Myocardial disease Flashcards

1
Q

LV dysfunction results in __________.

A

results in progressive remodeling of the ventricular chamber leading to dilation and a low ejection fraction

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2
Q

Describ what the hear looks like with the various types of cardiomyopathies?

dilated

hypertrophic

restrictive

A
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3
Q

What are the different forms of dilated cardiomyopathies?

A
  • inflammatory and non-inflammatory
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4
Q

What are the early symptoms of inflammatory myocarditis?

What does it progress to?

A
  • Early symptoms
    • fatigue
    • dyspnea
    • palpitations
  • Progresses to:
    • CHF
    • pulsus alterans- beat to beat variability in BP
    • tachycardia
    • pulmonary edema
  • *Usually complete recovery after treatment with abx!
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5
Q

Non-inflammatory cardiomyopathy usually manifests how? What is it usually cause by?

A
  • Manifests as CHF
  • Usually due to:
    • toxicity (ETOH)
    • idiopathic process
    • degenerative process
    • infiltrative process
    • post myocardial infarct
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6
Q

What are dilated cardiomyopathies usually characterized by?

What is the clinical picutre?

A
  • Characterized by
    • elevated filling pressures
    • failure of contractile strength
    • a marked inverse relationship btw arterial impedance stroke vol
  • Clinical picture: Forward failure (decreased CO)
    • fatigue
    • hypotension
    • oliguria
    • RAAS activated to increase circulating blood volume through Na and water retention
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7
Q

What are the differences between Left sided heart failure and right sided heart failure regarding dilated cardiomyopathies

A
  • Left sided HF
    • elevated filling pressures requires
    • Secondary mitral regurgitation caused by the dilation of the ventricle; causing orthopnea, pulm edema, and paroxysmal nocturnal dyspnea
  • Right sided HF
    • hepatomegaly
    • JVD
    • peripheral edema
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8
Q

What are the goals for anesthetic management of a patient with HF?

How would you treat hypotension?

Regional ok?

A
  • Goal is to prevent myocardial depression
    • HR- normal to elevated
    • Preload- normal to high
    • afterload- low
    • contractility- increased
  • Hypotension treated with ephedrine, phenylephrine, vasopressin–avoid fluid overload
  • Regional ok
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9
Q

What are some of the other names for hypertrophic cardiomyopathy?

A
  • Idiopathic hypertrophic subaortic stenosis (IHSS)- most common
  • Asymmetric septal hypertrophy
  • Hypertrophic obstructive cardiomyopathy
  • Muscular subaortic stenosis
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10
Q

What are the clinical features of hypertrophic cardiomyopathy?

A
  • Autosomal dominant trait- main defect is contractile elements of the heart: then an increase in the density of the Ca channels
  • majority of pts are asymptomatic, but symptoms include dyspnea, angina, syncope
  • 50% patients initially present with sudden death or cardiac arrest (often teens)
  • 75% have ventricular dysrhythmias, 25% SVT, 5-10% afib
  • anual mortality 3-8% (post op 1-3%)
  • Most patients become symptomatic in second and third decades of life
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11
Q

What is the pathophysiology of hypertrophic cardiomyopathy?

A
  • Main features of pathophysiology:
    • myocardial hypertrophy
    • Rapid LV ejection (80% in early systole)
    • dynamic left ventricular out flow tract obstruction
    • systolic anterior movement of mitral valve, causing regurgitation
    • diastolic dysfunction- can’t relax, doesnt fill well
    • sub-aortic pressure gradient
    • myocardial ischemia
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12
Q

What can make the LV outflow obstruction seen in hypertrophic cardiomyopathy worse?

A
  • decreased preload
    • dehydration
  • decreased afterload
  • increased contractility
    • exercise
  • **These reasons are why teenagers with hypertrophic cardiomyopathy can drop dead while exercising
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13
Q

What factors may impair contractility but improve systolic function in a pt with hypertrophic cardiomyopathy?

A
  • volume loading
  • vasoconstriction
  • myocardial depression
    • increased inhaled agents, these pts like this
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14
Q

Why may vasodilators be problematic for patients with Hypertrophic cardiomyopathy?

A
  • Most pts with hypertrophic cardiomyopathy have some degree of mitral regurg, which can be worsened with vasodilators
  • Vasoconstrictors attenuate obstruction and decrease the mitral regurgitation
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15
Q

Generally speaking, how do we treat patients with hypertrophic cardiomyopathies?

A
  • lots of gas
  • fluid loading
  • vasoconstriction
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16
Q

How is hypertrophic cardiomyopathy medically managed?

A
  • Beta blockers-
    • blunt sympathetically mediated increases in subaortic stenosis
    • decrease tachyarrhythmias
  • Calcium channel blockers
    • improve diastolic relaxation
17
Q

What are the ECHO findings in a pt with hypertrophic cardiomyopathy?

How is it managed surgically?

A
  • Echo findings:
    • thickened interventricular septum (IVS)
    • poor septal motion
    • anterior displacement of the mitral valve
  • Surgical treatment:
    • myomectomy
18
Q

What is the anesthetic management for a patient with IHSS?

A
  • IA are good because they decrease contractility
  • A-line- b/c of high risk of dysrhythmias
  • treat hypotension with alpha adrenergic agonists (phenylephrine) and volume
    • avoid ephedrine
  • Beta adrenergic agonists are contraindicated
  • promptly replace blood and fluids
  • avoid vasodilators
  • maintain NSR