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89 Cards in this Set

  • Front
  • Back
Congenital disorder predisposing one to ventricular tacharrhythmias
Long QT syndrome (QTc > 440msec)
JVD
> 7cm above sternal angle.
Suggests:
Right CHF
Pulmonary HTN
Volume overload
Tricuspid regurgitation
Pericardial disease
Kussmaul's sign
Increased JVD with inspiration
Suggests:
R ventricular infarction
Postoperative cardiac tamponade
Tricuspid regugitation
Constrictive pericarditis
Harsh systolic ejection murmur, radiating to carotids
Aortic Stenosis
Holosystolic murmur, radiating to axillae or carotids
Mitral regugitation
Midsystolic or late-systolic click
Mitral valve prolapse
Systolic murmurs (4)
Aortic stenosis
Mitral regurgitation
Mitral valve prolapse
Flow murmur : no disease
Diastolic murmurs (2)
ALWAYS ABNORMAL:
Aortic regurgitation
Mitral stenosis
Early decrescendo murmur
Aortic regurgitation
Mid-late low-pitched murmur
Mitral stenosis
S3 gallop
Dilated cardiomyopathy (floppy ventricle), mitral valve disease, or normal in younger patients in high output states (pregnancy)
S4 gallop
HTN, diastolic dysfunction (stiff ventricle), aortic stenosis, normal in younger athletes
Peripheral edema DDX (10)
R heart failure
Biventricular failure
Peripheral venous disease
Constrictive pericarditis
Tricuspid regurgitation
Hepatic disease
Lyphedema
Nephrotic syndrome
Hypoalbuminemia
Drugs
Peripheral pulses greater in the arms than legs
Coarcation
Heart problem with increased peripheral pulses (2)
Compensated aortic regurgitation
Patent ductus arteriosus
Pulses alternans
Alternating weak and strong pulses. Seen in : cardiac tamponade, impaired LV systolic function. Poor prognosis
Pulsus parvus et tardus
Weak and delayed pulse. Seen in aortic stenosis
Management of A-fib: ABCD
Anticoagulate
BBs
Cardiovert/CCBs
Digoxin
DDX for CHF: HEART FAILED
HTN
Endocrine
Anemia
Rheumatic heart disease
Toxins
Failure to take meds
Arrhythmia
Infection
Lung (PE)
Electrolytes
Diet (Excess Na+)
Treatment for symptomatic bradycardia
Atropine or pacemaker
PR interval > 200 msec
1st Degree AV block. No treatment necessary
Causes of 2nd Degree AV block MobitzI/Wenckebach) 6
Digoxin
BBs
CCBs
Increased Vagal Tone
Sinoatrial conduction disease
R coronary inscemia or infarction
Treatment for 2nd Degree AV block MobitzI/Wenckebach)
Stop offending drug
Atropine
Pacemaker
2nd Degree AV block Mobitz II DDX and TX
Fibrotic disease, acute, subacute or prior infarct

Treat with pacemaker
Progressive PR lengthening until a dropped beat occurs
2nd degree AV block Mobitz I/Wenckebach
Unexpected dropped beats without a change in PR interval
2nd Degree AV block, Mobitz II
3rd degree AV block (Complete) cause and treatment
No commincation between atria and ventricles. Cannon A waves. Treat with pacemaker
Disorder consisting of abnormalities in supraventricular impulse generation and conduction that lead to SVT and bradyarrhythmias
Sick Sinus Syndrome (SSS)
Most common indication for pacemaker placement
Sick sinus syndrome (SSS)
Acute A-fib DDX (PIRATES)
Pulmonary disease
Ischemia
Rheumatic heart disease
Anemia/Atrial myxoma
Thyrotoxicosis
Ethanol
Sepsis
No discernible P waves, with variable and irregular QRS response
A-fib

Treat with CCBs, BBs, amiodarone. Coumadin might be necessary.
Regular rhythm, sawtooth appearance of P waves, rate 240 - 300 bpm with varying degree of blockade
Atrial flutter

Treat with anticoagulation, rate control. Cardiovert if necessary
3 or more unique P-wave morphologies rate > 100 bpm
Multifocal atrial thacycardia

