Renal Flashcards

(41 cards)

1
Q

Types of glomerulonephritis

A
Minimal change disease
Focal segmental glomerulosclerosis
Membranous GN
IgA Nephropathy
Goodpasture's syndrome 
Etc
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2
Q

What is nephritic syndrome?

A

Inflammation in the kidneys, causing haematuria, oliguria, proteinuria, fluid retention

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3
Q

Criteria for Nephrotic syndrome

A
  1. Peripheral oedema
  2. Proteinuria
  3. Low serum albumin
  4. Hypercholesterolaemia
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4
Q

What is the most common cause of Primary Glomerulonephritis?

A

IgA Nephropathy

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5
Q

What is the most common cause of Glomerulonephritis overall?

A

Membranous glomerulonephritis

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6
Q

At what age does Membranous glomerulonephritis peak?

A

Bimodal peak- 20s + 60s

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7
Q

What is found on histology in Membranous glomerulonephritis?

A

IgG and complement deposits in basement membrane

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8
Q

What is Polycystic Kidney Disease?

A

Genetic condition where kidneys develop multiple fluid-filled cysts

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9
Q

What is the inheritance pattern of Polycystic Kidney Disease?

A

There is an autosomal dominant and an autosomal recessive type
- AD more common

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10
Q

How is Polycystic Kidney Disease diagnosed?

A

Kidney USS

Genetics

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11
Q

Which chromosome is affected in Autosomal recessive Polycystic Kidney Disease?

A

Chromosome 6

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12
Q

Features of Autosomal recessive Polycystic Kidney Disease

A

Oligohydramnios in pregnancy –> underdevelopment of lungs –> respiratory depression shortly after birth
Dysmorphic features- low set ears, flat nasal bridge
End-stage renal failure before adulthood

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13
Q

Complications of Autosomal dominant Polycystic Kidney Disease

A

Chronic loin pain, hypertension, cardiovascular disease, gross haematuria, renal stones, end-stage renal failure

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14
Q

Features of Autosomal dominant Polycystic Kidney Disease

A

Extra-renal manifestations- cerebral aneurysms, prostatic/ovarian/splenic/pancreatic/hepatic cysts, cardiac valve disease (MR), colonic diverticula, aortic root dilatation

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15
Q

What is the mutated gene in Autosomal dominant Polycystic Kidney Disease?

A

PKD1/2

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16
Q

Management of Polycystic Kidney Disease

A

Tolvaptan- slow progression of cysts and disease
Genetic counselling
Avoid anti-inflammatories + anticoagulation, contact sports
Analgesia for renal colic
Antihypertensives
Dialysis/transplant

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17
Q

What regular monitoring is needed in Polycystic Kidney Disease?

A

USS, renal function, hypertension monitoring

MR angiogram- for intracranial aneurysms

18
Q

General management of Glomerulonephritis

A

Immunosuppression

BP control- ACEi + ARB

19
Q

Presentation of nephrotic syndrome

A
Oedema
Frothy urine (proteinuria)
20
Q

Complications of nephrotic syndrome

A

Thrombosis
Hypertension
Hyperlipidaemia

21
Q

What is the most common cause of nephrotic syndrome in i) children and ii) adults?

A

Children- Minimal change disease

Adults- Focal segmental glomerulonephritis

22
Q

What is the peak age for IgA nephropathy (Berger’s disease)?

23
Q

Histology findings in IgA nephropathy (Berger’s disease)

A

IgA deposits and glomerular mesangial proliferation

24
Q

Causes of Membranous glomerulonephritis

A

Mostly idiopathic

Secondary to malignancy, rheumatoid disorders and drugs (NSAIDs)

25
What is post-streptococcal glomerulonephritis?
Presents 1-3 weeks after strep infection eg tonsilitis/impetigo Nephritic syndrome
26
Aetiology of Goodpasture syndrome
Anti-glomerular basement membrane antibodies attack glomerular and pulmonary basement membrane
27
Features of Goodpasture syndrome
1. Glomerulonephritis | 2. Pulmonary haemorrhage (haemoptysis)
28
Causes of Chronic Kidney Disease
Diabetes, hypertension, age, glomerulonephritis, polycystic kidney disease, meds eg NSAIDs, PPIs, lithium
29
Risk factors for Chronic Kidney Disease
Diabetes, hypertension, age, glomerulonephritis, polycystic kidney disease, meds eg NSAIDs, PPIs, lithium Smoking
30
Presentation of Chronic Kidney Disease
Usually asymptomatic | Pruritus, loss of appetite, nausea, oedema, muscle cramps, peripheral neuropathy, pallor, hypertension
31
How is Chronic Kidney Disease diagnosed?
eGFR- 2 tests 3 months apart
32
Investigations of Chronic Kidney Disease
Urinalysis- proteinuria (urine albumin:creatinine ratio >=3), haematuria eGFR Renal USS
33
Classification of Chronic Kidney Disease
``` By eGFR: 1) >90 2) 60-89 3) 30-59- mild-moderate 4) 15-29- severe 5) <15- kidney failure By albuminuria: 1) Albumin < 30 - A:Cr <3 2) Albumin 30-300 - A:Cr 3-30 3) Albumin < 300 - A:Cr >30 ```
34
Management of Chronic Kidney Disease
``` Slow progression: - Control diabetes + HTN - Treat glomerulonephritis Reduce risk of complications: - Exercise, healthy diet, stop smoking - Reduce water intake - Atorvastatin Treat complications: - Metabolic acidosis- sodium bicarbonate - Anaemia- iron supplement + erythropoeitin - Renal bone disease- vitamin D - Dialysis in end-stage - Renal transplant ```
35
Indications for acute renal dialysis
AEIOU: - Acidosis - Electrolyte abnormality - Intoxication - Oedema - Uraemia
36
What is Acute Kidney Injury?
Acute drop in kidney function - Cr rise >= 25mmol/L in 48hrs - Cr rise >50% in 7 days - Urine output < 0.5ml/hr/kg for 6 hours
37
Risk factors for Acute Kidney Injury
CKD, heart failure, diabetes, liver disease, age > 65, cognitive impairment, nephrotoxic meds (NSAIDs, ACEi), contrast
38
Causes of Acute Kidney Injury
Pre-renal: dehydration, hypotension, heart failure Renal: glomerulonephritis, interstitial nephritis, Acute tubular necrosis Post-renal: kidney stones, masses in abdomen/pelvis, ureter/urethral strictures, enlarged prostate/prostate cancer
39
Investigations of Acute Kidney Injury
Urinalysis, USSKUB
40
Management of Acute Kidney Injury
IV Fluid rehydration Stop nephrotoxic meds Relieve obstruction eg catheter Severe- dialysis
41
Complications of Acute Kidney Injury
Hyperkalaemia, fluid overload, metabolic acidosis | Uraemia --> encephalopathy/pericarditis