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650 Cards in this Set
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next step in mgmt: |
orchiectomy |
|
classic findings of HSP
|
palpable purpura
GI sx's (e.g. abd'l pain, vomiting, guaiac+, intussusception) renal disease transient arthritis/arthralgias |
|
What variables shift the Hb-O2 dissociation curve to the right
|
"CADET-face RT" |
|
what effect does a right shift on Hb-O2 curve have
|
Incr'd delivery of O2 to peripheral tissues
|
|
what is cause of anemia that develops after taking a sulfa drug
|
G6PD deficiency
|
|
what lab markers suggest anemia due to hemolysis
|
decr'd H&H with incr'd retics |
|
in hemolytic anemia, why is serum haptoglobin level der'd & serum LDH increased
|
Haptoglobin binds free Hb in blood
LDH spills out of hemolyzed RBC's |
|
characteristic findings in hereditary spherocytosis
|
jaundice & gallstones (2nd/2 elevated bilirubin)
splenomegaly anemia with incr'd retics & MCHC spherocytes on peripheral smear positive osmotic fragility test |
|
spherocytosis is a/w higher incidence of what lab abnormality
|
pseudohyperkalemia
(2nd/2 K+ spilling into blood when RBC's lyse after blood draw) |
|
tx of hereditary spherocytosis
|
folic acid 1mg qD
splenectomy (moderate to severe cases) RBC transfusion (extreme cases) |
|
Rx for diarrhea 2nd/2 E. histolytica
|
metronidazole (+ hydration)
|
|
Rx for diarrhea 2nd/2 G. Lamblia
|
metronidazole (+ hydration)
|
|
Rx for diarrhea 2nd/2 salmonella
|
quinolones or TMP-SMX (+ hydration)
|
|
Rx for diarrhea 2nd/2 shigella
|
quinolones or TMP-SMX (+ hydration)
|
|
Rx for diarrhea 2nd/2 campylobacter
|
erythromycin (+ hydration)
|
|
Rx for mild persistent asthma
|
ACUTE TX:
short-acting B2-agonist (i.e. albuterol) IV corticosteroids (for persistent sx's) LONG-TERM CONTROL: albuterol, prn inhaled glucocorticoid +/- leukotriene inhibitor (e.g. cromolyn) |
|
what is charcots triad indicative of & what are the components
|
Dx: cholangitis
TRIAD: jaundice RUQ pain Fever |
|
what is reynold's pentad indicative of & what are the components
|
Dx: cholangitis
PENTAD: jaundice RUQ pain Fever hypotension AMS |
|
Iron Def Anemia:
serum iron ferritin transferrin Fe/TIBC |
serum iron: decr'd
ferritin: decr'd transferrin: incr'd Fe/TIBC: < 12% |
|
Anemia of chronic disease:
serum iron ferritin transferrin Fe/TIBC |
serum iron: decr'd
ferritin: incr'd transferrin: decr'd Fe/TIBC: > 18% |
|
what is seen on blood smear of a patient with lead poisoning
|
microcytic
hypochromic basophilic stippling |
|
RBC disorder a/w:
schistocyte (fragmented RBC) |
hemolytic anemia
DIC TTP HUS |
|
RBC disorder a/w:
acanthocyte (spur cell) |
abetalipoproteinemia
|
|
RBC disorder a/w:
bite cell |
G6PD def
|
|
RBC disorder a/w:
basophilic stippling |
lead poisoning
B-thalassemia alcohol |
|
RBC disorder a/w:
peripheral neuropathy and ringed sideroblastic in BM |
lead poisoning
|
|
RBC disorder a/w:
hypersegmented neutrophils |
folate/B12 def
|
|
RBC disorder a/w:
heinz bodies (denatured Hgb in RBC) |
G6PD def
|
|
RBC disorder a/w:
burr cells |
uremia
|
|
MCV & anemia a/w:
mental status changes, neuropathy, constipation |
microcytic
lead poisoning |
|
MCV & anemia a/w:
heavy menses, strict vegetarians, ice pica |
microcystic
iron def |
|
MCV & anemia a/w:
dark urine, jaundice, hepatosplenomegaly |
normocytic
hemolytic anemia |
|
MCV & anemia a/w:
alcoholic, malnourished |
macrocytic
folate/B12 def |
|
what virus can cause aplastic anemia as well as erythema infectiosum disease (i.e. "fifth disease")
|
Parvovirus B19
|
|
what test is used to rule out urethral injury
|
retrograde cystourethrogram
|
|
lipid-lowering agent:
SE = facial flushing |
niacin
|
|
lipid-lowering agent:
SE = elevated LFT's, myositis |
statins
fibrates |
|
lipid-lowering agent:
SE = GI discomfort, bad taste |
bile acid sequestrants
(e.g. cholestyramine) |
|
lipid-lowering agent:
best effect on HDL |
niacin
|
|
lipid-lowering agent:
best effect on TG's |
fibrates
|
|
lipid-lowering agent:
best effect on LDL/cholesterol |
statins
|
|
lipid-lowering agent:
binds C. Diff toxin |
cholestyramine
|
|
which types of thalassemias are most commonly a/w pts of Mediterranean & AA/Asian descent
|
MEDITERRANEAN: B-Thal
AA/ASIAN: a-Thal |
|
What complication occurs in 10% of pts with sideroblastic anemia
|
myelodysplastic syndrome (aka "refractory anemia)
--> acute leukemia |
|
Besides Staph Aureus, which organism may be responsible for osteomyelitis in a sickle cell pt
|
salmonella
|
|
Which vaccines are particularly important in children with sickle cell disease
|
HiB
Pneumoccal Meningococcal Influenza Hep B |
|
What medication is used in the long-term management of sickle cell anemia
|
Hydroxyurea
|
|
drugs a/w elevated prolactin levels
|
METHYLDOPA
PSYCHIATRIC DRUGS phenothiazines haloperidol risperidone |
|
what substances cause hemolysis in px with G6PD def
|
primaquin
dapsone sulfonamides fava beans isoniazid nitrofurantoin high-dose ASA |
|
when would you expect eosinophillic casts in urine
|
acute interstitial nephritis, AIN
(i.e. allergic interstitial nephritis) |
|
differential dx for eosinophilia
|
"DNAAACP"
D = drugs (e.g. NSAIDS, PCN's/Ceph's) N = neoplasms A = allergies/asthma (churg-strauss), allergic bronchopulmonary aspergillosis A = adrenal insufficiency (Addison's) A = AIN (allergy-induced) C = CVD's (e.g. PAN, dermatomyositis) P = parasites (e.g. strongyloides, Ascaris --> Loeffler's eosinophilic pneumonitis) |
|
what is the management in a px with febrile neutropenia due to chemo
|
admit
culture start broad-spectrum antibiotics (e.g. cefepime/ceftazidine) |
|
what type of infection causes eosiniphilia
|
parasitic
|
|
immunoglobulin a/w eosinophilia
|
IgE
|
|
what type of hypersensitivity is good pasture
|
type II HSN
|
|
what is the treatment for type II hypersensitivity
|
anti-inflammatories
immunosuppressives (e.g. corticosteroids) possibly plasmaphoresis |
|
most important medication for anaphylaxis
|
epinephrine
|
|
Tx for anaphylaxis
|
ABC's
stop offending agent epinephrine IM or IV (for AW obstruction) H1/H2 blockers (for cutaneous sx's) bronchodilators steroids IVF's (for hypotension) |
|
Dx
45 yo with acute flank pain and hematuria |
nephrolithiasis
|
|
MCC of aortic stenosis in 50 y/o
|
congenital bicuspid aortic valve
|
|
MOA:
streptokinase |
activates tissue plasminogen --> cleaves fibrin clots
|
|
MOA:
aspirin |
Cox-2 inhibitor --> blocks plt aggregation
|
|
MOA:
clopidogrel |
inhibits ADP receptor
|
|
MOA:
abciximab |
Gp2b3a Inhibitor
|
|
MOA:
tirofiban |
Gp2b3a Inhibitor
|
|
MOA:
ticlopidine |
inhibits ADP receptor
|
|
MOA:
enoxaparin |
LMWH --> inhibits CF Xa
|
|
MOA:
eptifibatide |
Gp2b3a Inhibitor
|
|
classic triad of HUS
|
hemolytic anemia
uremia thrombocytopenia |
|
what is the pentad of TTP
|
hemolytic anemia
uremia thrombocytopenia neurologic sequelea fever |
|
lab test to monitor:
warfarin |
PT/INR
|
|
lab test to monitor:
heparin |
PTT
|
|
lab test to monitor:
LMWH |
doesn't need monitoring
(h/w it can be monitored with anti-CF Xa) |
|
drugs known to cause thrombocytopenia
|
heparin (HIT)
abciximab (GP2b3a inhibitor) carbamazepine, phenytoin, valproate cimetidine acyclovir, rifampin sulfonamides (e.g. sulfasalazine, TMP-SMX) procainamide, quinidine quinine, gold compounds |
|
1st line Rx for vWD
|
desmopressin, DDAVP (increases vWF secretion)
|
|
Rx for vWD that is severe or refractory
|
cryoprecipitate or Factor VIII
|
|
Rx for vWD with menorrhagia
|
OCP
|
|
MCC's of DIC
|
"STOP Making Thrombi"
S = sepsis T = trauma O = OB complications P = pancreatitis M = malignancy T = transfusions |
|
PLT's, BT, PT, PTT:
HUS/TTP |
PLT's: decr'd
BT: incr'd PT: normal PTT: normal |
|
PLT's, BT, PT, PTT:
hemophilia A or B |
PLT's: normal
BT: normal PT: normal PTT: incr'd |
|
PLT's, BT, PT, PTT:
vWD |
PLT's: normal
BT: incr'd PT: normal PTT: incr'd |
|
PLT's, BT, PT, PTT:
DIC |
PLT's: decr'd
BT: incr'd PT: incr'd PTT: incr'd |
|
PLT's, BT, PT, PTT:
warfarin use |
PLT's: normal
BT: normal PT: incr'd PTT: incr'd |
|
PLT's, BT, PT, PTT:
aspirin |
PLT's: normal
BT: incr'd PT: normal PTT: normal |
|
PLT's, BT, PT, PTT:
end stage liver disease |
PLT's: normal/decr'd
BT: normal/incr'd PT: incr'd PTT: incr'd |
|
what is the MC mutation that predisposes white pt's to venous thrombosis
|
Factor V Leiden mutation
|
|
Dx & Tx:
post-op pt with poor urine output, BUN 85, Cr 3 & clear lungs |
Dx: Prerenal azotemia (2nd/2 dehydration)
Tx: IVF's |
|
what infection causes aplastic crisis in sickle cell pt's
|
Parvovirus B19
|
|
Dx:
pt presents with glomerulonephritis plus b/l sensorineural deafness |
Alport's Syndrome
|
|
Tx of shock
|
IVF's & pressors
blood, urine, & sputum cultures (BEFORE starting antibiotics) CXR empiric antibiotics insulin drip continuous cardiac monitoring & central venous pressure measurments |
|
man returns from African safari c/o periodic fevers, chills, diaphoresis, muscle aches, & fatigue; how could he have avoided illness
|
prophylactic anti-malarials
|
|
Tx for infectious mononucleosis
|
