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208 Cards in this Set
- Front
- Back
MC cause of death from Acute Renal Failure
|
75% Infection
|
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Prerenal ARF
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Olliguria
High BUN/Cr ratio >20:1 High Urine osm >500 Low FeNa <1% Hyaline casts |
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Renal ARF
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Low BUN/Cr ratio <20:1
Low Urine osm < 350 (water resorption impaired) High FeNa >2% |
|
Nephrotoxins
|
Aminoglycosides
Radiocontrast NSAID Myoglobin Cisplatin Kappa/Gamma light chains |
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Tests of postrenal failure
|
physical - palpate bladder
U/S - obstruction, hydronephrosis catheter - check for urine |
|
MC deadly complication of early phase ARF
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hyperkalemic cardiac arrest + pulmonary edema
|
|
Level of symptomatic uremia
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BUN > 60
|
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Uremia features
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Hypertension
CHF Pericarditis Nausea, Vomiting Loss of apetite Lethargy Restless legs Asterixis Normocytic anemia Bleeding (low platelets) |
|
CRF Calcium/Phosphate
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HYPOcalcemia
HYPERphosphatemia High PTH |
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What is calciphylaxis
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Hyperphosphatemia may cause calcium and phosphate to precipitatevwhich causes vascular calcifications that may result in necrotic skin
lesions. |
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Major cause of mortality in CRF
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Infections
|
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Diet in CRF
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LOW protein
LOW salt (if HTN, CHF) LOW K, PO4, Mg HIGH Ca, Vit D |
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Ace Inhibitors in CRF
|
Used early on in CRF, may worsen hyperkalemia!!!
|
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Treatment of hyperphosphatemia in CRF
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calcium citrate (phosphate binder)
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Treatment of pruritus in CRF
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capsaicin cream
cholestyramine + UV light |
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Life threatening complications in CRF
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Hyperkalemia - get ECG
Pulmonary edema due to volume overload - check for weight gain Infection |
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Indications for dialysis
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Acidosis
Electrolytes - High K presists Intoxication - Methanol, Ethylene glycol, lithium, aspirin Overload - hypervolemia Uremia - pericarditis |
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AV fistula for dialysis
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B/t radial artery and veins in forearm
|
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How do you know AV fistula is ready to be used
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Audible bruit present
|
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Benefits of hemodialysis
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More efficient
Initiated more quickly |
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Disadvantages of hemodialysis
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Hypotension (fluid removed)
Hypoosmolarity (solute removed) Req vascular access Req anticoagulation with heparin |
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Advantages of peritoneal dialysis
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Patient can learn to do on own
Mimics kidney physiology more |
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Disadvantages of peritoneal dialysis
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Hyperglycemia/ Hypertriglyceridemia (high glucose load)
Peritonitis Req high motivation Increased abdominal girth |
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Patients on dialysis are lacking in what?
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Erythropoietin
Vit D |
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Complications hemodialysis
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Hypotension - ischemia
Hypoosmolarity - N/V, seizures First use syndrome Hemorrahge/Hematoma Infection Amyloidosis of B2 microglobulin |
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Complications of peritoneal dialysis
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Peritonitis
Abdo/Inguinal hernia Hyperglycemia Protein malnutrition |
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What is First Use Syndrome
|
Back pain, chest pain and reare anaphylaxis immediately when a new dialysis machine is used
|
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MC cause of nephrotic syndrome in adults
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Membranous nephropathy
|
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MC cause of nephrotic syndrome in kids
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Minimal change disease
|
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Treatment of asymptomatic transient proteinuria
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No treatment/tests
|
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Asymptomatic persistent protenuira
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Further workup required
First step is BP check and urine sediment examination |
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Urine dipstick for protein false negative
|
Only detects albumin, will not detect globulins (light chains in myeloma)
|
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Proteinuria on dipstick, next test to order?
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Urinalysis
|
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Urinalysis confirms protein, next test to order?
