Medicine - Renal Flashcards
what is an acute kidney injury (AKI)? how is it measured?
- an acute drop in kidney function| - serum creatinine
NICE criteria to diagnose an AKI?
- rise in creatinine of 20 micromol/L or more in 2 days (48 hours)- rise in creatinine of 50% or more in 7 days- urine output of less than 0.5ml/kg/h for over 6 hours
what is normal urine output?
0.5ml per kg per hour
risk factors for developing an AKI?
- chronic disease: CKD, HF, DM, liver disease- old age (>65)- cognitive impairment - drugs (NSAIDs, ACE-i)- contrast used in CT scans
how can the causes of AKI be classified? which is most common?
NAME?
examples of pre-renal causes of AKI?
NAME?
describe the pathophysiology of pre-renal AKI
- pathology causing reduced blood flow to the kidneys| - less blood gets filtered through them
describe the pathophysiology of renal AKI
- intrinsic disease of the kidney| - makes it less able to filter blood
examples of renal causes of AKI?
NAME?
describe the pathophysiology of post-renal AKI
an obstruction to outflow causes urine to build up in the kidney and reduce kidney function
examples of post-renal causes of AKI?
NAME?
investigations in AKI?
- urinalysis| - USS of urinary tract (?obstruction)
what might urinalysis show in AKI?
depends on underlying cause:- leukocytes and nitrites (infection)- protein and blood (acute tubular necrosis, infection)- glucose (diabetes)
how can AKI be prevented?
- avoid nephrotoxic meds where possible| - ensure adequate fluids are given
management of AKI?
treat underlying cause:- fluid rehydration (IV)- stop NSAIDs / antihypertensives - relieve obstruction (e.g. catheter to get past an enlarged prostate)if severe without clear cause, refer to renal
complications of AKI?
NAME?
which 2 complications could uraemia (secondary to AKI) cause?
- pericarditis| - encephalopathy
what is CKD?
permanent and progressive reduction in kidney function
causes / risk factors of CKD?
NAME?
drug causes of CKD?
NAME?
presentation of CKD?
NAME?
investigations for CKD?
NAME?
how must eGFR be done in order to diagnose CKD?
2 tests done 3m apart
what is a significant urine ACR reading in CKD? what does this mean?
- 3mg/mmol or more| - indicates proteinuria
what might urine dipstick show in CKD? why is this important?
- haematuria| - could be bladder Ca, investigate!!!!
which CKD patients should be offered renal USS?
NAME?
how is CKD staged?
G score for each eGFR:- G1 = >90- G2 = 60-89- G3a = 45-59- G3b = 30-44- G4 = 15-29- G5 = <15 (end-stage renal failure)
what is A score in CKD?
score based on the albumin : creatinine ratio
how is CKD diagnosed?
at LEAST eGFR <60, OR proteinuria
complications of CKD?
NAME?
when does a CKD patient need a renal referral?
- eGFR <30- ACR 70mg/mmol or more - accelerated disease- uncontrolled HTN despite 4 or more any-hypertensives
in CKD, what is classed as “accelerated disease”?
one of the following:- eGFR drops by 15- eGFR drops by 20%- eGFR drops by 15ml/minall within 1 year
how can the progression of CKD be slowed?
- optimise DM and HTN control| - treat glomerulonephritis
how can complications be reduced in CKD?
- exercise to maintain healthy weight- stop smoking - special dietary advice on phosphate, sodium, potassium and water intake - atorvastatin 20mg for CVD prevention
how are complications in CKD treated?
NAME?
first line drug for HTN in CKD? target BP?
- ACE-i| - <140/90
which electrolyte needs to be monitored closely in someone with CKD and on an ACE-i?
- serum K+| - hyperkalaemia can result from both of these
how does CKD cause anaemia?
healthy kidney cells should produce erythropoietin but they don’t in CKD
How should the iron deficiency in CKD be treated?
- erythropoietin| - IV iron used in dialysis patients
which bone diseases can arise from CKD?
NAME?
X-ray changes seen in CKD bone disease?
