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698 Cards in this Set
- Front
- Back
Vitamin A deficiency
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night blindness, dry skin
|
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Vitamin B1 (thiamine) def
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beriberi (polyneuritis, dilated cardiomyopathy, high output CHF, edema), Wernicke-Korsakoff syndrom
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Vitamin B2 (riboflavin) def
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angular stomatitis, cheilosis, corneal vascularization
|
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Vitamin B3 (niacin) def
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pellagra (diarrhea, dermatitis, dementia)
|
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Vitamin B5 (pantothenate) def
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dermatitis, enteritis, alopecia, adrenal insufficiency
|
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Vitamin B6 (pyridoxine) def
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convulsions, hyperirritability; required during administration of INH
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Vitamin B12 (cobalamin) def
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macrocytic, megaloblastic anemia, neurologic symptoms (optic neuropathy, subacute combined degneration, paresthesias), glossitis
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Vitamin C def
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scurvy (swollen gums, bruising, anemia, poor wound healing)
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Vitamin D def
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rickets in children, osteomalacia in adults (soft bones), hypocalcemic tetany
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Vitamin E def
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increased fragility of RBCs
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Vitamin K def
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neonatal hemorrhage, increase PT and aPP, normal BT
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biotin def
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dermatitis, enteritis, can be caused by ingestion of raw eggs or antibiotic use
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Folic acid def
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MOST COMMON VIT DEFICIENCY IN US; sprue, macrocytic, megaloblastic anemia without neuro signs
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Mg def
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weakness, muscle cramps, exacerbation of hypocalcemic tetany, CNS hyperirritability leading to tremors and choreoathetoid movement
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Selenium def
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Keshan disease (cardiomyopathy)
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unstable angina
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angina is new, worsening or occurs at rest
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Antihypertensive for a diabetic pt with proteinuria
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ACE I
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Beck's triad for cardiac tamponade
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hypotension, distant heart sounds and elevated JVD
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drugs that slow AV transmission
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beta blockers, digoxin, calcium channel blockers
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hypercholesterolemia tx that causes flushing and pruritis
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niacin
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tx for a-fib
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anticoagulation, rate control, cardioversion
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tx for v-fib
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immediate cardioversion
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autoimmune complication occurring 2-4 weeks post MI
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Dressler's syndrome: fever, pericarditis, increased ESR
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IV drug use with JVD and holosystolic murmur at left sternal border...tx?
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tx existing heart failure and replace tricuspid valve
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Diagnostic test for hypertrophic cardiomyopathy
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echocardiogram (showing thickened left ventricular wall and outflow obstruction)
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a fall in systolic BP of > 10mmHg with inspiration
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pulsus paradoxus (seen in cardiac tamponade)
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low-voltage, diffuse ST segment elevation
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classic ECG finding in pericarditis
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HTN =
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BP > 140/0 on three separate occasions two weeks apart
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8 surgically correctable causes of HTN
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renal artery stenosis, coarctation of the aorta, pheochromocytoma, Conn's syndrome, Cushings, unilateral renal parenchymal disease, hyperthyroidism and hyperparathyroidism
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indications for surgical repair of abd aortic aneurysm
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> 5.5 cm, rapidly enlarging, symptomatic, or ruptured
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Tx for acute coronary syndrome
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morphine, O2, sublingual nitroglycerin, AA, IV beta blockers, heparin
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metabolic syndrome
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abd obesity, high TGs, low HDL, HTN, insulin resistance, prothrombotic or pro-inflam states
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target LDL in pt with diabetes
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< 70
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signs of active ischemia during stress testing
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angina, ST-segment changes on EKG or decreased BP
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ECG findings suggesting MI
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ST elevation (depression means ischemia), flattened T waves and Q waves
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young pt has angina at rest with ST segment elevation, cardiac enzymes are nl
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prinzmetals angina
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common symptoms with silent MIs
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CHF, shock, and altered mental status
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diagnostic test for pulm embolus
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V/Q scan
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reverses effects of heparin
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protamine
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coagulation parameter affected by warfarin
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PT
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endocarditis prophylaxis regimens
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oral surgery - amoxicillin
GI/GU procedures: ampicillin and gentamicin before and amoxicillin after |
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6 P's of ischemia due to peripheral vascular disease
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pain, pallor, pulselessness, paralysis, parethesia and poikilothermia (cold)
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Virchow's triad
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stasis, hypercoagulability and endothelial damage
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most common cause of HTN in young women
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OCPs
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most common cause of HTN in young men
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excessive EtOH
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"stuck on" appearance
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seborrheic keratosis
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red plaques with silvery-white scales and sharp margins
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psoriasis
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most common type of skin cancer; lesion is pearly colored papule with a translucent surface and telangiectasias
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basal cell carcinoma
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honey crusted lesions
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impetigo
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febrile patient with history of diabetes presents with a red, swollen, painful lower extremity
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cellulitis
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+ Nikolsky's sign
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pemphigus vulgaris
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- Nikolsky's sign
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bullous pemphigoid
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55 year old obese pt presents with dirty, velvety patches on back of neck
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acanthosis nigricans; check fasting blood sugar to r/o diabetes
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Dermatomal distribution
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varicella zoster
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flat-topped papules
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lichen planus
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iris-like target lesions
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erythema multiforme
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presents with a herald patch, Christmas-tree pattern
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pityriasis rosea
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16 yo presents with an annular patch of alopecia with broken-off, stubby hairs
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alopecia areata (autoimmune process)
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pinkish, scaling, flat lesions on the chest and back; KOH prep has a "spaghetti and meatballs" appearance
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pityriasis versicolor
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four characteristics of nevus suggestive of melanoma
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asymmetry, border irregularity, color variation, large diameter
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premalignant lesion from sun exposure that can lead to squamous cell carcinoma
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actinic keratosis
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"dewdrop on a rose petal"
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lesions of primary varicella
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"cradle cap"
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seborrheic dermatitis...treat with antifungals
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associated with Propionibacterium acnes and changes in androgen level
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acne vulgaris
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painful, recurrent vesicular eruption of mucocutaneous surfaces
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herpes simplex
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inflammation and epithelial thinning of anogenital area, predominantly in postmenopausal women
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lichen sclerosus
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exophytic nodules on skin with varying degrees of scaling or ulceration; second most common type of skin cancer
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squamous cell carcinoma
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induction of p450 enzymes
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barbiturates, phenytoin, carbamazepine, rifampin, quinidine, griseofulvin
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inhibition of p450 enzymes
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cimetidine, ketoconazole, INH, grapefruit, erythromycin, sulfonamides
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Metabolism by p450 enzymes
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benzos, amide anesthetics, metoprolol, propranolol, nifedipine, phenytoin, quinidine, theophylline, warfarin, barbiturates
|
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increase risk of digoxin toxicity
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quinidine, cimetidine, amiodarone, calcium channel blockers
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competition for albumin binding sites
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warfarin, asa, phenytoin
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blood dyscrasias
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ibuprofen, quinidine, methyldopa, chemo agents
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hemolysis in G6PD deficient patients
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sulfonamides, INH, ASA, ibuprofen, nitrofurantoin, primaquine, pyrimethamine, chloramphenicol
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Gynecomastia
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spironolactone, estrogens, digitalis, cimetidine, chronic alcohol use, ketoconazole
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stevens johnson syndrome
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ethosuximide, sulfonamide
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photosensitivity
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tetracycline, amiodarone, sulfonamides
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drug induced SLE
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procainamide, hydralazine, INH, penicillamine, chlorpromazine, methyldopa, quinidine
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three most common causes of fever of unknown origin
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infection, cancer, and autoimmune disease
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four signs and symptoms of streptococcal pharyngitis
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fever, pharyngeal erythema, tonsillar exudate, lack of cough
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a nonsuppurative complication of strep infection that is not altered by treatment of primary infection
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postinfectious glomerulonephritis
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asplenic pts are particularly susceptible to these organisms
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encapsulated organisms - pneumococcus, meningococcus, H. flu and Klebsiella
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number of bacteria on a clean-catch specimen to diagnose UTI
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10 x 5 bacteria/mL
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health population susceptible to UTI?
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pregnant women...treat aggressively because of potential complications
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pt from california or arizona presents with fever, malaise, cough and night sweats...
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coccidiodomycosis, Amphotericin B
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nonpainful chancre
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primary syphilis
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"blueberry muffin" rash
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rubella
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meningitis in neonates...causes? tx?
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group B strep, E. coli, Listeria...tx with gentamycin and ampicillin
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meningitis in infants...causes? tx?
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pneumococcus, meningococcus, H. flu...
tx with cefotaxime and vanco |
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CSF - nl glucose and lymphocytic predominance
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aseptic (viral) meningitis
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numerous RBCs in serial CSF samples
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subarachnoid hemorrhage
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initially presents with pruritic papule with regional lymphadenopathy and evolves into black eschar after 7-10 days...
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cutaneous anthrax, tx with penicillin G or ciprofloxacin
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findings in tertiary syphilis
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tabes dorsalis, general paresis, gummas, argyll robertson pupils, aortitis, aortic root aneurysms
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cold agglutinins
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mycoplasma
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24 year old male with soft white plaques on tongue and back of throat
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candidal thrush...workup should include HIV...treat with nystatin oral suspension
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begin PCP proph in HIV + patient at what CD4 count?
MAC prophylaxis? |
PCP - < 200 (with TMP-SMX)
MAC - <50-100 (with clarithromycin/azithromycin) |
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risk factors for pyelonephritis
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pregnancy, vesicoureteral reflux, anatomic anomalies, indwelling catheters, kidney stones
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neutropenic nadir postchemo
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7-10 days
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classic physical findings of endocarditis
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fever, heart murmur, Osler's nodes, splinter hemorrhages, Janeway lesions, Roth's spots
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aplastic crisis in sickle cell disease
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Parvovirus B19
|
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ring-enhancing brain lesions on CT with seizures
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taenia solium (cysticercosis)
|
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branching rods in oral infection
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actinomyces israelii
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painful chancroid
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haemophilus ducreyi
|
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dog or cat bite
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pasteurella multocida
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gardener
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sporothrix schenckii
|
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pregnant women with pets
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toxoplasma gondii
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meningitis in adults
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neisseria meningitidis
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meningitis in elderly
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strep pneumo
|
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alcoholic with pneumonia
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klebsiella
|
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'currant jelly' sputum
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klebsiella
|
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infection in burn victims
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pseudomonas
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osteomyelitis from foot wound puncture
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pseudomonas
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osteomyelitis in sickel cell patients
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salmonella
|
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55 year old man who is a smoker and a heavy drinker presents with new cough and flulike symptoms...gram stain shows no organisms; silver stain of sputum shows gram neg rods...dx?
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legionella pneumonia
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middle aged man presents with acute-onset monoarticular joint pain and bilateral Bell's palsy...dx, tx?
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Lyme disease, Ixodes tick, doxycycline
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pt develops endocarditis 3 weeks after receiving prosthetic heart valve...organism?
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staph aureus or staph epidermidis
|
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Xeroderma pigmentosum (a/cancer)
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squamous cell and basal cell carinoma of the skin
|
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Gastric adenocarcinoma is a/w
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chronic atrophic gastritis, pernicious anemia, postsurgical gastric remnants
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Astrocytoma and cardiac rhabdomyoma a/w
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tuberous sclerosis (facial angiofibroma, seizures, mental retardation)
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Actinic keratosis a/w
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squamous cell carcinoma of the skin
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Barret's esophagus (chronic GI reflux)
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a/w esophagel adenocarcinoma
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Plummer Vinson Syndrome a/w
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first: Plummer Vinson syndrome is atrophic glossitis, eophageal webs, anemia...all due to iron deficiency
a/w squamous cell carcinoma of the esophagus |
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ulcerative colitis a/w
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colonic adenocarcinoma
|
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paget's disease of the bone a/w
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secondary osteosarcoma and fibrosarcoma
|
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immunodeficiency states a/w
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malignant lymphomas
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AIDS a/w (neoplasm)
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aggressive malignant NHLs and Kaposi's sarcoma
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autoimmune diseases (like myastenia) a/w
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benign and malignant thymomas
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acanthosis nigricans a/w
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visceral malignancy (stomach, lung, breast and uterus)
|
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dysplastic nevus a/w
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malignant melanoma
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four causes of microcytic anemia
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thalassemia, iron deficiency, anemia of chronic disease and sideroblastic anemia
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precipitants of hemolytic crisis in patients with G6PD deficiency
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sulfonamides, antimalarial drugs and fava beans
|
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most common inherited cause of hypercoagulability
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factor V Leiden mutation
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most common inherited hemolytic anemia
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hereditary spherocytosis
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diagnostic test for hereditary spherocytosis
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osmotic fragility test
|
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pure RBC aplasia
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diamond-blackfan anemia
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Fanconi's anemia
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anemia a/w absent radii and thumbs, diffuse hyperpigmentation, cafe-au-lait spots, microcephaly and pancytopenia
|
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meds and viruses that lead to aplastic anemia
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chloramphenicol, sulfonamides, radiation, HIV, chemotherpeutic drugs, hepatitis, parvo B19 and EBV
|
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how to distinguish polycythemia vera from secondary polycythemia
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both have increased hematocrit and RBC mass, but polycythemia vera has normal O2 sats and low EPO levels
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TTP pentad!!!
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fever, renal failure, anemia, thrombocytopenia and neurologic abnls
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HUS triad
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anemia, thrombocytopenia and acute renal failure
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treatment for TTP
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emergent large volume plasmapheresis, corticosteroids and antiplatelet drugs
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tx for ITP in kids
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usually resolves spontaneously, may require IVIG and/or corticosteroids
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changes in DIC
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elevated fibrin split products and D-dimer
decreased platelets, fibrinogen and hematocrit |
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14 year old girl with prolonged bleeding after dental surgery and with menses...nl PT, nl or increased PTT, increased bleeding time...dx?
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von Willebrand's disease, treat with desmopressin, FFP or cryoprecipitate
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60 year old AA male with bone pain...w/u for MM may reveal?
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monoclonal gammopathy, bence jones proteinuria, "punched out" lesions on x-ray of skull and long bones
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reed sternberg cells
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hodgkins lymphoma
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microcytic anemia with decreased serum iron, decreased TIBC and normal or increased ferritin
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anemia of chronic disease
|
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microcytic anemia with decreased serum iron, decreased ferritin and increased TIBC
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iron deficiency anemia
|
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80 yo male with fatigue, lymphadenopathy, splenomegaly and isolated lymphocytosis...wtf?
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CLL
|
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late, life-threatening complication of CML
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blast crisis (fever, bone pain, splenomegaly, pancytopenia)
|
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auer rods on blood smear
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AML
|
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AML subtype associated with DIC
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M3
|
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elec changes in tumor lysis syndrome
|
dec calcium, increased K, increased phosphate and increased uric acid
|
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treatment for AML M3
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retinoic acid
|
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heinz bodies?