rest & plenty of fluids
NSAIDS or Tylenol (for fever, sore throat, & malaise) gradual return to sports (incr'd risk of splenic rupture): NONCONTACT: 3 wks after sx onset CONTACT: 4 wks after sx onset |
|
what is the spectrum of conditions related to blood infections
|
bacteremia
SIRS sepsis severe sepsis septic shock multiple organ dysfxn syndrome |
|
definition:
bacteremia |
bacteria of any amount in the blood that does not meet criteria for SIRS
|
|
definition:
SIRS |
Systemic Inflammatory Response Syndrome (SIRS) WITHOUT an identified source of infection
(NOTE: criteria may be met due to other causes independent of infection or source may never be found) |
|
what are the 4 categories for SIRS criteria
|
temperature
tachycardia tachypnea WBC's |
|
how many of the SIRS categories must be present to meet the SIRS criteria
|
2 or more
|
|
What is the SIRS "temperature" criteria
|
> 38.3C or < 36.0C
|
|
What is the SIRS "tachycardia" criteria
|
HR > 90 bpm
|
|
What is the SIRS "tachypnea" criteria
|
RR > 20 bpm or PaCO2 < 32
|
|
What is the SIRS "WBC's" criteria
|
ANY 1 OF THE FOLLOWING:
> 12,000 > 10% bands < 4,000 |
|
Criteria:
SIRS |
CRITERIA: 2 or more of the following:
TEMPERATURE: > 38.3C < 36.0C TACHYCARDIA: HR > 90 TACHYPNEA: RR > 20 bpm PaCO2 < 32 WBC'S: > 12,000 > 10% bands < 4,000 |
|
definition:
sepsis |
SIRS WITH an identified source of infection;
(FYI: if SIRS criteria met & there is no obvious source of infection, w/u should include urine, blood, & sputum cultures) |
|
definition:
severe sepsis |
SEPSIS + 1 OF THE FOLLOWING:
organ dysfxn hypotension hypoperfusion |
|
what signs are evidence of organ dysfxn, hypotension &/or hypoperfusion seen in severe sepsis
|
lactic acidosis
SBP < 90 mmHg SBP drop > 40 mmHg |
|
definition:
septic shock |
SEVERE SEPSIS + hypotension , despite adequate fluid resuscitation
|
|
definition:
multiple organ dysfxn syndrome |
SEPTIC SHOCK + evidence of 2 or more organs failing
|
|
SUMMARIZE the spectrum of conditions related to blood infections with definition of each
|
BACTEREMIA: bacteria in the blood that does not meet criteria for SIRS
SIRS: 2+ criteria met WITHOUT source of infection identified SEPSIS: SIRS + source of infection identified SEVERE SEPSIS: sepsis + organ dysfxn, hypotension, or hypoperfusion SEPTIC SHOCK: severe sepsis + hypotension, despite adequate fluid resuscitation MULTIPLE ORGAN DYSFUNCTION SYNDROME: septic shock + evidence of 2+ organs failing |
|
classic EKG finding in PE
|
"S1Q3T3"
wide S in Lead I large Q in lead III inverted T wave in lead III |
|
Dx:
post op px with pain presents with hyponatremia and normal volume status |
SIADH (2nd/2 stress)
|
|
Rx for mild unconjugated hyperbilirubinemia
|
phototherapy
|
|
Rx for severe unconjugated hyperbilirubinemia
|
exchange transfusion
|
|
what is the initial HAART regimen
|
2 NRTI's + EITHER:
1 protease inhibitor 1 NNRTI may be add ritonavir |
|
antiretroviral a/w:
SE of lactic acidosis |
NRTI'S
|
|
antiretroviral a/w:
SE of GI intolerance |
protease inhibitors
|
|
antiretroviral a/w:
SE pancreatitis |
zalcitibine
didanosine stavudine ritonavir |
|
antiretroviral a/w:
SE of peripheral neuropathy |
zalcitibine
didanosine stavudine |
|
antiretroviral a/w:
SE of megaloblastic anemia |
zidovudine
|
|
antiretroviral a/w:
SE of rash |
NNRTI's
|
|
antiretroviral a/w:
SE of hyperglycemia, DM, lipid abnormalities |
protease inhibitors
(e.g. indinavir, sequinavir, amprinavir) |
|
antiretroviral a/w:
SE of BM suppression |
zidovudine
|
|
antiretroviral a/w:
given to pregnant woman with HIV |
HAART regimen with zidovudine
|
|
antiretroviral a/w:
regimen for occupational HIV exposure |
LOW-RISK: zidovudine + lamivudine
HIGH-RISK: 3-drug HAART regimen |
|
what bugs are tx prophylactically in AIDS pt's with CD4+ < 200 and what is rx is given
|
PCP: TMP-SMX
TOXOPLASMOSIS: TMP-SMX MAC: Macrolide (e.g. clarithromycin or azithromycin) |
|
Tx for acute toxoplasmosis in AIDS pt
|
pyrimethamine or sulfadiazine
|
|
HIV prophylaxis for TB
|
INH
|
|
AIDS criteria
|
ANY OF THE FOLLOWING:
HIV+ with CD4+ < 200 HIV+ with CD4+ < 15% of total lymphocytes HIV+ with "AIDS-defining illness" |
|
what are some examples of "AIDS-defining illness"
|
THERE ARE MANY (refer to SU p.144-145):
esophageal candidiasis PCP toxoplasmosis MAC |
|
tumor marker:
hepatocellular carcinoma |
AFP
|
|
tumor marker:
colon cancer |
CEA
|
|
tumor marker:
gastric cancer |
CEA
|
|
tumor marker:
pancreatic cancer |
CA 19-9
CEA |
|
tumor marker:
ovarian cancer |
CA-125
|
|
dx:
young black man with painless hematuria |
sickle cell trait
|
|
MCC of aortic stenosis in a 70 y/o
|
senile (i.e. degenerative) calcifications
|
|
labs in DIC
|
ELEVATED:
fibrin-split products D-dimers DECREASED: fibrinogen platelets hematocrit |
|
which type of RTA is a/w abnormal H+ secretion & nephrolithiasis
|
RTA I
|
|
what is the classic presentation of polycythemia vera
|
thrombosis
erythromelalgia (i.e. burning pain in hands & feet) pruritis (esp after warm bath/shower) facial plethora hepatosplenomegaly visual disturbances abnormal labs |
|
what visual distrubances are seen with polycythemia vera
|
blurred vision
amaurosis fugax scintillating scotoma ophthalmic migraine |
|
what lab abnormalities are seen with polycythemia vera
|
elevated H&H
elevated red cell mass basophilia leukocytosis thrombocytosis |
|
what is the Rx for polycythemia vera
|
phlebotomy
(FYI: induces a desirable iron def anemia --> DO NOT supplement with iron) |
|
what is used in px with polycythemia vera with high risk of thrombosis; which pts are considered "at risk"
|
hydroxyurea
"AT RISK": h/o thrombosis plts > 1,500,000 CV RF+ > 70 y/o |
|
what is used in px with polycythemia vera with refractory pruritis or refractory erythrocytosis
|
IFN-a
|
|
what tests will help in dx of MM
|
SPEP: monoclonal AB spike
UPEP: bence-jones proteins BM BX: incr'd plasma cells |
|
Dx
px with weight loss, pruritis, night sweats, hepatosplenomegaly, nontender cervical lymphadenopathy |
Hodgkin's lymphoma
|
|
Dx:
3 y/o girl presents with abd'l mass, hematuria, & HTN |
Wilm's tumor
|
|
Dx & Tx:
recent Cuban immigrant with sx's of malabsorption is found to also have megaloblastic anemia |
Dx: Tropical sprue
Tx: folate & antibiotics (e.g. tetracycline or sulfa) |
|
cell pathology a/w:
EBV |
Burkitt's lymphoma
|
|
cell pathology a/w:
reed sternberg cell, cervical lymphadenopathy, night sweats |
Hodgkin's lymphoma
|
|
cell pathology a/w:
bence jones proteins, osteolytic lesions, high Ca2+ |
MM
|
|
cell pathology a/w:
translocation 14:18 |
follicular lymphoma
|
|
cell pathology a/w:
MC lymphoma in US |
diffuse large B cell lymphoma
|
|
cell pathology a/w:
translocation 8:14 |
burkitt's lymphoma
|
|
cell pathology a/w:
translocations 9:22 |
philadelphia (CML or ALL)
|
|
cell pathology a/w:
MC hodgkin lymphoma |
nodular sclerosing
|
|
cell pathology a/w:
starry sky pattern due to phagocytosis of apoptotic tumor cells |
burkitt's lymphoma
|
|
cell pathology a/w:
high H&H, pruritis (esp after hot bath or shower), burning pain in hands or feet |
polycythemia vera
|
|
cell pathology a/w:
white cells with hair-like projections & splenomegaly |
hairy-cell leukemia
|
|
cell pathology a/w:
macrocytosis, hypogranular granulocytes with bilobed nuclei |
myelodysplastic syndrome
|
|
Rx for CML
|
imatinib
|
|
leukemia a/w:
MC in children (peak age 3-4 y/o) |
ALL
|
|
leukemia a/w:
MC in adults (avg age of onset 50 y/o) |
CLL
|
|
leukemia a/w:
philadelphia Chromosome is always present |
CML
|
|
leukemia a/w:
smudge cells |
CLL
|
|
leukemia a/w:
peripheral blasts are PAS+ and TdT+ |
ALL
|
|
leukemia a/w:
peripheral blasts are PAS-, MPO+ and have Auer rods |
AML
|
|
leukemia a/w:
pancytopenia in a down syndrome px |
ALL
|
|
lung cancer a/w:
elevated ACTH --> glucocorticoid excess --> Cushing's |
small cell lung cancer
|
|
lung cancer a/w:
elevated PTH related peptide --> hypercalcemia |
squamous cell lung cancer
|
|
lung cancer a/w:
elevated ADH --> SIADH --> hyponatremia |
small cell lung cancer
|
|
lung cancer a/w:
antibodies to presynaptic Ca2+ channels --> Lambert-Eaton syndrome |
small cell lung cancer
|
|
disease that causes glomerulonephritis with deafness
|
Alport's syndrome
|
|
MC adrenal tumor in children; lab study used to dx
|
MC = neuroblastoma
Dx'c = 24-hr urine --> incr'd VMA & HVA |
|
Dx:
4 y/o girl with URI & dangling thumbs, short stature, & hypopigmentation of some skin areas; labs reveal pancytopenia |
fanconi's anemia
|
|
Rx for neuroleptic malignant syndrome
|
DantroleneDopamine agonists (e.g. bromocriptine)
|
|
common complication of recurrent otitis media
|
hearing loss
|
|
Rx for DT's
|
long-acting benzos (e.g. chlordiazepoxide)
|
|
possible auto-antibodies a/w type 1 DM
|
anti insulin (IAA)anti islet cell cytoplasm (ICA)anti glutamic acid decarboxylase (GAD)anti tyrosine phosphatase (IA-2)
|
|
what lab test can be used in diabetic px to assess the adequacy of glycemic control over the last 3 months
|
HbA1c
|
|
leading cause of death in diabetics
|
CV disease
|
|
why must B-blockers be used with caution in diabetic pts
