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112 Cards in this Set
- Front
- Back
what is hypernatremia?
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Serum sodium > 145 mEq. Usually due to water loss
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presentation of hypernatremia
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>>thirst (due to hypertonicity) >>Neurologic symptoms ie. mental status changes, weakness, focal neurologic deficits, and seizures.
>>Examination reveals “doughy” skin |
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Hypernatremia causes—
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Diuretics
Dehydration Diabetes insipidus Docs (iatrogenic) Diarrhea Disease (e.g., kidney, sickle cell) |
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treatment for hypernatremia
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>>Treat the underlying causes >>replace free-water deficit with hypotonic saline, D5W, or oral water
>>Correction of chronic hypernatremia (> 36–48 hours) should occur gradually over 48–72 hours to prevent neurologic damage 2° to cerebral swelling. |
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Hyponatremia
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Serum sodium < 136 mEq/L.
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what are some of the causes of hypotonic hyponatremia. Osmolarity :High (> 295 mEq/L):
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Hyperglycemia, hypertonic infusion (e.g., mannitol).
■ |
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what are some of the causes ofnormal osmolarity with hyponatremia. Osmolarity : normal
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Normal (280–295 mEq/L): Hypertriglyceridemia, paraproteinemia
(pseudohyponatremia). |
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what are the 3 types of hypotonic with Low (< 280mEq/L):osmolarity
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Hypervolemic
Euvolemic Hypovolemic |
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Hypervolemic hyponatremic hypotonic: etiology and tx
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etiology: Renal failure, nephrotic syndrome, cirrhosis, CHF.
tx:Water restriction. |
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Euvolemic hyponatremic hypotonic: etiology and tx
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SIADH, hypothyroidism, renal failure, drugs, psychogenic polydipsia, adrenal insufficiency
Tx: Water restriction. |
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Hypovolemic hyponatremic hypotonic: etiology and tx
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Diuretics, vomiting, diarrhea, third spacing, dehydration.
Tx:Replete volume with normal saline |
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how should chronic hyponatremia be treated?
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Chronic hyponatremia (> 72 hours’ duration) should be corrected slowly (no more than 0.5–1.0 mEq/L/hr) in order to prevent central pontine
myelinolysis (quadriplegia and pseudobulbar palsy). |
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Hypervolemic hyponatremia is
caused by |
“nephrOSIS,
cirrhOSIS, and cardiOSIS.” |
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Hyperkalemia
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Serum potassium > 5 mEq/L
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Treatment of hyperkalemia—
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Values of > 6.5 mEq/L or ECG changes require emergent treatment.
C BIG K Calcium Bicarbonate Insulin Glucose Kayexalate |
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diagnosis of hyperkalemia
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>>Verify hyperkalemia with a repeat blood draw
>>ECG findings include tall, peaked T waves; PR prolongation; wide QRS; and loss of P waves Can progress to sine waves, ventricular fibrillation, and cardiac arrest. |
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Hypokalemia
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Serum potassium < 3.6 mEq/L
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presentation of hypokalemia
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Fatigue, muscle weakness or cramps, ileus,
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treatment of hypokalemia
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>>Treat the underlying disorder.
>>Oral and/or IV potassium repletion. >>Replace magnesium, as this deficiency makes potassium repletion difficult. |
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Causes of hypercalcemia
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CHIMPANZEES
Calcium supplementation Hyperparathyroidism Iatrogenic (e.g., thiazides)/Immobility Milk-alkali syndrome Paget’s disease Addison’s disease/Acromegaly Neoplasm Zollinger-Ellison syndrome (e.g.,MEN I) Excess vitamin A Excess vitamin D Sarcoidosis and other granulomatous disease |
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Hypercalcemia
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Serum calcium > 10.2 mg/dL. The most common causes are hyperparathyroidism and malignancy
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presentation of hypercalcemia
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bones (fractures), stones (kidney stones), abdominal groans
(anorexia, constipation), and psychiatric overtones (fatigue,depression) |
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treatment for hypercalcemia
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IV hydration followed by furosemide to ↑ calcium excretion.
■ Calcitonin, bisphosphonates (e.g., pamidronate), glucocorticoids, and dialysis are used for severe or refractory cases. Avoid thiazide diuretics, which ↑ tubular reabsorption of calcium |
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treatment of hypocalcemia
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TREATMENT
■ Treat the underlying disorder. ■ Magnesium repletion. ■ Administer oral calcium supplements; IV calcium for severe symptoms |
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hypocalcemia presentation
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Chvostek’s sign
Trousseau’s sign abdominal muscle cramps, dyspnea, tetany, perioral and acral paresthesias, |
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ECG hypocalcemia
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ECG may show a prolonged QT interval.