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intracellular inclusions seen in thalassemia, G6PD def and post-splenectomy
|
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Glanzmann's thrombasthenia
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AR disorder with defect in GPIIb/IIIa platelet receptor and decreased platelet aggregation
|
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virus associated with aplastic anemia in pts with sickle cell
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parvovirus B19
|
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25 year old AA male with sickle cell anemia has sudden onset bone pain...management?
|
O2, analgesia, hydration, and, if severe, transfusion
|
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significant cause of morbidity in thalassemia patients...tx?
|
iron overload; use deferoxamine
|
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elevated alpha feto protein
|
open neural tube defects (anencephaly, spina bifida), abdominal wall defects (gastroschisis, omphalocele), multiple gestation, incorrect gestational age, fetal death and placental abnormalities (placental abruption)
|
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abnormally low alpha fetoprotein
|
should do amniocentesis and karyotyping to rule out chromosomal abnormalities
|
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quad screen
|
alpha fetoprotein, inhibin A, estriol and beta-hCG
|
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decreased AFP, decreased estriol, decreased beta-hCG and decreased inhibin A
|
trisomy 18
|
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decreased AFP, decreased estriol, increased beta-hCG and increased inhibin A
|
trisomy 21
|
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reasons for amniocentesis
|
>35 years old, conjuction with abnl quad screen, Rh-sensitized pregnancy to obtain fetal blood type or detect fetal hemolysis, to evaluate fetal lung maturity via a lecithin-sphingomyelin ratio >2.5 or to detect presence of phosphatidylglycerol (done during 3rd trimester)
|
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chorionic villous sampling
|
can be done earlier - 10-12 weeks gestation...better diagnostic accuracy
dis: risk of fetal loss and inability to diagnose neural tube defects is 0.5% - 1% higher than with amnio limb defects a/w CVS performed earlier than 9 weeks |
|
percutaneous umbilical blood sampling
|
gett blood from umbilical vessels...used to diagnose fetal hemolytic disease and fetal infection
|
|
category A drugs (preg)
|
fine...no harm...ex: vit C
|
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cat B drugs (preg)
|
no risk in animal studies...ampicillin
|
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cat C drugs (preg)
|
drugs given only if potential benefit justifies potential risk to fetus...zidovudine
|
|
Cat D drugs (preg)
|
there are risks, but benefits from use in pregnant women may be acceptable despite the risk...PHENYTOIN
|
|
cat X drugs (preg)
|
just dont do it...no way.
isoretinoin |
|
fetal alcohol syndrome
|
growth restriction before and after birth, MR, midfacial hypoplasia, renal and cardiac defects...6 drinks/day have 40% risk
|
|
androgens/test der in pregnancy
|
virilization of females, advanced genital dev in males
|
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ACE-I in preg
|
can cause fetal renal tubular dysplasia and neonatal renal failure, oligohydramnios, IUGR, lack of cranial ossification
|
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coumadin in preg
|
BAD
nasal hypoplasia and stippled bone epiphyses, develop delay, IUGR, opthalmologic abnl |
|
Carbamazepine in preg
|
neural tube defects, fingernal hypoplasia, microcephaly, DD and IUGR
|
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folic acid antagonists in preg (methotrexate, aminopterin)
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increased spontaneous abortion
|
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cocaine in preg
|
bowel atresias in fetus, congenital malfms of heart, limbs, face and GU tract; microcephaly; IUGR, cerebral infarction
|
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DES in preg
|
clear cell adenocarcinoma of vagina or cervix, vaginal adenosis, abnl of cervix and uterus or testes, possible infertility
|
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Lead in preg
|
increase spont abortion rates, stillbirths
|
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Lithium in preg
|
congenital heart disease (Ebsteins anomaly)
|
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organic mercury in preg
|
cerebral atrophy, microcephaly, MR, spasticity, seizures and blindness
|
|
Phenytoin in preg
|
IUGR, MR, microcephaly, dysmorphic craniofacial features, cardiac defects fingernail hypoplasia
|
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Radiation in preg
|
microcephaly, MR, < 0.05 Gy to the fetus has no teratogenic risk
|
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Streptomycin and kanamycin in preg
|
hearing loss, CN VIII damage
|
|
tetracycline in preg
|
permanent yellow-brown discoloration of deciduous teeth, hypoplasia of tooth enamel
|
|
Thalidomide in preg
|
bilateral limb deficiencies, anotio and microtia, cardiac and GI abnormalities
|
|
Trimethadione and paramethadione in preg
|
cleft lip and cleft palate, cardiac defects, microcephaly, MR
|
|
Valproic acid in preg
|
neural tube defects (spina bifida), minor craniofacial defects
|
|
Vitamin A in preg
|
increased SAB rate, microtia, thymic agenesis, CV defects, craniofacial dysmorphism, microphthalmia, cleft lip or cleft palate, MR
|
|
CMV in preg
|
can cause in fetus: microcephaly, hydrocephaly, chorioretinitis, cerebral calcifications, IUGR, microphthalmos, MR and hearing loss
THE MOST COMMON CONGENITAL INFECTION |
|
Rubella in preg
|
to fetus: microcephaly, MR, cataracts, hearing loss, congenital heart disease
do NOT give immunization in pregnancy...live attenuated vaccine (no evidence of it doing sh*t, but dont give it still) |
|
Syphilis in preg
|
to fetus: fetal hydrops (severe), abnormalities of skin, teeth and bones (mild)
|
|
Toxo in preg
|
to fetus: microcephaly, hydrocephaly, cerebral calcifications, chorioretinitis
transmitted via raw meat or through exposure to infected cat feces |
|
Varicella in preg
|
to fetus: skin scarring, chorioretinitis, cataracts, microcephaly, hypoplasia of hands and feet, muscle atrophy
|
|
Bishop score
|
to see if cervix is favorable for both spontaneous and induced labor
dilation, effacement, station, cervical position and cervical consistency...> 8 is ready. |
|
early deceleration
|
apparent, gradual (onset to nadir less than 30sec) decrease in FHR with return to baseline that mirrors uterine contraction
causes: head compression from uterine contraction |
|
late deceleration
|
gradual onset decrease in FHR with return to baseline whose onset, nadir and recovery occur after the beg, peak and end of uterine ctx.
causes: uteroplacental insufficiency and fetal hypoxemia |
|
variable deceleration
|
an abrupt decrease in FHR below baseline lasting more than 15 sec but less than 2 min
cause: umbilical cord compression (most often secondary to oligohydramnios) |
|
bradycardia baseline
|
FHR below 110
causes: congenital heart malformations, severe hypoxia (2/2 uterine hyperstimulation, cord prolapse and rapid fetal descent) |
|
Tachycardia, FHR
|
FHR > 160...
causes: hypoxia, maternal fever and anemia |
|
BPP (biophysical profile)
|
5 parameters: breathing, fetal tone, movement, amniotic fluid volume and NST
8-10 is reassuring for fetal well being 6 is equivocal (most term preg) 0-4 is extremely worrisome for fetal asphyxia and strong consideration should be given for immediate delivery |
|
modified BPP
|
combines NST with the amniotic fluid index...considered normal with reactive NST and an AFI > 5cm
|
|
contraindications for regional anesthesia in preggers
|
refractory mat hypotension, maternal coagulopathy, mat use of heparin within 12 hours, untreated maternal bacteremia, skin infection over needle site and increased ICP caused by a mass lesion
|
|
maternal complications of pregestationl DM
|
DKA (1) and HHNK (2), preeclampsia/eclampsia, cephalopelvic disproportion, preterm labor, infection, polyhydramnios, postpartum hemorrhage, maternal mortality
|
|
fetal complications of maternal pregestational DM
|
macrosomia, cardiac and renal defects, neural tube defects (sacral agenesis), hypocalcemia, polycythemia, hyperbilirubinemia, IUGR, hypoglycemia with hyperinsulinemia, RDS, birth injury (shoulder dystocia), perinatal mortality
|
|
BP meds NOT to give in pregnancy
|
ACE-I or diuretics...
ACE-I can lead to uterine ischemia and diuretics can aggravate low plasma volume to the point of uterine ischemia |
|
complications a/w preeclampsia
|
prematurity, fetal distress, stillbirth, placental abruption, seizure, DIC, cerebral hemorrhage, serour retinal detachment, fetal/maternal death
|
|
severe preeclampsia
|
BP > 160/110
renal: proteinuria, >5gm/24hr cerebral: HA, somnolence Visual changes: blurred vision, scotomata hyperactive reflexes/clonus Hemolysis, elevated liver enzymes, thrombocytopenia (HELLP syndrome) give mag sulfate for prevention of seizures...watch out for toxicity - loss of DTRs, resp paralysis, coma...tx toxicity with IV calcium gluconate |
|
risk factors for placenta previa
|
prior C-sections, grand multiparous, advanced maternal age, multiple gestation, prior placenta previa
|
|
complications of placenta previa
|
increased risk of placenta accreta, vasa previa (fetal vessels crossing internal os)
preterm delivery, premature rupture of membranes, IUGR and congenital anomalies recurrence risk 4-6% |
|
oligohydramnios
|
AFI < 5cm
etiologies: fetal urinary tract abnl (renal agenesis, GU obstruction), chronic uteroplacental insufficiency and ROM a/w 40-fold increase in perinatal mortality; other complications include musculoskeletal abnormalities (eg clubfoot, facial distortion), pulmonary hypoplasia, umbilical cord compression and IUGR |
|
polyhydramnios
|
AFI >20
etiologies include: maternal DM, multiple gestation, isoimmunization, pulmonary abnormalities (eg cystic lung abnl), fetal anomalies (eg duodenal atresia, tracheoesophageal fistula, anencephaly) and twin-twin transfusion syndrome complications: preterm labor, fetal malpresentation, cord prolapse |
|
gestational trophoblastic disease
COMPLETE MOLES |
usually result from sperm fertilization of an empty ovum
46XX - paternally derived |
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Incomplete moles
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occur when normal ovum is fertilized by two sperm (or a haploid sperm that duplicates its chromosomes), contains fetal tissue
69XXY |
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history of ladies with gestational troph. dz
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first trimester uterine bleeding, hyperemesis gravidum, preeclampsia/eclampsia at < 24 weeks, uterine size greater than dates
no fetal HB detected, pelvic exam with enlarged ovaries (bilateral theca-lutein cysts) or expulsion of grapelike molar clusters risk factors: extremes of age, less than 20, more than 40, deficient in folate or beta-carotene and blood group |
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diagnosis of GTD
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markedly increased b-hCG (greater than 100,000)..."snowstorm" on US...
CXR: may have lung mets; D&C reveals cluster of grapes tissue |
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tx of GTD
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follow beta hCG, prevent pregnancy for one year
tx malignancy with chemo (methotrexate or dactinomycin) and residual uterine disease with hysterectomy; chemo and irradiation are cool/good |
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complications of GTD
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molar pregnancy may progress to malignant GTD...including invasive moles (10-15%) and choriocarcinoma (2-5%) with pulm mets or CNS mets
may see trophoblastic pulm nodules |
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to diagnose premature rupture of membranes
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sterile speculum exam shows pooling of amniotic fluid in vaginal vault, + Nitrazine paper test (paper turns blue in alkaline amniotic fluid)
+ fern test - ferning pattern is seen under a microscope after amniotic fluid dries on glass slide U/S to assess AFI do NOT perform digital vaginal exams in women who are not in labor or for whom labor in not immediately planned |
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to tx PROM
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term: check GBS and fetal presentation, can induce or wait 24-72 hrs
>34-36 wks: labor induction <32 wks: expectant management with bed rest and pelvic rest antibxs to prevent infxt prolong latency period in absence of infection antenatal corticosteroids: to promote fetal lung maturity in absence of intraamniotic infection prior to 32 weeks GA |
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uterine atony
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risk factors: uterine overdistention, exhausted myometrium, uterine infection, conditions interfering with contractions
dx: soft, enlarged, BOGGY uterus (most common cause of PPH...90%) tx: bimanual uterine massage, oxytocin, methergine (methylergonovine) if not hypertensive, Prostin (PGF2alpha) if not asthmatic |
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retained placental tissue
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another cause of PPH
risk factors: placenta accreta/increta/percreta, placenta previa, uterine leiomyomas, preterm delivery, previous c-section/curettage |
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primary syphilis
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10-60 days post exposure
chancre can tx primary or secondary: best is penicillin G, if allergic, can use tetracycline and doxycycline |
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secondary syphilis
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4-8wks after appearance of chancre, maculopapular rash (palms and soles); condylomata lata
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tertiary syphilis
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1-10 years after infection
granulomas (gummas) of the skin and bones, aortitis, neurosyphilis with meningovascular disease, paresis and tabes dorsalis must tx with penicillin...if allergice, desensitize pt. |
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herpes genitalis
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primary: malaise, myalgias and fever with vulvar burning/pruritis (2-5 days post exposure) followed by vesicular genital lesions (3-7 days post exposure)...shallow, painful ulcers with a red border
HSV 2 (85% genital lesions) Tzanck smear...presence of multinucleated giant cells with eosinophilic inclusion...viral culture is most sensitive tx: sitz baths and dryer...acyclovir, famciclovir or valacyclovir for primary or for suppressive tx for frequent recurrences |
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chancroid
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painful, nonindurated, purulent, hemorrhagic ulcers with painful inguinal lymphadenopathy
h. ducreyi tx: ceftriaxone, azithromycin, erythromycin or cipro |
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lymphogranuloma venereum
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primary: presents with painless, transient papule or shallow ulcer that can go unnoticed
secondary: inguinal syndrome - painful enlargement and inflammation of inguinal nodes with fever, malaise, HA and loss of appetite tertiary: anogenital syndrome, anal pruritis with discharge, proctocolitis, rectal stricture, rectovaginal fistula and elephantiasis L-serotype Chlamydia trachomatis tx: doxycycline 100mg BID x 21 days |
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granuloma inguinale
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raised, firm lesions
Calymmato-bacterium granulomatis tx: doxy, bactrim or cipro |
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condylomata acuminata (genital warts)
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raised cauliflower like lesions...in immunocompromised pts
HPV, HPV 6 and HPV 11 tx: surgical, chemical (TCA, podophyllin, 5-FU, podofilox), immunologic imiquimod) |
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molluscum
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poxviridae
tx with desiccation, cryotherapy, curettage or imiquimod |
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inpt antibiotics for PID
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1. cefoxitin or cefotetan and doxycycline x 14 days
2. clinda and gent x 14 days |
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outpt tx for PID
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1. cefoxitin with probenecid x 1 dose
2. ceftriaxone IM and doxycycline 3. ofloxacin and metronidazole |
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trichomonas
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protozoal flagellates affect the vagina, skene's duct and lower urinary tract...
STRAWBERRY PETECHIAE in upper vagina/cervix d/c: profuse, malodorous, yellow-green, frothy wet mount: motile trichomonads (slightly larger than WBCs) tx: single dose PO metronidazole or tinidazole complications: chorioamnionitis/endometritis, infection, preterm delivery, miscarriage, PID, cellulitis when invasive procedures done |
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risk factors for yeast infections
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diabetes, broad-spectrum antibiotic use, pregnancy steroids, HIV, OCP use, IUD use, young age at first intercourse, increased freq of intercourse
(avoid oral azoles in pregnancy) |
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vulvar cancer
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a/w HPV types 16, 18 and 31, diabetes, obesity, HTN, CV dz and immunosuppression
VIN (vulvar intraepithelial neoplasia)...dx with punch biopsy VIN III: carcinoma in situ about 87% are squamous cell carcinomas and 6% malignant melanomas...remainder are basal cell carcinoma and Paget's disease safe sex can help prevent this |
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ovarian cancer
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nulliparity, breast cancer, family history...