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24 hour Urine collection for albumin/cr
|
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Level of protein for microalbuminuria
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30 - 300 mg
NOT detected by dipstick |
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Most sensitive and specific test for microalbuminuria
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radioimunoassay
|
|
Best test of renal function
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Creatnine clearance
|
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Best test to detect renal obstruction, masses and cysts
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Renal ultrasound
|
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Test to detect chronic pyelonephritis
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Intravenous pyelogram
|
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When to do renal biopsy?
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No cause identified by less invasive tests
|
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Symptomatic proteinuria what vaccinations are recommended
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Influenza and Pneumococcus due to increased infections
|
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Best test to detect bladder cancer
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Cystoscopy = perform if suspicion is high even if cytology is negative on urine specimen
|
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What cancer is associated with Minimal Change disease
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Hodkin's and non Hodkins lymphoma
|
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Treatment of Minimal Change disease
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Steroids 4-8 weeks
|
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Treatment of Poststreptococcal GN
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Supportive - antihypertensives, loop diuretics
|
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Meds causing interstitial nephritis
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NSAIDs
penicillins furosemide, thazide sulfonamides phenytoin |
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Treatment Type I RTA
|
Sodium Bicarb (acidsosis0
Phosphate salt (excrete acid) |
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Treatment Type II RTA
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Sodium restriction (increases Na and Bicarb reabsorption)
|
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Hartnup disease defect
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Auto recessive
Decreased neutral aa absorption - tryptophan (nicotinamide deficiency) |
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Hartnup disease features
|
dermatitis
diarrhea ataxia psychiatric disturbance |
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Fanconi syndrome pathogenesis
|
proximal tubule defect (one of the causes of type 2 RTA)
|
|
Fanconi syndrome features
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glycosuria
phosphaturia (rickets, osteomalacia) proteinuria polyuria dehydration hypokalemia |
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Treatment of Fanconi anemia
|
Phophate
Potassium Alkali Salt Supplements Hydration |
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Confirmation test for polycystic kidney disease
|
U/S kidneys
CT/MRI alternative |
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Diagnosis of medullary sponge kidney
|
Intravenous Pyelogram
|
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Treatment of simple renal cysts
|
No Treatment (asymptomatic)
|
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Gold standard test for Renovascular HTN
|
Renal arteriogram - CONTRAINDICATED in renal failure
|
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In Renovascular HTN what test can be done in a patient with renal failure
|
MRA (dye is not nephrotoxic)
|
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Noninvasive study for renovascular HTN in people with good renal function
|
Captopril renal scintigram (scan)
|
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Diagnostic test for renal vein thrombosis
|
renal venography (definitive study) or IVP
|
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Treatment in renal vein thrombosis
|
Anticoagulation to prevent PE
|
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Risk Factors for Kidney stones
|
Low fluid intake (MC and preventable risk factor)
Fm Hx Gout, High PTH, type 1 RTA Loops, acetazolamide Chemo Male UTI |
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Which stones cannot be detected by KUB
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Uric acid - radiolucent
|
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What imaging is ordered for uric acid stone
|
CT
U/S kindneys IVP |
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What stones are MC in people with chronic UTI
|
Struvite (staghorn) due to PESK
Proteus Klebsiella Serratia Enterobacter |
|
Hexagon stone
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Cysteine
|
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Envelope stone
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Uric acid
|
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What vitamin defciency causes calcium oxalate stones
|
Pyridoxine
|
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Best initial test for kidney stones
|
KUB x ray
|
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Best test for kidney stones
|
CT (even radiolucent stones)
|
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Best test for defining degree of urinary tract obstruction
|
IVP - good for deciding if patient needs procedural therapy
|
|
Treatment of kidney stones
|
1st - Analgesia (Morphine, Ketorolac)
Fluid hydration Ab's if infected/UTI |
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When to admit someone with kidney stone?
|
Pain not controlled with oral med
Anuria (one kidney) Renal colic + UTI and or Fever Large > 1cm stone |
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Best method of treatment for stones >0.5cm but < 2cm
|
ESWL
|
|
Best method for treatment of stones >2cm
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Percutanous nephrolithotomy
|
|
Best initial test for urinary tract obstruction
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Kidney Ultrasound
|
|
What patients is IVP contraindicated in?
|
Pregnant
Allergies to contrast Renal Failure |
|
Best test for lower urinary tract obstruction
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Voiding cystourethrography
|
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When is Transrectal Ultrasound of Prostate indicated?
