nephrology + genitourinary Flashcards

(61 cards)

1
Q

what % of boys and girls get UTI before 6 years old

A

3-7% girls, 1-2% boys

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2
Q

complications pyelonephritis

A

damage growing kidney by forming a scar- hypertension and chronic renal failure

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3
Q

features UTI in infants

A

non specific- fever, vomiting, lethargy, poor feeding, jaundice, septicaemia, offensive urine, febrile convulsions

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4
Q

features UTI in children

A

dysuria and frequency, abdominal pain or loin tendernessm fever +- rigors, lethargy, d +v, haematuria, offensive urine, febrile convulsion, recurring enuresis

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5
Q

what differentiates pyelonephritis from cystitis

A

fever and systemic involvement

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6
Q

what is the best way to get a urine sample in infant

A

clean catch

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7
Q

what should you do with urine culture if

A

culture immediately. or refrigerate

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8
Q

what is the mode of infection in infant

A

haematogenous (older- bacteria from the gut flora)

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9
Q

commonest organisms UTI

A

e coli. others- klebsiella, proteus, pseudomonas, strep faecalis

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10
Q

what is vesicoureteric reflux

A

anomaly vesicoureteric junction. ureters displaced laterally, directly enter into bladder rather than at an angle (backward flow urine from bladder to kidneys)

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11
Q

what is mild VUR

A

reflex of urine into ureter only. on micturition

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12
Q

what is severe VUR

A

gross dilatation ureter, renal pelvis and calyces. reflux during bladder filling and voiding. assoc with intrarenal reflux

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13
Q

what has a high risk of causing scarring to the kidneys

A

intrarenal reflux

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14
Q

if bilateral scarring of kidneys what can occur

A

chronic renal failure. risk of HTN

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15
Q

when is investigation necessary in UTI

A

atypical or recurrent UTIs. septicaemia, poor urine flow, abdominal mass, incr creat, failure to respond to antibiotics within 48h. infection with non e coli organisms

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16
Q

investigations in UTI

A

ultrasound, DMSA (99Tc), MCUG (micturating cystourethrogam), MAG3 renogram, AXR

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17
Q

what is the best investigation for excluding reflux

A

MCUG

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18
Q

which scan is best for dynamic scan

A

MAG3

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19
Q

what can be done in first UTI

A

ultrasound

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20
Q

treatment UTI infant

A

cefotaxime. or amoxicillin + gentamicin

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21
Q

treatment lower UTI

A

trimethoprim 3 days. nitrofurantoin

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22
Q

treastment upper UT/ acute pyelonephritis

A

co amoxiclav for 7-10d or IV cefotaxime 2-4 days then oral for 7-10d

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23
Q

what can be used as prophylaxis

A

trimethoprim

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24
Q

what can enuresis be due to

A

lack of attention to bladder sensation, detrusor instability, bladder neck weakness, neuropathic bladder, UTI, constipation, ectopic ureter

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25
presentation ectopic ureter
girls who are dry at night but wet on getting up
26
investigations enuresis
urine sample, US, urodynamic studies, X ray, MRI
27
treatment enuresis
desmopressin. enuresis alarm
28
causes secondary enuresis
when lose previously achieved urinary continence- emotional upset, UTI, polyuria- DM, sickle cell
29
what is nephrotic syndrome
proteinuria, low albumin, oedema
30
signs nephrotic syndrome
periorbital oedema, scrotal or vulval leg or ankle oedema, ascites, breathless- effusion
31
investigations nephrotic syndrome
urine protein, FBC, ESR, U&Es, creat, albumin, complement, urine microscopy and culture, urinary Na, antistrepsolysin O or anti DNAase B titres and throat swab, hep B and C screen
32
what tests can detect group A strep
anti DNAase b titre, with anti strepsolysin O
33
what is steroid sensitive nephrotic syndrome
85-90% children with NS respond to corticosteroids. dont progress to renal failure. often precipitated by resp infections
34
features of steroid sensitive NS
age 1-10y, no macroscopic haematuria, normal bp, normal complement, normal renal function
35
management steroid sensitive NS
oral prednisolone 60mg/m/d reduce to 40 after 4 weeks then alternate days for 4 weeks then stop.
36
if steroid sensitive NS doesn't respond to corticosteroids or atypical what should be done
renal biopsy
37
what is the most common NS in children
minimal change disease
38
is minimal change disease responsive to steroid treatment
yes
39
complication of minimal change disease
hypovolaemia, low urinary Na, thrombosis, infection, hypercholesterolaemia
40
what can you treat hypovolaemia with in minimal change disease
IV albumin (colloid)
41
causes of steroid resistant NS
focal segmental glomerulonephritis, mesangiocapillary glomerulonephritis, membranous nephropathy
42
treatment focal segmental glomerulonephritis
cyclophosphamide, ciclosporin, tacrolimus, rituximab
43
associations membranous nephropathy
may precede SLE. associated with hep B. most remit spontaneously within 5 years
44
treatment oedema
diuretics, salt restriction, ACEi, NSAIDs
45
most common cause haematuria
UTI
46
signs glomerular haematuria
brown urine, deformed red cells and casts, proteinuria
47
signs lower UT haematuria
red. beginning or end of stream
48
when to do renal biopsy in haematuria
significant proteinuria, abnormal renal function, recurrent macroscopic haematuria, complement levels abnormal
49
non glomerular causes haematuria
trauma, stones, sickle cell, hypercalcuria, bleeding disorders, infection, renal vein thrombosis, tumours
50
glomerular causes haematuria
acute and chronic glomerulonephritis, IgA nephropathy, thin basement membrane disease, familial nephritis
51
investigations haematuria
urine microscopy and culture, protein and calcium excretion, US, U&Es, creat, Ca, PO4, albumin, FBC, platelets, clotting, sickle cell screen
52
if suspect alports what can you test
hearing
53
what is henoch schlonein purpura
acute immune complex mediated vasculitis
54
what precedes the purpura in HSP
URTI
55
symptoms HSP
purpura, arthritis/arthralgia, abdominal pain. renal involvement- glomerulonephritis, haematuria, proteinuria. intussusception, GI petechiae- haematemesis and malaena
56
presentation HSP
symmetrical rash over buttocks, extensor surfaces of arms and legs, ankles. trunk spared. usually have a fever. 3-10y. male : female 2:1
57
tests in HSP
ESR incr, IgA incr, proteinuria, ASO titres incr, U&E, BP.
58
complications HSP
massive GI bleeds, haemoptysis, acute renal failure
59
what is AKI characterised by
rapid rise in creat and development oliguria/anuria
60
what is haemolytic uraemic syndrome
acute microangiopathic haemolytic anaemia, thrombocytopaenia, renal failure + endothelial damage to glomerular capillaries.
61
what is typical HUS associated with
diarrhoea. more freq in summer months, typically occurs children