OCP use is protective. CA-125 for epithelial cancers AFP and b-hCG for germ cell cancers tx: TAH/BSO and peritoneal washing for cytology w or w/o pelvic and aortic node sampling, tumor debulking, chemo prevention: OCPs, prophylactic BSO with fm history most common cause of death is bowel obstruction |
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more on ovarian tumors
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pats with first-deg relative have 5% lifetime risk...with >2 relatives, risk is 7%
BRCA1 has 45% lifetime risk BRCA2 has 25% lifetime risk OCPs decrease risk!!! tumor marker CA-125...used only for progression and recurrence |
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Lynch II syndrome
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hereditary nonpolyposis colorectal cancer (HNPCC) is associated with increased risk of colon, ovarian, endometrial and breast cancer
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CA-125 in ovarian tumors
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premenopausal women: increased CA-125 may point to benign such as endometriosis
postmenopausal women: increased indicates an increased likelihood that the ovarian tumor is malignant any palpable ovarian or adnexal mass in a premenarchal or postmenopausal patient is suggestive of ovarian neoplasm |
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marker for ovarian epithelial tumor
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CA-125
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marker for endodermal sinue ovarian tumor
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AFP
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marker for ovarian tumor embryonal carcinoma
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AFP, hCG
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marker for ovarian tumor choriocarcinoma
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hCG
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marker for ovarian tumor dysgerminoma
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LDH
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marker for ovarian tumor granulosa cell
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inhibin!
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stress incontinence
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activities that increase intra-abd pressure
etiology: urethral sphincteric insufficiency due to laxity of pelvic floor musculature; common in multiparous women or after pelvic surgery tx: surgery places bladder neck into app anatomical location; swab test: greater than 30 degrees with increased intra-abd pressure |
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urge incontinence
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unexpected urge to void, unrelated to position or activity
etiology: detrussor hyperreflexia or sphincter dysfunction 2/2 inflammatory conditions or neurogenic d/o of bladder... tx: anticholinergics or TCAs oxybutynin |
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overflow incontinence
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chronic urinary retention
etiology: chronically distended bladder; increased intravesical pressure that just exceeds outlet resistance, allowing small amt of urine to dribble out tx: place urethral catheter in acute settings bethanecol and alpha blockers |
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primary causes of third trimester bleeding
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placental abruption and placenta previa
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classic U/S and gross appearance of complete hydatidiform mole
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snowstorm on U/S, "cluster of grapes" on gross exam
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molar pregnancy containing fetal tissue
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partial mole
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antibiotics with teratogenic effects
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tetracycline, fluoroquinolones, aminoglycosides and sulfonamide
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shortest AP diameter in pelvis
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obstetric conjugate: between sacral promontory and midpoint of symphysis pubis
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tx for postpartum hem
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uterine massage, if fails, oxytocin
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typical antibiotics for group B strep prophylaxis
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IV penicillin or ampicillin
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term for heaving bleeding during and between menstrual periods
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menometrorrhagia
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cause of amenorrhea with normal prolactin, no response to estrogen-progesterone challenge, history D&C
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Asherman's syndrome
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indications for med tx of ectopic preg
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stable, unruptured ectopic of <3.5cm at <6wks gestation
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med options for endometriosis
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OCPs, danazol, GnRH agonists
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lap findings in endometriosis
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chocolate cysts, powder burns
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most common location of ectopic preg
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ampulla of oviduct
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patient has increased vaginal discharge and petechial patches in upper vagina and cervix
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trichomonas vaginitis
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most common cause of bloody nipple discharge
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intraductal papilloma
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breast malignancy presenting as itching, burning and erosion of nipple
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Paget's
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annual screening for women with strong fm history of ovarian cancer
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CA-125 and transvaginal US
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30 year old has unpredictable urine loss...med options?
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anticholinergics (oxybutynin) or beta-adrenergics (metaproterenol) for urge incontinence
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most common cause of female infertility
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endometriosis
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two consecutive findings of atypical squamous cells of undet significance on pap...f/u?
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colposcopy and endocervical curettage
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breast cancer type that increases future risk of invasive carcinoma in both breasts
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lobular carcinoma in situ
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five thoracic causes of immediate death
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tension pneumo, cardiac tamponade, open pneumo, massive hemothorax and airway obstruction
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always suspect aortic disruption with...
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scapular, sternal or first and second rib fractures
CXR: widened mediastinum (>8cm), loss of aortic knob, pleural cap, deviation of trachia and esophagus to the right, depression of left main stem bronchus get CT or TEE before surgery aortography is gold standard |
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asystole
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give epinephrine and atropine
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v-fib or v-tach
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desyn shock then epi then shock then amio or lidocaine then shock then epi
if stable, amiodarone vasopressin can be given in place of 1st or 2nd dose of epi |
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pulseless electrical activity
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give epi and atropine
causes: hypovolemia, hypoxia, acidosis, hyper/hypokalemia, hypothermia, tablets, tamponade, thromobosis |
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emergent SVT
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unstable: electrical cardioversion
stable: control rate with maneuvers (valsalva, carotid sinus massage or cold stimulus) if resistant to maneuvers: adenosine |
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a-fib/flutter tx (ER)
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unstable: shock at 100J
stable: rate control with diltiazem or beta blockers, convert rhythm (<48 elect or chemical, >48 need to anticoagulate or do TEE) dont give nodal blockers if pt has WPW |
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bradycardia (ER)
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symptomatic: atropine and consider dopamine, epi or glucagon
if mobitz II or 3rd degree block present, place transvenous pacemaker |
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suspect smoke inhalation in...
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singed nose hairs, facial burns, hoarseness, wheezing or carbonaceous sputum
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fevers before POD 3 are unlikely to be infectious unless...
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clostridium or beta-hemolytic streptococci are involved
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CATCH 22
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cardiac abnormalities
abnormal facies thymic aplasia cleft palate hypocalcemia 22q11 deletion |
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tetralogy of fallot
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pulmonary stenosis, RVH, overriding aorta and VSD
most common cyanotic congenital heart disease in children risk factors: maternal PKU and CATCH 22 syndromes "tet spells" - hypoxemic episodes...children often squat for relief (increases systemic vascular resistance) CXR: "boot shaped" heart with decreased pulmonary vascular markings...EKG with right-axis deviation |
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breast bud dev age
testicular enlargment age |
breast bud dev: btw 8 and 13 years
testicular enlargement btw 9 and 11 years |
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Trisomy 21
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Downs
a/w duodenal atresia, Hirschsprung's and congenital heart disease (most common malformation is AV canal, which includes an ASD and VSD with mitral and tricuspid valve abnormalities 2/2 endocardial cushion defects) increased risk of ALL and early onset Alzheimer's, increased risk for atlantoaxial (C1-C2) instability |
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Edward's Syndrome
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Trisomy 18
severe MR, rocker-bottom feet, low-set ears, micrognathia, clenched hands and prominent occiput a/w congenital heart disease, may have horseshoe kidneys death usually occurs within one year of birth |
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Patau's syndrome
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Trisomy 13
severe MR, microphthalmia, microcephaly, cleft lip/palate, abnormal forebrain structures (holoprosencephaly), "punched out" scalp lesions and polydacyly a/w congenital heart disease death usually occurs within one year of birth |
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Klinefelter's
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45, XXY
inactivated X chromosome (Barr body) one of most common causes of hypogonadism in males presents with testicular atrophy; eunuchoid body shape; tall, long extremities; gynecomastia and female hair distributions |
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Turner's
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45, XO
most common cause of primary amenorrhea no barr body short stature, webbed neck, ovarian dysgenesis and coarctation of aorta...lymphedema of hands and feet in neonatal period may have horseshoe kidney buccal smear helpful normally Turners is 45 XO, but if 45 XY with turners, increased risk of gonadoblastoma - needs prophylactic bilateral gonadectomy |
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Phenylketonuria
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decreased phenylalanine hydroxylase or decreased tetrahydrobiopterin cofactor
screened for at birth - valid only after baby has had protein meal tyrosine becomes essential and phenylalanine builds up excess phenyl ketones MR, fair skin, eczema and a musty or mousy urine odor blonde-haired, blue-eyed infants a/w increased heart disease tx: decreased phenylalanine and increased tyrosine in diet, if mom with PKU wants to become pregnant, must restrict diet before conception |
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Fragile X syndrome
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an x-linked defect affecting the methylation and expression of FMR1 gene
second most common cause of genetic mental retardation presents with macro-orchidism; long face with large jaw; large everted ears and autism triplet repeat disorder that may show genetic anticipation |
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Fabry's
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x-linked recessive
deficiency of alpha-galactosidase A leads to accumulation of ceramide trihexoside in heart, brain and kidneys...renal failure and increased risk of stroke and MI |
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Krabbe's dz
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autosomal recessive
NO galactosylceramide and galactoside (due to galactosylceramidase deficiency) leads to accumulation of galactocerebroside in brain optic atrophy, spasticity and early death |
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Gaucher's dz
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AR
deficiency of glucocerebrosidase leads to glucocerebroside accumulation in the brain, liver, spleen and bone marrow (Gaucher's cells have characteristic "crinkled paper" enlarged cytoplasm) may have hepatosplenomegaly, anemia and thrombocytopenia type I more compatible with life...does not affect brain |
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Niemann-Pick dz
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AR
deficiency of sphingomyelinase which leads to buildup of sphingomyelin cholesterol in reticuloendothelial and parenchymal cells and tissues patients with type A die by age of 3 |
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Tay Sachs dz
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TAY SAX LACKS HEXOSAMINIDASE
no hexosaminidase leads to GM2 ganglioside accumulation, may appear nl until 3-6 months of age, weakness begins and development slows exaggerated startle response, death by age 3 cherry red spot on macula carrier rate is 1/30 Jews of European descent |
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Metachromatic leukodystrophy
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AR
deficiency of arylsulfatase A, accumulation of sulfatide in the brain, kidney, liver and peripheral nerves |
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Hurler's syndrome
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AR
def of alpha-L-iduronidase leads to corneal clouding and MR |
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Hunter's syndrome
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X-linked recessive (hunters need to see...no corneal clouding...to aim at the X.
def of iduronate sulfatase, milder form of Hurler's with no corneal clouding and mild MR |
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cystic fibrosis
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autosomal recessive
mutation in CFTR gene (chloride channel) on chromosome 7 with widespread exocrine gland dysfunction 15% infants have meconium ileus, other GI symptoms include greasy stools and flatulence, pancreatitis, rectal prolapse, esophageal varices and biliary cirrhosis other sym: type 2 DM, "salty taste", male infertility and unexplained hyponatremia at risk for fat-soluble vitamin def (vit A, D, E and K) 2/2 malabsorption...may have bleeding symptoms with vit K def |
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B cell deficiencies (peds)
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most common 50%
typicall present AFTER 6 months of age with recurrent sinopulmonary, GI and UTIs with encapsulated organisms (H flu, Strep pneumo, N. meningitidis); treat with IVIG X-linked agammaglobulinemia (Brutons), common variable immunodeficiency and IgA def |
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T cell def (peds)
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tends to present earlier (1-3 months) with opportunistic and low-grade fungal, viral and intracellular bacterial infections
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phagocytic def (peds)
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mucous mem infections, abscesses and poor wound healing
infections with catalase + organisms (staph aureus), fungi and gram - enteric org |
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X-linked agamma-globulinemia (Brutons)
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b cell deficiency only in boys
infections with encapsulated pseudomonas, strep pneumo and h. flu dx/tx: quantitative immunoglobulin levels; if low confirm with B and T cell subsets (no b cells, t cells often high) absent tonsils and other lymphoid tissues may be a clue tx with prophylactic antibodies and IVIG |
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common variable immunodeficiency
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immunoglobulin levels drop in 20s and 30s, usually combined B and T cell defect
increase pyogenic upper and lower respiratory infections; increased risk of lymphoma and autoimmune disease dx/tx: quantitative Ig levels; confirm with B and T cell subsets; treat with IVIG |
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IgA deficiency
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mild, the most common immunodeficiency
usually asymptomatic, recurrent infections anaphylactic transfusion rxt due to anti-IgA antibodies is a common presentation sinopulmonary and GI (giardia) - consequence of IgA's role in mucosal barrier protection dx: quantitative IgA levels; tx infections |
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Thymic aplasia (DiGeorge)
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cardiac, abnl facies, thymic aplasia, cleft palate, hypocalcemia and 22q11 del
defect in dev of 3rd/4th pharyngeal pouch, low set ears, anomolies of great vessels can present with tetany 2/2 hypocalcemia in first days of life way increased risk of infections with fungi and PCP dx: abs lymphocyte count, mitogen stim response, delayed hypersensitivity skin testing tx: bone marrow transplant and IVIG, PCP prophylaxis, thymus transplantation |
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Ataxia telangiectasia
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combined B and T cell messed up
oculocutaneous telangiectasias and progressive cerebellar ataxia - caused by DNA repair defect increased incidence of non-Hodgkin's lymphoma, leukemia and gastric carcinoma no spec tx; may require IVIG, depending on severity of Ig deficiency |
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Severe combined immunodeficiency (SCID)
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severe lack of B and T cells - adenosine deaminase deficiency
severe, frequent bacterial infections, chronic candidiasis and opportunistic infections tx with bone marrow transplant or stem cell transplant, IVIG...NEEDS PCP PROPHYLAXIS |
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Wiskott-Aldrich syndrome
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x-linked
(think twins at CHOC) less severe T and B cell dysfunction ECZEMA, increased IgE/IgA, decreased IgM and THROMBOCYTOPENIA classic presentation: bleeding, eczema and recurrent otitis media very increased risk of atopic disorders, lymphoma/leukemia and infection from strep pneu, staph aureus and H flu type b supportive tx, if severe, bone marrow transplant |
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Chronic Granulomatous Disease
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phagocytic defect
x-linked (2/3) or AR (1/3) with deficient superoxide production by PMNs and macrophages (mutation which causes loss or inactivation of NADPH oxidase) anemia, lymphadenopathy and hypergammaglobulinemia intracellular killing is deficient chronic skin, pulmonary, GI and UTIs; osteomyelitis and hepatitis infecting organisms are catalase +, increased risk of infection with aspergillus; may have granulomas of the skin and GI/GU tracts gm stain neutrophils filled with bacteria dx: abs neutrophil count with neutrophil assays NITROBLUE TETRAZOLIUM TEST treat with DAILY TMP-SMX IFN-gamma can decrease incidence of serious infection; poss bone marrow transplant and gene therapy |
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newborm with omphalitis with delayed separation of umbilical cord
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leukocyte adhesion deficiency
defect in chemotaxis of leukocytes recurrent skin, mucosal and pulmonary infections no pus with minimal inflammation in wounds (due to chemotaxis defect); high WBCs in blood; bone marrow transplant is curative |
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Chediak-Higashi syndrome
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phagocytic defect
AR d/o...defect in neutrophil chemotaxis THIS INCLUDES OCULOCUTANEOUS ALBINISM, NEUROPATHY AND NEUTROPENIA waaaay increased incidence of overwhelming infections with strep pyogenes, staph aureus and pseudomonas bone marrow is tx of choice |
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complement deficiencies
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present in children with congenital asplenia or splenic dysfunction (sickle cell disease)...recurrent bacterial infections with encapsulated organisms
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C1 esterase deficiency
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hereditary angioedema
AD d/o with recurrent episodes of angioedema lasting 2-72 hrs and provoked by stress or trauma can be life threatening if have airway edema dx/tx: total hemolytic complement to assess quantity and function of complement...purified C1 esterase and FFP can be used prior to surgery |
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Terminal complement def (C5-C9)
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inability to form membrane attack complex
recurrent meningococcal or gonococcal infections; rarely lupus or glomerulonephritis give men vaccine and app antibxs |
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conjunctivitis, rash, adenopathy, strawberry tongue, hands and feet (red, swollen, flaky skin) and fever > 40 for > 5 days
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KAWASAKI.
tx with high dose aspirin and IVIG (to prevent aneurysms) low dose aspirin is then continued, usually for 6 weeks (may use corticosteroids in IVIG refractory cases, not routinely used) |
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avoid live vaccines in immunocompromised and pregnant pts...