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PSA > 10, regardless of DRE
Abnormal DRE, regardless of PSA |
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How often would you follw up someone with PSA <4 and Negative DRE
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Annually
|
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If you can palpate a cancer on DRE what is the likelihood it has spread outside of the prostate
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70-80%
|
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Treatment of localized prostatic cancer
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Radical prostatectomy EXCEPT those < 10 years of life left, watchful waiting
|
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Treatment of locally invasive prostate cancer
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Radiation + Androgen deprivation (non curative)
|
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Treatment of metastatic prostate cancer
|
Decrease testosterone (orchiectomy, antiandrogens, LH agonists)
|
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Treatment of RCC
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radical nephrectomy - remove kidney, adrenal, Gerota fascia, and nodes along hilum
|
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Best test for diagnosing Transitional Cancer of the bladder
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Cystoscopy + Biopsy
|
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Treatment of Stage 0 TCC of bladder
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Intravesical Chemotherapy
|
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Treatment of Stage A TCC of bladder (involves lamina propria)
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Transurethral resection of tumor
|
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Treatment of Stage B and C TCC of bladder (muscle invasion/perivesicular fat invasion)
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Radical cystectomy + LN dissection + Remove prostate/uterus/ovaries/vaginal wall
|
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Germ cell tumor subtypes (95%)
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Seminoma - radiosensitive
Nonseminoma - Embryonal, Choriocarcinoma, Teratoma, Yolk Sac |
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Non Germ cell testicular tumor subtypes
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Leydig cell - most benign,if not surgical resection
Sertoli cell - benign |
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Which testicular tumor has high B-HCG
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Choriocarcinoma
|
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Which testicular tumor has high AFP
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Embryonal
|
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Treatment of testicular cancer
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Surgical removal of testicle (orchiectomy) via transinguinal approach (avoid seeding via scrotal approach)
|
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Seminoma treatment
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Inguinal orchiectomy + radiation (very sensitive)
|
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Nonseminoma treatment
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Orchiectomy + retroperitoneal LN dissection
|
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What reduces risk of penile cancer
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Circumcision
|
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What increases risk of penile cancer
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HSV
HPV 18 |
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Treatment of testicular torsion
|
Surgery < 6hours, BILATERAL orchioplexy to the scrotum if viable
Orchiectomy if nonviable testicle |
|
MC organisms causing epidydimitis in children and elderly?
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E. Coli
|
|
MC oraganism causing epidydymitis in young males
|
Chlamydia and Gonorrhea
|
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Treatment of subclavian steal
|
Surgical bypass
|
|
Definitive test for identyfing stenosis of vessels in head and neck
|
Magnetic resonance arteriogram
|
|
Contraindications to TPA
|
Uncontrolled HTN
Bleeding Anticoagulation Recent trauma/surgery |
|
What medication should be avoided 24 hours post tPA
|
Aspirin
|
|
What is the agent of choice for lowering BP in a stroke patient
|
Nitroprusside
- treat if >160-180/>105 |
|
When do you use mannitol in a stroke situation?
|
with increased ICP
NEVER prophylactically |
|
When do you use steroids in a stroke situation?