|
"masks" sympathetic sx's of hypoglycemiadecreases insulin release
|
|
what can cause hypoglycemia in a non-diabetic px
|
insulinoma (B-cell tumor)exogenous insulin or sulfonylureasalcoholfastingpituitary/adrenal insufficiency
|
|
what is the Somogyi effect
|
evening insulin dose is TOO HIGH --> HYPOGLYCEMIAhypoglycemia --> release of catecholaminescatecholamines --> high glucose in the mornings
|
|
what is the dawn phenomenon
|
evening dose is TOO LOW --> diminishing insulindiminishing insulin --> rising glucose (thru the night)rising glucose --> high glucose in the mornings
|
|
Rx other than stimulants for ADHD
|
TCA's (e.g. Imipramine, desipramine, & nortriptyline)bupropiona2-agonists (e.g. clonidine)
|
|
3 reasons for involuntary psychiatric hospitalization
|
danger to selfdanger to othersgravely disabled (e.g. catatonic schizophrenic)
|
|
what psychiatric condition occurs when a person travels a long distance and take a new name and has no memore or previous life
|
dissociative fugue
|
|
what are the DM'c drug classes
|
SulfonylureasThiazolidinediones (TZD's)BiguanidesIncretin mimeticsDPP-IV inhibitorsa-glucosidase inhibitorsMeglitinides
|
|
examples of med's within drug class:Sulfonylureas
|
GlyburideGlimeperideGlipizide
|
|
examples of med's within drug class:Thiazolidinediones (TZD's)
|
PioglitazoneRosiglitazone
|
|
examples of med's within drug class:Biguanides
|
Metformin
|
|
examples of med's within drug class:Incretin mimetics
|
ExenatideLiraglutide
|
|
examples of med's within drug class:DPP-IV inhibitors
|
SitagliptinSaxagliptinLinagliptin
|
|
examples of med's within drug class:a-glucosidase inhibitors
|
Acarbose
|
|
examples of med's within drug class:Meglitinides
|
RepaglinideNateglinide
|
|
what skin finding is a sign of insulin resistance
|
acanthosis nigricans(NOTE: acanthosis nigricans is also a/w occult malignancies)
|
|
diabetic Rx a/w:lactic acidosis
|
metformin (rare, but worrisome SE)
|
|
diabetic Rx a/w:MC SE is hypoglycemia
|
sulfonylureasmetglitinides
|
|
diabetic Rx a/w:oldest and cheapest oral agent
|
sulfonylureas
|
|
diabetic Rx a/w:often used in combination with otehr oral agents
|
metformin
|
|
diabetic Rx a/w:lowers TG and LDL
|
metformin
|
|
diabetic Rx a/w:not safe in HF
|
CHF:pioglitazone (TZD)rosiglitazone (TZD)INCR'D RISK OF MI:rosiglitazone (TZD)
|
|
diabetic Rx a/w:should not be used in px with increased Cr
|
metforminsulfonylureas
|
|
diabetic Rx a/w:avoid in px with inflammatory bowel disease
|
a-glucosidase inhibitors (e.g. acarbose)
|
|
diabetic Rx a/w:hepatic serum transaminase levels should be carefully monitored
|
TZD's (glitazones)metforminsulfonylureas
|
|
diabetic Rx a/w:no weight gain
|
metforminincretin mimetics (h/w cannot be given PO)
|
|
diabetic Rx a/w:metabolized by liver, good choice for those with renal failure
|
TZD's (glitazones)
|
|
diabetic Rx a/w:postprandial hyperglycemia
|
a-glucosidase inhibitors (acarbose)
|
|
what does GLP-1 do
|
decreases glucagonincreases insulindelays gastric emptying
|
|
what diabetic Rx increases GLP-1
|
INCRETIN MIMETICS:exenatideliraglutide
|
|
what does DPP-4 do
|
Inhibit GLP-1
|
|
what diabetic Rx inhibits DPP-4, indirectly increasing GLP-1 (i.e. inhibiting an "inhibitor)
|
DPP-IV Inhibitors = "--gliptins"(e.g. Sitagliptin, Saxagliptin, Linagliptin)
|
|
what diabetic Rx is an Amylin analog
|
pramlintide
|
|
what diabetic Rx can be used for both type 1 and type 2 DM
|
pramlintide
|
|
how can you Dx metabolic syndrome
|
Any 3 of the followingABDOMINAL OBESITY (waist circ.): M > 40; F > 35PRE-HTN: > 130/85HYPERGLYCEMIA: FBSG > 100 (or 2hr post PO glucose > 140)DYSLIPIDEMIA:TG's > 150HDL: M < 40; F < 50
|
|
what diabetic drug should be stopped before performing imaging with IV contrast
|
METFORMIN:d/c for 24 hrs prior to CT with contrastre-evaluate renal fxn before re-startingrestart 48 hrs after procedure (if renal fxn is back to baseline)
|
|
diabetic drug with MOA:decreases GI absorption or starch and disaccharides
|
a-glucosidase inhibitor (e.g. acarbose)
|
|
diabetic drug with MOA:stimulates insulin release
|
sulfonylureasmeglitinides
|
|
diabetic drug with MOA:decreases hepatic gluconeogenesis
|
metforminTZD's (glitazones)
|
|
diabetic drug with MOA:increases tissue glucose uptake and improves insulin sensitivity
|
TZD's (glitazones)
|
|
diabetic drug with MOA:mimics action of GLP-1
|
INCRETIN MIMETICS:exenatideliraglutide
|
|
diabetic drug with MOA:inhibits DPP-4
|
DDP-4 INHIBITORS = "--gliptins"(e.g. Sitagliptin, Saxagliptin, Linagliptin)
|
|
Which type of insulin is used in continuous infusion insulin pumps & in treatment of DKA
|
regular Insulin (used most commonly)very rapid-acting (e.g. Lispro, Aspart, Glulisine)
|
|
What must be kept in mind for a Type I DM'c pt that plans to begin a strenuous exercise program
|
Blood sugar is likely to drop during exercise as muscles take up more glucosePts's should always have a readily available source of glucosePt's should check glucose levels regularly: before exercising every hour during exercise after exercising
|
|
definitive tx for subdural and epidural hematoma
|
evacuation with burrhole
|
|
medication used to Dx symptomatic myasthenia gravis
|
edrophonium (i.e. tensilon test)
|
|
MCC of seizures in children 2-10 yo
|
febrileinfectiontraumaideopathic
|
|
signs and symptoms of DKA
|
metabolic acididosisvomiting (WITHOUT DIARRHEA)kussmal breathingfruity odor on breathpolyuria/polydipsiamental status change
|
|
Mgmt of DKA
|
Admit to ICUIVF'sinsulin (until anion gap closes)glucose (if BG drops before AG closes)Correct electrolytes (give KCl)Tx underlying d/o
|
|
what 2 tests can be used to confirm DKA
|
ABG'surine ketone
|
|
how to Dx diabetic gastroparesis
|
gastric emptying study
|
|
Rx for diabetic gastroparesis
|
DOC = metoclopramide (reglan)2nd line = erythromycin
|
|
Rx for proliferative diabetic retinopathy
|
laser photocoagulation+ glucose control
|
|
Rx for diabetic peripheral neuropathy
|
gabapentinpregabalinduloxetine+ glucose control
|
|
anti-HTN've that will reduce proteinuria and slow/prevent diabetic nephropathy
|
ACEIs/ARBs
|
|
what eye problems are diabetics at increased risk for developing
|
cataractsglaucomaretinal detachement
|
|
What is the equation for anion gap
|
AG = [Na+] - ([Cl-] + [HCO3-])
|
|
w/u for underlying cause of DKA
|
R/O INFECTION:blood/urine culturesCXRUA & toxicology screenR/O PANCREATITIS:amylaselipaseR/O MI (in pt's > 35-40 y/o):EKGtroponins x3
|
|
Rx for tourettes
|
fluphenazine (high-potency neuroleptic)pimozidetetrabenazine
|
|
Dxmuscle rigidity, fever and rhabdomyolysis in schizophrenic px
|
neuroleptic malignant syndrome
|
|
antidiabetic agent a.w lactic acidosis
|
metformin
|
|
Mgmt of thyroid storm
|
NON-PHARM:ICU admission (25-50% mortality)r/o infection (blood/urine cultures)aggressive hydration (except overt HF)PHARMACOLOGICAL:B-blockers (to control adrenergic stimulation)PTU/methimazole (block new hormone SYNTHESIS)Iodine (to block T4/T3 RELEASE from gland)Glucocorticoids (to reduce T4 --> T3 CONVERSION)
|
|
what Rx should be avoided in a pt with thyroid storm
|
aspirin(interferes with thyroid protein binding, generating MORE free thyroid)
|
|
Rx with MOA:decrease TH synthesis
|
PTU methimazole
|
|
Rx with MOA:decreases release of T4 & T3 from the gland
|
Iodine
|
|
Rx with MOA:decreases T4 conversion
|
PTUglucocorticoids
|
|
what thyroid abnormalities would you expect to find during pregnancy
|
incr'd TBG --> incr'd total T3 & T4normal free T3 & free T4
|
|
Dxpx with exophthalmos
|
graves
|
|
Rx for graves
|
PHARMACOLOGICAL:Methimazole or PTUDEFINITIVE TX'S:radioactive iodine/ablationsubtotal thyroidectomy
|
|
which thyroid dysfunction will radioactive iodine most likely result in hypothyroidism
|
GRAVE'S DISEASE:radioactive iodine is taken up by fxn'l tissue& in Grave's, the entire gland is hyperfxn'lNOTE: likely to happen in many thyroid d/o's tx'd with radioactive iodine, but Grave's is most likely b/c hyperfxn'l thyroid
|
|
what is the FIRST step in a pt with a palpable thyroid nodule
|
Check TSH, FT4Thyroid US (to measure size and assess for other nodules)
|
|
what should be done in a pt with a palpable thyroid nodule who's labs reveal hyperthyroid
|
radionucleotide uptake scan
|
|
what should be done in a pt with a palpable thyroid nodule who's labs reveal euthyroid
|
FNA
|
|
what should be done in a pt with a palpable thyroid nodule who's labs reveal hypothyroid
|
thyroid replacementmonitor for decrease in nodule size (if nodule persists after thyroid replacement --> FNA)
|
|
what should be done in a hyperthyroid px with cold radionucleotide uptake scan
|
FNA
|
|
what should be done in a hyperthyroid px with hot radionucleotide uptake scan
|
tx as hyperthyroidism (i.e. B-blocker, PTU/Methimazole, Iodide, Glucocorticoids)
|
|
what should be done if a FNA of thyroid nodule is malignant
|
surgery
|
|
what should be done if FNA of thyroid nodule is benign
|
repeat US every 6 monthsif increase in size --> repeat FNA
|
|