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live vaccine: oral polio vaccine, varicella, MMR
(exception: may give MMR and varicella in HIV peeps) |
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Croup
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3 months to 3 years
acute viral inflammatory disease, primarily subglottic space parainfluenza 1 (most common), 2 and 3, RSV; influenza and adenovirus bacterial superinfection may progress to tracheitis hx: prodromal URI symptoms, low-grade fever, mild dyspnea, inspiratory stridor that worsens with agitation, hoarse voice and characteristic barking cough (usually at night) dx: CLASSIC STEEPLE SIGN FROM SUBGLOTTIC NARROWING - not sens or spec may need nebulized RACEMIC EPINEPHRINE! |
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Epiglottitis
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supraglottic infection
used to be H. flu, now strep pneumo, nontypable H flu and viral agents CAN BE LIFE THREATENING hx: acute-onset high fever, dysphagia, drooling, muffled voice, insp retractions, cyanosis and soft stridor pts sit with neck hyperextended and chin protruding, leaning forward must secure airway before looking in!! will see cherry red swollen epiglottis and arytenoids thumbprint sign TRUE EMERGENCY - endotracheal intubation or tracheostomy and IV antibiotics (ceftriaxone or cefuroxime) |
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most common organisms in childhood bact meningitis
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Strep pneumo, N. meningitidis (will give petechial rash) and E. coli
(enteroviruses are most common agents in viral meningitis - all ages, risk factors are sinofacial infections, trauma and sepsis) can give empiric tx: ceftriaxone, vancomycin and ampicillin neonates should get ampicillin and cefotaxime or gentamycin older: ceftriaxone and vanco |
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erythema infectiosum (5th disease)
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parvovirus B19
fever absent or low grade slapped cheek, erythematous, pruritic, maculopapular rash starts on arms and spreads to trunk and legs, WORSENS WITH FEVER AND SUN EXPOSURE complications: arthritis, hemolytic anemia, encephalopathy, congenital infection a/w fetal hydrops and death aplastic crisis may be precipitated in children with increased RBC turnover (sickle cell anemia, hereditary spherocytosis) or in those with decreased RBC production (severe iron def) |
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measles
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paramyxovirus
prodrome: low grade fever with cough, coryza and conjunctivitis...koplik's spots on buccal mucosa rash: head towards feet complications: otitis media, pneumonia, laryngotracheitis, subacute sclerosing panencephalitis |
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Rubella
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prodrome: asymptomatic...
rash: also starts on face and goes downwards; in contrast with pts with measles, rubella often have low grade fever and do not seem ill |
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Roseola
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HHV 6 (herpes)!
prodrome: acute onset of high fever, no other symptoms for 3-4 days rash: MACULOPAPULAR RASH APPEARS AS FEVER BREAKS, begins on trunk and spreads to face and extremities comp: FEBRILE SEIZURES |
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Hand-foot-and-mouth disease
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Coxsackie A
oral ulcers, maculopapular vesicular rash on hands and feet, sometimes on buttocks |
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duodenal atresia
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completel or partial failure of the duodenal lumen to recanalize during gestational weeks 8-10
polyhydramnios in utero; bilious emesis within hours after first feeding; a/w Down syndrome and other cardiac/GI abnormalities (like annular pancreas, malrotation and imperforate anus) double bubble sign surgery to repair |
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AML can present with a chloroma
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-- greenish soft-tissue tumor of the skin or spinal cord
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neuroblastoma
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embryonal tumor of neural crest origin
<1year old...70% have distant mets at presentation a/w neurofibromatosis, Hirschsprung's and N-myc oncogene NONTENDER abd mass (may cross midline), horners syndrome, HTN or cord compression (from paraspinal tumor) elevated 24 hr urinary catecholamines (VMA and HVA) |
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Wilms tumor
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renal tumor of embryonal origin, 2-5 years old
a/w Beckwith Wiedemann syndrome (hemihypertrophy, macroglossia, visceromegaly), neurofibromatosis and WAGR (wilms, aniridia, GU and MR) ASYMPTOMATIC, NONTENDER, smooth abd mass abd pain, fever, HTN and microscopic/gross hematuria are seen |
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Ewing's sarcoma
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neuroectodermal origin...from bone
mostly in Caucasian male adolescents a/w chrom 11:22 translocation local pain and swelling commonly target midshaft of long bones - femur, pelvis, fibula and humerus (descen order) systemic stuff: fever, anorexia, fatigue LYTIC BONE LESION (ONION SKIN IF TUMOR PENETRATES THROUGH CORTEX) |
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"sunburst" lytic bone lesions
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osteosarcoma - from osteoblasts of mesenchymal origin
male adolescents systemic symptoms are RARE (as compared with Ewings) METAPHYSES OF LONG BONES (ewings is midshaft)...distal femur, proximal tibia and proximal humerus...mets to lungs in 20% pts increased LDH is worse prognosis increaed alk phosp |
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most common type of tracheoesophageal fistula
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esophageal atresia with distal TEF (85%)...cannot pass NG tube
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not contraindications to vaccines
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mild illness and/or low grade fever, current antibiotic therapy and prematurity
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neonate has meconium ileus
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CF or Hirschsprung's
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bilious emesis within hours after first feeding
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duodenal atresia
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infant has high fever and onset of rash as fever breaks...babys at risk for what?
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febrile seizures (roseola infantum)
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chronic resp infections, nitroblue tetrazolium test is positive
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chronic granulomatous disease
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child has eczema, thrombocytopenia and high levels of IgA
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Wiskott-Aldrich syndrome
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4 month old infant has life-threatening Pseudomonas infection
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bruton's x-linked agammaglobulinemia
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sudden onsent of mental status changes, emesis and liver dysfunction after taking aspirin
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Reye's syndrome
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child has loss of red light reflex...
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suspect retinoblastoma
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vaccines at 6 month visit
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HBV, DTaP, IPV, PCV
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cause of neonatal RDS
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surfactant deficiency
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red "currant jelly" stools
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intussusception
|
|
congenital heart disease that causes secondary HTN
|
coarctation of the aorta
|
|
first line tx for otitis media
|
amoxicillin x 10 days
|
|
most common pathogen causing croup
|
parainfluenza virus 1
|
|
homeless child small for his age, peeling skin and swollen belly
|
Kwashiorkor
|
|
defect in x-linked syndrome with MR, gout, self mutilation and choreoathetosis
|
Lesch-Nyhan syndrome (purine salvage problem with HGPRTase deficiency)
|
|
machinery murmur in newbord
|
PDA
|
|
farmer's lung
|
spores of actinomycetes from moldy hay
|
|
bird fancier's lung
|
antigens from feathers, excreta, serum
|
|
mushroom worker's lung
|
spores of actinomycetes from compost
|
|
malt worker's lung
|
spores of Aspergillus clavatus in grain
|
|
Grain handler's lung
|
grain weevil dust
|
|
Bagassosis
|
spores of actinomycetes from sugarcane
|
|
Air condition lung
|
spores of actinomycetes from air conditioners
|
|
Asbestosis
|
work involving SHIPBUILDING, tile or brake linings, insulation, construction...presents 15-20yrs after initial exposure
CXR: linear opacities of lung bases and interstitial fibrosis, CALCIFIED PLEURAL PLAQUES indicative of benign pleural disease comp: increased risk of mesothelioma (rare) and lung cancer; risk of lung cancer is higher in smokers |
|
Coal mine disease
|
CXR: small nodular opacities (<1cm) in upper lung zones; restrictive lung disease
progressive massive fibrosis |
|
Silicosis
|
works in mines or quarries with glass, pottery or silica
CXR: small (<1cm) nodular opacities in upper lung zones; EGGSHELL CALCIFICATIONS restrictive lung disease increased risk of TB, annual skin test progressive massive fibrosis |
|
Berylliosis
|
work in high-tech fields such as aerospace, nuclear and electronic plants; ceramic industries; foundries; plating facilities; dental material sites, dye manufacturing
CXR: diffuse infiltrates, hilar adenopathy requires chronic steroid treatments |
|
usual interstitial pneumonia
|
most common form of interstital pneumonia
|
|
causes of obstructive pulmonary disease
|
asthma, bronchiectasis, cystic fibrosis and tracheal or bronchial obstruction
|
|
asthma
|
REVERSIBLE airway obstruction 2/2 bronchial hyperreactivity, airway inflammation, mucous plugging and SM hypertrophy
peak flow is diminished; FEV/FVC is decreased, residual volume and TLC increased CXR: hyperinflation methacholine challenge: test for bronchial hyperresponsiveness; useful when PFTs are normal |
|
Isoproterenol
|
nonspecific beta agonist
relaxes bronchial SM (beta 2); tachycardia (beta 1) is an adverse effect |
|
beta 2 agonists
|
albuterol: relaxes bronchial SM, used in acute attacks
Salmeterol: long acting agent for prophylaxis |
|
methylxanthines
|
Theophylline
likely causes bronchodilation by inhibiting phosphodiesterase, thereby decreasing cAMP hydrolysis usage is limited due to narrow therapeutic index (cardiotoxicity and neurotoxicity) |
|
Ipratropium
|
muscarinic antagonists
competitive block of muscarinic receptors, prevents bronchoconstriction |
|
Cromolyn
|
prevents release of mediators from mast cells; useful for exercise-induced bronchospasm, effective only in prophylaxis of asthma; not effective during an acute asthmatic attach...toxicity is rare
|
|
Beclomethasone
|
corticosteroid used in asthma
inhibits synthesis of virtually all cytokines; inactivate NF-kB, transcription factor that induces production of TNF-alpha, among other inflammatory agents inhaled corticosteroids are first line tx for long term control of asthma |
|
Zileuton
Zafirlukast |
antileukotrienes
zileuton: 5-lipoxygenase pathway inhibitor; blocks conversion of arachidonic acid to leukotrienes zafirlukast: blocks leukotriene receptors |
|
Bronchiectasis
|
DILATION OF BRONCHI, permanent fibrosis, remodeling...caused by cycles of infection and inflammation of bronchi/bronchioles...
hx: cough with frequent bouts of yellow or green sputum production...a/w hx of pulm infections (pseudo, h flu and TB), and lots of other stuff... CXR: TRAM LINES (parallel lines outlining dilated bronchi as a result of peribronchial inflammation and fibrosis), increased bronchovascular markings and HONEYCOMBING high res CT: DILATED AIRWAYS...and ballooned cysts at end of bronchus |
|
Chronic bronchitis
|
productive cough for > 3 months per year for 2 consecutive years
BLUE BLOATER - PRODUCTIVE COUGH, cyanosis with mild dyspnea; pts often overweight with peripheral edema...barrel chest, use of acc chest muscles, JVD, end-exp WHEEZING or muffled breath sounds |
|
Emphysema
|
terminal airway destruction and dilation that may be due to SMOKING (centrilobular) or to alpha-1-antitrypsin deficiency (panlobular)
PINK PUFFER - dyspnea, pursed lips, thin wasted appearance parenchymal bullae or subpleural blebs |
|
an increased A-a gradient indicates...
|
V/Q mismatch or a diffusion impairment.
(random...in hypercapnic pts, increase minute ventilation...if give more O2, may suppress hypoxic resp drive) |
|
ARDS
|
ACUTE ONSET, ratio PaO2/FiO2 < 200, diffuse infiltration, swan ganz wedge pressure < 18mmHg (non-cardiogenic pulm edema)
2/2 endothelial injury, common causes are sepsis, pneumonia, aspiration, multiple blood transfusions, inhaled/ingested toxins and trauma...overall mortality is 30-40% minimize injury induced by mechanical ventilation by ventilating with low tidal volumes...use PEEP to recruit collapsed alveoli and titrate PEEP and FiO2 to achieve adequate oxygenation |
|
pulmonary HTN
|
mean pulmonary art pressure > 25mmHg (nl 15mmHg)
causes: left sided heart failure, mitral valve disease, congenital heart disease with L to R shunt, hypoxic vasoconstriction (2/2 chronic lung disease), increased resistance in pulm veins, thromboembolic disease...remodeling 2/2 structural lung disease loud, palpable S2 (often split)...systolic ejection murmur, S4 or parasternal heave |
|
CXR for PE
|
may show atelectasis, pleural effusion...HAMPTONS HUMP: wedge shaped infarct, WESTERMARKS SIGN: oligemia in embolized lung zone
|
|
EKG in PE
|
not diagnostic, sinus tach
classic triad of S1Q3T3 - acute right heart strain with an S wave in lead I, a Q wave in lead III and inverted T in III - uncommon! |
|
lung nodules...char favoring malignancy
|
age > 45-50; smoking history, history of malignancy, new or larger lesions, absence of calcifications or irregular calcifications, > 2cm, irregular margins
|
|
Characteristics favoring benign lung nodule
|
age < 35, no change from old films, central/uniform/laminated/popcorn calcifications, size < 2cm, smooth margins
|
|
lung cancer NOT associated with smoking
|
bronchoalveolar carcinoma
(an adenocarcinoma) |
|
small cell lung cancer
|
highly correlated with cigarette exposure
central location neuroendocrine origin; a/w paraneoplastic syndromes commonly presents with mets (intrathoracic and extrathoracic sites such as brain, liver and bone) paraneoplastic processes a/w small cell lung cancer: Cushing's (ACTH), SIADH leading to hyponatremia, peripheral neuropathy, subacute cerebellar degeneration, myasthenia (eaton-lambert syndrome) |
|
non small cell lung cancer
|
less propensity to metastasize
paraneoplastic: hypertrophic pulmonary osteoarthropathy, digital clubbing |
|
adenocarinoma of the lung
|
MOST COMMON TYPE OF LUNG CANCER
PERIPHERAL location includes bronchoalveolar carcinoma which is a/w multiple nodules, interstitial infiltration and prolifer sputum production paraneo: thrombophlebitis, nonbacterial verrucous endocarditis, hypercoagulability |
|
squamous cell carcinoma of the lung
|
central location; 98% are in smokers
paraneoplastic: HYPERCALCEMIA (PTHrP) |
|
large cell/neuroendocrine carcinomas of the lung
|
least common; a/w poor prognosis
a/w gynecomastia |
|
lung cancer can present with...