|
NEVER, harmful not helpful
|
|
2 types of hemorrhagic stroke
|
Intracerebral hemmorhage - bleed into the parenchyma
Subarachnoid hemmorhage - bleed into CSF outside parenchyma |
|
What is the association between cocaine and stroke
|
Young patients
ICH, SAH and Ischemic Stroke |
|
Best initial test for SAH
|
CT non contrast
|
|
Best definitive test for SAH
|
Lumbar Puncture
|
|
What is the best test for identifying site of bleeding in SAH
|
Cerebral Angiogram
|
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What psychiatric diagnosis is Tourette's associated with
|
OCD and ADHD
|
|
Treatment of Tourette's
|
1st - Pimozide, Haloperidol
2nd - Clonidine |
|
Most important risk factor for dementia
|
Increasing age
|
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What area of the brain is affected by Biswanger disease (vascular dementia)
|
Subcortical white matter degeneration
|
|
Why is donezepil preferred over tacrine in Alzheimers Disease
|
1x/day dosing
more improvement in congitive and behavioral domains less SE |
|
How many times a day is Tacrine dosed
|
4x/day
|
|
Has ginko and lecithin been proven to be effective in Alzheimers
|
NO
|
|
What vitamin may be beneficial in Alzheimers
|
Megadose >2000 units Vitamin E
|
|
Is HRT good for Alzheimers?
|
Associated with lower risk of developing Alzheimers
|
|
What medication class exacerbates symptoms of Dementia with Lewy bodies
|
Neuroleptics
|
|
Features of Delirium
|
Rapid deterioration of MS (hour-days)
Fluctuating LOC Abnormal vital signs |
|
What time of day is delirium the worst?
|
Sundowning - night
|
|
What can you test with the Doll's Eye reflex
|
Check if brainstem is intact - also intact if respiraiton is normal
|
|
Cause of bilateral fixed + dialated pupils
|
Sever anoxia
|
|
Cause of unilateral fixed + dialated pupil
|
Herniation with CNIII compression
|
|
Cuase of pinpoint pupils
|
Narcotics
Intracerebral hemmorhage |
|
GCS - Eye opening categories (out of 4)
|
No Opening - 1
Open to PAIN - 2 Open to VOICE - 3 Open Spontanously - 4 |
|
GCS - Motor response categories (out of 6)
|
No movement - 1
Decerebrate (extension) - 2 Decorticate (flexion) - 3 Withdraw to pain - 4 Localize to pain - 5 Obeys command - 6 |
|
GCS - Verbal response categories (out of 5)
|
No sound - 1
Inconmprehensible - 2 Inappropriate words - 3 Appropriate confused - 4 Appropriate orientated - 5 |
|
Describe locked in syndrome
|
Fully aware
Capable of feeling pain Completely Paralyzed |
|
What area is affected in Locked In syndrome
|
Ventral pons
|
|
Features of Uncal (transtentorial) Herniation
- uncus compresses midbrain |
CN III compression - Ipsilateral anisocoria, sluggish pupil, dialated
Contralateral hemiparesis |
|
Features of Tonisllar herniation
- cerebellar tonsils compress medulla |
compression of cardiorespiratory centres - rapid death
|
|
Braindeath criteria
|
Irreversible abscence of brain and brainstem function (apnea)
No brainstem reflex (gag, caloric, cornea, doll's eye) Core temp > 32 Clinical or Imaging evidence of cause of braindeath x2 repeated exams or EEG (isoelectric activity - silence) |
|
Who has right to turn off life support in braindeath
|
Physician (in most states)
|
|
What is vegetative state
|
Complete coma
Eyes Open and appear aawke Random head/limb movements |
|
Most common presenting complaint in MS
|
Decreased sensation or parasthesias
Fatigue |
|
Features of Optic Neuritis in MS
|
monoocular vision loss
pain on eye movement central scotoma decreased light reaction |
|
Features of Internuclear Opthalmoplegia
|
Ipsilateral medial rectus palsy (adduction defect)
Horizontal nystagmus of abducting eye |
|
What is needed for MS diagnosis
|
2 episodes of symptoms
2 white matter lesions |
|
Laboratory diagnosis of MS
|
2 episodes of symptoms
At least 1 white matter lesion on MRI Abnormal CSF |
|
Which variant of MS appears later in life > 40 years old
|
Primary Progressive
|
|
Test of choice for MS diagnosis
|
MRI - number of lesions not necessarily proportional to severity or speed of disease progression
|
|
EMG of MS patients what do you see
|
Evoked potentials show slow conduction due to demyelination
|
|
Treatment of Acute MS attack
|
High dose IV corticosteroids shorten duration but not alter disease course
|
|
How long does an untreated MS attack take to resolve
|
approx. 6 weeks
|
|
What is the most effective MS treatment
|
Interferon B-1a
|
|
What should be used for primary progressive
|
Immunosuppresants like MTX or Cyclophosphomide
|
|
What is seen on CSF of patients with Guillian Barre
|
Elevated Protein with NORMAL cell count
|
|
Rx of Guillian Barre
|
IV Immunoglobulin or Plasmapheresis
No STEROIDS, harmful |
|
MC adult primary CNS tumor
|
Glioma
Meningioma 2nd |
|
Features of Myelofibrosis
|
Teardrop cells
Splenomegaly Bleeding, Infections |
|
What does myelofibrosis often progress to?
