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650 Cards in this Set

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next step in mgmt:
25 y/o man dx'd with a solitary testicular mas by US

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"

C: incr'd
A: incr'd altitiude/acid (i.e. decr' pH)
D: incr'd DPG3
E: exercise
T: incr'd temp

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
normal MCV
decr'd haptoglobin
incr'd indirect bilirubin
incr'd LDH

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
alpha-1 adrenergic blockers - Prazosin or Terazosin (Tamsulosin least effect on HTN but least side effects overall)
Migranes
BB
Osteoporosis
Thiazides
Ashtma/COPD
C:BB
Pregnancy
C: Thiazides-decrease blood volume, ACEI/ARB-Teratogenic
Gout
C: Diuretic increase UA
Depression
C: BB may worsten symptoms
Secondary HTN
Identify the cause and treat
Hypertensive Urgency
high BP with mild symptoms lower in 24hrs Tx Captopril PO, Clonodine PO
HTN Emergency
high BP with end organ damage lower bp in 1 hr Tx Labetalol Nitroprusside
Malignant HTN
high BP with progressive RF, encephalopathy/papiledema

normal systemic vascular resistance

~1000-1600 dyne*sec/cm

CVP
3-5cc
RA
0-8
Pulmonary
32-48/16-24
LA PCWP
8-10
LV
140/8-10
Aorta
120/80
systolic RA RV Pul LA LV
RA3-Pul25/10-LA10-LV140/10-A120/80
Shock
general rule all have low CO except septic shock
Cardiogenic
MI, Arrythmias
Right
inc CVP PCWP dec CO inc TPR, responds to IVF inc CWP

Left

inc CVP dec PCWP CO TPR, responds to IVF inc CWP
Tamponade
inc CVP PCWP dec CO inc TPR, no response
Lung (PE, Air Embolus, Pn Thx, ARDS
inc CVP dec PCWP CO inc TPR, no reponse
Hypovolemic
everything low except TPR, responds to IVF inc CWP
Septic
everthing low excetp CO, responds to IVF -only one with a high mixed V-O2 body is using lactic acid not O2
Neurogenic
everything low, no responce to IVF
Aortic Aneurysm
MC Atherosclerosis Connective tissue dz - cystic medial necrosis Syphillis - vasovasorum inflammation.
AAA
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
Aortic Dissection
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
Leg pain that improves with rest, resting leg pain if severe, dry skin, ulcers.
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
tortuosity of veins, edema, ulcerations.
Tx exercise, compression hosiery, leg elevation.
palpable, warm, pulsating masses
AVM, risk of thrombus, surgical removal if symptomatic
deep leg pain, swelling warmth
DVT, rf prolonged inactivity, pregnancy, OCP, tobacco. inflammation-thombophlebitis Radio: US or Contrast venography. Tx leg elevations, heparin-warfarin, comp: PE 40% mortality
palpable purpura or ulcers on skin, hematuria, HTN, joint pain
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
new onset headache, jaw claudication, scalp pain, temporal tenderness
Temporal Arteritis, women >50, inc ESR, temp artery bpx: inflammation in vessel media and lymphocytes, giant cell in adventitia. Elevated ESR, tx Prednisone
decrease carotid and limb pulses
Takayasu's arteritis, inflammation of aorta, bpx plasma lymphocytes in adventitia. tx corticosteroids Comp: cerebrovascular or MI
Asthmatic symptoms older px, fatigue, malaise
Churge Strauss allergic angiitis, eosinophils in biopsy and cbc. Tx Corticosteroids
recent upper respiratory infection, arthritis, palpable purpura, abdominal pain
children, IgA vasculitis, Tx self limiting or Corticosteroids for GI symptoms
desquamation of hands and feet, lymphadenopathy, conjunctival lesions, maculopapular rash
Kawasaki's necrotizing inflamation, young children, coronary vasculitis- aneurysm, MI sudden death. Tx ASA IVIg
CRASH and Burn
Conjunctivits, Rash, Adenopathy, Strawberry tongue, Hand and Foot, Burn >40-5d
pansystolic murmur at lower left sternal border
VSD, most common cong disease. Echo, small follow large-close before eisenmenger's
wide fixed S2 systolic ejection murmur at upper left border
ASD, untreated ASD, surgery when pulmonary blood flow is twice that of systemic. Comp: Eisenmenger's, RV dysfunction, Pul HTN, arrythmias
machinery murmer 2nd intercostal space, bounding pulses
PDA; rf prematurity, high altitude, rubella, maternal prostaglandins. CXR: cardiomegaly, Echo: LA and LV, DX: Angiogram Tx: Indomethacin closure, surgical if unrespnsive
cyanosis worsens with closure of PDA, loud S2
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
cyanosis, failure to thrive, HF, systolic murmur at lower left sternal border, loud S1 S2 bounding pulses
Persitent Truncus Arteriousis, CXR: Boot shaped heart, Dx: angio or echo for dx. Tx Surgery
downs syndrome
Endocardial cushion defect, ASD/VSD and single atrio Dx:Echo. Tx surgery
cyanosis, dysnea, fatigue, child squates to releive hypoxemic event
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