|
Horner's: miosis, ptosis and anhidrosis in patients with Pancoast's tumor at apex of the lung
superior vena cava syndrome: obstruction of SVC with supraclavicular venous engorgement Hoarseness: due to recurrent laryngeal nerve involvement Paraneoplastic syndromes |
|
tx of small cell lung cancer
|
unresectable
chemotherapy is mainstay of tx. usually metastasized at time of diagnosis |
|
tx of non-small cell lung cancer
|
surgical resection in early stages (IA, IB, IIA, IIB and poss IIIA)
supplement surgery with radiation and chemo palliation for symptomatic but unresectable disease |
|
causes of transudate pleural effusion
|
CHF, cirrhosis or nephrotic syndrome
(increased pulm cap wedge pressure, dec oncotic pressure) |
|
exudative pleural effusion
|
causes: pneumonia (parapneumonic effusion), TB, malignancy, pulmonary embolism, collagen vascular disease (RA, SLE), pancreatitis, trauma
2/2 increased pleural vascular permeability ratio of pleural to serum protein is >0.5 ratio of pleural to serum LDH is >0.6 pleural fluid LDH is more than 2/3 of upper normal limit of serum LDH |
|
parapneumonic effusion
|
complicated in setting of + gram stain or culture OR pH < 7.2 OR a glucose level of <60
presence of PUS indicates an EMPYEMA |
|
primary spontaneous pneumothorax
|
due to rupture of subpleural apical blebs
usually found in tall, thin young males |
|
secondary pneumothorax
|
due to COPD, TB, trauma, PCP and iatrogenic factors (thoracentesis, subclavian line placement, positive pressure mechanical ventilation, bronchoscopy)
|
|
tension pneumo
|
pulmonary or chest wall defect that acts as a one-way valve, drawing air into the pleural space including penetrating trauma, infection and positive pressure mechanical ventilation
immediate needle decompression (2nd intercostal space at midclavicular line), then chest tube presents with respiratory distress, falling O2 sats, hypotension, distended neck veins and tracheal deviation |
|
normalizing PCO2 in patient with asthma exacerbation
|
fatigue and impending respiratory failure
|
|
dyspnea, lateral hilar lymphodenopathy on CXR, noncaseating granulomas, increased ACE and hypercalcemia
|
sarcoidosis
|
|
honeycomb pattern on CXR
|
diffuse interstitial pulmonary fibrosis; supportive care, steroids may help
|
|
treatment for SVC syndrome
|
radiation
|
|
tall white male presents with acute shortness of breath
|
spontaneous pneumothorax, spontaneous regression, supplemental O2 may be helpful
|
|
hypoxemia and pulmonary edema with normal pulmonary cap wedge pressure
|
ARDS
|
|
increased risk of what infection with silicosis?
|
TB
|
|
classic CXR findings for pulmonary edema
|
cardiomegaly, prominent pulmonary vessels, Kerley B lines, 'bats-wing' appearance of hilar shadows and perivascular and peribronchial cuffing
|
|
causes of hyperkalemia
|
1. spurious: hemolysis of blood samples, fist clenching in blood draws, rhabdo
2. decreased excretion - renal insufficiciency, drugs (spironolactone, triamterene, ACEIs, trimethoprin, NSAIDs, mineralocorticoid def/type IV RTA) 3. cellular shifts: tissue injury, insulin deficiency, acidosis, drugs (succinylcholine, digitalis, arginine, beta blockers) |
|
hx of hyperkalemia
|
N/V, intesintal colic, areflexia, weakness, flaccid paralysis and paresthesias
|
|
EKG: peaked T waves, PR prolongation, wide QRS and loss of P waves
can progress to sine waves, ventricular fibrillation and cardiac arrest |
HYPERKALEMIA, biotch.
|
|
tx of hyperkalemia
|
C BIG K
calcium gluconate!!! (for cardiac cell membrane stabilization) bicarbonate and/or insulin + glucose to temporarily shift potassium into cells kayexalate and loop diuretics to remove potassium from the body beta agonists - promotes cellular reuptake of potassium |
|
causes of hypokalemia
|
1. transcellular shifts - insulin, beta 2 agonists, alkalosis, familial hypokalemic periodic paralysis
2. GI losses - diarrhea, chronic laxative abuse, vomiting, NG suction 3. renal losses - diuretics (loop or thiazide), primary mineralocorticoid excess or secondary hyperaldosteronism, decreased circulating volume, Bartter's syndrome, drugs (eg gentamycin, amphotericin), DKA, hypomagnesemia, type I RTA (defective distal H+ secretion) consider RTA in setting of metabolic acidosis |
|
hx of hypokalemia
|
muscle weakness, cramps, fatigue, hyporeflexia, paresthesias, rhabdomyolysis and ascending paralysis
|
|
EKG- T wave flattening, U wave (additional wave after the T wave) and ST segment depression can lead to AV block and subsequent cardiac arrest
|
hypokalemia
|
|
tx of hypokalemia
|
replete K and also magnesium - as hypomagnesia complicates potassium repletion
|
|
cause of hypercalcemia
|
calcium supplementation, hyperparathyroidism, iatrogenic (thiazides), immobility, milk-alkali syndrome, paget's disease, addisons disease/acromegaly, neoplasm, zollinger-ellison syndrome (MEN 1), excess vitamin A, excess vitamin D, sarcoidosis
(can see short QT with hypercalcemia) |
|
abd muscle cramps, dyspnea, tetany, perioral and acral paresthesias and convulsions
|
hypocalcemia
Chvostek's sign - tapping of facial nerve Trousseau's sign - carpal spasm after arterial occlusion of BP cuff may show PROLONGED QT INTERVAL... |
|
causes of increased anion gap
|
methanol.
uremia. DKA. Paraldehyde. Intoxication. Lactic acidosis. Ethylene glycol. Salicylates. if normal anion gap: diarrhea, glue sniffing, RTA or hyperchloremia |
|
early aspirin ingestion can cause...
|
respiratory alkalosis
|
|
causes of metabolic alkalosis with compensation
|
vomiting, diuretic use, antacid use or hyperaldosteronism
|
|
renal tubular acidosis
|
net decrease in either tubular H+ secretion or HCO3- reabsorption that leads to a NON-ANION GAP METABOLIC ACIDOSIS
three main types of RTA, type IV (distal) is the MOST COMMON FORM!!! |
|
type I RTA
|
distal - defect in H+ secretion
etiologies: hereditary, amphotericin, cirrhosis, autoimmune disorders, sickle cell disease and lithium Tx: potassium citrate complications: nephrolithiasis |
|
type II (proximal) RTA
|
defect in HCO3- resorption
etiologies: hereditary, carbonic anhydrase inhibitors, Fanconi's syndrome, MM Tx: potassium citrate Complications: rickets, osteomalacia |
|
Type IV (distal) RTA
|
defect is aldosterone deficiency or resistance leads to defects in sodium reabsorption and H+/K+ excretion
etiologies: hyporeninemic hypoaldosteronism; chronic kidney disease from DM, HTN and HIV tx: furosemide, fludrocortisone, and low potassium diet in pts with aldosterone def complications: hyperkalemia |
|
acute interstitial nephritis
|
fever, arthralgias, and a pruritic, erythematous rash...methicillin is the classic association
|
|
FeNa < 1%, Urine sodium < 20, urine specific gravity > 1.020 or a BUN/Creatinine ratio > 20 suggest...
|
pre-renal etiology of acute renal failure
|
|
indications for urgent dialysis
|
acidosis
electrolyte abnormalities (hyperkalemia) ingestions - salicylates, theophylline, methanol, barbiturates, lithium, ethylene glycol overload - fluid uremic symptoms - pericarditis, encephalopathy, bleeding, nausea, pruritis and myoclonus |
|
hyaline casts (urine sediment)
|
normal finding, but increased amount suggests volume depletion
prerenal |
|
red cell casts, dysmorphic red cells
|
glomerulonephritis
intrinsic renal disease |
|
white cells, eosinophils
(urine sediment) |
allergic interstitial nephritis, atheroembolic disease
intrinsic |
|
granular casts, renal tubular cells, "muddy-brown cast"
|
ATN
intrinsic |
|
white cells, white cell casts
|
pyelonephritis
postrenal etiology |
|
carbonic anhydrase inhibitor
|
acetazolamide
acts on proximal convuluted tubule mech: inhibits carbonic anhydrase, increases H+ reabsorption, blocks Na/H exchange side effects: hyperchloremic metabolic acidosis, sulfa allergy |
|
osmotic agents
(ie. mannitol, urea) |
acts on entire tubule
increases tubular fluid osmolarity side effects: pulmonary edema 2/2 CHF and anuria |
|
Loop agents
(furosemide, ethacrynic acid, bumetanide, torsemide) |
acts on ascending loop of henle
inhibits Na/K/Cl transporter side effects: water loss, metabolic alkalosis, decreases potassium, decreases calcium, OTOTOXICITY, sulfa allergy (not ethacrynic acid - hyperuricemia) |
|
thiazide agents
(HCTZ, chlorothiazide) |
acts on distal convoluted tubule
inhibits Na/Cl transporter side effects: water loss, metabolic alkalosis, decreases sodium, decreases potassium, increases glucose, increases CALCIUM, increases uric acid, sulfa allergy, pancreatitis |
|
K sparing agents
|
spironolactone, triamterene, amiloride
acts on cortical collecting tubule mech: aldosterone receptor antagonist (spironolactone) blocks sodium channels (triamterene, amiloride) side effects: metabolic acidosis, increases potassium, antiandrogenic effects - including gynecomastia (spironolactone) |
|
nephritic syndrome in general
|
d/o of glomerular inflammation, aka glomerulonephritis
classic findings: oliguria, macroscopic/microscopic hematuria (smoky-brown urine), HTN and EDEMA!!! (may have small amt of proteinuria) pts have decreased GFR with elevated BUN and creatinine; measure complement, ANA, ANCA and anti-GBM antibody levels... tx: HTN, fluid overload and uremia; corticosteroids are useful in reducing glomerular inflammation in some cases |
|
nephrotic syndrome in general
|
PROTEINURIA (> 3.5 g/day), generalized EDEMA, HYPOALBUMINEMIA and HYPERLIPIDEMIA
about 1/3 cases from systemic diseases like DM, SLE or amyloidosis hx: generalized edema, FOAMY URINE, increased susceptibility to infection and predisposition to hypercoagulable states...increased risk of venous thrombosis and pulmonary embolism tx: protein and salt restriction, ACE inhibitors decrease proteinuria and diminish progression... vaccinate with 23-polyvalent pneumococcus vaccine (PPV23) - patients at increased risk of Strep pneumo |
|
list of causes of nephritic syndrome
|
Immune complex - postinfectious glomerulonephritis, IgA nephropathy (Berger's dz)
Pauci immune - Wegener's granulomatosis Anti-GBM disease - Goodpasture's syndrome and Alport's syndrome |
|
list of causes of nephrotic syndrome
|
minimal change, focal segmental glomerular sclerosis, membranous nephropathy, diabetic nephropathy, lupus nephritis, renal amyloidosis, membranoproliferative nephropathy
|
|
post infectious glomerulonephritis
|
NEPHRITIC
a/w recent group A beta hemolytic streptococcal infection (within 2 weeks) hx: oliguria, edema, HTN, smoky brown urine LOW SERUM C3!!!!, increased ASO titer, lumpy-bumpy immunofluorescence |
|
IgA nephropathy (Berger's disease)
|
MOST COMMON TYPE
NEPHRITIC a/w upper resp or GI infections, commonly seen in young men; may be seen in HSP episodic gross hematuria or persistent microscopic hematuria NORMAL C3 tx: glucocorticoids for select pts, ACEIs in pts with proteinuria 20% progress to ESRD |
|
Wegener's granulomatosis
|
NEPHRITIC (pauci-immune)
granulomatous inflammation of the respiratory tract and kidney with necrotizing vasculitis hx: fever, weight loss, hematuria, hearing disturbances, resp and sinus symptoms, cavitary pulmonary lesions bleed and lead to HEMOPTYSIS C-ANCA!!! (cell mediated immune response)...renal biopsy shows segmental necrotizing glomerulonephritis with few immunoglobulin deposits on immuno-fluorescence tx: high dose corticosteroids and cytotoxic agents; pts have frequent relapses |
|
Goodpasture's
|
Nephritic
Anti-GBM disease glomerulonephritis with pulmonary hemorrhage; peak incidence in men in their mid-20s HEMOPTYSIS, dyspnea, possible resp failure LINEAR ANTI-GBM DEPOSITS on immunofluorescence; iron def anemia; hemosiderin-filled macrophages in sputum; pulm infiltrates on CXR tx: plasma exchange tx, pulsed steroids, may progress to ESRD |
|
Alport's syndrome
|
nephritic
hereditary glomerulonephritis; presents in boys 5-20 yrs of age asymptomatic hematuria a/w NERVE DEAFNESS and eye disorders GBM splitting on EM tx: progresses to renal failure; anti-GBM nephritis may recur s/p transplant |
|
minimal change disease
|
most common nephrotic syn in children, idiopathic, 2' causes include NSAIDs and hematologic malignancies
tendency towards infections and thrombotic events light mic is NORMAL EM: FUSION of EPITHELIAL FOOT PROCESSES with lipid laden renal cortices tx: steroids - excellent prognosis |
|
focal segmental glomerular sclerosis
|
nephritic
idiopathic, IV drug use, HIV infection, obesity typical pt is young black male with uncontrolled HTN microscopic hematuria; biopsy - sclerosis in capillary tufts tx: prednisone, cytotoxic tx |
|
most common nephropathy in caucasian adults
|
MEMBRANOUS NEPHROPATHY
2' causes includes solid tumor malignancies (esp in pts > 60 yrs old) and immune complex disease a/w HBV, syphilis, malaria and gold SPIKE AND DOME 2/2 granular deposits of IgG and C3 at BM tx: prednisone and cytotoxic therapy for severe disease |
|
Kimmelstiel-Wilson lesions
increased mesangial matrix |
diabetic nephropathy
two forms: diffuse hyalinization and nodular glomerulosclerosis long standing, poorly controlled DM with evidence of retionpathy or neuropathy tx: tight control of blood sugars; ACEIs for type I and ARBs for type 2 |
|
Lupus nephritis
|
WHO types I-IV
both nephrotic and nephritic severity of renal disease often determines overall prognosis... proteinuria or RBCs on UA ma be found during evaluation of SLE patients mesangial proliferation, subendothelial immune complex deposition tx: prednisone and cytotoxic therapy may decrease disease progression |
|
Renal amyloidosis
|
primary (plasma cell dyscrasias) and secondary (infectious or inflammatory) are most common
pts with MM or chronic inflam dz (RA, TB) CONGO RED STAIN; APPLE GREEN birefringence under polarized light tx: prednisone and melphalan; bone marrow transplant may be used for MM |
|
membranoproliferative nephropathy
|
a/w HCV, dammit!!! cryoglobulinemia, lupus and subacute bacterial endocarditis
slow progression to renal failure TRAM TRACK, double layered BM; type I has subendothelial deposits and mesangial deposits; all three types have low serum C3 tx: corticosteroids and cytotoxic agents may help |
|
calcium oxalate/calcium phosphate stones
|
most common stones (most common are calcium oxalate)
etiology: idiopathic hypercalciuria, elevated urine acid 2/2 to diet and 1' hyperparathyroidism, alkaline urine radiopaque! tx: hydration and thiazide diuretic |
|
Struvite stones
|
9%
triple phosphate stones a/w urease-producing organisms (Proteus, Klebsiella), form staghorn calculi, alkaline urine, radiopaque, increased ammonia tx: hydration, tx UTI if present |
|
Uric acid stones
|
7%
a/w gout and high purine turnover states acidic urine (pH < 5.5) RADIOLUCENT (cannot see on x-ray) tx: hydration, alkalinize urine with citrate, which is converted to HCO3 in the liver; dietary purine restriction and allopurinol |
|
Cystine stones
|
least common
hexagonal crystals 2/2 defect in renal transport of certain amino acids (COLA - cystine, ornithine, lysine and arginine) HEXAGONAL CRYSTALS radiopaque tx: hydration, alkalinize urine, penicillamine |
|
AR PCKD
|
less common but more severe
infants and young children with renal failure, liver fibrosis and portal hypertension; may lead to death in first few years of life |
|
AD PCKD
|
most common
starts to be sympt > 30 yrs old a/w increased risk of cerebral aneurysm, especially in pts with + fm history extrarenal complications: hepatic cysts, valvular heart disease, colonic diverticula, abd wall and ing hernia hx: PAIN AND HEMATURIA, other findings - HTN, hepatic cysts, cerebral berry aneurysms, diverticulosis and mitral valve prolapse |
|
cryptorchidism
|
failure of testes to descend into scrotum
prematurity is a huge risk factor bilateral cryptorchidism is a/w oligospermia and infertility tx: orchiopexy after age one (in all but 1% of males, testes will descend by that age) but before age 5 (to preserve fertility) if discovered later, tx with orchiectomy to avoid risk of testicular cancer |
|
risk factors for erectile dysfunction
|
DM, atherosclerosis, meds (beta-blockers, SSRIs), HTN, heart disease, surgery or radiation for prostate cancer and spinal cord injury
|
|
tx of erectile dysfunction
|
Sildenafil (Viagra), Vardenafil (Levitra) and Tadalafil (Cialis)
phosphodiesterase-5 inhibitors that prolong action of cGMP-mediated SM relaxation and increase blood flow in the corpora cavernosa...effective but contraindicated in pts taking nitroglycerin testosterone is useful for pts with hypogonadism of testicular or pituitary origin; discouraged for pts with normal testosterone levels |
|
tx of BPH
|
medical therapy with alpha-blockers (terazosin) and 5-alpha-reductase inhibitors (finasteride) to reduce mild to moderate symptoms
TURP (transurethral resection of the prostate) or open prostatectomy for pts with moderate to severe symptoms |
|
major side effect of alpha blockers (for BPH)
|
orthostatic hypotension
|
|
leading causes of cancer death in men
|
1. lung cancer
2. prostate cancer 3. colorectal cancer 4. pancreatic cancer 5. leukemia |
|
tx of metastatic prostate cancer
|
androgen ablation (eg. GnRH agonists, orchiectomy, flutamide) and chemotherapy
|
|
differential for hematuria
|
strictures, stones, infection, inflammation, infarction, tumor, trauma and TB
|
|
lets talk about bladder cancer
|
most frequent malignant tumor of urinary tract
transitional cell carcinoma risk factors: smoking, diets rich in meat and fat, schistosomiasis, chronic tx with cyclophosphamide and exposure to aniline dyes (benzene derivative) hx: GROSS HEMATURIA - most common presenting symptom dx: CYSTOSCOPY WITH BX IS DIAGNOSTIC..IVP tx: depends on extent of spread beyond the bladder mucosa... superficial cancers: complete transurethral resection or intravesicular chemo with mitomycin C or BCG (TB vaccine) |
|
renal cell carinoma...whhhatt.
