WHAT WENT WRONG?
The middle
layer of the heart wall that contains cardiac muscle (myocardium)
weakens and
stretches, causing the heart to lose its pumping strength and become
enlarged. The
heart remains functional; however, contractions are weak, resulting
in decreased
cardiac output. Most are idiopathic and not related to the major causes
of heart
disease. The three types of cardiomyopathy are:
1. Dilated
cardiomyopathy (common): The heart muscle thins and enlarges,
which leads to
congestive heart failure. Progressive hypertrophy and dilatation
result in
problems with pumping action of ventricles.
2.
Hypertrophic cardiomyopathy: The ventricular heart muscle thickens, resulting
in outflow
obstruction or restriction. There is some blood flow present.
3. Restrictive
cardiomyopathy (rare): The heart muscle becomes stiff and restricts
blood from
filling ventricles, usually as a result of amyloidosis, radiation,
or myocardial
fibrosis after open-heart surgery.
PROGNOSIS
Prognosis is
variable. Sudden cardiac death is a possible outcome in dilated or
hypertrophic cardiomyopathy;
arrhythmia is often a precursor to sudden death.
HALLMARK SIGNS AND SYMPTOMS
• Asymptomatic—Many
clients with hypertrophic cardiomyopathy (HCM)
are
asymptomatic. Those with signs do not present until their mid-twenties.
• Dyspnea—The
most frequent symptom is shortness of breath due to increase
pressure in
the lungs. The heart may not sufficiently relax resulting in higher
pressure and a
backup of blood into the lungs.
• Angina—Clients
experience chest pain related to increase oxygen demand
of the extra
heart muscle and due to thick, narrowing coronary blood vessels
within the
heart’s wall
• Syncope—Fainting
is caused by heart arrhythmias related to the inability of
the cardiac
muscle to conduct electrical impulses.
• Sudden
death—Young adults are at risk of sudden death during physical
exercise
resulting from ventricular fibrillation, which is a cardiac arrhythmia.
• Abnormal
heart sounds
• Murmur,
which is the sound of turbulence results from abnormal blood flow
• S3,
which is a third heart sound commonly heard in heart failure. S3 is a
soft sound
made by the vibration of the ventricular wall when the ventricle
fills too
rapidly. S3 is heard after the S2 heart sound and is best found
over the apex
of the left ventricle, which is the fourth intercostal space
along the
mid-clavicular line
• S4,
which is the heart sound heard before the S1 heart sound is the result
of the heart
being too stiff. This is vibration of the valves and the ventricular
walls when the
atria contracts and the ventricles fill.
INTERPRETING TEST RESULTS
• Chest
x-ray (CXR) shows enlarged heart, pulmonary congestion.
• Echocardiography
shows left ventricular hypertrophy (LVH) and dysfunction
in dilated and
hypertrophic cardiomyopathy; small ventricular size and
function in
restrictive cardiomyopathy.
• Electrocardiogram:
ST changes, conduction abnormalities, LVH.
• Left
ventricular hypertrophy shows as a broad QRS wave, usually in leads
4, 5, and 6 because
of high voltage.
• Cardiac
catheterization—to measure chamber pressures, cardiac output, ventricular
function, but
is often unable to add to information that has already
been received from
echocardiogram.
• Exercise
testing may show poor cardiac function not evident in a resting
state.
TREATMENT
Treatment is
based on the specific cause. Avoiding the offending drug/treatment is
imperative.
Manage the underlying disease and provide cardiac support; however,
few therapies
can halt the process of cardiomyopathy.
• Change
to a low-sodium diet.
• Beta
adrenergic blockers—cause the heart to beat slowly, allowing more
time for
ventricular filling and improve contractile function:
• propranolol,
nadolol, metoprolol (for hypertropic cardiomyopathy)
• Angiotensin-converting
enzyme (ACE) inhibitors—to decrease left ventricular
filling
pressures.
• Calcium
channel blockers—reduced cardiac workload by increasing contractile
ability:
• verapamil
(for hypertrophic cardiomyopathy)
• Diuretics
reduce fluid retention:
• furosemide,
bumetanide, metolazone (for dilated cardiomyopathy)
• spironolactone
(aldosterone antagonist)
• Administer
inotropic agent to enable the heart to have greater contractile
force:
• dobutamine
• milrinone
• digoxin
(for dilated cardiomyopathy)
• Administer
oral anticoagulant to reduce the coagulation of blood:
• warfarin
(for dilated and hypertrophic cardiomyopathy)
• Implantable
cardioverter-defibrillator for high risk.
• Myectomy—incision
into septum and removal of tissue.
DIAGNOSES
• Activity
intolerance
• Impaired
gas exchange
• Decreased
cardiac output
INTERVENTION
• Place
patient in a semi-Fowler’s position for comfort, which eases respiratory
effort.
• Record
intake and output of fluids.
• Monitor
vital signs to assess for increased respiratory rate, arrythmias.
• Monitor
electrocardiogram to look for changes from previous tracing.
• Explain
to the patient: fluids restriction may be necessary as heart failure is
a concurrent
disease with dilated cardiomyopathy.
• Record
daily weight and call physician if weight increases 3 lbs (1.4 kg).
• No
smoking or drinking alcohol.
• No
straining during bowel movements.
• Increase
exercise.
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