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
single umbilical artery
if no other abnormality then likely not a problem associated abnormalities with renal abnormalities: - ear abnormalities, GU, pulmonary hypoplasia, imperforate anus, scoliosis
26
Definition of hypertension urgency
>99th percentile BP headache or vomiting but no signs of end organ damage tx: IV or PO
27
hypertension emergency
>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
How fast should you decrease the BP?
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
Aside from nifedipine, 3 other meds for acute BP
nitro labetalol hydralazine
30
Most common cause of nephrotic syndrome in children
minimal change disease
31
What is the treatment for minimal change disease
steroids
32
In a child with nephrotic syndrome, when to biopsy
if steroids fail, or if older age
33
BP in nephrotic syndrome
should be nomal (although can be elevated in 25%, but shouldn't be in typical minimal change disease (baby nelson)
34
Treatment of rhabdo
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
Why do you get polyuria with ATN?
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
Abdominal compartment syndrome
abdominal compartment 1. low u/o 2. hypotension 3. resp distress because of increased abdominal pressure
37
How to measure abdominal compartment pressure?
bladder probe - manometer - on the end of a foley
38
increased anion gap
mudpiles i is isoniazzid and iron non anion gap: is RTA and diarrhea
39
Bartters syndrome
loop of henle problem autosomal recessive metabolic alkalosis - present with persistent vomiting, polyuria and polydipsia
40
kid not peeing and hyponatremic | urine SP gravity 1.020 (concentrated)
fluid restrict 1L/m2/24 hours
41
4 year old with hematuria on two urine dips, has a grandfather with renal stones
urine calcium/creatinine ratio | >0.2 think of stones
42
random microscopic hematuria
check BP, repeat the urine (2 more times), check for protein
43
proteinuria - false positive
antiseptic agent if urine is alkaline if the dipstick stays there too long
44
most common cause of persistent proteinuria
orthostatic proteinuria test for this diagnosis: first morning urine x 2/3 urine protein/Cr ratio <0.2 then confirms diagnosis
45
when to refer to paediatric surgeon for undescended testicle
should refer by 6 months (most descent by 4 months?, somewhere else says 9 months) 2 complications: - infertility - undetected cancer/cancer
46
5 month old with UTI, 2 indications for prophylaxis
1. high grade reflux 2. obstruction - ie PUV reasons for urology 1. hypertension 2. impaired renal function3. renal abnormalities
47
reducible hernia, when to refer?
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