what should be done if FNA of thyroid nodule is intermediate
|
repeat US every 6 monthsif increase in size --> repeat FNA
|
|
what should be done if FNA of thyroid nodule is nondiagnostic
|
repeat FNA
|
|
what lab abnormalities necessitate obtaining a thyroid function test to rule out thyroid disease
|
hyperlipidemia (hypothyroid incr's LDL & total ch'ol)hyponatremiaelevated CPK
|
|
hyperthyroidism a/w:tender thyroid
|
Subacute thyroiditis (aka De Quervain Thyroiditis)
|
|
hyperthyroidism a/w:pretibial myxedema
|
graves
|
|
hyperthyroidism a/w:pride in recent weight loss
|
exogenous abuse
|
|
hyperthyroidism a/w:palpation of single thyroid nodule
|
toxic thyroid adenoma (aka Plummer Ds)
|
|
hyperthyroidism a/w:palpation of multiple thyroid nodules
|
multinodular goiter
|
|
hyperthyroidism a/w:recent iodine IV contrast study
|
Jod Basedow Phenomenon(aka iodine-induced hyperthyroidism)
|
|
hyperthyroidism a/w:eye changes
|
graves
|
|
hyperthyroidism a/w:history or thyroidectomy
|
excess TH replacement
|
|
lab abnormality a/w bacterial meningitis
|
incr'd WBCs WITH POSSIBLE:left shift on CBC (bandemia)leukopeniamild hyponatremia
|
|
RX for DKA
|
IVF'sIV insulin (until AG closes & NO ketones)IV glucose (prevent hypoglycemia)Replace electrolytes (Mg2+, Ca2+, K+, & phosphate)
|
|
disorder a/w child who has history of theft, vandalism and violence
|
conduct disorder
|
|
How do you tx a px who has hyperPTH who refuses or cant have surgery
|
ADEQUATE HYDRATION (to avoid renal stones)MINIMIZE BONE RESORPTION:exercisebisphosphonatesCa2+ (1000mg/day)Vit D (400 - 600 IU/day)PREVENT WORSENING HYPERCALCEMIA BY AVOIDING:thiazide diureticslithiumvolume depletionprolonged bed rest Ca2+ ingestion (>1000mg/day)ROUTINE MONITORING:serum Ca2+ q6 mosserum Cr q12 mos BMD of hip, L-spine, & forearm q12 mos
|
|
what are oral phosphate binders for px with hyperphosphatemia 2nd/2 hyperPTH
|
Ca2+ carbonate Ca2+ acetate
|
|
MCC's of hyperPTH
|
adenoma (single PT gland)hyperplasia (x4 PT glands)
|
|
how will vit D def affect Ca, PTH, P
|
decr'd Caincr'd PTHdecr'd P
|
|
why might PTH be increased in renal disease
|
renal ds --> decr'd vit D conversion --> decr'd Ca absorption (gut) --> incr'd PTH
|
|
what happens to phosphate in px with hyperPTH and renal disease
|
increases
|
|
likely cause of increased PTH, decreased Ca and increased P
|
renal failure
|
|
Ca2+, Phos, Alk phos, PTH in:pagets
|
Ca2+: normalPhos: normalAlk phos: incr'dPTH: normal
|
|
Ca2+, Phos, Alk phos, PTH in:osteomalacia/rickets
|
Ca2+: decr'dPhos: decr'dAlk phos: nl/incr'dPTH: incr'd
|
|
Ca2+, Phos, Alk phos, PTH in:chronic renal failure
|
Ca2+: decr'dPhos: incr'dAlk phos: nl/incr'dPTH: incr'd
|
|
Ca2+, Phos, Alk phos, PTH in:osteoporosis
|
Ca2+: normalPhos: normalAlk phos: normalPTH: normal
|
|
Ca2+, Phos, Alk phos, PTH in:osteopetrosis
|
Ca2+: normalPhos: normalAlk phos: normalPTH: normal
|
|
Ca2+, Phos, Alk phos, PTH in:primary hyperPTH
|
Ca2+: incr'dPhos: decr'dAlk phos: incr'dPTH: incr'd
|
|
Ca2+, Phos, Alk phos, PTH in:hypoPTH
|
Ca2+: decr'dPhos: incr'dAlk phos: normalPTH: decr'd
|
|
Ca2+, Phos, Alk phos, PTH in:pseudohypoPTH
|
Ca2+: decr'dPhos: incr'dAlk phos: normalPTH: incr'd
|
|
what is the disease a/w shortened 4th and 5th digits
|
albrights hereditary osteodystrophy
|
|
what are the indications for surgical parathyroidectomy
|
SYMPTOMATIC:bonesstonesgroanspsychiatric overtonesINCR'D [Ca2+]:> 1.0 mg/dl above upper limits of nlDECR'D Cr Cl (reduced by 30%) --> incr'd CrAGE < 50 y/oBMD:T-score < -2.5 (at any site)
|
|
If parathyroid adenoma is found & surgery is indicated, what is removed
|
REMOVAL of ONLY the gland containing adenomaBIOPSY of 1 - 3 other glands
|
|
If parathyroid hyperplasia is found & surgery is indicated, what is removed
|
REMOVAL of 3 & 1/2 glands SURGICALLY "CLIP" the remaining 1/2 (or forearm autotrasplantation in cases of high recurrence e.g. Men type 1 & IIa)
|
|
what happens to phosphate in pts with hyperPTH caused by renal ds
|
HYPERPHOSPHATEMIA (2nd/2 kidney's inability to excrete phosphate)
|
|
Dxpx with exophthalmos, pretibial myxedema and decreased TSH
|
graves
|
|
worrisome SE of ADHD Rx, Atomoxetine
|
incr'd suicidal ideationhepatic injury
|
|
what are common SE or atypical antipsychotics
|
fewer mvmt SE'sfewer anticholinergic SE'sWt gain --> DM/DKA (esp, Olanzapine)
|
|
Rx for prolactinoma
|
DOPAMINE AGONISTS:cabergolinebromocriptine or pergolide
|
|
Rx for female with prolactinoma > 3cm with desire to be pregnant
|
withhold DA agonisttransphenoidal surgery (even if DA agonist is effective)
|
|
what are common complications of acromegaly
|
cardiac failureDMspinal cord compressionoptic nerve compressionarthropathy
|
|
screening test for acromegaly
|
IGF-1 levels
|
|
confirmatory test for acromegaly
|
oral glucose suppression test(75g glucose --> measure GH at 1hr & 2hr;[GH] > 1ng/mL = acromegaly)
|
|
what should be done if a px tests positive for acromegaly
|
pituitary MRI to evaluate for mass or empty sella (MCC of acromegaly = pituitary adenoma)
|
|
what should be done in empty sella syndrome
|
nothing/reassurance
|
|
Rx for acromegaly
|
1ST LINE = OCTREOTIDE(somatostatin analog: inhibits GH secretion)2ND LINE = CABERGOLINE (DA agonist: inhibits PRL & GH secretion)3RD LINE = PEGVISOMANT (GH receptor antagonist)DEFINITIVE TX: transphenoidal resection
|
|
What is typical hyperprolactinoma presentation
|
MALES:incr'd PRL --> decr'd LH/FSH --> decr'd Testosteronedecr'd LH/FSH --> HYPOGONADISMdecr'd Testosterone --> FATIGUE, LOW LIBIDOFEMALES:incr'd PRL --> decr'd LH/FSH --> decr'd E2/Progesterone --> AMENORRHEA GALACTORRHEA
|
|
what Rx cause elevated prolactin levels
|
PHENOTHIAZINES:thioridazineprochlorperazinepromothiazineOTHER ANTIPSYCHOTICS:risperidonehaloperidolMETHYLDOPAVERAPAMIL
|
|
next step in management of a px with non-drug-induced hyperprolactinemia
|
MRI of brain (r/o pituitary adenoma)TSH levels (r/o hypothyroidism)
|
|
what visual field deficit is a/w prolactinoma
|
bitemporal hemianopsia
|
|
what is a lactotroph adenoma
|
prolactinoma
|
|
what is a somatotroph adenoma
|
growth hormone secreting adenoma
|
|
Rx for hypercalcemia
|
IVF's --> urinate Ca2+ outloops (e.g. furosemide)
|
|
Dxpx with hearing loss and vertigo, examination shows a greyish white pearly lesion involving the TM
|
cholesteatoma
|
|
what marker is most accurate to Dx an androgen-producing tumor in a woman
|
DHEA-S (NOTE: DHEA-S made ONLY by adrenals;DHEA & testosterone made by adrenals & ovaries)
|
|
what are the elctrolyte abnormalities found in hyperaldosteronism
|
hypokalemiamildly elevated Na+metabolic alkalosis
|
|
what is the hyperaldosteronism triad
|
TRIAD:HTNhypokalemiametabolic alkalosis
|
|
what is the most specific lab finding in making the Dx of primary hyperaldosteronism
|
HIGH PAC:PRC RatioPAC is incPRC is dec(NOTE:PAC = plasma aldosterone concentrationPRC = plasma renin concentration)
|
|
what steroid is used to replace aldosterone
|
fludracortisone (100 x stronger than aldosterone)
|
|
what steroid is most like cortisol
|
Hydrocodone (has glucocorticoid & mineralcorticoid action)
|
|
What is the MC pituitary tumor & what is the rx
|
MC = ProlactinomaTx = bromocriptine, cabergoline, or pergolide
|
|
Dx:16 y/o with left arm paralysis (no medical cause is found) after her boyfriend dies in a MVA
|
Conversion d/o
|
|
What effect would giving a B-Blocker have on a pt with HTN due to pheochromacytoma
|
Worsen HTN due to unopposed a1-activity
|
|
What is the likely condition of a female infant with virilization of the genitalia & hypotension
|
21a-hydroxylase def --> CAH
|
|
What serum lab abnormalities would you see in 17a-hydroxylase deficiency & in 21a-hydroxylase deficiency
|
17a-HYDROXYLASE DEFICIENCY:hypokalemiamild hypernatremia+ HTN21a-HYDROXYLASE DEFICIENCY:hyperkalemiahyponatremia+ hypotension
|
|
Dx:A pt with acromegaly is found to have elevated Ca2+ on a blood draw during a w/u of his peptic ulcer
|
DX: MEN I ("3 P's"):acromegaly = pituitary d/oelevated Ca2+ = hyperparathyroidismpeptic ulcer = gastrin-secreting tumor (ZES)
|
|
What is involved in MEN I Syndrome
|
Mnemonic: "3 P's"parathyroid hyperplasiapituitarypancrease (islet) or GI
|
|
What is involved in MEN IIa Syndrome
|
Mnemonic: "1M + 2 P's"medullary thyroid carcinomaparathyroid hyperplasiapheochromacytoma
|
|
What is involved in MEN IIb Syndrome
|
Mnemonic: "2 M's + 1P"medullary thyroid carcinomamucosal neuromaspheochromacytoma
|
|
What oncogene is involved with the MEN Syndromes & with which type is it associated
|
RET Proto-Oncogenea/w Men IIa & Men IIb
|
|
What are the MCC's of eosinophilia |
Mnemonic: "DN-AAA-CP" (D-N triple-A C-P):DrugsNeoplasmsAllergic causes (allergies, asthma, Churg-Strauss)Addison's DsAcute Interstitial NephritisCVD'sParasitic Infections (including Loeffler's Eosinophilic Pneumonitis 2nd/2 Ascaris Lumbricoides)
|
|
causes of secondary HTN
|
pheochromacytomahyperaldosteronismexcess glucocorticoidscushing's syndromerenal artery stenosisCAH (11a-OH & 17a-OH def's)CKDOCPcoarctation of aorta
|
|
The most common cause of hypothyroidism.
