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112 Cards in this Set

  • Front
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what is hypernatremia?
Serum sodium > 145 mEq. Usually due to water loss
presentation of hypernatremia
>>thirst (due to hypertonicity) >>Neurologic symptoms ie. mental status changes, weakness, focal neurologic deficits, and seizures.
>>Examination reveals “doughy” skin
Hypernatremia causes—
Diuretics
Dehydration
Diabetes insipidus
Docs (iatrogenic)
Diarrhea
Disease (e.g., kidney,
sickle cell)
treatment for hypernatremia
>>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.
Hyponatremia
Serum sodium < 136 mEq/L.
what are some of the causes of hypotonic hyponatremia. Osmolarity :High (> 295 mEq/L):
Hyperglycemia, hypertonic infusion (e.g., mannitol).
what are some of the causes ofnormal osmolarity with hyponatremia. Osmolarity : normal
Normal (280–295 mEq/L): Hypertriglyceridemia, paraproteinemia
(pseudohyponatremia).
what are the 3 types of hypotonic with Low (< 280mEq/L):osmolarity
Hypervolemic
Euvolemic
Hypovolemic
Hypervolemic hyponatremic hypotonic: etiology and tx
etiology: Renal failure, nephrotic syndrome, cirrhosis, CHF.
tx:Water restriction.
Euvolemic hyponatremic hypotonic: etiology and tx
SIADH, hypothyroidism, renal failure, drugs, psychogenic polydipsia, adrenal insufficiency
Tx: Water restriction.
Hypovolemic hyponatremic hypotonic: etiology and tx
Diuretics, vomiting, diarrhea, third spacing, dehydration.
Tx:Replete volume with normal saline
how should chronic hyponatremia be treated?
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).
Hypervolemic hyponatremia is
caused by
“nephrOSIS,
cirrhOSIS, and cardiOSIS.”
Hyperkalemia
Serum potassium > 5 mEq/L
Treatment of hyperkalemia—
Values of > 6.5 mEq/L or ECG changes require emergent treatment.
C BIG K
Calcium
Bicarbonate
Insulin
Glucose
Kayexalate
diagnosis of hyperkalemia
>>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.
Hypokalemia
Serum potassium < 3.6 mEq/L
presentation of hypokalemia
Fatigue, muscle weakness or cramps, ileus,
treatment of hypokalemia
>>Treat the underlying disorder.
>>Oral and/or IV potassium repletion.
>>Replace magnesium, as this deficiency makes potassium repletion difficult.
Causes of hypercalcemia
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
Hypercalcemia
Serum calcium > 10.2 mg/dL. The most common causes are hyperparathyroidism and malignancy
presentation of hypercalcemia
bones (fractures), stones (kidney stones), abdominal groans
(anorexia, constipation), and psychiatric overtones (fatigue,depression)
treatment for hypercalcemia
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
treatment of hypocalcemia
TREATMENT
■ Treat the underlying disorder.
■ Magnesium repletion.
■ Administer oral calcium supplements; IV calcium for severe symptoms
hypocalcemia presentation
Chvostek’s sign
Trousseau’s sign
abdominal muscle cramps, dyspnea, tetany, perioral and
acral paresthesias,
ECG hypocalcemia
ECG may show a prolonged QT interval.
Dx: patient who
develops cramps and tetany
following thyroidectomy.
hypocalcemia
how are the calcium levels in hypoalbuminemia
Serum calcium may be falsely
low in hypoalbuminemia
Hypomagnesemia
Serum magnesium < 1.5 mEq/L
treatment for hypomagnesemia
IV and oral supplements.
■ Hypokalemia and hypocalcemia will not correct without magnesium correction
↑ anion gap— caused by what diseases
MUDPILES
Methanol
Uremia
DKA
Paraldehyde
Intoxication
Lactic acidosis
Ethylene glycol
Salicylates
pH < 7.4 pCO2 >40
Respiratory acidosis
Hypoventilation
Acute lung disease
Chronic lung disease
Opioids, narcotics, sedatives
Weakening of respiratory
muscles
pH < 7.4 pCO2 <40 with normal anion gap
Normal anion gap (8–12 mEq/L)
–Diarrhea
–Glue sniffing
–Renal tubular acidosis
–Hyperchloremia
pH < 7.4 pCO2 <40
⇧Anion gap
–Renal failure
–Lactic acidosis
–Ketoacidosis (DM)
–Aspirin ingestion
pH > 7.4 PCO2 < 40 mmHg
Respiratory alkalosis
–Hyperventilation
–Aspirin ingestion (early)
pH > 7.4 PCO2 > 40 mmHg
Metabolic alkalosis with
compensation
–Vomiting
–Diuretic use
–Antacid use
–Hyperaldosteronism
Pre renal:

Intrinsic:
↓ renaI Intrinsic

Injury within the nephron unit.