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Dx: patient who
develops cramps and tetany following thyroidectomy. |
hypocalcemia
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how are the calcium levels in hypoalbuminemia
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Serum calcium may be falsely
low in hypoalbuminemia |
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Hypomagnesemia
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Serum magnesium < 1.5 mEq/L
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treatment for hypomagnesemia
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IV and oral supplements.
■ Hypokalemia and hypocalcemia will not correct without magnesium correction |
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↑ anion gap— caused by what diseases
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MUDPILES
Methanol Uremia DKA Paraldehyde Intoxication Lactic acidosis Ethylene glycol Salicylates |
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pH < 7.4 pCO2 >40
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Respiratory acidosis
Hypoventilation Acute lung disease Chronic lung disease Opioids, narcotics, sedatives Weakening of respiratory muscles |
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pH < 7.4 pCO2 <40 with normal anion gap
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Normal anion gap (8–12 mEq/L)
–Diarrhea –Glue sniffing –Renal tubular acidosis –Hyperchloremia |
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pH < 7.4 pCO2 <40
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⇧Anion gap
–Renal failure –Lactic acidosis –Ketoacidosis (DM) –Aspirin ingestion |
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pH > 7.4 PCO2 < 40 mmHg
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Respiratory alkalosis
–Hyperventilation –Aspirin ingestion (early) |
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pH > 7.4 PCO2 > 40 mmHg
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Metabolic alkalosis with
compensation –Vomiting –Diuretic use –Antacid use –Hyperaldosteronism |
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Pre renal:
Intrinsic: |
↓ renaI Intrinsic
Injury within the nephron unit. |
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Postrenal:
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Urinary outflow obstruction. Generally, both kidneys must be obstructed in order to → a significant ↑ in BUN and creatinine.
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etiology: An FeNa < 1%, a UNa < 20, a specific gravity > 1.020, or a BUN/creatinine ratio > 20
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prerenal etiology
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White cells, eosinophils: etiology and classification
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etiology: Allergic interstitial nephritis, atheroembolic disease
classification is intrinsic |
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Hyaline casts: etiology and classification
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etiology: Normal finding, but ↑ amount suggests volume depletion.
classification is Prerenal |
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Red cell casts, dysmorphic red cells
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Glomerulonephritis
Intrinsic |
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Granular casts, renal tubular cells,
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ATN
Intrinsic |
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White cells, white cell casts
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Pyelonephritis
Postrenal |
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Indications for urgent dialysis
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AEIOU
Acidosis Electrolyte abnormalities (hyperkalemia) Ingestions (salicylates, theophylline, methanol, barbiturates, lithium, ethylene glycol) Overload (fluid) Uremic symptoms (pericarditis, encephalopathy, bleeding, nausea, pruritus, myoclonus |
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hematuria, hypertension, and oliguria. DDx
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nephritic syndrome
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tx of nephrotic syndrome
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Corticosteroids are useful in reducing glomerular inflammation in some
cases |
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nephrotic syndrome
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proteinuria (≥ 3.5 g/day), generalized edema, hypoalbuminemia, and hyperlipidemia
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Membranous nephropathy: most common in what group of people an biopsy
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The most common nephropathy in caucasian adults
“Spike-and-dome” appearance |
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tx for nephrotic syndrome
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Protein and salt restriction, diuretic therapy, antihyperlipidemics.
■ ACEIs ↓ proteinuria and diminish the progression of renal disease in patients with diabetic nephropathy. ■ Vaccinate with 23-polyvalent pneumococcus vaccine (PPV23), as patients are at ↑ risk of Streptococcus pneumoniae infection. |
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Dx for nephrolithiasis
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Obtain an AXR in patients with known radiopaque stones and possibly a renal ultrasound to look for obstruction as well as for pregnant patients, in
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tx for calcium oxalate stones
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Hydration, thiazide diuretic.
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(Mg-NH4-PO4) tx
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Hydration; treat UTI
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uric acid: tx and type of stone
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Hydration; alkalinize urine
Acidic urine (pH < 5.5). Radiolucent. with citrate, which is converted to HCO3 in the liver; dietary purine restriction and allopurinol. |
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cystine stones tx
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from homocytenuria
Hydration, alkalinize urine, penicillamine. |
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dx of stones
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Noncontrast abdominal CT scans may diagnose stones and other causes
of flank pain. ■ An IVP can be used to confirm the diagnosis if there is a lack of contrast filling below the stone |
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initial treatment of stones
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Hydration and analgesia are the initial treatment.