|
Hashimoto's thyroiditis
|
|
Lab findings in Hashimoto's thyroiditis.
|
high TSH, low T4,antimicrosomal antibodies
|
|
Exophalamos, pretibial myxedema, & ⇩TSH
|
Grave's disease
|
|
The most common cause of Cushing's syndrome.
|
Iatrogenic steroid administration. (2nd most common is Cushing's disease)
|
|
A patient presents w/ signs of hypocalcemia, high phosphorus, & low PTH.
|
Hypoparathyroidism
|
|
"Stones, bones, groans, psychiatric overtones."
|
Signs & symptoms of hypercalcemia.
|
|
A patient complains of headache, weakness, & polyuria; exam reveals hypertension & tetany. Labs reveal hypernatremia, hypokalemia, & metabolic alkalosis.
|
Primary hyperaldosteronism (due to Conn's syndrome or bilateral adrenal hyperplasia)
|
|
A patients presents with tachycardia, wild swings in BP, headache, diaphoresis, altered mental status, & a sense of panic.
|
Pheochromocytoma
|
|
Should α- or β-antagonists be used first in treating pheochromocytoma?
|
α-antagonists(phentolamine & phenoxybenzamine)
|
|
A patient w/ a history of lithium use presents with copious amounts of dilute urine.
|
Nephrogenic diabetes insipidus (DI)
|
|
Treatment of central diabetes insipidus.
|
Administration of DDAVP ⇩serum osmolality & free water restriction
|
|
A postoperative patient w/ significant pain presents with hyponatremia & normal volume status.
|
SIADH due to stress
|
|
An antidiabetic agent associated w/ lactic acidosis.
|
Metformin
|
|
A patient presents w/ weakness, nausea, vomiting, weight loss, & new skin pigmentation. Labs show hyponatremia & hyperkalemia. Treatment?
|
Primary adrenal insufficiency (Addison's disease).Treat with replacement glucocorticoids, mineralcorticids, & IV fluids.
|
|
Goal hemoglobin A1c for a patient w/ DM.
|
<7.0
|
|
Treatment of DKA. |
Fluids, insulin, & aggressive replacement of electrolytes (e.g. K+)
|
|
What are β-blockers contraindicated in diabetics? |
They can mask symptoms of hypoglycemia. (How?) |
|
overdose of what causes metabolic acidosis and retinal damage leading to blindness
|
methanol
|
|
what electrolyte abnormalities are found in hyperaldosteronism
|
metabolic alkalosishypokalemiamild hypernatremia
|
|
MC coronary artery to become occluded
|
LAD
|
|
ECG leads that correspond to occlusion of LAD
|
V2-V4
|
|
in which phase of the cardiac cycle do coronary arteries fill with blood
|
diastole
|
|
how can you calculate mean arterial pressure
|
2/3 diastole + 1/3 systoleCO x TPR
|
|
what electrophysiologic reason could make a QRS complex become wider
|
origin of depolarization is distal to AV nodedelay along the ventricular conduction system
|
|
Dx, Rx and MCC:otoscopy of a child presenting with acute onset of ear pain reveals large reddish vesicles on the TM
|
Dx: bullous myringitisMCC: mycoplasmaRx: macrolides
|
|
Dx & Rxburn px with cherry red flushed skin, O2 sat is normal but carboxyhemogllobin is elevated
|
Dx: CO2 PoisoningTx: 100% O2 or hyperbaric O2
|
|
Rxpatient with aldosterone deficiency
|
fludrocortisone
|
|
EKG finding that is suggestive of myocardial ischemia during exercise
|
**ST depression > 1mmST elevationU-wave inversion
|
|
if angina or ischemia occurs during a stress test, what test should follow
|
coronary angiography with possible angioplasty
|
|
how do statins reduce the incidence of myocardial infarction
|
lower LDLanti-inflammatory effectsinhibit plt thrombus formationimprove coronary endothelial function
|
|
lipid lowering agent:SE flushing
|
niacin
|
|
lipid lowering agent:SE elevated LFT and myositis
|
statins and fibrates
|
|
lipid lowering agent:SE of GI discomfort, bad taste
|
bile acid sequestrants
|
|
lipid lowering agent:best for HDL
|
niacin
|
|
lipid lowering agent:best for TGs
|
fibrates
|
|
lipid lowering agent:best for LDL/cholesterol
|
statins
|
|
lipid lowering agent:binds to C difficile
|
cholestyramine
|
|
LDL recommendations for px based on their CAD risk factors
|
0 - 1 RF's: LDL < 1602+ RF's: LDL < 130CAD/Eq: LDL <100
|
|
what are risks for CAD
|
tabacco useHTN or currently on a antihypertensiveHDL < 40FHx of CAD (males < 55 & females < 65)AGE (males > 45 & females > 55)
|
|
how can the "flushing" reaction of niacin be prevented
|
ASA (1/2 - 1 hr before taking niacin)NSAID's (1/2 - 1 hr before taking niacin)continued use(flushing reaction will subside with time)take it in the eveningtake with a low-fat snackavoid hot beverages & spicy foods
|
|
with what are chvostek and trousseau sign assoc'd
|
hypocalcemia
|
|
area of the brain lesioned:contralateral hemiballismus
|
subthalamic nucleus
|
|
area of the brain lesioned:hemispatial neglect syndrome
|
non-dominant parietal lobe
|
|
area of the brain lesioned:coma
|
reticular activating system, RAS (i.e. pontine lesion)
|
|
area of the brain lesioned:poor repitition
|
arcuate fasciculus
|
|
area of the brain lesioned:poor comprehension
|
Wernicke's area
|
|
area of the brain lesioned:poor vocal expression
|
broca's area
|
|
Rx for prinzmetal angina
|
**Dihydropyridine CCB's (nifedopine, amlodipine)Non-dihydropyridine CCB's (verapamil, diltiazem)NitratesAVOID: non-selective B-Blockers (e.g. propranolol)ASA
|
|
most likely cause of chest painST segment elevation only during brief episodes of CP
|
prinzmetal angina
|
|
most likely cause of chest painlocalized with one finger
|
costochondritis
|
|
most likely cause of chest painchest wall tenderness on palpation
|
musculoskeletal
|
|
most likely cause of chest painrapid onset sharp CP that radiates to the scapula
|
aortic dissection
|
|
most likely cause of chest painrapid onset sharp CP in 20 y/o with assoc'd dyspnea
|
spontaneous pneumothorax
|
|
most likely cause of chest painoccurs after meals, improved with antacids
|
GERDesophageal spasm
|
|
most likely cause of chest painsharp pain lasting hours to days and somewhat relieved by sitting forward
|
pericarditis
|
|
most likely cause of chest painpain worsened by deep breathing or motion
|
pleuritic or musculoskeletal
|
|
most likely cause of chest painalong dermatome
|
Herpes zoster (pain may appear before the rash)
|
|
most likely cause of chest painMCC of noncardiac CP
|
GERDmusculoskeletal
|
|
most likely cause of chest painacute onset dyspnea, tachycardia, confusion in hospitalized pt
|
pulmonary embolism
|
|
most likely cause of chest painpain began a day following the start of an intense exercise program
|
musculoskeletal
|
|
most likely cause of chest painwidened mediastinum on CXR
|
aortic dissection
|
|
which patient population is more likely to have atypical angina during episode of myocardial ischemia
|
diabeticswomenelderly
|
|
how does nitroglycerin work acutely in cardiac ischemic episodes
|
PERIPHERAL VENOUS VASODILATION -->decr'd preloaddecr'd cardiac O2 demandNOTE: with ACUTE ISCHEMIA, coronary arteries are already maximally dilated, therefore, NTG cannot further dilate them!