Postrenal:
Urinary outflow obstruction. Generally, both kidneys must be obstructed in order to → a significant ↑ in BUN and creatinine.
etiology: An FeNa < 1%, a UNa < 20, a specific gravity > 1.020, or a BUN/creatinine ratio > 20
prerenal etiology
White cells, eosinophils: etiology and classification
etiology: Allergic interstitial nephritis, atheroembolic disease
classification is intrinsic
Hyaline casts: etiology and classification
etiology: Normal finding, but ↑ amount suggests volume depletion.
classification is Prerenal
Red cell casts, dysmorphic red cells
Glomerulonephritis
Intrinsic
Granular casts, renal tubular cells,
ATN
Intrinsic
White cells, white cell casts
Pyelonephritis
Postrenal
Indications for urgent dialysis
AEIOU
Acidosis
Electrolyte abnormalities
(hyperkalemia)
Ingestions (salicylates, theophylline, methanol, barbiturates, lithium, ethylene glycol) Overload (fluid)
Uremic symptoms
(pericarditis, encephalopathy,
bleeding, nausea, pruritus, myoclonus
hematuria, hypertension, and oliguria. DDx
nephritic syndrome
tx of nephrotic syndrome
Corticosteroids are useful in reducing glomerular inflammation in some
cases
nephrotic syndrome
proteinuria (≥ 3.5 g/day), generalized edema, hypoalbuminemia, and hyperlipidemia
Membranous nephropathy: most common in what group of people an biopsy
The most common nephropathy in caucasian adults
“Spike-and-dome” appearance
tx for nephrotic syndrome
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.
Dx for nephrolithiasis
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
tx for calcium oxalate stones
Hydration, thiazide diuretic.
(Mg-NH4-PO4) tx
Hydration; treat UTI
uric acid: tx and type of stone
Hydration; alkalinize urine
Acidic urine (pH < 5.5). Radiolucent. with citrate, which is converted to HCO3 in the
liver; dietary purine restriction and allopurinol.
cystine stones tx
from homocytenuria
Hydration, alkalinize urine,
penicillamine.
dx of stones
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
initial treatment of stones
Hydration and analgesia are the initial treatment.
presentation of PCKD
Pain and hematuria,hypertension, hepatic cysts, cerebral berry
aneurysms,
management of PCKD
Prevent complications and ↓ the rate of progression to end-stage renal disease. Early management of UTIs and control of BP
Dx of PCKD
Based on ultrasound or CT scan
management of ESRD in PCKD
Dialysis and renal transplantation are used to manage patients with endstage renal disease.
RTA type I: complications and tx
Treatment: Potassium citrate.
Complications: Nephrolithiasis.
RTA type II: complications and tx
Treatment: Potassium citrate.
Complications: Rickets, osteomalacia.
RTA type IV: complications and tx
Treatment: Furosemide, fludrocortisone, and low-potassium diet in patients with aldosterone deficiency.
Complications: Hyperkalemia
types of uretharal reflux
■ 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
common presentation of urethral reflux
Patients present with recurrent UTIs
Dx: of urethral reflux
Perform a voiding cystourethrogram

All children < 7 years of age presenting with their first UTI should undergo a voiding cystourethrogram
to screen for reflux.
management of reflux
>>Treat infections aggressively.
>>Treat mild reflux with daily prophylactic antibiotics until reflux resolves at puberty. >>Ureteral implantation may be considered in severe reflux.
complication of reflux
Inadequate treatment can → progressive renal
scarring and end-stage renal disease.
how to diagnose DI
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
Tx for central and nephrogenic DI
Treat the underlying cause.
■ Central DI: Administer DDAVP intranasally.
■ Nephrogenic DI: Salt restriction and ↑ water intake are the 1° treatment.
