General Renal, AKI and CKD Flashcards

1
Q

Recurrent frank haematuria 1-2 days after an upper respiratory infection

A

IgA nephropathy

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2
Q

Nephritic syndrome (haematuria, fall in GFR, hypertension) 1-3 weeks after an infection

A

Post-infective glomerulonephritis

Typically post-streptococcal

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3
Q

Skin or joint involvement

A

Suggests secondary to underlying condition eg. SLE or vasculitis

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4
Q

Obesity and renal problems

A

Associated with focal segmental glomerulosclerosis

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5
Q

Anti-glomerular basement membrane antibody

A

Goodpastures disease

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6
Q

Anti-neutrophil cytoplasmic antibodies - ANCA

A

Systemic vasculitis

Check for specificity against MPO (myeloperoxidase) or protease 3 (PR3)

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7
Q

Antinuclear antibodies with specificity for ds DNA

Low complement levels

A

SLE

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8
Q

Abnormal lung function tests with renal problems

A

Can be Goodpastures syndrome - blood in alveoli absorbs CO used to measure gas transfer - therefore raises gas transfer coefficient

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9
Q

Other signs of drug-induced acute interstitial nephritis

A

Maculopapular rash, fever or eosinophilia

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10
Q

Symptoms/signs of acute interstitial nephritis

A

May be loin pain from stretching of renal capsule

Mild proteinuria, microscopic haematuria, white blood cells casts and eosinophils in urine

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11
Q

Ultrasound in acute interstitial nephritis

A

Slightly enlarged kidneys

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12
Q

Tubular/interstitial causes of acute kidney injury

A

Drugs (NSAIDs, aminoglycoside antibiotics, ACEi or ARB, PPIs)
Radiological contrast
Rhabdomylosis - myoglobin
Haemolysis - haemoglobin
Systemic/renal infection - infiltration
Gout- excess urate production - urate crystals precipitate in tubules
Tumour lysis syndrome following chemo

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13
Q

Signs of chronic kidney injury

A

Small kidneys

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14
Q

When to refer kidney injury to nephrologist

A

Hyperkalaemia in oligoanuric patient,
Hyperkalaemia or fluid overload not reponsive to medical treatment
Urea >40
Suspected glomerulonephritis (blood or protein on urinalysis)

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15
Q

Signs of glomerular disease on urine dip

A

Protein or blood

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16
Q

Presence of Bence Jones proteins in urine

A

Myeloma

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17
Q

General management of AKI

A

Aim for euvolaemia

Stop nephrotoxic drugs (NSAIDs, ACEi, gentamicin, amphotericin, metformin if creatinine >150)

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18
Q

Management of pre-renal AKI

A

Correct volume depletion
Treat sepsis
If shock - consider ITU

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19
Q

Management of post-renal AKI

A

Catheterise
CT of renal tract if needs be
Urology referral if obstruction

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20
Q

Management of intrinsic renal AKI

A

Refer to nephrology if glomerulonephritis or tubulointerstitial disease suspected

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21
Q

Management of uraemia in AKI

A

May need dialysis if severe or complications eg. encephalopathy, pericarditis

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22
Q

Management of acidaemia in AKI

A

Sodium bicarbonate PO or IV

23
Q

Management of hyperkalaemia in AKI

A

Give calcium gluconate (cardioprotective)
Give insulin and glucose - get K+ into cells
Salbutamol same affect as insulin/glucose but more needed and tachycardia is a risk
If acidotic - give sodium bicarbonate

24
Q

Definition of Chronic Kidney Disease

A

Impaired renal function >3 months based on abnormal structure or function
or GFR 3 months without evidence of kidney damage

25
Classification of CKD
Done according to GFR
26
Stage 1 CKD
>90ml/min - therefore normal but with evidence of renal damage eg. proteinuria or haematuria
27
Stage 2 CKD
60-89 Slight decrease with signs of renal damage IF ALL kidney tests are normal at this GFR then there is no CKD
28
Stage 3 CKD
30-59 - with or without signs of renal damage
29
Stage 4 CKD
15-29 with or without
30
Stage 5 CKD
Below 15
31
End stage renal failure
GFR
32
Causes of CKD x5
``` Diabetes- type 2 more than type 1 Glomerulonephritis Unknown Hypertension or renovascular disease Pyelonephritis ```
33
Screening for CKD in which patients
``` AT RISK HTN DM CVD Structural renal disease Recurrent UTIs Multisystem disorders eg. SLE Family history of ESRF ```
34
Hx in CKD - looking for cause
PMHx of risk factors DHx FHx Systems review for systemic disorder or malignancy
35
Hx in CKD - current state
Uraemic symptoms - anorexia, vomiting, restless legs, fatigue, weakness, pruritus, bone pain Women - amenorrhea Men - impotence
36
Examination of CKD
``` Pallor Uraemic tinge - yellow Purpura and excoriations HTN Cardiomegaly ```
37
Signs of bone problems in CKD
Renal bone disease - bone pain, especially in lower back, hips and legs Often associated with proximal myopathy and soft tissue calcification
38
Haemotological complications of CKD
Anaemia - inadequate erythropoietin production Therefore give erythropoietin SC or IV - only works if iron, folate and B12 are normal Bleeding times increased - can give synthetic vasopressin (desmopressin) to transiently reduce bleeding time
39
Vascular complications in CKD
Many have DM Also hypertension - hypervolemia from salt and water retention Or due to excess renin production
40
Skin complication in CKD
Itch - calcium phosphate deposition in skin | Also ureamia- can get uremic frost
41
GIT in CKD
Peptic ulcer no more common in CKD but gastrin elevated - nausea, vomiting, anorexia and heartburn Higher incidence of oesophagitis and angiodysplasia
42
Endo in CKD
Men - loss of libido, impotence and low sperm count | Women - loss of libido, reduced ovulation and infertility
43
Immunological in CKD
Function is impaired in severe CKD and infection common | Uremia suppresses function of immune cells
44
Lipid in CKD
Hyperlipidaemia - higher in patients on peritoneal dialysis than haemolysis
45
Cardiac in CKD
Pericarditis can occur and more likely if urea or phosphate are high Fluid overload and HTN - left ventricular hypertrophy or dilated cardiomyopathy
46
Management of CKD
Restrict dietary potassium, phosphate and sodium and water BP management Treat complications
47
Neuro in CKD
Cramps, restless legs Peripheral neuropathy Myopathy Depression and anxiety
48
Fused podocytes on electron microscopy - proliferative or non-proliferative glomerulonephritis
Non-proliferative
49
Syndrome caused by proliferative and non-proliferative glomerulonephritis
``` Proliferative = nephritic syndrome Non-proliferative = nephrotic syndrome ```
50
What do you see on electron microscopy of rapidly progressive glomerulonephritis
Crescents | eg. goodpastures and systemic vasculitis
51
What do you see on electron microscopy of membranous IgA nephropathy
thickening of glomerular basement membrane
52
How is Alports syndrome inherited?
X-linked dominant usually
53
Most common and important infective agent in transplant of solid organs
CMV