Renal II Flashcards

1
Q

Most common cause of AKI

A

Acute tubular necrosis

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2
Q

Two main causes of ATN

A

Ischaemia

Nephrotoxins

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3
Q

Examples of cases in which ischaemia occurs causing ATN

A

Shock

Sepsis

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4
Q

Nephrotoxins which can cause ATN

A

Aminoglycosides
Myoglobin secondary to rhabdomyolysis
radiocontrast agents
lead

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5
Q

Features of ATN

A

features of AKI: raised urea, creatinine, potassium

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6
Q

What might be seen on urinalysis in ATN

A

Muddy brown casts

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7
Q

Mx of ATN

A

Supportive management
IV fluids
Stop nephrotoxic medications
Treat complications

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8
Q

What is interstitial nephritis

A

inflammation of the space between cells and tubules (the interstitium) within the kidney.

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9
Q

How does acute interstitial nephritis present

A

AKI
HTN

Rash
Fever
Eosiniphilia(hypersensitivity reaction)

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10
Q

what causes acute interstitial nephritis

A

Drugs (e.g. NSAIDS or antibiotics)

Infection

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11
Q

Mx of acute interstitial nephritis

A

Treat underlying cause

Steroids

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12
Q

How does chronic tubulointerstitial nephritis present

A

chronic inflammation of the tubules and interstitium. It presents with chronic kidney disease.

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13
Q

What is HUS

A

Occurs when there is thrombosis in small blood vessels throughout the body. This is usually triggered by a bacterial toxin called the shiga toxin.

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14
Q

HUS triad

A

Haemolytic anaemia
Acute kidney injury
Low platelet count (thrombocytopenia)

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15
Q

Most common cause of HUS

A

toxin produced by the bacteria e. coli 0157 called the shiga toxin. Shigella also produces this toxin and can cause HUS

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16
Q

What can increase risk of HUS

A

Use of antibiotics and anti-motility medications such as loperamide to treat the gastroenteritis

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17
Q

Presentation of HUS

A

Brief gastroenteritis with bloody diarrhoea

Reduced urine output

Haematuria

Abdominal pain

Lethargy and irritability

Confusion

HTN

Bruising

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18
Q

Mx of HUS

A

Supportive mx
Antihypertensives
Blood transfusions
Dialysis

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19
Q

Pathophys of type 1 RTA

A

pathology in the distal tubule. The distal tubule is unable to excrete hydrogen ions.

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20
Q

Causes of RTA 1

A
genetic 
SLE
Sjogren's 
Primary biliary cirrhosis 
Hyperthyroidism 
Sickle cell disease
21
Q

Presentation of RTA 1

A

Failure to thrive in children
Hyperventilation to compensate for the metabolic acidosis
Chronic kidney disease
Bone disease (osteomalacia)

22
Q

IX - RTA 1

A

Hypokalaemia
Metabolic acidosis
High urinary pH (above 6)

23
Q

Rx of RTA 1

A

Oral bicarbonate

24
Q

RTA 2 pathophys

A

Pathology in the proximal tubule. The proximal tubule is unable to reabsorb bicarbonate from the urine into the blood. Excessive bicarbonate is excreted in the urine

25
Main cause of RTA 2
Fanconi's syndrome
26
RTA 2 - IX
Hypokalaemia Metabolic acidosis High urinary pH (above 6)
27
Mx of RTA 2
Oral bicarb
28
What is RTA 4 caused by
caused by reduced aldosterone Can be due to adrenal insufficiency, ACE inhibitors/spironolactone or systemic conditions such as SLE/diabetes/HIV
29
RTA 4 - IX
Hyperkalaemia High chloride Metabolic acidosis Low urinary pH
30
Mx of RTA 4
Fludrocortisone Sodium bicarbonate Treatment of hyperkalaemia may be required
31
Indications for acute dialysis - AEIOU
A – Acidosis (severe and not responding to treatment) E – Electrolyte abnormalities (severe and unresponsive hyperkalaemia) I – Intoxication (overdose of certain medications) O – Oedema (severe and unresponsive pulmonary oedema) U – Uraemia symptoms such as seizures or reduced consciousness
32
Indications for long term dialysis
End stage renal failure (CKD stage 5)
33
Options for maintenance dialysis
Continuous Ambulatory Peritoneal Dialysis Automated Peritoneal Dialysis Haemodialysis
34
Complications of peritoneal dialysis
Bacterial peritonitis Peritoneal sclerosis Weight gain Psychosocial effects
35
What does rhabdomyolysis cause release of
Myoglobin (causing myoglobinurea) Potassium Phosphate Creatine kinase
36
Causes of rhabdomyolysis
Prolonged immobility Extremely rigorous exercise Crush injuries Seizures
37
signs and symptoms of rhabdomyolysis
``` Muscle aches and pain Oedema Fatigue Confusion (particularly in elderly frail patients) Red-brown urine ```
38
Mx of rhabdomyolysis
IV fluids IV sodium bicarbonate IV mannitol (increases GFR) Manage electrolyte disturbances
39
What is polycystic kidney disease(PCK)
genetic condition where the kidneys develop multiple fluid-filled cysts
40
Types of PCK
Autosomal recessive and dominant
41
Diagnosis of PCK
kidney ultrasound scan and genetic testing
42
Extra-renal manifestations of PCK
Cerebral aneurysms Hepatic, splenic, pancreatic, ovarian and prostatic cysts Cardiac valve disease (mitral regurgitation) Colonic diverticula Aortic root dilatation
43
Complications of PCK
``` Chronic loin pain Hypertension Cardiovascular disease Gross haematuria Renal stones End-stage renal failure ```
44
Mx of PCK
``` Tolvaptan(slows progression of cysts) Antihypertensives Analgesia Antibiotics Dialysis ```
45
Definition of AKI
a rise in serum creatinine of 26 micromol/litre or greater within 48 hours a 50% or greater rise in serum creatinine known or presumed to have occurred within the past 7 days a fall in urine output to less than 0.5 ml/kg/hour for more than 6 hours in adults and more than
46
Diagnosis of amyloidosis
Congo red staining: apple-green birefringence serum amyloid precursor (SAP) scan biopsy of skin, rectal mucosa, or abdominal fat
47
Features of amyloidosis in renal disease
Commonly presents as nephrotic syndrome (e.g. 70% present with proteinuria in AL amyloidosis). Common in AA amyloidosis (in 80% of cases) & AL amyloidosis, but less likely in ATTR amyloidosis.
48
Neurological presentation of amyloidosis
Ischaemic stroke | Peripheral & autonomic neuropathy