Thiazide diuretics
SIADH tx.
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.
BPH diagnosis
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.
tx for BPH: mild, moderate and severe symptoms
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.
what is the major side effect of α-
blockers?
orthostatic hypotension
what are the Leading causes of
cancer death in men:
1. Lung cancer
2. Prostate cancer
3. Colorectal cancer
4. Pancreatic cancer
5. Leukemia
presentation of prostate cancer.
Usually asymptomatic,urinary retention,back pain due to bone metastases. DRE may reveal a palpable nodule or an area of induration.
Dx of prostate cancer
>>↑ 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
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
recommended screening method for prostate cancer
annual DRE after the age
of 50 is the recommended
screening method for prostate
cancer.
Differential for hematuria
S2I3T3
Strictures
Stones
Infection
Inflammation
Infarction
Tumor
Trauma
TB
most common presenting symptom of bladder cancer
Gross hematuria is the most common presenting symptom.
diagnostic test for bladder cancer
>>UA often shows hematuria
>>IVP can examine the upper urinary tract as well as defects in bladder filling.
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.
tx: for bladder cancer: Superficial cancers:
Complete transurethral resection or intravesicular
chemotherapy with mitomycin-C or BCG (the vaccine for TB).
tx: for bladder cancer
Large, high-grade recurrent lesions:
Intravesicular chemotherapy.
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.
tx: for bladder cancer
Patients with distant metastases:
Chemotherapy alone.
hematuria, flank pain, and a palpable flank mass. Dx
renal cell carcinoma
presentation of renal cell carcinoma
>>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.
Dx of renal cell carcinoma
Ultrasound and/or CT to characterize the renal mass
Tx for renal cell carcinoma
>>Surgical resection may be curative in localized disease
>>chemotherapy 15%-30%
presentation of testicular cancer
>>painless enlargement of the testes
>>ages of 15 and 30
>>seminomas: 40 and 50 years of age.
testicular cancer etiology and RF
ET:germ cells, and virtually all are malignant.
RF: Cryptorchidism: ↑ risk of neoplasia in both testes. and Klinefelter’s syndrome
diagnosis of testicular cancer: next best step, evaluation of metastasis, tumor markers
>>Testicular ultrasound.
■ CXR and abdominal/pelvic CT to evaluate for metastasis.
■ Tumor markers are useful in diagnosis and in monitoring treatment response.
β-hCG in testicular carcinoma: Dx
↑ in choriocarcinoma and 10% of seminomas.
α-fetoprotein (AFP)
↑ nonseminomatous germ cell
tumors, particularly endodermal sinus (yolk sac) tumors.
treatment for testicular cancer:
main therapy
>>Radical orchiectomy.
testicular cancer: nonseminomatous germ cell tumors tx
>>Platinum-based chemotherapy is used for nonseminomatous germ cell tumors.
testicular cancer: seminoma tx
>>Seminomas are exquisitely radiosensitive and also respond to chemotherapy.
what is cryptochodism
Failure of the testes to fully descend into the scrotum.
RF of cryptochodism
Prematurity
Bilateral cryptochodism what is it associated with
oligospermia and infertility
cryptochordism presentation
>>Testes cannot be manipulated into the scrotal sac with gentle pressure
>>testes is palpated anywhere along the inguinal canal or in the abdomen.
tx for cryptochordism
Orchiopexy after age one but before age five (to preserve fertility).
If it is later in life: orchiectomy to decrease risk of testicular cancer
Erectile dysfunction RF
DM, atherosclerosis, medications
causes of ED
>>medication use
>>nocturnal or early-morning erections (if present, it is nonorganic)
>>neurologic dysfunction
>>hypogonadism
test for ED
>>Check prolactin, as elevated prolactin can →↓androgen activity
>>Testosterone and gonadotropin levels may be abnormal
physiological ED tx
psychotherapy or sex
therapy involving discussion and exercises with the appropriate partner.
organic ED tx
sildenafil (Viagra) and vardenafil (Levitra)
when would you use testosterone therapy for tx of ED?
Testosterone is a useful therapy for patients with hypogonadism of testicular or pituitary origin;
tx for ED who failed medical therapy
Vacuum pumps, intracavernosal injections, and surgical implantation of
semirigid or inflatable penile prostheses