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presentation of PCKD
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Pain and hematuria,hypertension, hepatic cysts, cerebral berry
aneurysms, |
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management of PCKD
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Prevent complications and ↓ the rate of progression to end-stage renal disease. Early management of UTIs and control of BP
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Dx of PCKD
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Based on ultrasound or CT scan
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management of ESRD in PCKD
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Dialysis and renal transplantation are used to manage patients with endstage renal disease.
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RTA type I: complications and tx
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Treatment: Potassium citrate.
Complications: Nephrolithiasis. |
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RTA type II: complications and tx
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Treatment: Potassium citrate.
Complications: Rickets, osteomalacia. |
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RTA type IV: complications and tx
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Treatment: Furosemide, fludrocortisone, and low-potassium diet in patients with aldosterone deficiency.
Complications: Hyperkalemia |
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types of uretharal reflux
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■ Mild reflux (grades I–II): No ureteral or renal pelvic dilatation. Often
resolves spontaneously. ■ Moderate to severe reflux (grade III–V): Ureteral dilatation with associated calyceal blunting in severe cases |
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common presentation of urethral reflux
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Patients present with recurrent UTIs
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Dx: of urethral reflux
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Perform a voiding cystourethrogram
All children < 7 years of age presenting with their first UTI should undergo a voiding cystourethrogram to screen for reflux. |
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management of reflux
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>>Treat infections aggressively.
>>Treat mild reflux with daily prophylactic antibiotics until reflux resolves at puberty. >>Ureteral implantation may be considered in severe reflux. |
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complication of reflux
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Inadequate treatment can → progressive renal
scarring and end-stage renal disease. |
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how to diagnose DI
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During a water deprivation test, patients excrete a high volume of dilute urine.
■ Desmopressin acetate (DDAVP) challenge: ■ Central DI: DDAVP (a synthetic analog of ADH) challenge will ↓ urine output and ↑ urine osmolarity. ■ Nephrogenic DI: DDAVP challenge will not significantly ↓ urine output. ■ MRI may show a pituitary or hypothalamic mass in central DI |
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Tx for central and nephrogenic DI
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Treat the underlying cause.
■ Central DI: Administer DDAVP intranasally. ■ Nephrogenic DI: Salt restriction and ↑ water intake are the 1° treatment. Thiazide diuretics |
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SIADH tx.
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Restrict fluid and address the underlying cause.
■ Na < 110 mEq/L) or the patient is significantly give hypertonic saline. ■ Demeclocycline can help normalize serum sodium by antagonizing the action of ADH in the collecting duct. |
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BPH diagnosis
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DRE to screen for masses; if findings are suspicious, evaluate for prostate cancer.
■ UA and urine culture to rule out infection and hematuria. ■ Creatinine levels to rule out obstructive uropathy and renal insufficiency. |
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tx for BPH: mild, moderate and severe symptoms
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Reassurance for mild symptoms.
■ Medical therapy with α-blockers (terazosin) and 5α-reductase inhibitors (finasteride) to reduce mild to moderate symptoms. ■ Transurethral resection of the prostate (TURP) or open prostatectomy forpatients with moderate to severe symptoms. |
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what is the major side effect of α-
blockers? |
orthostatic hypotension
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what are the Leading causes of
cancer death in men: |
1. Lung cancer
2. Prostate cancer 3. Colorectal cancer 4. Pancreatic cancer 5. Leukemia |
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presentation of prostate cancer.
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Usually asymptomatic,urinary retention,back pain due to bone metastases. DRE may reveal a palpable nodule or an area of induration.
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Dx of prostate cancer
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>>↑ PSA (> 4 ng/mL)
>>Definitive diagnosis ultrasound-guided transrectal biopsy >>Tumors are graded by the Gleason histologic system, 10 is the highest grade. >>metastases: CXR and bone scan |
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treatment for protate cancer:
>>low grade tumors: >>↑ risk of incontinence and/or impotence: >>metastatic disease: >>for progress of treatment: |
>>low grade tumors: Watchful waiting
>>↑ risk of incontinence and/or impotence: Radical prostatectomy and radiation therapy >>metastatic disease: androgen ablation >>PSA for progress of treatment |
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recommended screening method for prostate cancer
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annual DRE after the age
of 50 is the recommended screening method for prostate cancer. |
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Differential for hematuria
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S2I3T3
Strictures Stones Infection Inflammation Infarction Tumor Trauma TB |
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most common presenting symptom of bladder cancer
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Gross hematuria is the most common presenting symptom.