Treat underlying disorder (COPD, hypoxemia), cerapamil, BBs
Ectopic beats from ventricular foci. Associated with hypoxia, hyperthyroidism, electrolyte abnormalities
Premature ventricular contraction (PVC)
3 or more consecutive PVCs with wide QRS complexes in a regular rapid rhythm. AV dissociation. Associated with MI, CAD, and structural heart disease
Ventricular tachycardia
Treat with cardioversion and antiarrhythmics (amiodarone, lidocaine, procainamide)
Totally eratic wide-complex tracing associated with CAD, structural heart disease and cardiac arrest
Ventricular fibrilation

Treat with immediate electrical cardioversion and ACLS protocol
Polymorphous QRS; VT with rates 150 - 250 associated with long QT syndrome, proarrhythmic response to meds, hypokalemia, and congenital deafness
Torsades de pointes

Treat with correcting cause. Give magnesium and cardiovert if unstable
Stage A of CHF
Have risk factors but no signs or symptoms

Manage risk factors, ACEIs for those with HTN, PAD, and DM
Stage B of CHF
Structural heart disease (prior MI, valvular disease, etc.) without symptoms

Treat: ACEIs and BBs
Stage C of CHF
Structural heart disease with symptoms of CHF

Treat: ACEIs, BBs, digitalis, and low Na+ diet
Stage D of CHF
Marked symptoms at rest despite maximal medical therapy

Treat: mechanical assist devises, heart transplant, continuous IV inotropic drugs, and hospice
Diuretic that can cause hyperglycemia and hyperlipidemia
Thiazide
Diuretic that can cause hyperkalemia
K+ sparing, Spironolactone, triamterene, amiloride
Treatment for acute pulmonary congestion in CHF (PLOMN)
Position upright
Lasix (Furosemide)
Oxygen
Morphine
Nitrates
Indication for an implantable biventricular cardiac defibrillator (ICD)
EF < 30%
and
CAD
2 Most common causes of secondary dilated cardiomyopathy
Ischemia
Long-standing HTN