|
adenocarcinoma from tubular epithelial cells
tumors can spread along renal vein to the IVC and can metastasize to lung and bone risk factors: male gender, smoking, obesity, acquired cystic kidney disease in ESRD and von Hippel-Lindau disease |
|
classic triad of RCC
|
hematuria, flank pain and palpable flank mass
many have fever...varicocele is common ANEMIA IS COMMON AT PRESENTATION, BUT POLYCYTHEMIA 2/2 increased EPO production may be seen in 5-10% pts |
|
testicular cancer shiznit.
|
95% derive from germ cells and virtually all are malignant
cryptorchidism a/w increased risk of neoplasm in both testes Klinefelter's also risk factor most common malignancy in men 25-34 hx: painless enlargement of testes seminomas peak b/t 40-50yo |
|
beta-hCG in test. cancer
|
always elevated in choriocarcinoma and elevated in 10% seminomas
|
|
alpha-fetoprotein in test. cancer
|
often elevated in nonseminomatous germ cell tumors, particularly endodermal sinus (yolk sac) tumors
|
|
testicular seminomas
|
exquisitely radiosensitive and also respond to chemotherapy
(platinum based chemo for nonseminomatous germ cell tumors) |
|
renal tubular acidosis a/w abnormal H+ secretion and nephrolithiasis
|
Type I (distal) RTA
|
|
RTA a/w abnormal HCO3 and rickets
|
Type II (proximal) RTA
|
|
RTA a/w aldosterone defect
|
Type IV (distal) RTA
|
|
"doughy skin"
|
hypernatremia
|
|
differential of hypervolemic hyponatremia
|
cirrhosis, CHF, nephritic syndrome
|
|
most common causes of hypercalcemia
|
malignancy and hyperparathyroidism
|
|
hematuria, hypertension and oliguria
|
nephritic syndrome
|
|
proteinuria, hypoalbuminemia, hyperlipidemia, hyperlipiduria and edema
|
nephrotic syndrome
|
|
presence of red cell casts in urine sediment
|
glomerulonephritis/nephritic syndrome
|
|
waxy casts in urine sediment and Maltese crosses (seen with lipiduria)
|
nephrotic syndrome
|
|
drowsiness, asterixis, nausea and pericardial friction rub
|
uremic syndrome seen in pts with renal failure
|
|
low urine specific gravity in presence of high serum osmolality
|
DI
|
|
testicular cancer a/w beta-hCG and alpha fetoprotein
|
choriocarcinoma
|
|
salicylate ingestion - what type of acid-base d/o?
|
anion gap acidosis and primary respiratory alkalosis due to central respiratory stimulation
|
|
acid-base disturbance commonly seen in pregnant women
|
respiratory alkalosis
|
|
three systemic diseases that lead to nephrotic syndrome
|
DM, SLE and amyloidosis
|
|
elevated EPO, elevated Hct and normal O2 sats suggest?
|
RCC or other EPO-producing tumor; evaluate with CT scan
|
|
L4 nerve root
|
motor: foot dorsiflexion (tibialis anterior)
reflex: patellar sensory: medial aspect of lower leg |
|
L5 nerve root
|
motor: big toe dorsiflexion (extensor hallucis longus), foot eversion (peroneu muscles)
no reflex a/w L5 sensory: dorsum of the foot and lateral aspect of the lower leg |
|
S1 nerve root
|
Motor: plantar flexion (gastrocnemius/soleus), gluteus maximus (hip extension)
Reflex: achilles Sensory: plantar and lateral aspects of the foot |
|
most common spot for Herniated Disk
|
L4-L5 and L5-S1
|
|
cauda equina syndrome
|
bowel or bladder dysfunction (urinary overflow incontinence), impotence and saddle-area anesthesia
surgical emergency!! |
|
spinal stenosis
|
usually 2/2 degenerative joint disease
leg cramping worse at rest, with standing and with walking (pseudo or neurogenic claudication) symptoms improve with flexion at the hips and bending forward if refractory to med tx, may do surgical laminectomy - achieves significant short term success, but many have recurrence of symptoms |
|
anterior dislocation of the shoulder
|
most common
AXILLARY ARTERY AND NERVE are at risk patients hold arm in external rotation tx: reduction followed by sling and swath; recurrent dislocations may need surgical repair |
|
posterior dislocation of the shoulder
|
a/w seizure and electrocusions
can injure RADIAL ARTERY pts hold arm in internal rotation |
|
posterior hip dislocation
|
MOST COMMON!! (>90%)
occurs via posteriorly directed force on an internally rotated, flexed, adducted hip (dashboard injury) a/w risk of sciatic nerve injury and avascular necrosis tx: closed reduction followed by abduction pillow/bracing...evaluate with CT scan after reduction |
|
anterior hip dislocation
|
not that common
can injury obturator nerve |
|
Colles' fracture
|
distal radius...fall on outstretched hand...dorsally displaced, dorsally angulated fracture
tx: closed reduction by application of long-arm cast open reduction if fracture is intra-articular |
|
Scaphoid (carpal navicular) fracture
|
MOST COMMONLY FRACTURED CARPAL BONE
may take two weeks for radiographs to show fracture... assume fracture if tenderness in ANATOMICAL SNUFF BOX tx: thumb spica cast; if displacement or navicular nonunion present - tx with open reduction (if displacement) with proximal 3rd scaphoid fractures, AVN may result from disruption of blood flow |
|
boxer's fracture
|
5th metacarpal neck fracture
2/2 trauma of closed fist tx: closed reduction with ulnar gutter splint; percutaneous pinning if fracture is excessively angulated if skin is broken - assume infection by human oral pathogens...surgical irrigation, debridement and IV antibiotics (covering Eikenella) |
|
Humerus fracture
|
RADIAL NERVE PALSY - wrist drop and loss of thumb abduction
tx: hanging arm cast vs. coaptation splint and sling functional bracing |
|
Nightstick fracture
|
ulnar shaft fracture resulting from self defense
tx: open reduction and internal fixation (ORIF) if significanly displaced |
|
Monteggia's fracture
|
diaphyseal fracture of proximal ulna with subluxation or radial head
tx: ORIF of the shaft fracture (due to poor fracture diaphyseal blood supply) and closed reduction of radial head |
|
Galeazzi's fracture
|
diaphyseal fracture of radias with dislocation of distal radioulnar joint
from direct blow to radius tx: ORIF of radius and casting of fracture forearm in supination to reduce distal radioulnar joint |
|
hip fracture
|
increased risk with osteoporosis...presents with shortened and externally rotated leg
DISPLACED FEMORAL NECK FRACTURES: a/w increased risk of AVN, nonunion and DVTs tx: ORIF with parallel pinning of femoral neck; displaced fractures in elderly pts ma require hip hemiarthroplasty anticoagulate to decrease likelihood of DVTs |
|
femoral fracture
|
direct trauma...beware of fat emboli - fever, change in mental status, dyspnea, hypoxia, petechiae and decreased platelets
tx: intramedullary nailing of the femur; irrigate and debride open fractures |
|
achilles tendon rupture
|
sudden "pop" like a rifle shot; more likely with decreased physical deconditioning
exam: limited plantar flexion and a + Thompson's test (pressure on the gastrocnemius leads to absent foot plantar flexion) tx: surgically followed by long leg cast for 6 weeks |
|
ACL injury
|
results from noncontact twisting mechanism, forced hyperextension or impact to an extended knee, + anterior drawer and Lachman tests; r/o meniscal or MCL injury
tx: generally surgical with graft from patellar or hamstring tendons |
|
PCL injury
|
from forced hyperextension
+ posterior drawer test tx: operative for highly competitive athletes |
|
Meniscal tears
|
from acute twisting injury or degenerative tear in elderly pts
clicking or locking may be present joint line tenderness and + McMurray's test operative for younger pts with significant tears or older pts whose symptoms did not respond to conservative management |
|
Nursemaid's elbow
|
radial head subluxation that typically occurs as a result of being pulled or lifted by the hand
presents with pain and refusal to bend the elbow tx: manual reduction by gentle supination of the elbow at 90 degrees of flexion; no immobilization |
|
Supracondylar humerus fracture
|
tends to occur at 5-8 yrs old
proximity to brachial artery increases risk of Volkmann's contracture (results from compartment syndrome of the forearm) tx: cast immobilization; closed reduction with percutaneous pinning if significantly displaced |
|
Osgood-Schlatter dz
|
overuse apophysitis of tibial tubercle, localized pain, especially with quadriceps contraction, in active young boys
tx: decrease activity for 2-3 months or until asymptomatic; neoprene brace may provide symptomatic relief |
|
salter-harris fracture
|
fractures of growth plates in children
5 different types types III-V: surgical repair to prevent complications such as leg length inequality |
|
Developmental dysplasia of the hip
|
aka: congenital hip dislocation
can result in subluxed, dislocatable or dislocated femoral heads...can lead to early degenerative joint disease of the hips dislocations result from poor development of the acetabulum and hip 2/2 lax musculature and EXCESSIVE UTERINE PACKING in the flexed and adducted position (eg. breech presentation) --> excessive stretching of the posterior hip capsule and adductor muscle contracture |
|
History of developmental dysplasia of hips
|
FIRST BORN FEMALES in BREECH POSITION
|
|
Barlow's maneuver
|
DDH
pressure placed on inner aspect of abducted thigh and hip is then adducted - audible "clunk" as femoral head dislocates posteriorly |
|
Ortolani's maneuver
|
thighs are gently abducted from midline with ant pressure on greater trochanter...SOFT CLICK signifies reduction of femoral head into acetabulum
|
|
other stuff with DHH (rando)
|
Allis (Galeazzi's) sign: knees are at unequal heights when hips and knees are flexed (dislocated side is lower)
Asymmetric skin folds and limited abduction of the affected hip |
|
Tx of DDH
|
early detection is critical
u/s may be helpful, esp after 10 weeks of age radiographs unreliable until pts > 4months because of radiolucency of neonatal femoral head < 6months: splint with PAVLIK HARNESS (maintains hip flexed and abducted)...dont flex hips >60 degrees to prevent AVN 6-15months: spica cast 15-24 months: open reduction followed by spica cast complications: joint contractures and AVN of femoral head without tx, significant defect is likely in patients < 2 yrs of age |
|
Legg-Calve Perthes Disease
|
idiopathic AVN of the femoral head
most commonly in boys 4-10yo usually self-limited with symptoms lasting < 18 months history/PE: asymptomatic at first, but pts can develop painless limp; if there is pain - groin or anterior thigh, or referred to the knee LIMITED ABDUCTION AND INTERNAL ROTATION, atrophy of affected leg; usually unilateral - 85-90% tx: OBSERVATION if limited femoral head involvement or full ROM if extensive or decrease ROM - consider bracing, petrie cast or an osteotomy prognosis good if pt < 5yo and has full ROM, decreased fem head involvement and stable joint |
|
Slipped Capital Femoral Epiphysis (SCFE)
|
separation of proximal femoral epiphysis through growth plate --> medial and posterior displacement of femoral head (relative to femoral neck)
may be 2/2 imbalance btw growth hormone and sex hormones risk factors: obesity, age, 11-13 yrs old, male gender and african american ethnicity a/w hypothyroidism hx: acute or insidious THIGH or KNEE PAIN and a PAINFUL LIMP acute cases present with restricted ROM and commonly INABILITY TO BEAR WEIGHT bilateral in 40-50% cases limited internal rotation and abduction of hip...on flexion of hip, obligatory external rotation 2/2 physical displacement...further loss of internal rotation with hip flexion Dx: BOTH hips in AP and FROG-LEG LATERAL VIEWS reveal POSTERIOR AND MEDIAL DISPLACEMENT of femoral heads r/o hypothroidism with TSH tx: no weight bearing; gentle closed reduction in acute slips ext fixation - surgical pinning where it lays...lesseens risk of AVN and chondrolysis complications: ANV of fem head, chondrolysis and premature hip osteoarthritis --> hip arthroplasty |
|
Osteosarcoma
|
2nd most common primary malignant tumor of bone (1st is MM)
METAPHYSEAL areas of DISTAL FEMUR, PROXIMAL TIBIA and proximal humerus...often mets to lungs some cases preceeded by Paget's; risk factors include male gender and age 20-30 presents as progressive and eventually intractable PAIN THAT IS WORSE AT NIGHT dx: CODMANS TRIANGLE (periosteal new bone fmt at diaphyseal end of lesion) SUNBURST PATTERN of osteosarcoma (Ewing's has onion skinng) tx: limb sparing surgical procedures and pre/post-op chemo (methotrexate, doxorubicin, cisplatin and ifosfamide), may need amputation |
|
Colchicine
|
inhibits chemotaxis and is most effective when used early during a gout flare (use is limited by a narrow therapeutic window)
|
|
causes of hyperuricemia
|
increased cell turnover (hemolysis, blast crisis, tumor lysis, myelodysplasia, psoriasis)
cyclosporine, dehydration, diabetes insipidus, diet (increased red meat, alcohol), diuretics, lead poisoning, Lesch Nyhan syndrome, salicylates (low dose), starvation |
|
Reactive arthritis
|
Reiter's syndrome
disease of young men, characteristic arthritis, uveitis, conjunctivitis and urethritis... usuall follows infection with Campylobacter, Shigella, Salmonella, Chlamydia or Ureaplasma |
|
ank spon
|
HLA B27
tx: NSAIDs (indomethacin) or for refractory cases - tumor necrosis factor inhibitors may have anterior uveitis and heart block |
|
dermatomyositis
|
may have heliotrope rash, "shawl sign" - rash involving shoulders, upper chest and back, Gottron's papules - papular rash with scales located on the dorsa of the hands, over bony prominences
|
|
Felty's syndrome
|
RA, splenomegaly and neutropenia
|
|
Rheumatoid Arthritis
|
chronic, destructive inflammatory arthritis with SYMMETRIC involvement of both large and small joints...causes synovial hypertrophy and pannus formation...leads to erosion of adjacent cartilage, bone and tendons...
