Renal Flashcards

1
Q

Pre-renal causes of AKI

A

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

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2
Q

Renal (Intrinsic) causes of AKI

A

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

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3
Q

Post-renal causes of AKI

A

Anything that obstructs urine flow below level of renal calyx:

Stones
Clots
Malignancy 
BPH
Strictures 
Retroperitoneal fibrosis
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4
Q

Criteria for AKI stage 1

A

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

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5
Q

Criteria for AKI stage 2

A

Creatinine 2x baseline
OR
Urine output < 0.5ml/Kg/Hr for 12+ hours

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6
Q

Criteria for AKI stage 3

A
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
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7
Q

Complications of AKI

A
Uraemia 
Hyperphosphataemia 
Hyperkalaemia 
Prolonged chronic kidney disease 
Metabolic acidosis
Electrolyte imbalances
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8
Q

Investigating AKI

A
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

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9
Q

CKD symptoms

A
Fatigue
Nocturia 
Hypertension
Hameaturia and/or proteinuria 
Nausea and vomiting
Itching 
Breathlessness 
Late stages:
Seizures
Reduced GCS
Kussmaul's respiration 
Muscle twitching
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10
Q

CKD Complications

A

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

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11
Q

CKD Stages + eGFR + Symptoms

A

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

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12
Q

Causes of CKD

A
Diabetes
Interstitial disease
Glomerular disease 
Hypertension
Systemic inflammatory disease 
Congenital conditions 
Renal artery stenosis
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13
Q

Treating CKD

A

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

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14
Q

Investigating CKD

A

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

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15
Q

ADPKD Symptoms

A
Hypertension
Abdominal/flank pain 
Haematuria 
Palpable kidneys 
Hepatomegaly 
Headache 
Heart murmur 
Hernia
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16
Q

Required for diagnosis of nephrotic syndrome

A

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

17
Q

Causes of nephrotic syndrome in paediatrics

A

Minimal change disease (a form of glomerulonephritis)

Non-Hodgkins lymphoma (rare)

Membranoproliferative glomerulonephritis (rare)

18
Q

Causes of nephrotic syndrome in younger adults

A

Focal segmental glomerulosclerosis (a form of glomerulonephritis)

Minimal change disease (a form of glomerulonephritis)

Diabetic nephropathy

19
Q

Causes of nephrotic syndrome in older adults

A

Membranous nephropathy - often secondary to another pathology such as malignancy, SLE, HBV, reaction to medications etc.

Diabetic nephropathy

20
Q

Conditions classified as Glomerulonephritis

A
Minimal change disease 
Membranous glomerulonephritis 
Focal segmental glomerulosclerosis 
Segmental glomerulosclerosis 
Immunoglobulin A nephropathy
21
Q

Focal segmental glomerulosclerosis pathology

A

Injury to podocytes in glomeruli

Immune mediated

Secondary via viral infection, drugs, renal mass etc.

22
Q

Membranous glomerulonephritis pathology

A

Immune mediated disease of glomerular basement membrane

23
Q

Risk factors for renal stones

A
Anatomical deformities 
Gout
Hypertension
Dehydration 
High salt diet 
Immobilisation
24
Q

Renal stone composition

A

Calcium oxalate and calcium phosphate

Uric acid

Struvite - magnesium, ammonia and phosphate

Cysteine

25
Q

UTI Pathogens

A
E.Coli
Enteroccoci 
Klebsiella
Proteus 
Pseudonomas (catheter)