|
|
why shouldnt chest pain relieved by nitroglycerin be diagnostic of cardiac nature
|
can also relieve esophageal spasm and GERD
|
|
MOA:streptokinase
|
converts plasminogen --> plasmin --> degrades fibrin
|
|
MOA:aspirin
|
irreversibly inhibits COX 1 - 2 --> prevents plt aggregation
|
|
MOA:clopidogrel
|
ADP receptor blocker --> prevents plt aggregation
|
|
MOA:abciximab
|
GP IIb/IIIa Inhibitor --> prevents plt aggregation
|
|
MOA:tirofiban
|
GP IIb/IIIa Inhibitor --> prevents plt aggregation
|
|
MOA:ticlopidine
|
ADP receptor blocker --> prevents plt aggregation
|
|
MOA:enoxaparin
|
catalyzes activation of antithrombin
|
|
MOA:eptifibatide
|
GP IIb/IIIa Inhibitor --> prevents plt aggregation
|
|
cause of hyperthyroidism: extremely tender thyroid gland
|
subacute thyroiditis (i.e. De Quervain's)
|
|
cause of hyperthyroidism:pretibial myxedema
|
Grave's disease
|
|
cause of hyperthyroidism:pride in recent wt loss, medical professional
|
exogenous thyroid use
|
|
cause of hyperthyroidism:palpation of single thyroid nodule
|
toxic thyroid adenoma
|
|
cause of hyperthyroidism:palpation of multiple thyroid nodules
|
multinodular goiter
|
|
cause of hyperthyroidism:recent study using IV contrast dye
|
job-basedow phenomenon
|
|
cause of hyperthyroidism:proptosis, ocular edema, & ocular injection
|
Grave's disease
|
|
cause of hyperthyroidism:h/o thyroidectomy or radioablation of thyroid
|
excess thyroid hormone replacement
|
|
Rx of opioid overdose
|
naloxonenaltrexone
|
|
classic presentation of aspirin overdose
|
n/v & dehydrationtinnitushyperthermiaAMSrespiratory alkalosis (hyperventilation) --> mixed respiratory acidosis & metabolic acidosis with high AG
|
|
first line treatment for growth hormone-secreting pituitary adenoma
|
transsphenoidal tumor resection
|
|
meds for all post-MI outpatients
|
ASA or clopidogrelB-BlockersACEI/ARBstatinaldosterone antagonist
|
|
Rx proven to reduce mortality following MI
|
B-BlockersACEI's/ARB'sStatins
|
|
what labs should be ordered in patients suspected of having an MI
|
SERIAL CARDIAC ENZYMES:3 sets of Troponin-I q8 hrs3 sets of CKMB q8 hrs
|
|
MCC of death in patients with acute myocardial infarction
|
arrhythmia (V-Fib)
|
|
What is timeline for thrombolytics to be given in MI vs CVA
|
MI: 12 hrs after onset of sx'sCVA: 3 hrs after onset of sx's
|
|
EKG leads & involved vessel:anterior wall MI
|
LEADS: V2 - V4VESSEL: LAD
|
|
EKG leads & involved vessel:septal MI
|
LEADS: V1 - V3VESSEL: LAD
|
|
EKG leads & involved vessel:inferior wall MI
|
LEADS: II, III, aVFVESSEL: posterior descending
|
|
EKG leads & involved vessel:lateral wall MI
|
LEADS: I, aVL, V5, V6VESSEL: LAD/left circumflex
|
|
Dxpx has HTN, mild hypernatremia, hypokalemia, metabolic alkalosis
|
PRIMARY HYPERALDOSTERONISM:Conn's Syndromeb/l adrenal hyperplasia
|
|
antidote for:salicylates
|
activated charcoalNa+Bicarbdialysis
|
|
antidote for:B-Blocker
|
atropineglucagonCa2+insulin & dextroseatropine
|
|
antidote for:digoxin
|
activated charcoalDig Fab fragments
|
|
antidote for:iron
|
deferoxamine
|
|
antidote for:copper
|
penicillamine
|
|
antidote for:t-PA and Streptokinase
|
aminocaproic acid
|
|
Rx for MI due to cocaine overdose
|
Benzo's (e.g. Lorazepam)CCB's** DO NOT GIVE B-BLOCKERS
|
|
type of heart block:PR interval is longer than .2 sec (5 small boxes)
|
1st degree
|
|
type of heart block:no relationship between P and QRS
|
3rd degree
|
|
type of heart block:PR interval becomes progressively longer until beat dropped
|
2nd degree - Type I (aka Weinckebach's)
|
|
type of heart block:PR interval fixed but with occasional blocked beats
|
2nd degree - Type II
|
|
which heart block needs a pacemaker
|
2nd degree - Type II3rd degree
|
|
an EKG shows complete independence of P waves and QRS, what is the next best step
|
Dx: 3rd degree blockTx: pacemaker
|
|
pathology with EKG:narrow QRS not a/w P wavesrate of 60 bpm
|
junctional rhythm
|
|
pathology with EKG:narrow QRS not a/w P waverate > 60 but < 100
|
accelerated junctional rhythm
|
|
pathology with EKG:narrow QRS not a/w P waverate > 100
|
junctional tachycardia
|
|
What is the tx for premature atrial contractions (PAC's)
|
observationreduce caffeinestop smokingr/o hyperthyroidism
|
|
px has atrial fib with rapid ventricular rate, he had a chronic atrial fib previously, what should be done before cardioversion
|
transesophageal echo (to look for atrial thrombus)
|
|
which endocrine disorder can cause atrial fib
|
hyperthyroidism
|
|
what is the drug of choice for acute onset atrial fib with rapid ventricular rate in a px with WPW
|
procainamideelectrical cardioversion
|
|
Dx for multifocal atrial bradycardia (MFAB)
|
3+ different P wave morphologies< 60 bpm
|
|
Dx for wandering pacemaker (aka multifocal atrial rhythm)
|
3+ different P wave morphologies< 100 bpm
|
|
Dx for multifocal atrial tachycardia (MFAT)
|
3+ different P wave morphologies> 100 bpm
|
|
what is the drug of choice for paroxysmal supraventricular tachycardia
|
carotid massageIV adenosine
|
|
pathology with EKG:wide QRS not a/w P wavesrate 20-40
|
ventricular rhythm
|
|
pathology with EKG:wide QRS not a/w P waves rate > 40 but < 100
|
accelerated ventricular rhythm
|
|
pathology with EKG:wide QRS not a/w P waverate > 100
|
ventricular tachy
|
|
pathology with EKG:chaotic, no p-waves, no QRS
|
V fib
|
|
pathology with EKG:erratic QRS that varies in amplitude in a repeating pattern (sinusoidal)
|
torsades
|
|
antiarrhythmic that should be avoided in px with preexisting lung disease
|
Amiodarone
|
|
What are some common SE's with the use of amiodarone & what should be monitored
|
Pulmonary fibrosis (monitor PFT's & diffusion capacity before starting & q 6 months)Liver damage (monitor LFT's)Hyper/hypothyroidism (monitor TFT's)
|
|
what are the classes of anti-arrhythmics
|
"SoBe PoCa"CLASS I: Na+ channel blockers ("So" = sodium)CLASS II: B-Blockers ("Be" = Beta)CLASS III: K+ channel blockers ("Po" = potassium)CLASS IV: CCB's ("Ca" = calcium)OTHER: Adenosine
|
|
generally, what arrhythmias do each anti-arrhythmic class tx
|
CLASS I: V-Tach (lidocaine)CLASS II:PVC'sA-fib/flutterMATV-TachCLASS III:A-fib/flutterCLASS IV:A-fib/flutterPSVTMATADENOSINE:PSVT (unless 2nd/2 WPW)
|
|
What is Rx for SVT vs SVT 2nd/2 WPW
|
SVT: AdenosineSVT 2ND/2 WPW:amiodaroneprocainamidecatheter ablation of accessory pathway**DO NOT GIVE ADENOSINE
|
|
area of the brain lesioned:resting tremor
|
basal ganglia
|
|
area of the brain lesioned:intention tremor
|
cerebellar hemisphere
|
|
area of the brain lesioned:hyperorality, hypersexuality, disinhibited behavior
|
b/l amygdala
|
|
area of the brain lesioned:personality changes
|
frontal lobe
|
|
area of the brain lesioned:dysarthria
|
cerebellar vermis
|
|
area of the brain lesioned:agraphia, acalculia, & finger agnosia
|
L parietal (dominant)
|
|
organism a/w with causing infection in burn px
|
pseudomonas aeruginosa
|
|
Rx for atrial fib of unknown duration
|
RATE CONTROL:B-BlockerNon-DHP CCB (e.g. verapamil)DigoxinANTICOAGULATE:WarfarinHeparin
|
|
what are Kerley B lines and what are they associated with
|
subpleural interstitial (interlobular septa) thickeningseen on CXR in periphery of the lower lung zones2nd/2 pulmonary edemaETIOLOGIES:LV failure, mitral valve diseaselymphatic obstruction, lymphangitis, carcinomatosisasbestosis, sarcoidosis
|
|
what is the normal range for the ejection fractionwhat EF is considered HF
|
nl = 55-75 %HF < 55%
|
|
what two cardiovascular diseases have the biggest risk factors for CHF
|
HTNCAD
|
|
what ECG finding may indicate a very early stage HF
|
LVH
|
|
what lab markers are used to help Dx acute exacerbations of CHF
|
BNP
|
|
what medications are important in the outpatient Rx for chronic congestive heart failure
|
**ACEI's (& certain ARB's)**B-Blockers (bisoprol, carvedilol, metoprolol XR)**Aldosterone Antagonist (e.g. spironolactone)Loop diuretics (e.g. furosemide)Digoxinloopsaldosterone -digoxin
|
|
Rx for acute exacerbations of CHF
|
DISCONTINUE B-BLOCKERS (during exacerbation)"LMNOP"loopsmorphinenitratesoxygenposition/pressors (e.g. dobutamine)
|
|
in which population are triptans contraindicated
|
CADprinzmetal anginapregnancy
|
|
what drugs block transmission through AV node
|
B-BlockersNon-DHP CCB's (e.g. verapamil, diltiazem)digoxin
|
|
what causes stones, bones, groans and psychic overtones
|
hypercalcemia (MCC = hyperparathyroidism)
|
|
what valves have blood flowing during systole
|
aortic & pulmonic valves
|
|
what valves have blood flowing during diastole
|
mitral & tricuspid valves
|
|
what are the systolic heart murmurs
|
AS/PSMR/TRVSD/MVP
|
|
what are the diastolic heart murmurs
|
MS/TSAR/PR
|
|
what is next step in mgmt in w/u of a low-grade systolic murmur in an otherwise healthy, asx'c pt
|
no further w/u
|
|
what is next step in mgmt in w/u of a diastolic murmur in an otherwise healthy, asx'c pt
|
echocardiogram
|
|
type of heart murmur:diastolic murmur heard best at LLSB, that increases with inspiration
|
tricuspid stenosis
|
|
type of heart murmur:late diastolic murmur with an opening snap (no change with inspiration)
|
mitral stenosis
|
|
type of heart murmur:systolic murmur heard best in the 2nd RICS, parasternal
|
aortic stenosis
|
|
type of heart murmur:systolic murmur heard best in the 2nd LICS, parasternal
|
pulmonic stenosis
|
|
type of heart murmur:late systolic murmur best heard at the apex
|
MVP
|
|
type of heart murmur:diastolic murmur with widened pulse pressure
|
aortic regurg
|
|
type of heart murmur:holosystolic murmur that is louder with inspiration at the LLSB
|
tricuspid regurgVSD
|
|
type of heart murmur:holosystolic murmur heard at the apex and radiates to the axilla
|
mitral regurg
|
|
what is the MCC of CP in a pt with sudden tearing CP radiating to the back
|
aortic dissection
|
|
increased skin pigmentation is seen in pts with which kind of adrenal insufficiency
|
primary adrenal insufficiency (aka Addison's)
|
|
what are the classic sx's of Parkinson's
|
resting tremor ("pill rolling")cog-wheel rigiditymask-like faciesshuffling gaitpostural instability
|
|
What is Kussmaul sign
|
Definition: JVD with inspirationPathology: decr'd capacity of RVDiseases: constrictive pericarditis >> tamponade
|
|
What is Pulsus Paradoxus
|
Definition: decr'd SBP with inspiration ( > 10 mmHg) Pathology: decr'd capacity of LVDiseases: tamponade >> pericarditis
|
|
What is Beck's Triad & when is it seen
|
Seen with TAMPONADEJVD (decr'd capacity of RV)hypotension (decr'd capacity of LV)distant heart sounds