risk factors: female, age 35-50 and HLA-DR4!! hx: insidious onset of morning stiffness for > 1 hr with painful, warm swelling of multiple symmetric joints wrists, MCP and PIP joints)... ulnar deviation BAKERS CYSTS (palpable popliteal mass), vasculitis, atlantoaxial subluxation, carpal tunnel syndrome, rheumatoid nodules, keratoconjunctivitis sicca, pulm nodules, inflam endocarditis |
|
tx of RA
|
NSAIDS - reduced or d/c'ed if tx successful with DMARDS (disease modifying antirheumatic drugs)
DMARDS should be started early...first line are hydroxychloroquine, sulfasalazine, methotrexate and azithioprine...2nd line include rituximab (anti-CD20) and leflunomide |
|
anticentromere antibodies
|
CREST
|
|
anti-Scl 70 antibodies
|
a/w with poor prognosis of scleroderma
|
|
CREST
|
calcinosis, Raynaud's, esophageal dysmotility, sclerodactyly and telangiectasias
(diffuse form - pulmonary fibrosis) can tx Raynaud's with calcium channel blockers mortality 2/2 pulmonary hypertension and complications of pulmonary HTN |
|
criteria for SLE
|
DOPAMINE RASH
discoid rash, oral ulcers, photosensitivity, arthritis, malar rash, immunologic criteria, neurologic symptoms (lupus cerebritis, seizures), elevated ESR, renal disease, + ANA, serositis, hematologic abnormalities |
|
anti-ds DNA and anti-Sm antibodies
|
LUPUS
|
|
+ antihistone antibodies
|
drug induced SLE
|
|
neonatal SLE
|
+ anti-Ro antibodies
|
|
drugs that cause a lupus syndrome
|
chlorpromazine, hydralazine, INH, methyldopa, penicillamine, procainamide, quinidine
|
|
hip and back pain along with stiffness that improves with activity over the course of the day and worsens at rest
|
suspect ankylosing spondylitis
check HLA-B27 |
|
arthritis, conjunctivitis and urethritis in young men...dx?
associated organisms? |
Reactive (reiter's) arthritis
a/w Campylobacter, Shigella, Salmonella, Chlamydia and Ureaplasma |
|
active 13 year old boy with anterior knee pain...
|
Osgood Schlatter disease
|
|
complication of scaphoid fracture
|
avascular necrosis
|
|
signs of radial nerve damage
|
wrist drop, loss of thumb abduction
|
|
first born female who was born in breech position found to have asymmetric skin folds on her newborn exam...whats up?
|
developmental dysplasia of the hip
if severe, consider a Pavlik harness to maintain abduction |
|
11 year old obese, African American boy presents with sudden onset of limp...dx, w/u?
|
slipped capital femoral epiphyses
AP and frog-leg lateral view |
|
most common primary malignant tumor of bone
|
multiple myeloma
|
|
pemphigus
|
pemphigus vulgaris
intraepidermal blister that leads to widespread painful erosions MUCOUS MEMBRANE antibodies against desmoglein molecules responsible for keratinocyte adherence leading to loss of cellular attachment MIDDLE AGED (40-60) + Nikolsky's sign ACANTHOLYIS - intraepidermal split with free-floating keratinocytes in blister |
|
Bullous pemphigoid
|
separation at epidermal BM
60-80 years old antibodies against bullous pemphigoid antigen, superficially in BM zone BLISTERS ARE STABLE - roof consists of nearly normal epidermis IgG and C3 at dermal-epidermal junctions autoantibodies against BM glycoproteins BP230 and BP 180 - Nikolsky's sign mucous membranes NOT involved |
|
HSV 1
|
oral labial lesions
primary: typically presents in infancy with widespread, severe herpetic gingivostomatitis with oral erosions |
|
HSV 2
|
genital lesions
often presents in adults with bilateral, erosive vesicular lesions with edema and lymphadenopathy |
|
verrucae (warts)
|
many different types of HPV
usually benign, some subtypes of HPV (especially 16 and 18) can lead to squamous malignancies cauliflower like...grows downward dx: acetowhitening... tx: destruction of tissue by curettage, cryotherapy or acid keratolytics... genital warts tx locally with podophyllin, trichloroacetic acid, imiquimod or 5-FU |
|
Pityrosporum orbiculare
|
yeast that causes Tinea Versicolor
normal on skin...pathogenic type called Malassezia furfur KOH preparation of scale that reveals "spaghetti and meatballs" pattern of hyphae and spores tx: selenium sulfide daily for one week, followed by application once weekly for prophylaxis |
|
pyrethrin
|
aka: RID
tx of head and pubic lice |
|
Scabies
|
Sarcoptes scabiei - tiny arthropod mates on skin surface
female digs passage into stratum corneum and lays eggs...burrowing leads to pruritis... hx: intense pruritis especially at night; hands, axillae and genitals...exam: mite's track can sometimes be seen along with erythematous, excoriated papules Tx: 1-2 applications of PERMETHRIN oral IVERMECTIN also effective... pruritis may persist for two weeks after treatment...symptomatic tx should be used after this |
|
Lichen planus
|
violaceous, flat-topped, polygonal papules
may have Wickham's striae (white stripes), especially on mucous membranes Koebner's phenomenon - lesions that appear at the site of trauma...initially on genitalia histology: "lichenoid pattern" - band of T lymphocytes at the epidermal-dermal junction with damage to the basal layer tx: mild cases with corticosteroids P disease: planar, purple, pruritic, persistent, polygonal, penile, perioral, puzzling and Koebner's phenomenon |
|
"christmas tree pattern"
|
Pityriasis Rosea
acute dermatitis that is pink and scaly etiology unknown, may be due to viral infection with human herpesvirus 7 (HHV7) HERALD PATCH "cigarette paper" asymptomatic...heal without tx in 2-3 weeks...can use skin lubrication, topical antipruritics and systemic antihistamines |
|
class of drugs that may cause syndrome of muscle rigidity, hyperthermia, autonomic instability and EPS
|
antipsychotics (neuroleptic malignant syndrome)
|
|
side effects of corticosteroids
|
acute mania, immunosuppression, thin skin, osteoporosis, easy bruising, myopathies
|
|
treatment for DTs
|
benzodiazepines
|
|
tx for acetaminophen OD
|
N-acetylcysteine
|
|
Tx for opiod overdose
|
Naloxone
|
|
Tx for benzo overdose
|
Flumazenil
|
|
Tx for neuroleptic malignant syndrome
|
Dantrolene or bromocriptine
|
|
Tx for malignant hypertension
|
nitroprusside
|
|
Tx of AF
|
rate control rhythm conversion and anticoagulation
|
|
Tx of SVT
|
if stable, rate control with carotid massage or other vagal stimulation...if unsuccessful, consider adenosine
|
|
causes of drug induced SLE
|
INH, penicillamine, hydralazine, procainamide, chlorpromazine, methyldopa and quinidine
|
|
blood in the urethral meatus or high-riding prostate
|
bladder rupture or urethral injury
|
|
test to rule out urethral injury
|
retrograde cystourethrogram
|
|
radiologic evidence of aortic rupture or dissection
|
widened mediastinum (>8cm), loss of aortic knob, pleural cap, tracheal deviation to the right, depression of left main stem bronchus
|
|
acceptable urine output in trauma pt
|
50cc/hr
|
|
acceptable urine output in stable patient
|
30cc/hr
|
|
cannon "a" waves
|
third degree heart block
|
|
signs of neurogenic shock
|
hypotension and bradycardia
|
|
signs of increased ICP
|
Cushings triad...
hypertension, bradycardia and abnormal respirations |
|
decreased CO, decreased pulmonary capillary wedge pressure, increased peripheral vascular resistance
|
hypovolemic shock
|
|
increased CO, decreased PCWP, decreased PVR
|
septic or anaphylactic shock
|
|
tx of cardiogenic shock
|
identify cause; pressors (eg dopamine)
|
|
tx of anaphylactic shock
|
diphenhydramine or epinephrine 1:1000
|
|
supportive tx for ARDS
|
continuous positive airway pressure
|
|
signs of air embolism
|
pt with chest trauma who was previously stable suddenly dies
|
|
trauma series
|
AP chest, AP/lateral C-spine, AP pelvis
|
|
4 D's of posterior circulation strokes
|
Diplopia
Dizziness Dysphagia Dysarthria |
|
MCA strokes
|
aphasia (dominant hemisphere), neglect (nondominant hemisphere), contralateral paresis and sensory loss in the FACE and ARM, gaze preference toward the side of the lesion, homonymous hemianopia
|
|
ACA stroke
|
contralateral paresis and sensory loss in the LEG, amnesia, personality changes, foot drop, gait dysfunction, cognitive changes
|
|
PCA stroke
|
homonymous hemianopia, memory deficits, dyslexia/alexia
|
|
Basilar artery stroke
|
coma, "locked in" syndrome, cranial nerve palsies, apnea, visual crap, drop attacks, dysphagia, dysarthria, vertigo, "crossed" weakness and sensory loss affecting the ipsilateral face and contralateral body
|
|
neuro deficients in polio and Werdnig Hoffman
|
LMN lesions only 2/2 destruction of anterior horns; flaccid paralysis
|
|
multiple sclerosis
|
demyelination
scanning speech, intention tremor and nystagmus |
|
ALS
|
combined upper and lower motor neuron lesions with no sensory deficits
|
|
tabes dorsalis
|
tertiary syphilis
degeneration of dorsal roots and dorsal columns; impaired proprioception, locomotor ataxia |
|
subarachnoid hemorrhages
|
2/2 trauma, berry aneurysms, AVM or trauma in circle of willis (often at the MCA)
|
|
hx of subarachnoid hemorrhage
|
acute onset, intensely painful "thunderclap" headache often followed by neck stiffness
may have had sentinel bleed days to weeks earlier marked by HA, neck stiffness and N/V 2/2 leaking aneurysm LP if CT - to look for RBCs, xanthochromia (yellowish CSF due to breakdown of RBCs), increased protein from RBCs and increased ICP |
|
tx of subarachnoid hemorrhage
|
prevent rebleeding, keep SBP <150
prevent vasospasm and associated neurologic deterioration by giving calcium channel blockers, IV fluids and pressors to maintain BP give phenytoin for seizure prophylaxis decrease ICP (CN III palsy with pupil involvement is a/w Berry aneurysms) |
|
subdural hematomas
|
typically follows head trauma leading to rupture of bridging veins and accumulation of blood btw dura and arachnoid membranes...common in elderly and alcoholics
hx: headache, changes in mental status, contralateral hemiparesis and ipsilateral pupillary dilation CT: Crescent shaped, concave hyperdensity that does NOT cross suture midline tx: surgical evacuation if symptomatic |
|
epidural hematomas
|
usually 2/2 lateral skull fracture --> tear of middle meningeal artery
hx: immediate loss of consciousness leads to a lucid interval (minutes to hours) then to a coma with hemiparesis...ultimately a "blown pupil" (watch out for impending brain stem compression)... CT: lens-shaped CONVEX hyperdensity limited by sutures |
|
Tx of migraine headaches
|
abortive therapy: triptans - 1st line, metoclopramide; consider symptomatic tx for nausea
prophylactic: beta-blockers (propranolol), TCAs (amitriptyline), CCBs and valproic acid |
|
tx of cluster HA
|
acute: high flow O2, ergots, sumatriptans, intranasal lidocaine, corticosteroids
prophylactic: ergots, CCBs, prednisone, lithium, valproic acid and topiramate |
|
Lambert-Eaton Myasthenic Syndrome
|
small cell lung carcinoma risk factor (60%)
Dx: repetitive nerve stimulation shows incremental response, autoantibodies to presynaptic calcium channels and a chest CT indicative of lung neoplasm Tx: tx small cell lung carcinoma; tumor resection may reverse symptoms; Guanidine hydrochloride is mainstay of tx; anticholinesterases may also improve symptoms |
|
scanning speech, intranuclear ophthalmoplegia and nystagmus
|
MS
|
|
MS
|
can have optic neuritis (painful loss of vision)
Lhermittes sign may be present - sharp pain traveling up and down neck with flexion MRI: multiple, asymmetric, periventricular white matter lesions (Dawsons fingers), esp in corpus callosum increase IgG in CSF tx: steroids, avonex/rebif (interferon alpha), betaseron (interferon alpha 1b) and copaxone (copolymer 1) mitoxantrone... alt tx: cyclophosphamide, IVIG and plasmapharesis symptomatic therapy: baclofen for spasticity, cholinergics for urinary retention, anti-cholinergics for urinary incontinenct or amitriptyline for painful paresthesias glatiramer acetate - suppresses T-cells against myelin |
|
ropinirole or pramipexole
|
dopamine agonists
side effect of pramipexole: uncontrolled gambling |
|
selegiline
|
MAO-B inhibitor...may be neuroprotective and may decrease need for levodopa
|
|
Dural tails
|
meningioma
from dura mater or arachnoid |
|
Medulloblastoma
|
primitive neuroectodermal tumor
common in children arises from 4th ventricle and increases ICP HIGHLY MALIGNANT; may seed the subarachnoid space posterior vermis sign - truncal dystaxia |
|
Neurofibromatosis 1
|
AD, chromosome 17
aka: von Recklinghausen's syndrome cafe au lait spots, freckling in axillary or inguinal area, optic glioma, two lisch nodules (pigmented iris hamartomas), bone abnormality, first degree relative with NF1 clinically evident by age 15 |
|
NF 2
|
AD, chromosome 22
BILATERAL ACOUSTIC NEUROMAS first degree relative with NF2 unilateral acoustic neuromas neurofibromas, meningiomas, gliomas or schwannomas seizures, skin nodules, cafe au lait spots clinically evident by age 20 |
|
tuberous sclerosis
|
AD
convulsive seizures, "ash leaf" hypopigmented lesions, MR sebaceous adenomas (small red nodules on nose and cheeks in butterfly shapes) shagreen patch (rough papule in lumbosacral region with an orange-peel consistency) two retinal lesions: mulberry tumors and phakomas (round, flat, gray lesions) lots of systems can be involved...CHF from rhabdomyoma...renal involvement may include hamartomas, angiomyolipomas or rarely, RCC head CT: calcified tubers within cerebrum in the periventricular area renal CT: angiomyolipomas (causing cystic or fibrous pulmonary changes) |
|
Brocas
|
d/o of language production, including writing with intact comprehension
posterior inferior frontal gyrus is messed...often 2/2 left superior MCA stroke impaired repetition, frustration, arm and face hemiparesis |
|
Wernickes
|
d/o of language comprehension with intact yet nonsensical production
sensory aphasia left posterior superior temporal (perisylvian) lobe...2/2 inferior/posterior MCA preserved fluency, impaired repitition and comprehension..."word salad"...lack of awareness... may have right upper homonymous quadrantanopia 2/2 involvement of Meyer's loop |
|
Locked in syndrome
|
pts awake and alert but can move only eyes and eyelids
a/w central pontine myelinolysis, brain stem stroke and advanced ALS |
|
persistent vegatative state
|
normal sleep-wake cycles but lack of awareness of self or the environment
most commonly caused by trauma with diffuse cortical injury or hypoxic ischmic injury |
|
Wernicke's encephalopathy
|
encephalopathy, ophthalmoplegia (nystagmus, lateral rectus palsy, conjugate gaze palsy) and ataxia
pts: alcoholics, hyperemesis, starvation, renal dialysis and AIDS can be elicited by high dose glucose administration |
|
closed angle glaucoma
|
risk factors: PUPILLARY DILATION (prolonged time in darkened area, stress, meds), anterior uveitis and lens dislocation
hx: presents with EXTREME PAIN and blurred vision HARD, RED EYE seen...pupil dilated and nonreactive to light MEDICAL EMERGENCY that may lead to blindness...need to decrease intraocular pressure with acetazolamide and then pilocarpine...laser iridotomy |
|
open angle glaucoma
|
risk factors: age > 40, african american ethnicity, diabetes and myopia
hx/PE: initially asymptomatic; frequent lens changes...defect in peripheral visual fields...CUPPING of optic disk almost always bilateral dx: tonometry, look at optic nerve...diseased trabecular meshwork that obstructs proper drainage of the eye...gradulal loss of vision...tunnel vision tx: frequent optho exams...topical beta blockers - timolol, betaxolol to decrease aqueous humor production or with pilocarpine to increase aqueous outflow can use carbonic anhydrase inhibitors... |
|
Central retinal artery occlusion
|
sudden, painless unilateral blindness...cherry-red spot on the fovea, retinal swelling and retinal arteries that may appear bloodless
tx: THROMBOLYSIS within 8 hrs of symptom onset...decrease intraocular pressure through drainage of anterior chamber...may use IV acetazolamide to improve retinal perfusion...if no tx, may have retinal infarction and permanent blindess may result |
|
Central retinal vein occlusion
|
subacute monocular visula loss..."blood and thunder", cotton wool spots...edema/optic disk swelling...dilated veins
tx: laser photocoagulation has variable results |
|
most common primary sources of mets to the brain
|
lung, breast, skin (melanoma), kidney and GI tract
|
|
most common cause of seizures in children (2-10yo)
|
infection, febrile seizures, trauma and idiopathic
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most common cause of seizures in adults (18-35)
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trauma, alcohol withdrawal and brain tumor
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Kluver-Bucy syndrome (amygdala)
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hyperphagia, hypersexuality, hyperorality and hyperdocility
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SSRIs
(fluoxetine, sertraline, paroxetine, citalopram, escitalopram) |
indications: depression and anxiety; first line for generalized anxiety disorder, OCD and PTSD
side effects: nausea, GI upset, somnolence, sexual dysfunction, tremor, diarrhea, and agitation SEROTONIN SYNDROME: if SSRIs are used with MAOIs - fever, myoclonus, mental status changes, cardiovascular collapse |
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buspirone
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indications: generalized anxiety disorder, OCD and PTSD
