USMLE Step 1 Flashcards
Most common causes of Meningitis in Older Pts
S. pneumoniae N. meningitis H. influenzae type b S. agalactiae (group B) L. monocytogenes
Metronidazole adverse reaction
disulfiram-like reaction (pt should avoid alcohol)
bacterial vaginosis
organism: G. vaginalis
clinical findings: gray watery discharge, vaginal pH > 4.5, positive KOH whiff test
Microscopic findings: clue cells
treatment: metronidazole
Trichomoniasis
clinical findings: green-yellow discharge, strawberry cervix, dyspareunia
Vaginal pH: > 4.5
microscopy: motile trichomonads
treatment: metronidazole
vulvovaginal candidiasis
clinical findings: thick white discharge
vaginal pH: <4.5
microscopy: pseudohyphae
treatment: fluconazole
Vitamin C is a cofactor for what reaction?
It is a cofactor the propyl hydroxylase. It catalyzes the formation of hydroxyproline and hydroxylysine from proline and lysine. This relates to the development of symptoms seen in scurvy
ALK
adenocarcinoma of the lung
BRAF
melanoma, non Hodgkin lymphoma, papillary thyroid
c-MYC
Burkitt lymphoma
HER2/neu
breast and gastric carcinomas
JAK2
chronic myeloproliferative disorders
KRAS
colon cancer, lung cancer, pancreatic cancer
RET
MEN 2A (pheochromocytoma, medullary thyroid, parathyroid) MEN 2B (pheochromocytoma, medullary thyroid, mucosal neuromas), papillary thyroid cancer
APC
colorectal cancer (associated with FAP)
BRCA1 and BRCA2
breast and ovarian cancer
MEN1
MEN1 (pituitary, parathyroid, pancreatic)
NF1
NF1 (cafe au leit spots, leisch nodules, fibrodysplasia of bone, pernicious puberty)
NF2
NF2 (meningeoms, schwannomas, ependymomas)
Rb
retinoblastoma and osteosarcoma
TP53
Li-Fraumeni syndrome; associated with most cancers
VHL
von Hippel-Lindau disease (renal cell carcinoma, cardiac rhabdomyosarcoma, liver cysts)
What drug class is used for cervical ripening?
Prostaglandin analogs (-prost)
Treatment for Lyme disease
doxycycline amoxicillin (pregnant women and children younger than 8 years old)
Penicillin MOA
block transpeptidase cross-linking of peptidoglycan in the cell wall
Doxycycline (tetracycline) MOA
blocks attachment of aminoacyl-tRNA at the 30S ribosomal subunit
Clindamycin MOA
blocks translocation at the 50S ribosomal subunit
Vancomycin MOA
inhibits cell wall peptidoglycan formation by binding the D-Ala-D-Ala portion of the cell wall
What class of diuretics can lead to hypercalcemia?
Thiazide diuretics (eg chlorthalidone). Decreased intracellular Na activates the Na/Ca antiporter. Leads to decreased intracellular Ca which causes enhanced calcium reabsorption within the convoluted tubule
Osteoprotegerin MOA
Acts as a physiologic decoy receptor that decreases binding of RANK-L to RANK. Inhibition of this reduces differentiation and survival of osteoclasts
A-I
HDL
B-48
chylomicrons, chylomicron remnants
B-100
IDL, LDL, VLDL
C-II
HDL, IDL, VLDL, chylomicrons
Apolipoprotein E
HDL, IDL, VLDL, Chylomicrons, chylomicron remnants
Acute Intermittent Porphyria
Affected enzyme: porphobilinogen deaminase
accumulated substrate: porphobilinogen and aminolevulinic acid (ALA)
Clinical presentation of acute intermittent porphyria
abdominal pain
polyneuropathy
port wine colored urine
psych disturbance
Exacerbation of acute intermittent porphyria
alcohol, tobacco, P-450 inducers
Porphyria cutanea tarda
affected enzyme: uroporphyrinogen decarboxylase
risk factor: Hep C
accumulated substrate: uroporphyrin
Clinical presentation of porphyria cutanea tarda
blistering cutaneous photosensitivity
hyperpigmentation
tea-colored urine
symptoms exacerbated by alcohol
Switch to what drug following HIT?
