Renal Flashcards
Pre-renal causes of AKI
Reduced perfusion as a result of either circulatory changes or a reduction in glomerulus perfusion pressure leading to a reduced eGFR:
Hypovolaemia (haemorrhage, dehydration, burns etc.)
Hypotension (shock)
Fluid overload (cirrhosis, CCF, nephrotic syndrome)
Reduced cardiac output (shock, MI, arrhythmia, CCF)
Vascular changes (renal stenosis or thrombosis)
Drugs such as ACE-I’s and NSAIDS
Renal (Intrinsic) causes of AKI
Anything which impacts the parenchyma of the kidneys and may occur as a result of chronic pre or post renal pathologies:
Glomerular damage (glomerulonephritis, IgA nephropathy, thrombosis, uraemic syndrome
Acute interstitial nephritis
Acute tubular necrosis
Vasculitis
Post-renal causes of AKI
Anything that obstructs urine flow below level of renal calyx:
Stones Clots Malignancy BPH Strictures Retroperitoneal fibrosis
Criteria for AKI stage 1
Rise in creatinine of at least 26 mol/L in 48 hours
OR
Creatinine rise to 50%+ of baseline in 7 days
OR
Urine output < 0.5ml/Kg/Hr for 6+ hours
Criteria for AKI stage 2
Creatinine 2x baseline
OR
Urine output < 0.5ml/Kg/Hr for 12+ hours
Criteria for AKI stage 3
Creatinine 3x baseline OR Rise of 1.5 baseline to at least 355 micromol/L OR Urine output < 0.3ml/Kg/Hr for 24 hours OR Anuria for 12+ hours
Complications of AKI
Uraemia Hyperphosphataemia Hyperkalaemia Prolonged chronic kidney disease Metabolic acidosis Electrolyte imbalances
Investigating AKI
U&E's with creatinine FBC CRP LFTs - hepatorenal syndrome? Clotting Creatine Kinase - rhabdomyolysis? VBG
Urine dip and cultures
Monitor urine output
Fluid challenge
ECG especially if potassium deranged
Renal US - if obstruction suspected or no cause obvious
CT/MRI is US suggests obstruction or not cause obvious
CKD symptoms
Fatigue Nocturia Hypertension Hameaturia and/or proteinuria Nausea and vomiting Itching Breathlessness
Late stages: Seizures Reduced GCS Kussmaul's respiration Muscle twitching
CKD Complications
Anaemia from erythropoietin deficiency
Renal osteodystrophy due to PTH rising in response to hypokalaemia and hyperphosphataemia
Vitamin D deficiency
Cardiovascular disease
Protein malnutrition
Metabolic Acidosis
Oedema
Hyperkalaemia
CKD Stages + eGFR + Symptoms
Stage 1 - Damage but eGFR normal - Asymptomatic
Stage 2 - Damage with eGFR 60-89 - Asymptomatic
Stage 3a - eGFR 45-59 - Can be asymptomatic
Stage 3b - eGFR 30-44 - Anaemia
Stage 4 - eGFR 15-29 - Electrolyte disturbances
Stage 5 - eGFR < 15 - Significant complications
Causes of CKD
Diabetes Interstitial disease Glomerular disease Hypertension Systemic inflammatory disease Congenital conditions Renal artery stenosis
Treating CKD
Stage 1-2 with no uraemia
1) ACE-I/ARB or non-dihyrdopyridine CCB
2) Statin
Additional HTN control if needed
Glycaemic control if needed
Stage 3-4 with no uraemia
Same as above + education on renal replacement (e.g. dialysis, transplantation)
Stage 5 OR any stage with uraemia
1) Dialysis
2) Kidney Transplant
If anaemic: Erythropoietin stimulating agent, Fe
If hyperparathyroidism: phosphate binder, calcium mimetic, vitamin D
Investigating CKD
eGFR - stage of CKD
U&E’s - electrolytes, especially K+
ECG - arrhythmia etc.
Bone profile - hyperparathyroidism, hypocalcaemia, hypoalbuminaemia
FBC - anaemia
Urinalysis - protein and blood in urine
HbA1c - glucose control
Lipids - lipid control
Renal US +/- Bx
ADPKD Symptoms
Hypertension Abdominal/flank pain Haematuria Palpable kidneys Hepatomegaly Headache Heart murmur Hernia
Required for diagnosis of nephrotic syndrome
1) Proteinuria (3.5g+ in 24 hours)
2) Hypoalbuminaemia (less than 30g/L)
3) Peripheral oedema
Hyperlipidaemia and thrombotic disease often seen but not diagnostic
Urine lacks cells and casts
Persistent proteinuria as a single symptom is considered nephrotic range and tends to indicate glomerulopathy
Causes of nephrotic syndrome in paediatrics
Minimal change disease (a form of glomerulonephritis)
Non-Hodgkins lymphoma (rare)
Membranoproliferative glomerulonephritis (rare)
Causes of nephrotic syndrome in younger adults
Focal segmental glomerulosclerosis (a form of glomerulonephritis)
Minimal change disease (a form of glomerulonephritis)
Diabetic nephropathy
Causes of nephrotic syndrome in older adults
Membranous nephropathy - often secondary to another pathology such as malignancy, SLE, HBV, reaction to medications etc.
Diabetic nephropathy
Conditions classified as Glomerulonephritis
Minimal change disease Membranous glomerulonephritis Focal segmental glomerulosclerosis Segmental glomerulosclerosis Immunoglobulin A nephropathy
Focal segmental glomerulosclerosis pathology
Injury to podocytes in glomeruli
Immune mediated
Secondary via viral infection, drugs, renal mass etc.
Membranous glomerulonephritis pathology
Immune mediated disease of glomerular basement membrane
Risk factors for renal stones
Anatomical deformities Gout Hypertension Dehydration High salt diet Immobilisation
Renal stone composition
Calcium oxalate and calcium phosphate
Uric acid
Struvite - magnesium, ammonia and phosphate
Cysteine