others: Chagas, wet beri beri, thyroid dysfunction, acromegaly, pheo, cocaine, myocarditis, post-partum, coxackievirus, HIV, etc.
Gradual development of CHF symptoms, displacement of left ventricular impulse, JVD, S3/S4 gallop, LBBB, sinus tachycardia, low-voltage QRS
Dilated cardiomyopathy
Most common cause of sudden death in young healthy athletes
Hypertrophic obstructive cardiomyopathy. Autosomal dominant in 50%
Syncope, dyspnea, palplitations, angina, sustained apical impulse, S4 gallop, systolic ejection crescendo-decrescendo murmur that increases with decreased preload (valsalva).
Hypertrophic obstructive cardiomyopathy
Asymmetrically thickened left ventricular wall and dynamic obstruction of blood flow, LVH, mitral regurgitation, left atrial enlargement
Hypertrophic obstructive cardiomyopathy
Treatment for hypertrophic obstructive cardiomyopathy
BBs
CCBs 2nd line
Causes of restrictive cardiomyopathy (4)
Sarcoidosis
Amyloidosis
Hemochromatosis
Scarring and fibrosis (radiation or doxorubicin)
Rapid early filling with a normal EF, LBBB, fibrosis or infiltration on biopsy
Restrictive cardiomyopathy
Young women at rest in the early morning, sharp pain in chest with pressure, ST-segment elevation in absence of cardiac enzyme elevation
Prinzmetal's (variant) angina. Caused by vasospasm of coronary vessels.
New onset chest pain, occurs with less exertion or a rest, ST-changes, no elevation in cardiac enzymes
Unstable angina, possible impending infarction.
Medications that have a mortality benefit in treating angina (2)
BBs
ASA
Indication for heparin, angiography and possible percutaneous coronary intervention (PCI) or CABG
Chest pain refractory to meds
TIMI score >3
Troponin elevation
ST changes > 1mm
Treatment for STEMI (6 meds)
ASA
BBs (not if also CHF, instead use ACEIs)
Clopidogrel (plavix)
Morphine
Nitrates
O2
Non-pharmacologic tx for STEMI
Angiography and PCI
Hypercholesterolemia (4)
Total cholesterol > 200
LDL >130
HDL < 40
Triglycerides > 500
Drug therapy for stage 1 HTN (BP 140/90)
Thiazide diuretic - first line
ACEIs
BBs
CCBs
or combo
Drug therapy for stage 2 HTN (BP 160/100)
2 drug combo
Usually thiazie + ACEIs, BB, or CCB
HTN
Unexplained hypokalemia
Metabolic alkalosis
Conn's syndrome (Hyperaldosteronism)
Usually due to an aldosterone-producing adrenal adenoma. Remove tumor.
Tumors causing HTN (4)
Pheo (adrenal gland tumor)
Aldosterone-producing adrenal adenoma (Conn's syndrome)
ACTH-producing pituitary tumor (Cushing's disease)
Ectopic ACTH-producing tumor (Cushing's syndome)
HTN
Progressive renal failure
Encephalopathy with papilledema
Malignant HTN
Treatment for HTN urgencies
Oral BBs, clonidine, ACEIs
Gradually lower BP over 24 - 48 hours
Treatment for hypertensive emergencies
IV labetalol, nitroprusside, nicardipine. Gradually lower mean arterial pressure by no more than 25% over first 2 hours
Signs of pericarditis (PERIC)
Pulsus paraodxus
ECG changes
Rub
Increased JVP
Chest pain
Causes of pericarditis CARDIAC RIND
Collagen vascular disease
Aortic dissection
Radiation
Drugs
Infections
Acute renal failure
Cardiac (MI)
Rhematic fever
Injury
Neoplasms
Dressler's syndrome
Pleuritic chest pain, dyspnea, cough, fever. Pain worsens in supine position with inspiration. Pericardial friction rub.
Pericarditis
Excess fluid in pericardial sac leading to compromised ventricular filling and decreased cardiac output.
Cardiac tamponade
JVD
Hypotension
Distant heart sounds
Beck's triad for acute cardiac tamponade
Kussmaul's sign
JVD on inspiration
Electrical alternans on ECG
Diagnostic for cardiac tamponade
Treatment for cardiac tamponade
Volume expansion with IV fluids
Pericardiocentesis
Possible balloon pericardiotomy and pericardial window
Aortic aneurysms most common association and location
Atherosclerosis
Below renal arteries
Indication for surgical repair of aortic aneurysm
Abdominal > 5.5 cm
Thoracic > 6 cm
or rapidly enlarging
Aortic dissection association and location
HTN, males, 40 - 60
Above aortic valve and distal to left subclavian artery
Pulsus parvus et tardus, single or paradoxically split S2 sound, systolic murmur radiating to carotids
Aortic stenosis
Blowing diastolic murmur at L sternal border, mid-diastolic rumble (Austin Flint murmur), widened pulse pressure, Musset's sign (head bob with heart beat), Corrigan's sign (water-hammer pulse), Duroziez's sign (femoral bruit)
Aortic regurgitation
Causes of aortic regurgitation CREAM
Congenital
Rheumatic damage
Endocarditis
Aortic dissection/aortic root dilation
Marfan's syndrome
Opening snap and mid-diastolic murmur at apex, pulmonary edema
Mitral valve stenosis. Rhematic fever most common cause.
Holosystolic murmur radiating to axillae
Mitral valve regurgitation. Rheumatic fever or chordae tendineae rupture after MI
DeBakey classification for aortic dissections
I: Both ascending and descending
II: Only ascending
III: Only descending (can be treated medically)
Stanford classification for aortic dissections
A: Ascending aorta
B: All other types
Virchow's Triad
Hemostasis
Endothelial damage
Hypercoagulability
6 P's of acute ischemia
Pain
Pallor
Pulselessness
Paralysis
Paresthesia
Poikilothermia
Immigrant presenting with progressive swelling of lower extremities bilaterally with no cardiac abnormalities
Filariasis
Treatment for lymphedema
Exercise
Massage therapy
Pressure garments
Diuretics are relatively contraindicated