alternative non-heparin, non-warfarin anticoagulants. This can include direct thrombin inhibitors and indirect factor Xa inhibitors
Mirtazapine MOA
alpha2 antagonist, 5-HT2 and 5-HT3 antagonist, H1 antagonist
acetaminophen
N-acetylcysteine (NAC)
anticholinergic toxicity
physostigmine (AChE inhibitor, crosses BBB)
Benzodiazepines
flumazenil
beta blockers
atropine
glucagon
carbon monoxide
100% O2
cyanide
nitrite + thiosulfate
digoxin
anti-digoxin antibody fragments
heparin
protamine sulfate
lead
dimercaprol
EDTA
succimer (for children)
Methanol and ethylene glycol
fomepizole
ethanol
dialysis
methemoglobin
methylene blue
vitamin C
opioids
naloxone
salicylates
sodium bicarbonate
dialysis
serotonin syndrome
dantrolene (also for malignant hyperthermia)
TCAs
sodium bicarbonate
warfarin
vitamin K
fresh frozen plasma (if rapid reversal is needed)
Urea cycle produces what amino acid
arginine
Albendazole MOA
inhibition of microtubule synthesis by inhibiting tubulin polymerization
Treatment for latent TB
9 month course of isoniazid monotherapy
treatment for active TB
9 month course of rifampin, isoniazid, pyrazinamide, and ethambutol
Treatment for hypertensive emergency and MOA
Nitroprusside: increases cGMP via direct release of NO
Fenoldopam: dopamine D1 agonist
diagnosis of A. lumbricoides
visualization of characteristic eggs in concentrated stool samples
Function and associations of Apolipoprotein E
- Clearance of lipoprotein and chylomicron remnants from circulation
- IDL,HDL,VLDL, chylomicrons and chylomicron remnants
- associated with late-onset Alzheimer disease
- type 3 familial dyslipidemia
function of apolipoprotein A-I
- structural protein for HDL
* activation of LCAT
Apolipoprotein B-48
required for the assembly and secretion of chylomicrons
*chylomicrons and chylomicron remnants
Apolipoprotein B-100
- LDL, IDL, VLDL
- assembly and secretion of VLDL
- type 2 familial dyslipidemia
apolipoprotein C-II
- cofactor for lipoprotein lipase
* dysfunction leads to type 1 familial dyslipidemia
Functions of Vitamin C
antioxidant
collagen synthesis
conversion of dopamine to norepinephrine
facilitates iron absorption
Treatment for MDD
first line: cognitive behavioral therapy, SSRI
second line: bupropion (contraindicated in a pt with hx of seizures
Differentiate between failed regression of allantois and vitelline duct.
allantois: urinary leakage through the umbilicus
vitelline duct: purulent or feculent umbilical drainage
Marfan syndrome
pathology: AD, FBN1 gene, chromosome 15
Marfan syndrome clinical presentation
major criteria: ectopia lentis (up and out), dilation of aortic root, aortic dissection
mitral valve prolapse in majority of pts
Adverse effect of Mannitol
Pulmonary edema
heart failure
dehydration
electrolyte imbalance
What drug/drug class would enhance the effects of levodopa/carbidopa?
Selegiline (MAO-B inhibitor) slows metabolism of levodopa. Avoid use if pt is on an SSRI
Signs of decreased synthetic function of the liver
- decreased albumin
- increased PTT
- increased unconjugated bilirubin
Which inflammatory cytokines cause an increase in levels of acute phase reactants?
IL-6, IL-1, and TNF-alpha
IL-1
secreted by: macrophage
USMLE association: causes inflammation
IL-6
secreted by: macrophage
USMLE association: increase ESR and CRP
TNF-alpha
secreted by: macrophage
USMLE association: cachexia in malignancy, maintain granulomas in Tb
IL-8
secreted by: macrophage
USMLE: association: recruits neutrophils
IL-12
secreted by: macrophage
USMLE association: activated NK cells
IL-2
secreted by: all T cells
USMLE association: stimulate T cell and NK cell proliferation
IL-3
secreted by: all T cells
USMLE association: growth and differentiation of bone marrow stem cells
Interferon-gamma
secreted by: Th1 cells
USMLE association: stimulates macrophages, stimulates granuloma formation, activate NK cells
IL-4
secreted by: Th2 cells USMLE association: T cell differentiate into Th2 cells, class switching of antibodies
IL-5
secreted by: Th2 cells
USMLE association: growth and differentiation of eosinophils
IL-10
secreted by: Th2 cells
USMLE association: IL-10 and TGF-beta are the main anti-inflammatory cytokines
Topoisomerase inhibitors: drug name and target
etoposide: II
teniposide: II
irinotecan: I
topotecan: I
Muscle activity involved in micturition
Relaxation of the levator ani muscles and contraction of detrusor muscle
Hunter syndrome
inheritance: x-linked recessive
pathophysiology: deficiency of iduronate-2-sulfatase
accumulated substance: heparan sulfate and dermatan sulfate
Why can’t newborns synthesize vitamin K?
Lack intestinal flora that are seen in adults. Will have bleeding issues and require IM vitamin K injections after birth
Clinical features of Digeorge syndrome
CATCH-22
- cardiac defects
- abnormal facies
- thymic dysplasia
- cleft palate
- hypocalcemia
Folate deficiency clinical features
- megaloblastic anemia without neurologic symptoms (differentiate from B12)
- in pregnancy, neural tube defects
- hyper segmented neutrophils
- increased homocysteine
Niacin (B3) deficiency clinical features
diarrhea, dermatitis, dementia
glossitis
Vitamin A deficiency clinical features
Nyctalopia (night blindness)
xeropthalmia
keratomalacia
complete blindness