deck 2 Flashcards

1
Q

hyponatremic hypovolemia

A
diarrhea
emesis
burns
third spacing
urine na - low (cause you are concentrating)
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2
Q

hypervolemia hyponatremia

A
CHF
nephrotic syndrome
renal failure
sepsis if leaky
decreased albumin from protein losing enteropathy
cirrhoses
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3
Q

euvolemic hyponatremia

A
SIADH
water intoxication - psychogenic or dilute formula
glucose
hypothyroidism
glucocorticoid deficiency
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4
Q

8 month old baby with gastroenteritis. Na 160, Cl elevated, Bicarb 14, HR 220, BP 60/30. What is your initial management. Once stable what is your ongoing fluid management?

A
ABCs 20 cc/kg NS
then ongoing fluid management once stable 
determine how long to correct Na over - 
initial Na 145-157 correct over 24 hours
158-170 over 48 hours
171 -183 72 hours
184-196 over 96 hours 

correction rate 10-12 mmol/day
typically fluid D5 1/2 normal saline with 20 KCl
1.25-1.5 maintenance (because they are dehydrated)
check your sodium often

Change in Serum Sodium
= (Fluid Sodium - Serum Sodium) / (Total Body Water + 1)
Total Body Water = (Wt in kg * % Water)

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5
Q

noctural enuresis

A

2 parents with enuresis, 75% chance of enuresis
causes for nocturnal enuresis:
delayed maturation in cortical mechanism
sleep disorders
OSA
severe constipation
Don’t make as much ADH at night

Motivational therapy – limited evidence, try it
Fluid restrict, void before bed, caffeine
If doesn’t work, conditioning therapy – 30-60%, curative
Alarm system, usually better in kids > 6-7
meds - symptomatic
1st line DDAVP
2nd oxybutinin
3rd imipramine

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6
Q

Struvite stone, which organism

A

proteus
foreign body
urinary stasis

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7
Q

protein in a teenage girl

A

1st test - 1st AM urine x 2 then move on to other tests

in general if 3+ on dipstick more likely to be a fixed proteinuria, more likely to be a glomerular or tubular issue

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8
Q

when do sperm die in torsion

A

4-6 hours

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9
Q

painless testicular masses

A
varicocele
hydrocele
spermatocele
inguinal hernia
idiopathic
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10
Q

painful scrotal masses

A

epididymitis
testicular torsion/appendicular torsion
orchitis
trauma

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11
Q

most common flank mass

A

hydronephrosis

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12
Q

most common abdo mass

A

multicystic dysplastic kidney

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13
Q

types of rhabdo

A
  1. exertional
  2. non trauma exertional - hyperthermia, metabolic
  3. non trauma non exertional - drugs, toxins, , infections
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14
Q

What is DMSA

A

functional and anatomical information
better visualizes focal renal parenchymal abnormalities
also can compare kidney function between the two
look for scarring and pyelo

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15
Q

What is MAG3

A

look at obstructive and non obstructive hydronephrosis, as well as different function between the two kidneys

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16
Q

3 things VCUG can tell you

A
  1. reflux
  2. PUV
  3. bladder shape and function
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17
Q

Alport’s disease

A

X linked dominant in 85% the rest are different types
start on high frequency loss
eye stuff - anti - lento conus (eye stuff), macular flex, corneal erosion, anterior lenticonus is pathognomic for Alport’s
renal disease - hypertension
type 4 collagen
prognosis for boys: 15% by 15 years old, 75% by age 30, hearing loss is gradual
for ladies - mild in general, some can have findings later in life (milder)

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18
Q

Prognostic factors in Alport’s

A
  1. gross hematuria
  2. nephrotic syndrome
  3. on biopsy have prominent glomerular basement membrane thickening
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19
Q

What percentage of patients with nocturnal enuresis will spontaneously improve each year?

A

15% per year

20
Q

Do acute hydroceles hurt?

A

might have discomfort, but should be okay and tolerate feedings

21
Q

Causes of HUS

A
Infectious causes of HUS:
- E. coli, S. pneumo, Shigella , HIV 
Medications 
- chemo (cyclosporine and tacrolimus)
Genetic HUS
Any disease with microvascular disease
- lupus, HELLP, antiphospholid
22
Q

Places you can get organism

A
uncooked meat
well water
contaminate vegetables
unpasteurized milk/apple cider 
petting farms 
(usually E. coli, sometimes shigella)
23
Q

What is the incidence of CNS involvement in HUS?

