Urology Potpourri Flashcards

1
Q

what classifies microhematuria?

A

> 3 RBCs per hpf on microscopic UA

*postive dipstick should ALWAYS be confirmed w/ microcsopic

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2
Q

evaluation for asymptomatic hematuria

A
  • CT urography

- can get US if pt is pregnant

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3
Q

asymptomatic hematuria is . . .

A

CA until proven otherwise

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4
Q

RF for malignancy

A
  • > 35 yrs
  • smoking
  • occupational exposure to chemicals
  • chronic indwelling foley
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5
Q

when to refer to urology

A

-hematuria in absence of obvious cause

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6
Q

anticoagulated patients and hematuria

A

-do not assume blood is related to the meds, these pts still need work up

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7
Q

clinical presentation of stone

A

sudden onset of sharp pain to ipsilateral side w/ radiation to pelvis or labia/scrotum

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8
Q

when do stones cause pain?

A
  • only when they are obstructing

- if nonobstructing, consider other cause of pain

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9
Q

gold standard imaging for stone

A

CT abd/pelvis without contrast

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10
Q

important point about uric acid stone

A

they are radiolucent

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11
Q

stone size likely to pass on its own

A

4 mm or less have 95% chance of passing

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12
Q

aditional tx when waiting to pass stone

A
  • flomax .4 mg PO daily

- give pt a strainer

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13
Q

indications for prompt tx of a stone

A
  • prolonged complete or high grade unilateral obstruction
  • any b/l obstruction
  • any obstruction in a solitary kidney or w/ urinary infection or sepsis
  • obstruction w/ rising creatinine
  • intractable pain, n/v
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14
Q

ureteroscopic extraction

A
  • outpatient
  • preferred option if stone is infected
  • only option if stone is below bony pelvis
  • generally needs stent placement for 7-10 days following
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15
Q

ESWL

A
  • outpatient
  • stones MUST be visible on KUB
  • stone broken up w/ US waves then fragments passed by pt
  • stent placed
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16
Q

when is ESWL contraindicated?

A
  • pregnancy
  • coagulopathy
  • urinary infection
  • obesity
  • large renal a. or AAA >4 cm
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17
Q

percutaneous nephrolithomy (PCNL)

A
  • for staghorn calculi or stones >2cm
  • access through nephrostomy tube
  • 1-2 night stay in hospital
  • higher risk of complication
18
Q

types of stones

A
  • caclium oxalate (MC)
  • calcium phosphate
  • uric acid (radiolucent)
  • struvite (associated w/ infection; staghorn)
  • cystine (too hard for ESWL )
19
Q

w/u for metabolic evaluation of stones

A
  • 24 hr urine
  • labs: BMP, Ca, PTH, uric acid, phosphorus
  • dipstick UA
20
Q

stone prevention guidelines

A
  • WATER WATER WATER (UOP of 2-2.4 L/day)
  • reduce Na intake
  • reduce dietary oxalate
  • moderate Ca intake
21
Q

hypogonadism

A

low serum testosterone and clinical sx

22
Q

T level indication for tx

A

-no tx indicated for a T level >350

23
Q

when to draw serum T

A
  • early morning

- always confirm w/ 2 lab draws

24
Q

sx of low T

A
  • low libido
  • fatigue
  • ED
  • infertility
  • muscle loss
  • altered mood disturbances
25
Q

interstitial cystitis

A
  • diagnosis of exclusion in pts w/ urgency, frequency, and dysuria for >6mos
  • chronic inflammatory condition of the bladder
  • no cure
  • have high suspicion in women w/ chronic UTI sx and neg culture
26
Q

lifestyle changes in interstitial cystitis

A
  • IC diet
  • reduce stress
  • daily exercise
27
Q

meds for interstitial cystitis

A
  • elmiron, elavil, atarax, H2 blockers
  • anti-inflammatory meds, pyridium
  • NEVER narcotics
28
Q

alternative tx for interstitial cystitis

A
  • cystocscopty w/ hydrodistension
  • bladder instillations
  • neuromodulation
  • intravesical botox
  • urinary diversion - extremely last resort
29
Q

presentation of renal cell carcinoma

A
  • most found incidentally during eval of unrelated medical issue
  • typically asymptomatic
30
Q

classic triad in renal cell carcinoma

A
  • flank mass
  • hematuria
  • pain

*generally indicated advanced dz

31
Q

imaging for renal cell carcinoma

A
  • renal US
  • CT abdomen w/ and w/o
  • MRI w/ gadolinium
32
Q

RF for RCC

A
  • smoking
  • obesity
  • HTN
  • horseshoe kidney
  • aquired cysts from chronic renal failure
33
Q

what is the main genetic RF for RCC?

A

von Hippel lindau

34
Q

risk of mets with RCC

A
  • increases w/ size

- <4cm is typically confined to kidney

35
Q

common sites of met in RCC

A
  • lungs
  • bone
  • regional lymph nodes
  • liver
  • adrenal glands
  • contralateral kidney
  • brain
36
Q

tx of RCC

A
  • surgical excision is only cure

- if not a canidate for surgery: surveillance

37
Q

radical nephrectomy

A
  • removal of everything contained w/i Gerota’s fascia
  • may include adrenal gland and regional lymph nodes
  • open or laparoscopic
38
Q

renal sparing surgery options

A
  • partial nephrectomy
  • enucleation
  • ablation
39
Q

partial nephrectomy

A
  • tumor removed w/ margin of normal tisssue

- preferred option based on long term data

40
Q

enucleation

A

-tumor removed by dissecting b/w the tumor pseudocapsule and nl kidney

41
Q

ablation

A
  • tumor destruction w/o excision

- higher risk of recurrence

42
Q

when to consider the surgeries that don’t remove the entire kidney:

A
  • solitary kidney
  • b/l renal tumors
  • poor renal fxn
  • definitive diagnois of benign tumor
  • tumor < 7 cm