|
|
What is the classic appearance of the heart on CXR of a pt with pericardial effusion
|
enlarged, globular heart ("water bottle" shaped)
|
|
What is the tx for cardiac tamponade
|
immediate pericardiocentesis
|
|
What disease has signs of heart failure + DM + elevated LFT's
|
HEMOCHROMATOSIS:Fe2+ deposition in heart --> dilated/restrictive cardiomyopathyFe2+ deposition in pancrease --> DMFe2+ deposition in liver --> incr'd LFT's
|
|
in what scenarios might you see kussmaul sign
|
Kussmaul sign = incr'd JVD with inspirationconstrictive pericarditisrestrictive cardiomyopathycardiac tamponadeRV infarctmassive PE
|
|
what are the symptoms of neuroleptic malignant syndrome
|
AMSmuscle rigidityhyperthermiaautonomic instabilityrhabdomyolysis
|
|
what is the treatment of neuroleptic malignant syndrome
|
d/c neurolepticcooling (for hyperthermia)dantrolene (or bromocriptine or amantadine)IVF's (to prevent rhabdomyolysis)
|
|
what are the common viruses of myocarditis
|
echovirusadenovirusEBV/CMVcoxsackieinfluenza
|
|
Dx:S. american with cardiomegaly and achalasia
|
chagas disease (trypanosoma cruzi)
|
|
what is the bug that causes Chagas Ds & what are the common findings
|
Bug: trypanosoma cruziSx's: cardiomegaly, mega-esophagus (a/w achalasia), mega-colon
|
|
what are the major jones criteria for rheumatic heart disease
|
joint pain (arthropathy)heart (pancarditis)subcutaneous noduleserythema marginatumsydenham chorea
|
|
What bugs should be considered with high suspicion of endocarditis but cultures are negative
|
"HACEK" organisims:haemophilusactinobacilluscardiobacteriumeikenellakingella
|
|
what study is used to visualize a vegetation in a heart valve
|
TEE
|
|
Describe the 4 peripheral signs of endocarditis:
|
JANEWAY LESIONS:PAINLESS petechiae on palm/solesOSLER'S NODES:PAINFUL nodules on fingers/toesROTH SPOTS:retinal hemorrhagesSPLINTER HEMORRHAGES:petechiae under the nails
|
|
Dx:hypocalcemia, high phosphorus, & low PTH
|
hypoparathyroidism
|
|
what is the classic EKG finding in pericarditis
|
Global ST elevation (i.e. seen in all leads)PR interval depression
|
|
what commonly causes heart failure in young patients
|
myocarditis
|
|
What is pre-HTN
|
120-139/80-89
|
|
when should pre-HTN be tx'd
|
H/O OF COMORBIDITY:CV diseaseDMCKDend-organ damage
|
|
what is the most effective in reducing BP
|
Weight loss
|
|
what is the MCC of renal artery stenosis
|
fibromuscular dysplasia
|
|
screening test for renal artery stenosis
|
MRA of renal arteries
|
|
gold standard to Dx renal artery stenosis
|
renal arteriogram
|
|
what does renal artery stenosis show on radiologicimaging
|
"beads-on-a-string" appearance
|
|
MCC of secondary HTN
|
renal disease (CKD, ESRD, RAS)
|
|
most likely cause of secondary HTN:HTN in arms but low BP in legs
|
coarctation of aorta
|
|
most likely cause of secondary HTN:proteinuria
|
renal disease
|
|
most likely cause of secondary HTN:hypokalemia
|
primary hyperaldosteronismRAS
|
|
most likely cause of secondary HTN:tachycardia, diarrhea, heat intolerance
|
hyperthyroidism
|
|
most likely cause of secondary HTN:hyperkalemia
|
renal failure
|
|
most likely cause of secondary HTN:episodic sweating and tachycardia
|
pheochromocytoma
|
|
what lab marker is used to help dx acute CHF exacerbation
|
BNP
|
|
w/u for underlying cause of DKA
|
R/O INFECTION:blood/urine cultures, UA, CXRR/O DRUGS:tox screenR/O PANCREATITIS:amylase/lipaseR/O MI:EKGcardiac enzymes x 3
|
|
what is the preferred initial antihypertensive in a px with no comorbidities
|
thiazide
|
|
first line antihypertensive:diabetes
|
ACEI's/ARB's
|
|
first line antihypertensive:heart failure
|
ACEI'sB-BlockersAldosterone antagonist
|
|
first line antihypertensive:BPH
|
a1-Blocker
|
|
first line antihypertensive:LV hypertrophy
|
ACEI's/ARB's
|
|
first line antihypertensive:hyperthyroidism
|
B-Blocker (e.g. propranolol)
|
|
first line antihypertensive:osteoporosis
|
thiazides
|
|
first line antihypertensive:benign essential tremor
|
B-Blocker (e.g. propranolol)
|
|
first line antihypertensive:post-menopausal woman
|
thiazides
|
|
first line antihypertensive:migraines
|
B-BlockersCCB's (e.g. verapamil)
|
|
SE of antihypertensive:first dose orthostatic hypotension
|
a-Blockers
|
|
SE of antihypertensive:hypertrichosis
|
minoxidil
|
|
SE of antihypertensive:dry mouth, sedation, severe rebound HTN
|
clonidine (a2-agonist)
|
|
SE of antihypertensive:bradycardia, impotence, asthma exacerbation
|
non-selective B-Blocker
|
|
SE of antihypertensive:reflex tachycardia
|
vasodilators (eg. hydralazine, nitrates)
|
|
SE of antihypertensive:cough
|
ACEI's
|
|
SE of antihypertensive:avoid in px with sulfa allergy
|
loopsthiazides
|
|
SE of antihypertensive:angioedema
|
ACEI's
|
|
SE of antihypertensive:development of drug-induced lupus (anti-histone AB's)
|
hydralazine
|
|
SE of antihypertensive:cyanide toxicity
|
Na+ nitroprusside
|
|
what is dilated by:hydralazine
|
arteries
|
|
what is dilated by:CCB
|
arteries & veins
|
|
what is dilated by:nitroprusside
|
arteries & veins
|
|
what is dilated by:nitroglycerin
|
venodilation
|
|
what is the MCC of cushings syndrome
|
#1 exogenous glucocorticoids#2 pituitary ACTH-secreting tumor (i.e. Cushing's Ds)
|
|
what is the Parkland burn formula
|
4mL x body wt in kg x %BSA:1/2 given in 1st 8 hrs1/2 given over following 16 hrs
|
|
what is becks triad for cardiac tamponade
|
JVD (decr'd capacity of RV)hypotension (decr'd capacity of LV)distant heart sounds
|
|
hypoperfusion and resultant tissue ischemia are the concern in shock pt'swhat is the chemical marker for this
|
lactate
|
|
what complications can arise from the use of vasopressors such as NE in treating shock
|
ischemia/necrosis of fingertips/toesmesenteric ischemiarenal failure
|
|
pathophysiology of shock:cardiogenic
|
failure of the pump
|
|
pathophysiology of shock:extracardiogenic
|
compression of the pump
|
|
pathophysiology of shock:hypovolemic
|
not enough fluid to pump
|
|
pathophysiology of shock:anaphylactic
|
widespread vasodilation in response to allergen
|
|
pathophysiology of shock:neurogenic
|
widespread vasodilation due to loss of autonomic-regulated vascular tone
|
|
pathophysiology of shock:septic
|
widespread vasodilation due to massive release of inflammatory mediators
|
|
CO, SVR, PCWP:cardiogenic shock
|
CO: decr'dSVR: incr'dPCWP: incr'd(source: Step-Up-to-Med, 2nd ed)
|
|
CO, SVR, PCWP:hypovolemic shock
|
CO: decr'dSVR: incr'dPCWP: decr'd(source: Step-Up-to-Med, 2nd ed)
|
|
CO, SVR, PCWP:neurogenic
|
CO: decr'dSVR: decr'dPCWP: decr'd(source: Step-Up-to-Med, 2nd ed)
|
|
CO, SVR, PCWP:septic
|
CO: incr'dSVR: decr'dPCWP: decr'd(source: Step-Up-to-Med, 2nd ed)
|
|
what are the 2 MC SE's of statin use & assoc'd labs
|
hepatotoxicity: elevated LFTsmyositis: elevated CPK
|
|
which BP medication should be avoided in px with ischemic stroke or SAH b/c of the increase in ICP
|
nitroprussidenitroglycerin
|
|
what are the indications for surgical repair of aortic aneurysm
|
diameter > 5.5 cm for mendiameter > 5.0 cm for womendiameter increase by more than 5 mm in 6 monthssx'c (e.g. tenderness, pain in abdomen or back)
|
|
What are the components of management of peripheral artery disease (PAD)
|
smoking cessationexercise (to increase collateral flow)glucose & BP controlcilastozol (improve flow to LE & decr claudication)ASA or clopidogrel + statin (to reduce CV events)
|
|
how do confirm Dx of aortic dissection
|
CT - chest with contrast
|
|
Who should be screened for an AAA
|
MEN 65-75 y/o with h/o smokingSX'C PT's (e.g. pulsatile abdominal mass)
|
|
What study should be ordered for a pt suspected of having a AAA
|
ultrasound
|
|
what is the next best step in the management of a px with a DVT that has a high likelihood of falling
|
IVC filter
|
|
How is Kawasaki's dx'd
|
Fever + 4/5 "CRASH" sx'sConjuctivitis (b/l, non-exudative, painless)Rash (truncal)Adenopathy (cervical LN's)Strawberry tongue + diffuse mucous membrane erythemaHands and Feet: edema with induration, erythema, or desquamation
|
|
how is kawasaki treated
|
IVIGhigh-dose aspirin (acute phase)low-dose aspirin (48-hrs after fever resolution)echocardiogram(during acute phase + 6-8 wks later)
|
|
vasculitis a/w:weak pulse on upper extremity
|
takayasu's
|
|
vasculitis a/w:necotizing immune complex inflammation of visceral/renal vessels
|
PAN
|
|
vasculitis a/w:young male smokers
|
buerger's
|
|
vasculitis a/w:young asian women
|
takayasu's
|
|
vasculitis a/w:young asthmatics
|
churg-strauss
|
|
vasculitis a/w:infants and young children, involves coronary arteries
|
kawasaki
|
|
vasculitis a/w:MCC of vasculitis
|
temporal arteritis
|
|
vasculitis a/w:a/w Hep B infection
|
PAN
|
|
vasculitis a/w:occlusion of opthalmic artery that leads to blindness
|
temporal arteritis
|
|
vasculitis a/w:unilateral headache, jaw claudication
|
temporal arteritis
|
|
what autoimmune complication occurs 2-4 weeks post-MI
|
dressler syndrome --> pericarditis (fever, incr'd ESR)
|
|
what type of psychotherapy is used to treat phobias, obsessive compulsive disorders and panic disorders
|
cognitive behavioral therapy
|
|
ebsteins anomoly is a/w
|
maternal lithium use
|
|
what is found in ebsteins anomaly
|
tricuspid leaflets are displaced into RVhypoplastic RV & dilated RAtricuspid regurg, wide split S2patent foramen ovale (80%)
|
|
for which arrhythmias are pt's with ebstein's anomaly at incr'd risk; what causes this incr'd risk
|
SVT & WPW2nd/2 dilated right atrium
|
|
Dx:6 week old infant present to ER with irritability and signs of L sided heart failureEKG finds a left sided MI
|
Dx: anomolous origin of the L main coronary artery(arises from pulmonary artery rather than the aorta)
|
|
MC congenital heart defect
|
VSD
|
|
what is used to close a PDA
|
indomethacin
|
|
what is used to keep PDA open in px with TOGV
|
prostaglandin E
|
|
what are the abnormalities a/w tetrology of fallot
|
VSDoverriding aortapulmonary stenosis (RV outflow obstruction)RVH
|
|
what heart defect are down syndrome patients higher risk of getting |
endocardial cushion defect
|
|
What are the unique structures of the fetal circulation that close after birth |
umbilical vein & 2 umbilical arteries ductus venosus foreman ovale ductus arteriosus |
|
Primary/Essential HTN |
>140/>90 on 3 separate occasions. obesity, tobacco, salt diet. Retinal-arterovenous nicking, cotton wool spots, retinal hemorrhages. Tx 1-Wt loss, salt restriction, alcohol reduction 2- Diuretic (thiazide) then add drug to affect the comorbid condition (ACEI/BB-CAD, ACEI-DM, CCB-vasospasms) |
