Patients with chronic kidney disease pass normal volumes of urine. Precise restriction of fluid intake is only required for patients with oliguria. The usual recommendation is for a daily intake equal to the daily urinary output plus 500 mL (for insensible losses).
    • Patients should avoid binge drinking and be vigilant in replacing extra fluid losses in hot weather and during episodes of diarrhoea or vomiting.
    • Severe acute volume overload may require high dose loop diuretics or dialysis.
    • Dietary restriction to 60 mmol/day each of sodium and potassium is appropriate but compliance is greatly improved with sensible and flexible dietary advice.
    • Loop diuretics (with the addition of a thiazide diuretic if resistant) improve sodium balance and blood pressure.
    • Hyperkalaemia is treated with dialysis if the potassium level rises above 7 mmol/L. Otherwise treatment is directed towards the cause, e.g. excess fruit, chocolate or coffee, gastrointestinal haemorrhage, acidosis or tissue necrosis. Hyperkalaemia with the GFR still above 10 mL/min may be due to hyporeninaemic hypoaldosteronism in patients with diabetes, hypoadrenalism or as a result of treatment with ACE inhibitors.
  • Anaemia:
    • Erythropoietin is given with iron. The serum ferritin is monitored throughout treatment and iron is stopped if the ferritin level becomes too high, e.g. above 500 mcg/L.
    • Early erythropoietin therapy may prevent left ventricular hypertrophy.
    • The timing for initiation of treatment remains uncertain. The haemoglobin level is usually maintained at or above 11 g/dL.
  • Acidosis:
    • Chronic acidosis aggravates hyperkalaemia, inhibits protein synthesis and accelerates calcium loss from bone.
    • Treated with sodium bicarbonate as long as the patient can tolerate the increased sodium load. Additional sodium may cause fluid overload and worsen hypertension.
  • Hyperphosphatemia:
    • Occurs late in chronic kidney disease.
    • Treated with dietary restriction, dietary phosphate binders and calcium carbonate.
  • Hypocalcaemia:
    • Prescribe calcium supplements, with or without calcitriol.
  • Hyperparathyroidism:
    • Reduce hyperphosphataemia by diet and phosphate binders.
    • Prescribe 1,25-dihydroxycholecalciferol and maintain a normal calcium level.
    • Secondary hyperparathyroidism starts early in chronic renal failure and is difficult to treat when it becomes established.
    • Secondary hyperparathyroidism may lead to tertiary hyperparathyroidism if not treated effectively.
  • Malnutrition:
    • Must be avoided, although protein restriction can slow progression of renal failure.
    • Restriction of dietary protein slows the progress of glomerulosclerosis in residual nephrons in animal experimental models.
    • There remains controversy as to the benefits of protein restriction for treatment. Although patients are advised against high-protein diets, low-protein diets are not usually recommended and the emphasis is to maintain good nutrition.


Document references
  1. Royal College of General Practitioners; Introducing eGFR- Promoting good CKD management
  2. The Renal Association; UK Guidelines for the management of Chronic Kidney Disease. June 2005.

Internet and further reading
  • Verrelli M; Chronic Renal Failure. eMedicine, June 2006.
Acknowledgements EMIS is grateful to Dr Colin Tidy for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2008.
DocID: 1959
Document Version: 20
DocRef: bgp681
Last Updated: 7 Feb 2008
Review Date: 6 Feb 2010






















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