Renal/Uro Flashcards

1
Q

CKD definition

A

reduction in kidney function (eGFR <60) and/or structural kidney damage that persists for 3+ months

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2
Q

CKD stages

A

based on serun eGFR

G1 90+ normal and high
G2 60-89 mild reduction related to normal range for a young adult
G3a 45-59 mild to moderate reduction
G3b 30-44 moderate to severe reduction
G4 15-29 severe reduction
G5 <15 end-stage kidney failure

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3
Q

CKD pathophysiology

A

chronic damage to the glomeruli which causes various types of remodelling

causes:
DM
HTN
meds eg NSAID
primary glomerular diseases
obstructive uropathies
systemic disease eg SLE

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4
Q

CKD presentation

A

generally unwell (fatigue, SOB, cramps)
polyuria, oliguria, nocturia
pallor, cachexia, malnourished
hypertensive, oedema, flank masses if PKD,
frothy urine

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5
Q

CKD Ix

A

first test- urine dipstick to look for blood and exclude UTI
ACR urinalysis
serum Cr
eGFR (repeat in 6mo then 3mo)
- no meat 12 hours before test
BMI, lipids, HbA1c, lipid profile
renal USS

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6
Q

AD polycystic kidney disease pathophysiology

A

AD condition, multiple cysts in kidneys, destroys parenchyma

PKD1, PKD2

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7
Q

ADPKD presentation

A

middle age
large bilateral flank masses
haematuria
hypertension
associations (aneurysm > SAH), CKD

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8
Q

ADPKD diagnosis

A

USS shows multiple cysts in kidney, sometimes also liver

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9
Q

types of renal artery stenosis

A

atherosclerotic
fibromuscular dysplasia

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10
Q

renal artery stenosis epidemiology

A

men with ASCVD risk factors
young women

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11
Q

renal artery stenosis presentation

A

resistant hypertension
flash pulmonary oedema

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12
Q

renal artery stenosis diagnosis

A

1st: duplex USS
most useful: CTA
gold standard: DSA

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13
Q

renal cell carcinoma pathophysiology

A

malignancy of kidney
most common type is clear cell adenocarcinoma
originates from PCT cells

gene deletion of chr3 (acquired or inherited as part of vHL syndrome)

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14
Q

renal cell carcinoma presentation

A

50-70 yrs
triad: flank pain, haematuria, palpable mass
maybe FLAWS
Internist tumours (paraneoplastic syndrome)

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15
Q

renal cell carcinoma diagnosis

A

CT scan

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16
Q

amyloidosis pathophysiology

A

multisystem disease due to deposition of abnormal amyloid proteins

type 1 is AL
type 2 is AA
familial is ATTR

17
Q

amyloidosis presentation

A

multisystem
key ones are cardiomyopathy and amyloid kidney disease

18
Q

amyloidosis diagnosis

A

gold standard is biopsy, fat pad most easily accessible
- congo red
- apple green birefringence under polarised light

19
Q

common causes of UTI

A

most common overall - E.coli

young women - S.saprophyticus
ppl with chronic UTI and staghorn kidney stone - P.mirabilis

Klebsiella

20
Q

UTI presentation

A

dysuria, polyuria, urgency
suprapubic discomfort
delirium, confusion in elderly
change in urine appearance

21
Q

red flags for upper UTI

A

fever
costovertebral angle tenderness
vital sign derangements

22
Q

UTI investigations

A

1st: urine dip
- unreliable in women >65 and if catheterised
- if positive for nitrite or leukocyte of RBC likely UTI
- if neg for nitrite and positive for WBC send for culture to confirm
- if neg for all nitrite, WBC and RBC consider other diagnosis

send urine sample for culture if pregnant, plastic, paediatric, persistent or peeing blood

23
Q

UTI mx

A

assess for sepsis risk or risk of upper UTI
simple analgesia
nitrofurantoin or trimethoprim 1st line for uncomplicated UTI
no improvement after 48 hrs - pivmecillinam

24
Q

UTI complications

A

upper UTI (pyelonephritis) > septic shock
renal abscess
renal papillary necrosis