VALUE!
how does CKD cause secondary hyperparathyroidism?
the parathyroid glands respond to the low Ca by secreting more PTH
management of renal bone disease in CKD?
NAME?
AEIOU: indications for acute dialysis in AKI patients
NAME?
features of uraemia indicating dialysis?
- seizures| - reduced consciousness
2 indications for long-term dialysis?
- ESRF (CKD stage 5)| - any acute indications continuing long-term
what are the 3 main types of dialysis?
NAME?
which factors are taken into account when choosing a method for dialysis?
NAME?
which factors are taken into account when choosing a method for dialysis?
NAME?
complications of peritoneal dialysis?
NAME?
which 2 methods are there to access blood flow in order to carry out haemodialysis?
- tunnelled cuff catheter| - AV fistula
complications of an AV fistula?
NAME?
what is STEAL syndrome?
inadequate blood flow to limb distal to AV fistula (it literally STEALS the blood rip)
describe the scar left by a renal transplant
hockey stick scar over ipsilateral iliac fossa
describe the scar left by a renal transplant
hockey stick scar over ipsilateral iliac fossa
what is the immunosuppressant regime used after a kidney transplant? hint: there are 3
NAME?
how long is the immunosuppressant regime continued for after a renal transplant?
lifelong
complications of a renal transplant?
NAME?
features of nephritic syndrome?
NAME?
features of nephrotic syndrome?
- peripheral oedema- proteinuria (>3g/day)- frothy urine- low serum albumin- hypercholesterolaemia
define glomerulonephritis
an umbrella term used to describe any condition which causes inflammation of the glomerulus
define interstitial nephritis. what are the 2 main diagnoses?
NAME?
define glomerulosclerosis
NAME?
list 3 causes of glomerulosclerosis
NAME?
management of glomerulonephritis?
- steroids| - ACE-i / ARB
complications of untreated nephrotic syndrome?
NAME?
most common cause of nephrotic syndrome in children?
minimal change disease
most common cause of nephrotic syndrome in adults?
focal segmental glomerulosclerosis
what is IgA nephropathy?
- Berger’s disease| - most common cause of primary glomerulonephritis
when does IgA nephropathy typically present?
in 20s
what is seen on histology in IgA nephropathy?
- IgA deposits| - glomerular mesangial proliferation
what is the most common type of glomerulonephritis overall?
membranous glomerulonephritis
how does post-strep GN present?
- patient <30 years old- weeks after a strep infection - nephritic syndrome presentation- full recovery
which streptococcal infections could be followed by post-strep GN?
- tonsillitis| - impetigo
key feature of diabetic nephropathy?
proteinuria
how is diabetic nephropathy prevented?
it is screened for using albumin:creatinine ratio (ACR) and UEs
management of diabetic nephropathy?
NAME?
how does acute interstitial nephritis present?
delayed onset, 2-40 days after drug trigger:- AKI- HTN- rash- fever- eosinophilia- transient arthralgia in some
causes of acute interstitial nephritis?
infection but mostly drugs:- ABx- NSAIDs- diuretics- rifampicin - allopurinol- PPIs
management of acute interstitial nephritis?
- remove underlying cause| - steroids
pathophysiology of acute tubular necrosis?
ischaemia / toxins causing death of epithelial cells of the renal tubules
causes of acute tubular necrosis? (hint: split into ischaemic and nephrotoxic)
ischaemic:- shock- sepsis- dehydration nephrotoxic:- radiology contrast dye- gentamicin- NSAIDs - lithium - statins- ACE-i, ARBs- heroin
investigation and findings in acute tubular necrosis?
urinalysis shows “muddy brown casts”
management of acute tubular necrosis? hint: same as other AKIs
NAME?
pathophysiology of type 1 renal tubular acidosis?
NAME?
causes of type 1 renal tubular acidosis?
- genetic - SLE- sjogren’s syndrome- PBC- hyperthyroidism - sickle cell anaemia - marfan syndrome
how does type 1 renal tubular acidosis present?
NAME?
investigation findings in renal tubular acidosis (type 1 and type 2)?
- low K+- metabolic acidosis- urinary pH >6 (high)
management of renal tubular acidosis (types 1 and 2)?