|
DM
|
ACEI C: Thiazides-inc glucoseC: BB-mask hypoglycemia
|
|
CHF
|
ACEI/Diuretics C: CCB may exacerbate HF
|
|
Post MI
|
BB/ACEI decreae mortality
|
|
BPH
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alpha-1 adrenergic blockers - Prazosin or Terazosin (Tamsulosin least effect on HTN but least side effects overall)
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Migranes
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BB
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Osteoporosis
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Thiazides
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Ashtma/COPD
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C:BB
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Pregnancy
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C: Thiazides-decrease blood volume, ACEI/ARB-Teratogenic
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Gout
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C: Diuretic increase UA
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Depression
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C: BB may worsten symptoms
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Secondary HTN
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Identify the cause and treat
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Hypertensive Urgency
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high BP with mild symptoms lower in 24hrs Tx Captopril PO, Clonodine PO
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HTN Emergency
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high BP with end organ damage lower bp in 1 hr Tx Labetalol Nitroprusside
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Malignant HTN
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high BP with progressive RF, encephalopathy/papiledema
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normal systemic vascular resistance |
~1000-1600 dyne*sec/cm |
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CVP
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3-5cc
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RA
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0-8
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Pulmonary
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32-48/16-24
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LA PCWP
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8-10
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LV
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140/8-10
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Aorta
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120/80
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systolic RA RV Pul LA LV
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RA3-Pul25/10-LA10-LV140/10-A120/80
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Shock
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general rule all have low CO except septic shock
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Cardiogenic
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MI, Arrythmias
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Right
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inc CVP PCWP dec CO inc TPR, responds to IVF inc CWP
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Left |
inc CVP dec PCWP CO TPR, responds to IVF inc CWP
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Tamponade
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inc CVP PCWP dec CO inc TPR, no response
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Lung (PE, Air Embolus, Pn Thx, ARDS
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inc CVP dec PCWP CO inc TPR, no reponse
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Hypovolemic
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everything low except TPR, responds to IVF inc CWP
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Septic
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everthing low excetp CO, responds to IVF -only one with a high mixed V-O2 body is using lactic acid not O2
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Neurogenic
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everything low, no responce to IVF
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Aortic Aneurysm
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MC Atherosclerosis Connective tissue dz - cystic medial necrosis Syphillis - vasovasorum inflammation.
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|
AAA
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screen >65 who ever smoked. pulsating, abdominal mass, abd bruits. US, CT/MRI for accurate localization and size. TX <5 follow symptomatic or >6 surgery. Complication Ischemic colitis, stroke, paraplegia, renal insufficiency
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Aortic Dissection
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ripping chest pain , decreased peripheral pulses, CXR/Echo/CT Gold St:Angiogram wide mediastinum, A-ascending aorta tx surgery : B: distal to subclavian decrease bp treat medically
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Leg pain that improves with rest, resting leg pain if severe, dry skin, ulcers.
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Peripheral Vascular Dz: HTN, DM, CAD. Ankle Brachial Index <1, <0.4 severe. US for locating stenosis, Arteriogram, Tx Exercise, foot exams, ASA, pentoxifyllin or cilostazol, bypass if severe (resting pain, necrotic foot) Prolonged ischemia - amputation dont be afraid to choose it
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tortuosity of veins, edema, ulcerations.
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Tx exercise, compression hosiery, leg elevation.
|
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palpable, warm, pulsating masses
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AVM, risk of thrombus, surgical removal if symptomatic
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deep leg pain, swelling warmth
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DVT, rf prolonged inactivity, pregnancy, OCP, tobacco. inflammation-thombophlebitis Radio: US or Contrast venography. Tx leg elevations, heparin-warfarin, comp: PE 40% mortality
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palpable purpura or ulcers on skin, hematuria, HTN, joint pain
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PAN, rf: HepB/C young, everything but lungs involved, LAB: inc WBC ESR, Dec Hgb, protienuria, hematuria, p-ANCA, Dx biopsy artery. Radio: angiogram with numerous aneurysms. Tx corticosteroids
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new onset headache, jaw claudication, scalp pain, temporal tenderness
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Temporal Arteritis, women >50, inc ESR, temp artery bpx: inflammation in vessel media and lymphocytes, giant cell in adventitia. Elevated ESR, tx Prednisone
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decrease carotid and limb pulses
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Takayasu's arteritis, inflammation of aorta, bpx plasma lymphocytes in adventitia. tx corticosteroids Comp: cerebrovascular or MI
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Asthmatic symptoms older px, fatigue, malaise
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Churge Strauss allergic angiitis, eosinophils in biopsy and cbc. Tx Corticosteroids
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recent upper respiratory infection, arthritis, palpable purpura, abdominal pain
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children, IgA vasculitis, Tx self limiting or Corticosteroids for GI symptoms
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desquamation of hands and feet, lymphadenopathy, conjunctival lesions, maculopapular rash
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Kawasaki's necrotizing inflamation, young children, coronary vasculitis- aneurysm, MI sudden death. Tx ASA IVIg
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CRASH and Burn
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Conjunctivits, Rash, Adenopathy, Strawberry tongue, Hand and Foot, Burn >40-5d
|
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pansystolic murmur at lower left sternal border
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VSD, most common cong disease. Echo, small follow large-close before eisenmenger's
|
|
wide fixed S2 systolic ejection murmur at upper left border
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ASD, untreated ASD, surgery when pulmonary blood flow is twice that of systemic. Comp: Eisenmenger's, RV dysfunction, Pul HTN, arrythmias
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machinery murmer 2nd intercostal space, bounding pulses
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PDA; rf prematurity, high altitude, rubella, maternal prostaglandins. CXR: cardiomegaly, Echo: LA and LV, DX: Angiogram Tx: Indomethacin closure, surgical if unrespnsive
|
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cyanosis worsens with closure of PDA, loud S2
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Transposition of GV, incompatidble with life-PDA or VSD, apert's syndrome, CXR: narrow heart base, abnormal pulmonary markings, Dx: Echo for dx, Tx: Prosta E2 to keep open. Balloon atrial septostomy to widen VSD, promp surgical correction
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cyanosis, failure to thrive, HF, systolic murmur at lower left sternal border, loud S1 S2 bounding pulses
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Persitent Truncus Arteriousis, CXR: Boot shaped heart, Dx: angio or echo for dx. Tx Surgery
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downs syndrome
|
Endocardial cushion defect, ASD/VSD and single atrio Dx:Echo. Tx surgery
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cyanosis, dysnea, fatigue, child squates to releive hypoxemic event
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Teratology of Fallot, rf trisomies and cri du chat, PROV Pul stenosis, RVH, Overiding aorta, VSD. CXR boot shaped heart, Tx PG E2, O2, propanolol, fluids and morphine knee to chest for acute episode. Surgical correction
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