|
AML, poor prognosis
|
|
Rx of Myelofibrosis
|
Multiple transfusions
EPO Splenectomy (pain paliation) BM transplant |
|
Define Essential Thrombocytosis
|
Plt > 600,000
|
|
Features of Essential Thrombocytosis
|
Thrombosis (VVA)
Bleeding (defective platelets) Splenomegaly Pseudohyperkalemia Increased Bleed Time |
|
What is erythromelalgia
|
Burning pain and erythema of extremities due to microvascular occlusions
- feature of essential thrombocytosis |
|
Rx of Essential Thrombocytosis
|
Antiplatelet Drugs - Anagrelide or Low dose ASA
Hydroxyurea (severe disease) |
|
Causes of Myelodysplastic Syndromes
|
Idiopathic MC
Radiation Immunosuppresants |
|
What is seen in a Myelodysplastic BM
|
Dysplastic cells with blasts or ringed sideroblasts
|
|
What is seen in a Myelodysplastic peripheral smear?
|
Normal MCV
Low Retic Howell Jolly bodies Basophilic Stippling Large agranular platelets |
|
Rx of Myelodysplastic syndromes
|
RBC/Plt transfusions
EPO G-CSF (adjunct) VIt supplements B6, B12, Folate Immunosuppresants BM transplat (only cure) |
|
Major Criteria of Polycythemia Vera
|
Elevated RBC mass
O2 Sat >92% Splenomegaly (2 major + 2 minor for dx) |
|
Minor Criteria of Polycythemia Vera
|
Thrombocytosis >400
Leukocytosis >12 x 10 (9) LAP >100 B12 > 900 (2 major + 2 minor for dx) |
|
Clinical features of PV
|
Headache,Pruritus, Dizzy, Weak, Dyspneic (all due to hyperviscosity)
DVT, CVA, MI, Portal V thrombosis Bleeding (GI/GU, ecchymoses) Spleno/Hepatomegaly Hypertension |
|
Lab features of PV
|
Elevated RBC count, Hb, Hct
Thrombocytosis, Leukocytosis Low EPO High B12 Hyperuricemia |
|
How do you confirm diagnosis of PV
|
BM Biopsy
|
|
Rx of Polycythemia Vera
|
Repeat phlebotomy
Hydroxyurea or Rec Interferon ALFA (for myelosuppresion) |
|
Subtypes of Hodgkins Lymphoma
|
Nodular Sclerosing MC, women
Mixed Cellularity (lots of RS cells) Lymphocyte predominant (few RS cells) Lymphocyte depleted (worst prognosis) |
|
What is Ann Arbor Staging (Hodgkins lymphoma)
- B symptoms worsen prognosis |
Stage 1 - single node
Stage 2 - >2 node, same side of diaphram Stage 3 - both sides of diaphram Stage 4 - disseminated |
|
Hodgkin's Features
|
Painless lymphadenopathy
Continuous spread |
|
Dx of Hodgkin's Lymphoma
|
LN Biopsy with RS cells + presence of inflammatory cell infiltrates (NOT seen in Non-Hodgkin's)
|
|
Rx of Hodkin's Lymphoma
|
Stage 1, 2, 3A - Radiotherapy
Stage 3B, 4 - Radiotherapy + Chemotherapy |
|
Risk factors for Non Hodgkin's Lymphoma
|
HIV/AIDS
Immunosuppresion (organ transplant recipients) EBV, HTLV-1 infection H. Pylorii gastritis (gastric lymphoma) Hashimoto's/Sjorgens (assoc with MALToma) |