side effects: seizures with chronic use, no tolerance, dependence or withdrawal |
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TCA toxicity
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convulsions, coma and cardiac arrythmias
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Atypicals (for psych)
Buproprion, venlafaxine, Mirtazapine, Nefazodone and Trazodone |
indications: depression, anxiety and chronic pain
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side effect of Bupropion
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decreased seizure threshold; minimal sexual side effects; CONTRAINDICATED IN BULIMICS
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side effects of venlafaxine
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diastolic hypertension
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side effect of Mirtazapine
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atypical
weight gain, sedation |
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side effects of Nefazodone
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atypical
sedation, HA and dry mouth |
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side effects of Trazodone
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aytpical
highly sedating, priapism |
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TCAs
nortriptyline, desipramine, amitriptyline and imipramine |
indications: depression, anxiety disorder, chronic pain, migraine and enuresis (imipramine)
side effects: LETHAL with OD owing to cardiac arrhythmias...monitor for 3-4 days in the ICU after OD ANTICHOLINERGIC EFFECTS - dry mouth, constipation, urinary retention and sedation |
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phenelzine and tranylcypromine
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MAOIs
indication: depression, especially atypical Side effects - hypertensive crisis if taken with high-TYRAMINE foods (cheese, red wine) sexual side effects, orthostatic hypotension, weight gain |
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chronic lithium use...
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hypothyroidism and nephrotoxicity
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lamotrigine can lead to a...
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life threatening skin rash
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Typical antipsychotics
haloperidol, droperidol, fluphenazine, thioridazine, chlorpromazine |
indications: psychotic d/o, acute agitation, acute mania and Tourette's syndrome
side effects: EPS!!! HYPERPROLACTINEMIA ANTICHOLINERGIC EFFECTS - drug mouth, urinary retention and constipation seizures, hypotension, sedation and QTc prolongation |
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side effect of Thioridazine
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typical antipsychotic
irreversible retinal pigmentation |
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Neuroleptic malignant syndrome
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fever, muscle rigidity, autonomic instability, clouded consciousness
stop medication, go to ICU Dantrolene or bromocriptine |
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Atypical antipsychotics
clozapine, risperidone, quetiapine, olanzapine, ziprasidone and aripiprazole |
indicaitons: 1st line for schizophrenia - fewer EPS and anticholinergic effects
Clozapine is reserved for severe tx resistance and severe tardive dyskinesia; AGRANULOCYTOSIS side effects of atypicals: weight gain, Type 2 DM, somnolence, sedation and QTc prolongation |
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Lithium toxicity
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ataxia, dysarthria and delirium
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Lithium
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mood stabilizer, used for acute mania (in combo with antipsychotics); prophylaxis in bipolar disorders and augmentation in depression tx
side effects: thirst, polyuria, diabetes insipidus, tremors, weight gain, hypothyroidism, nausea, diarrhea, seizures, teratogenicity (if used in first trimer), acne and vomiting |
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Carbamazepine
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2nd line mood stabilizer; anticonvulsant
side effects: nausea, skin rash, leukopenia, AV block rarely, aplastic anemia (monitor CBC biweekly), Stevens-Johnson syndrome |
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Valproic acid
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bipolar d/o and anticonvulsant
side effects: GI (N/V), tremor, sedation, alopecia, weight gain rarely - pancreatitis, thrombocytopenia, fatal hepatotoxicity and agranulocytosis |
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Lamotrigine
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2nd line mood stabilizer; anticonvulsant
side effects: blurred vision, GI distress, Steven Johnson syndrome |
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acute dystonia
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involuntary muscle contraction or spasm (eg. torticollis, oculogyric crisis)
tx: anticholinergics (benztropine or diphenhydramine); to prevent, administer these meds prophylactically |
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akathisia
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subjective/objective restlessness - perceived as being distressing
tx: decrease neuroleptics and try beta-blockers (propranolol) benzos or anticholinergics may help |
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Dyskinesia
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pseudoparkinsonism (eg. shuffling gait, cogwheel rigidity)
tx: give an anticholinergic (benztropine) or a dopamine agnost (amantadine); decrease dose of neuroleptic or d/c |
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Tardive dyskinesia
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stereotypic oral facial movements...likely from dopamine receptor sensitization...often irreversible (50%)
tx: d/c or decrease dose of neuroleptic; consider changing neuroleptic (to clozapine or risperidone) GIVING ANTICHOLINERGICS OR DECREASING NEUROLEPTICS MAY INITIALLY WORSEN TARDIVE DYSKINESIA |
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evolution of EPS
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4 hours: acute dystonia
4 days: akinesia 4 weeks: akathisia 4 months: tardive dyskinesia |
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Cluster A personality d/o
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weird...
paranoid, schizoid (loner) and schizotypal |
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Cluster B pers d/o
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wild...
Borderline, histrionic, narcissistic and antisocial |
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Cluster C pers d/o
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worried and wimpy
obsessive compulsive, avoidant and dependent |
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Rett's disorder
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genetic neurodegenerative d/o of FEMALES with progressive impairment (language, head growth, coordination, ataxia, seizures, MR) AFTER 5 MONTHS NORMAL DEVELOPMENT
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Childhood disintegrative disorder
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severe developmental REGRESSION after > 2 years of normal development (eg. language, motor skills, social skills, bladder/bowel control, play)
males > females |
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Tourette's syndrome
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a/w ADHD, learning disorders and OCD
multiple motor tics (blinking, grimacing) and vocal tics, occurring many times a day, recurrently for > 1 year with social or occupational impairment tx: dopamine receptor antagonists (haloperidol, pimozide) or clonidine...stimulants can worsen or precipitate tics |
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substance dependence
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tolerance
withdrawal symptoms attempts to cut down use or abstain - fails (dependence differs from abuse b/c has physical manifestations) |
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alcohol withdrawal
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tremor, tachycardia, hypertension, malaise, nausea, seizures, DTs and agitation
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opiod intoxication
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euphoria leading to apathy, CNS depression, constipation
PUPILLARY CONSTRICTION and respiratory depression (life-threatening OD) naloxone/naltrexone will block opioid receptors and reverse effects (beware of antagonist clearing before opioids...particularly long-acting opioids like methadone) |
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opioid withdrawal
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dysphoria, insomnia, anorexia, myalgias, fever, lacrimation, diaphoresis, dilated pupils, rhinorrhea, piloerection, nausea, vomiting, stomach cramps, diarrhea and yawning
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amphetamine intoxication
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PUPILLARY DILATION, psychomotor agitation, impaired judgment, HTN, tachycardia, fever, diaphoresis, anxiety, angina, euphoria...arrhythmias, hallucinations, seizures
can give haldol for severe agitation and symptom targeted meds (like antiemetics, NSAIDs) |
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amphetamine withdrawal
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postuse "crash" with anxiety, lethargy, HA, stomach cramps, hunger, fatigue, depression/dysphoria, sleep disturbance, nightmares
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PCP intoxication
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ASSAULTIVENESS
VERTICAL/HORIZONTAL NYSTAGMUS belligerence, psychosis, violence, impulsiveness, psychomotor agitation, HTN, impaired judgement, ataxia, seizures, delirium give benzos or haldol for severe symptoms |
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PCP withdrawal
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may have recurrence of intoxication symptoms due to reabsorption in the GI tract; udden onset of severe, random violence
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galactorrhea, impotence, menstrual dysfunction and decreased libido
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patient on dopamine antagonist
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key side effects of atypical antipsychotics
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weight gain, type 2 DM and QT prolongation
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a young wt lifter receive IV haldol and complaints that his eyes are deviated sideways...dx? tx?
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acute dystonia (oculogyric crisis); tx with benztropine or diphenhydramine
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med to avoid in pts with history of alcohol withdrawal seizure
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neuroleptics
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5 month old girl has decreased head growth, truncal dyscoordination and decreased social interaction
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Rett's disorder
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violent patient with horizontal and vertical nystagmus
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phencyclidine hydrochloride intoxication (PCP)
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man has repeated, intense urges to rub his body against unsuspected passengers on a bus
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frotteurism (a paraphilia)
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live, attenuated vaccines
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MMR, polio (sabin), yellow fever
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Inactivated (killed) vaccines
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cholera, influenza, HAV, polio (Salk) and rabies
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Toxoid vaccine
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diphtheria, tetanus
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Subunit vaccines
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HBV, pertussis, Streptococcus pneumoniae, HPV, meningococcus
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Conjugate vaccines
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Hib, Strep pneumoniae
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number of true positives divided by number of patients with the disease
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sensitivity
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sensitive tests have few false negatives and are thus used to...
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rule OUT a disease
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cross sectional survey - incidence or prevalence?
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prevalence
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cohort study - incidence or prevalence
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incidence and prevalence
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case control study - incidence or prevalence?
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neither
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difference btw cohort and case-control study
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cohorts can be used to calculate relative risk, incidence and odds ratio
case control studies used to calculate odds ratio |
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attributable risk?
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incidence ratio of a disease in exposed minus IR of disease in unexposed
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Relative risk?
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incidence rate of disease in population exposed to facor divided by incidence rate of those not exposed
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Odds ratio?
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likelihood of a disease among individuals exposed to a risk factor compared to those who have not been exposed
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number needed to treat?
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1 / (rate in untreated group - rate in treated group)
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patients where screening for colorectal cancer is initiated early...
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patients with IBD, those with FAP/hereditary nonpolyposis colorectal cancer, and those who have first degree relatives with adenomatous polyps (< 60 years old) or colorectal cancer
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percentage of cases within one SD of the mean? two SDs? three SDs?
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68%
95.5% 99.7% |
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postnatal mortality?
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number of death from 28 days to one year per 1000 live births
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infant mortality?
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number of deaths from birth to one year of age per 1000 live births (neonatal + postnatal mortality)
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perinatal mortality?
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number of deaths from 20 weeks' gestation to one month of life per 1000 total births
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maternal mortality?
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number of deaths during pregnancy to 90 days postpartum per 100,000 live births
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involuntary psychiatric hospitalization can be undertaken for which three reasons?
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danger to self, danger to others or gravely disturbed (unable to provide for basic needs)
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when can a physician refuse to continue treating a pt on grounds of futility?
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no rationale for treatment, maximal intervention is failing, given intervention has already failed and tx will not achieve goals of care
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conditions where confidentiality can be overriden...
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real threat of harm to third parties, suicidal intentions, certain contagious diseases; elder and child abuse
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10 yr old child presents in status epilepticus, but parents refuse tx on religious grounds...
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tx because disease represents immediate threat to the child's life...then seek a court order
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