A

the majority have CNS involvement, most are mild - lethargy, irritability, non specific encephalopathic features, seizures, stroke
microvascular thrombosis

24
Q

What’s the prognosis for HUS?

A

<5% mortality but 50% of children need dialysis during the acute phase
70% fully recover, 30% have chronic renal insufficiency

25
Q

single umbilical artery

A

if no other abnormality then likely not a problem
associated abnormalities with renal abnormalities:
- ear abnormalities, GU, pulmonary hypoplasia, imperforate anus, scoliosis

26
Q

Definition of hypertension urgency

A

> 99th percentile BP
headache or vomiting but no signs of end organ damage
tx: IV or PO

27
Q

hypertension emergency

A

> 99th percentile BP with encephalopathy, seizures or renal dysfunction
fragile vessels and the blood pounding them, lots of pressure
wrecks your organs like a typhoon.
tx: must be IV

28
Q

How fast should you decrease the BP?

A

don’t go too fast because you don’t want to reduce the perfusion to the organ
goal of 25% decrease over the 1st 8 hours
normalization over the next 48 hours
regardless of whether they are still symptomatic

29
Q

Aside from nifedipine, 3 other meds for acute BP

A

nitro
labetalol
hydralazine

30
Q

Most common cause of nephrotic syndrome in children

A

minimal change disease

31
Q

What is the treatment for minimal change disease

A

steroids

32
Q

In a child with nephrotic syndrome, when to biopsy

A

if steroids fail, or if older age

33
Q

BP in nephrotic syndrome

A

should be nomal (although can be elevated in 25%, but shouldn’t be in typical minimal change disease (baby nelson)

34
Q

Treatment of rhabdo

A

either dialysis or mannitol (to help with osmotic diuresis)
because doesn’t act on the kidneys
(vs lasix actually acts on stuff)
benefit of mannitol is not established

35
Q

Why do you get polyuria with ATN?

A

3 phases

  1. acute decrease in GFR with sudden increase in BUN/Cr
  2. maintenance - severe sustained reduction in GFR
  3. recovery - tubular function restored - increase in u/o volume at that point
36
Q

Abdominal compartment syndrome

A

abdominal compartment

  1. low u/o
  2. hypotension
  3. resp distress because of increased abdominal pressure
37
Q

How to measure abdominal compartment pressure?

A

bladder probe - manometer - on the end of a foley

38
Q

increased anion gap

A

mudpiles
i is isoniazzid and iron
non anion gap: is RTA and diarrhea

39
Q

Bartters syndrome

A

loop of henle problem
autosomal recessive
metabolic alkalosis - present with persistent vomiting, polyuria and polydipsia

40
Q

kid not peeing and hyponatremic

urine SP gravity 1.020 (concentrated)

A

fluid restrict 1L/m2/24 hours

41
Q

4 year old with hematuria on two urine dips, has a grandfather with renal stones

A

urine calcium/creatinine ratio

>0.2 think of stones

42
Q

random microscopic hematuria

A

check BP, repeat the urine (2 more times), check for protein

43
Q

proteinuria - false positive

A

antiseptic agent
if urine is alkaline
if the dipstick stays there too long

44
Q

most common cause of persistent proteinuria

A

orthostatic proteinuria
test for this diagnosis: first morning urine x 2/3
urine protein/Cr ratio <0.2 then confirms diagnosis

45
Q

when to refer to paediatric surgeon for undescended testicle

A

should refer by 6 months (most descent by 4 months?, somewhere else says 9 months)
2 complications:
- infertility
- undetected cancer/cancer

46
Q

5 month old with UTI, 2 indications for prophylaxis

A
  1. high grade reflux
  2. obstruction - ie PUV

reasons for urology
1. hypertension 2. impaired renal function3. renal abnormalities

47
Q

reducible hernia, when to refer?

A

does not resolve spontaneously, early repair reduces the chance of incarceration, should do within 6-12 months of life
70% of incarcerated occur in the first year of life
can get testicular atrophy from inguinal hernia
for the routine hernia, operation should be done shortly after diagnosis