|
Immune causes of platelet destruction
|
ITP
HIT 2 Drugs SLE HIV assoc |
|
Non Immune causes of platelet destruction
|
HUS
TTP DIC HIT 1 |
|
Features of HIT1
|
<48 hours, direct platelet aggregation
|
|
Treatment of HIT 1
|
No treatment necessary
|
|
Features of HIT 2
|
3-12 days, Ab mediated platelet injury
|
|
Treatment of HIT 2
|
Stop Heparin asap
|
|
Mechanism of ITP
|
IgG against platelets
|
|
Acute form of ITP features
|
Children
Preceeded by viral infections Self limited 80% |
|
Chronic form of ITP features
|
Adults (MC women 20-40)
Rarely remits spontanously |
|
What do you see in bone marrow in patients with ITP
|
Increase megakaryocytes and platelet assoc-Ig G
|
|
Rx of ITP
|
Corticosteroids
IV Immune Globulin (binds IgG) Splenectomy (chronic ITP) |
|
Mechanism of TTP
|
Hayline microthrombi occlude small vessels and cause mechanical damage to RBC
|
|
TTP Prognosis
|
Life threatning if untreated within MONTHS
|
|
Lab features of TTP
|
normal PT and PTT (no consumption of clotting factor)
|
|
Features of TTP
|
Fever
Anemia (hemolytic) Renal failure Thrombocytopenia Neuro sx transiently |
|
Rx of TTP
|
Large volume Plasmapheresis ASAP
2nd line - steroids + splenectomy |
|
Role of transfusions in TTP
|
CONTRAINDICATED
|
|
Features of Bernard Soulier syndrome
|
Auto RECESSIVE
def GP1b-IX (platelet adhesion) |
|
Features of Glanzmann's Thromboasthenia
|
Auto RECESSIVE
def GPIIb-IIIa (platelet aggregation) |
|
Features of Von Willebrand
|
Auto DOMINANT
def vWF factor (platelet aggregation and adhesion) MC inherited bleeding disorder |
|
Cliniical features of Von Willebrand
|
epistaxis
easy bruising scratches/cuts gingival bleeds menorrhagia |
|
Random causes of impaired platelet function
|
Uremia
NSAID Aspirin |
|
Laboratory features of Von Willebrand
|
Inc Bleeding Time
Inc aPTT (but can be N) Low ristocetin platelet aggregation Low fVIII |
|
Rx of Von Willebrand
|
DDAVP - induces vWF secretion
Factor VIII concentrate |
|
Do you use cryoprecipitate in Von Willebrand
|
NO - risk of viral transmission
|
|
Clincal features of Hemophilia
|
Hemarthosis (MC knee)
Intracranial bleed (must evaluate all head trauma urgently) Hematomas Hematuria Hemospermia |
|
How do you detect presence of Factor VIII Inhibitor
|
Mix normal plasma with hemophiliac - PTT should normalize if not an INHIBITOR is present
|
|
Lab features of hemophilia
|
Inc aPTT
|
|
Rx hemophilia acute hemarthosis
|
Analgesia with codeine/acetaminophen
Immobilize, ice, non weight bearing |
|
Rx hemophilia A
|
Factor VIII concentrate
DDVAP in mild disease |
|
Is DDVAP treatment helpful in hemophilia B?
|
No, only helps fVIII release
|