9. Paediatric nephrology Flashcards

1
Q

What are the major diseases in paediatric nephrology?

A

Proteinuria/Haematuria- (glomerular disease, nephrotic syndrome, nephritic syndrome

AKI- heamolytic uraemic syndrome

CKD- developmentla abnomrlaities, repflux nephropahty/UTI

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2
Q

What are 5 functions of the kidneys?

A
Waste handling
Water handling
Salt balance
Acid base control
Endocrine functions (RBC, BP, bone growth)
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3
Q

What does proteinuria signify?

A

Glomerular injury

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4
Q

What is nephritic syndrome?

A

Increasing haematuria

Intravascular overload

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5
Q

What is nephrotic syndrome?

A

Increasing proteinuria
Intravascular depletion
Leads to hypoalbuminaemia
Oedema increasing third space fluid volume as water isn’t pulled into blood vessels

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6
Q

What aspects of the glomerulus are affected by acquired glomerulopathy?

A

Common conditions:

Minimal change disease- podocyte (epithelial cell

Post infectious glomerulonephritis (basement membrane)

Heamolytic uraemic syndrome- endothelial cell

IgA nephropathy- mesangial cell (cells that filter the basement membrane)

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7
Q

What are the different ways to measure proteinuria?

A

Dipstix- measures concentration (>3+ abnormal), has a lot of false positives adn negatives

Protein:creatinine ratio- early mornignurine best, normal range <20mg/mmol. Nephrotic range >250mg/mmol

24 hour urine collection (gold standard)- Nephrotic range >1g/m2/24 hours

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8
Q

Describe a run of the mill, absolute classic nephrotic case in children.

A

gastroenteritis 10 days prior
3-4 days of a swollen face (worse in the mornings)
One eye closed, swollen legs
No allergies
Inflated weight, pitting oedema, ascites, pleural effusions
Frothy urine
low albumin, normal creatinine on bloods

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9
Q

What are the typical features of a nephrotic syndrome

A

age 1-10 years
normal blood pressure
no frank haematuria
normal renal function

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10
Q

What are atypical features of nephrotic syndrome

A

Abnormal renal function, steroid resistance and suggestions of an autoimmune disease are atypical features and warrant a renal biopsy

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11
Q

What are the treatments of nephrotic syndrome and what are the side effects?

A

Prednisolone 8 weeks

personality change
increased susceptibity to infection
hypertension
GI distress
reduced growth/osteoperosis
sleep disturbance
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12
Q

What are the different types of steroid resistant nephrotic syndrome

A

Acquired- focal segmental glomeruloscerosis (FSGS)
Podocyte loss
Progressive inflammation and sclerosis

Congenital- infant presentations
NPHS1- nephrin
NPHS 2- podocin
Podocyte loss

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13
Q

How do you identify haematuria

A

Macroscopic (seen by naked eye) investigate
Microscopic (dipstick adequate) investigate if positive on two or more occasions or if stix positive and microscopy negative

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14
Q

What are the causes haematuria?

A
Systemic clotting disturbances
Renal glomerulonephrtits
Tumour
Wilm's nephroblastoma
Cysts
Malignancies-sarcomas
Stones
UTI's
Trauma
Urethritis
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15
Q

What investigations would you do on a child if glomerulonephritis was suspected?

A

Increased waste accumulation (high creatinine)
Electrolytes looking for hyponatremia and hyperkalaemia
Full blood count looking for anaemia and heamolysis
Exclude UTI with urine culture
protein:creatnine ratio to look for nephrotic syndrome

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16
Q

What are the clinical features of glomerulonephritis?

A
Haematuria and proteinuria
Reduced GFR
Oliguria
Fluid overload
Raised JVP
Oedma
Hypertension
Worsebing renal failure
17
Q

Describe the pathogensis of post infectious glomerulonephritis?

A

Group A strep infection
Antigens of the disease binds in the glomerulus,
This leads to a humeral and cellular immune response
This activates an alternative compliment pathway

18
Q

How do you diagnose post infectious glomerulonephritis?

A
Bacterial culture
Positive ASOT (strep antibody test)
Low C3 abnormalities
Remember- differential diagnosis
May not always be post streptococcal
19
Q

How do you treat post infectious glomerulonephritis?

A

Antibiotics
Support the 5 renal functions (electrolyte/acid base balance)
Overload/hypertension (diuretics)

20
Q

What is Henoch schonlein purpura?

A

IgA related autoimmune disease
Can affect the blood vessels (vasculitis) or kindeys (glomuerulonephritis)
Presents with purple purpura
Occurs due to URTI or drugs

21
Q

How do you treat IgA vasculitis?

A

treat symptoms e.g. joints, guts
Glucocorticoid therapy- not helpful in mild nephritis
May help with gastrointestinal involvement
Imunosuppresion in moderate to severe renal disease
Long term hypertension and proteinuria screening

22
Q

How do you confirm IgA nephropathy?

A

Diagnosis through a clinical picture (negative autoimmune workup, normal compliment)
Confirmation biopsy

23
Q

How do you treat IgA nephropathy

A

Mild disease ACE inhibitors

Moderate to severe- immune suppresion

24
Q

What is meant by an acute kidney injury?

A

Abrupt loss of kidney function, resulting in the retention of urea and other nitrogenous waste products and in the dysregualtion of extracellular volume and electrolytes

25
Q

What are the different classes of acute kidney injury?

A

AKI 1- Creatinine 1.5-2x reference
AKI 2- measured creatinine 2-3x reference creatinine
AKI 3- serum creatinine> 3x reference creatinine

26
Q

How do you manage AKI’s?

A

Monitor )peadiatric early warning score (BP, urine output, weight)

Maintain good hydration

Minimise drugs

(3 M’s)

27
Q

What are the three classes of causes of acute kidney injuries?

A

Pre renal- perfusion problem
Renal- multiple causes
Post renal- obstructive uropathies

28
Q

What are renal causes of an AKI?

A

Glomerular disease- Heamolytic ureamic syndrome, glomerulonephritis

Tubular injury- acute tubular necrosis
Drugs

Interstitial nephritis- NSAIDS, autoimmune, drugs