PO bicarbonate
pathophysiology of type 2 renal tubular acidosis?
pathology of proximal tubule making it unable to reabsorb bicarbonate
main cause of type 2 renal tubular acidosis?
fanconi syndrome
which group of people is fanconi syndrome most associated with?
Ashkenazi Jews
features of fanconi syndrome?
NAME?
what causes type 4 renal tubular acidosis?
low aldosterone
investigation findings in type 4 renal tubular acidosis?
NAME?
most common type of renal tubular acidosis?
type 4
causes of type 4 renal tubular acidosis? hint: these all lower aldosterone levels
NAME?
management of type 4 renal tubular acidosis?
- fludrocortisone (mineralocorticoid, so mimics aldosterone) - sodium bicarbonate - treat hyperkalaemia (IV insulin w/ glucose + calcium gluconate)
what is haemolytic uraemic syndrome (HUS)? what causes this?
- thrombosis in all the small vessels around the body| - caused by shiga toxin
features of HUS? hint: classic triad
NAME?
where does the shiga toxin come from?
either E. coli or shigella infection
presentation of HUS?
NAME?
management of HUS?
- medical emergency!- anti-hypertensives- blood transfusions- dialysis
prognosis of HUS?
- 10% mortality rate| - approx 75% make a full recovery
what do muscle cells release when they die? (features of rhabdomyolysis)
NAME?
complication of potassium release from rhabdomylosis?
NAME?
causes of rhabdomyolysis?
NAME?
presentation of rhabdomyolysis?
NAME?
investigations and findings in rhabdomyolysis?
- CK (raised, remains high for 1-3 days) - urine dipstick (positive for blood due to myoglobin)- UEs (AKI, hyperkalaemia)- ECG (hyperkalemia changes)
management of rhabdomyolysis?
NAME?
main complication of hyperkalaemia?
- arrhythmias| - particularly VF
causes of hyperkalaemia?
NAME?
drug causes of hyperkalaemia?
NAME?
what can cause a falsely raised potassium in a blood test?
haemolysis of the sample
ECG signs in hyperkalaemia?
NAME?
management of acute hyperkalaemia?
NAME?
management of less urgent hyperkalaemia?
NAME?
at what level of K+ does hyperkalaemia need to be managed urgently?
- > 6mmol/L with ECG changes, OR:| - >6.5 mmol/L regardless of ECG
what is polycystic kidney disease (PKD)? what does it cause?
genetic condition where the kidneys develop fluid-filled cysts
which other organs can have cysts in them in PKD?
NAME?
extrarenal findings in ADPKD?
NAME?
what is the mode of inheritance of PKD?
- there are both autosomal dominant and recessive forms| - autosomal dominant (ADPKD) is more common
how is PKD diagnosed?
- USS of kidneys| - genetic testing
which genes are associated with autosomal dominant PKD?
- PKD-1 (chrom 16), majority| - PKD-2 (chrom 4)
complications of PKD?
- chronic loin pain- HTN- CVD- gross haematuria- renal stones- ESRF aged 50
management of PKD?
NAME?
what is haemolytic uraemic syndrome (HUS)? what causes this?
- thrombosis in all the small vessels throughout the body| - caused by shiga toxin
how does autosomal recessive PKD (ARPKD) present?
NAME?
renal features of ADPKD?
NAME?
most common complication of dialysis?
dialysis-induced hypotension
criteria for stage 1 AKI?
either:- Cr >1.5x baseline- UO <0.5ml/kg/hr for 6h
criteria for stage 2 AKI?
either: - Cr >2x baseline- UO <0.5ml/kg/hr for 12h
criteria for stage 3 AKI?
any of these:- Cr >3x baseline- Cr >354- UO <0.3ml/kg/hr for 24h- anuria for 12h
which other conditions are associated with focal segmental glomerular sclerosis?
- IgA nephropathy (berger’s disease)- HIV- sickle cell disease
first line renal replacement therapy in ESRF? why is this preferred?
NAME?
which variables are taken into account to calculate eGFR?
NAME?