Chronic Kidney Disease (CKD) Flashcards

1
Q

What are the Sx of CKD?

A

Often asymptomatic until advanced (fatigue/anorexia)
Polyuria/nocturia
Restless legs syndrome
Sexual dysfunction
Nausea & Pruritis
Yellow pigmentation, encephalopathy, pericarditis
Pedal/pulmonary oedema

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2
Q

What are the signs of CKD?

A

Pallor due to anaemia
Excoriations due to pruritis
HTN/fluid overload signs
Pericardial rub

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3
Q

What are the appropriate initial investigations for CKD?

A

Bloods - FBC, U&E, LFTs, Ca, PO4, PTH, Glucose
Urinalysis & MCS - quantify proteinuria, exclude infection
24h urinary protein - assess severity
CXR - suspected pulmonary oedema
Renal USS - suspected obstructive causes

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4
Q

How is CKD diagnosed?

A

Two tests 3/12 apart showing reduced eGFR

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5
Q

How is CKD staged?

A

According to eGFR

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6
Q

Describe Stage 1 CKD

A

eGFR >90
Normal kidney function
Urine findings/structural abnormalities/genetic traits point to kidney disease

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7
Q

Describe Stage 2 CKD

A

eGFR 60-89
Mildly reduced kidney function
Urine findings/structural abnormalities/genetic traits point to kidney disease

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8
Q

Describe Stage 3 CKD

A

eGFR 30-59

Moderately reduced kidney function

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9
Q

Describe Stage 4 CKD

A

eGFR 15-29

Severely reduced kidney function

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10
Q

Describe Stage 5 CKD

A

eGFR <15

V. severe/established renal failure

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11
Q

What is eGFR?

A

An estimate of GFR based on a plasma level of creatinine

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12
Q

What are the common causes of CKD?

A
DM (20-40%)
HTN
AKI
Renal Disease
   -Polycystic kidney disease
   -Chronic glomerulonephritis
   -Chronic pyelonephritis
Obstructive uropathy
Renovascular disease
Drugs (NSAIDs)
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13
Q

What additional specialist investigations may be required in CKD?

A

DTPA scan (investigates vascular supply)
Renal biopsy
Bone imaging

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14
Q

What are the management options for CKD?

A
Treat reversible causes (obstruction, nephrotoxic drugs)
BP/DM control
   -BP <130/80 OR <125/75 if proteinuric
   -ACEIs 1st line, also statin + ld aspirin
Complication control
   -EPO
   -ca/vit D supplementation
   -K+ restriction if hyperkalaemic
Renal replacement therapy (Stage 5)
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15
Q

When should renal replacement therapy be started?

A

Any symptomatic CKD Stage 5 pt

-often try to delay dialysis

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16
Q

What are the three main complications of CKD?

A

Renal anaemia
Renal bone disease
2o HTN

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17
Q

What is the underlying pathophysiology of renal anaemia in CKD?

A

Loses ability to secrete EPO –> anaemia

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18
Q

How is renal anaemia managed?

A

Recombinant EPO as part of renal replacement therapy

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19
Q

What factors contribute to renal anaemia?

A

CKD
Bone marrow toxins
Increased blood loss
Abnormal red cell membrane

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20
Q

What is the underlying pathophysiology of renal bone disease in CKD?

A

Low vit D –> hypocalcaemia, hyperphosphataemia, osteomalacia –> 2o hyperparathyroidism –> cyst formation & marrow fibrosis –> 3o hyperparathyroidism –> osteopenia

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21
Q

How can osteopenia be detected radiologically?

A

Pseudofractures

Subperiosteal erosions

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22
Q

How is renal bone disease managed?

A

Restrict dietary phosphate
Give phosphate binders
AdCal supplementation

23
Q

What is the underlying pathophysiology of 2o HTN in CKD?

A

Overactivation of RAAS –> HTN
Thickened renal artery walls (afferent)
Chronic ischaemia, progressive loss of glomeruli

24
Q

What are the different options for renal replacement therapy?

A

Haemodialysis
Peritoneal dialysis
Transplantation

25
What is haemodialysis?
Diffusion of solutes b/w blood & dialysate - flow in opposite directions - semi-permeable membrane b/w
26
How is vascular access typically achieved for haemodialysis?
Arteriovenous Fistula - wrist/cubital fossa - can also use double lumen venous lines
27
How often must haemodialysis occur?
4hrs, 3x/wk, normally in hospital
28
What is the main issue in haemodialysis?
Haemodynamic instability during dialysis
29
What is haemofiltration?
Variant of haemodialysis where blood is continuously filtered across highly permeable membrane - more efficient - more haemodynamically stable - more expensive
30
How is peritoneal dialysis performed?
2l of isotonic/hypertonic solution inserted into peritoneal cavity -equilibrates w/ blood in peritoneal capillaries through peritoneal membrane
31
How often must peritoneal dialysis occur?
3-4x/daily Fluid drained after 4-6hrs -can be performed at night (automated peritoneal dialysis)
32
What is the main risk of peritoneal dialysis?
Peritonitis
33
What are the complications of dialysis?
``` Mortality 20% Infection CVD Renal bone disease/anaemia Bleeding Renal malignancies ```
34
What factors must be measured in a patient assessment pre-transplantation?
Virology/TB status (active infection = contraindication) Blood group/HLA monitoring Full systemic examination (co-morbid disease = contraindication)
35
What are the potential complications of renal transplantation?
Operative complications Rejection Ciclosporin/tacrolimus toxicity (immunosuppressants) Infection/malignancy (immunosupression)
36
What are the potential operative complications of renal transplantation?
Bleed Thrombosis Infection Urinary leaks
37
Describe the risk of rejection in renal transplantation
Risk highest in 3mo Lifelong immunosuppression Episodes of rejection reversible Immunological tolerance develops
38
What malignancies are most likely post renal transplant?
Skin cancer Anal cancer Lymphoma
39
What is the prognosis of a renal transplant?
Good | 1yr graft survival rate 80-95%
40
What three ways can DM affect the kidney?
Direct glomerular damage Ischaemia Ascending infection
41
Describe direct glomerular damage caused by DM
Basement membrane thickening - increased leakiness of capillary wall - proteinuria - glomerular hyalinisation --> CKD
42
How is polycystic kidney disease inherited?
AD or AR | -AD more common (1/800)
43
What is the long term consequence of PKD?
Both kidneys replaced by enlarging fluid filled cysts
44
How do ADPKD sufferers present?
Systemic HTN CKD Abdo swelling (bilateral, ballotable kidneys) Renal failure (later in life)
45
Where else may cysts develop in ADPKD?
Liver Lungs Pancreas
46
How do ARPKD sufferers present?
Earlier onset | Chronic renal failure earlier in life
47
What is the potential effect of liver cysts in PKD?
Portal HTN | Fibrosis
48
What is the main condition associated w/ PKD?
Berry aneurysms --> SAH
49
How is PKD managed?
As CKD | Screen for berry aneurysms
50
What are the two forms of chronic interstitial nephritis?
Reflux associated | Obstructive
51
Describe reflux associated chronic interstitial nephritis
Incompetent vesicoureteric valves -predisposition to inflammation/scarring Presents in eraly adulthood w/ deteriorating renal funcn
52
Describe obstructive chronic interstitial nephritis?
Recurrent episodes of infection due to anatomical abnormality/stone
53
What are the histological hallmarks of chronic interstitial nephritis?
Irregular areas of scarring | Chronic inflammatory infiltrate
54
What drugs typically require dose reduction in the presence of a decreased eGFR?
``` Gentamicin Cephalosporins Heparin Lithium Opiates Digoxin ```