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diagnostic test for bladder cancer
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>>UA often shows hematuria
>>IVP can examine the upper urinary tract as well as defects in bladder filling. |
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tx: for bladder cancer
Carcinoma in situ: |
Carcinoma in situ: Intravesicular chemotherapy.
■ Superficial cancers: Complete transurethral resection or intravesicular chemotherapy with mitomycin-C or BCG (the vaccine for TB). ■ Large, high-grade recurrent lesions: Intravesicular chemotherapy. ■ Invasive cancers without metastases: Radical cystectomy or radiotherapy for patients who are deemed poor candidates for radical cystectomy or with unresectable local disease. ■ Patients with distant metastases: Chemotherapy alone. |
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tx: for bladder cancer: Superficial cancers:
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Complete transurethral resection or intravesicular
chemotherapy with mitomycin-C or BCG (the vaccine for TB). |
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tx: for bladder cancer
Large, high-grade recurrent lesions: |
Intravesicular chemotherapy.
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tx: for bladder cancer
Invasive cancers without metastases: |
Radical cystectomy or radiotherapy
for patients who are deemed poor candidates for radical cystectomy or with unresectable local disease. |
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tx: for bladder cancer
Patients with distant metastases: |
Chemotherapy alone.
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hematuria, flank pain, and a palpable flank mass. Dx
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renal cell carcinoma
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presentation of renal cell carcinoma
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>>Anemia is common at presentation, but polycythemia due to ↑ erythropoietin
production may be seen in 5–10% of patients. >>fever and Varicocele in men >>hematuria, flank pain, and a palpable flank mass. |
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Dx of renal cell carcinoma
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Ultrasound and/or CT to characterize the renal mass
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Tx for renal cell carcinoma
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>>Surgical resection may be curative in localized disease
>>chemotherapy 15%-30% |
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presentation of testicular cancer
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>>painless enlargement of the testes
>>ages of 15 and 30 >>seminomas: 40 and 50 years of age. |
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testicular cancer etiology and RF
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ET:germ cells, and virtually all are malignant.
RF: Cryptorchidism: ↑ risk of neoplasia in both testes. and Klinefelter’s syndrome |
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diagnosis of testicular cancer: next best step, evaluation of metastasis, tumor markers
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>>Testicular ultrasound.
■ CXR and abdominal/pelvic CT to evaluate for metastasis. ■ Tumor markers are useful in diagnosis and in monitoring treatment response. |
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β-hCG in testicular carcinoma: Dx
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↑ in choriocarcinoma and 10% of seminomas.
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α-fetoprotein (AFP)
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↑ nonseminomatous germ cell
tumors, particularly endodermal sinus (yolk sac) tumors. |
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treatment for testicular cancer:
main therapy |
>>Radical orchiectomy.
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testicular cancer: nonseminomatous germ cell tumors tx
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>>Platinum-based chemotherapy is used for nonseminomatous germ cell tumors.
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testicular cancer: seminoma tx
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>>Seminomas are exquisitely radiosensitive and also respond to chemotherapy.
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what is cryptochodism
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Failure of the testes to fully descend into the scrotum.
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RF of cryptochodism
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Prematurity
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Bilateral cryptochodism what is it associated with
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oligospermia and infertility
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cryptochordism presentation
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>>Testes cannot be manipulated into the scrotal sac with gentle pressure
>>testes is palpated anywhere along the inguinal canal or in the abdomen. |
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tx for cryptochordism
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Orchiopexy after age one but before age five (to preserve fertility).
If it is later in life: orchiectomy to decrease risk of testicular cancer |
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Erectile dysfunction RF
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DM, atherosclerosis, medications
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causes of ED
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>>medication use
>>nocturnal or early-morning erections (if present, it is nonorganic) >>neurologic dysfunction >>hypogonadism |
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test for ED
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>>Check prolactin, as elevated prolactin can →↓androgen activity
>>Testosterone and gonadotropin levels may be abnormal |
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physiological ED tx
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psychotherapy or sex
therapy involving discussion and exercises with the appropriate partner. |
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organic ED tx
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sildenafil (Viagra) and vardenafil (Levitra)
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when would you use testosterone therapy for tx of ED?
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Testosterone is a useful therapy for patients with hypogonadism of testicular or pituitary origin;
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tx for ED who failed medical therapy
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Vacuum pumps, intracavernosal injections, and surgical implantation of
semirigid or inflatable penile prostheses |