Sunday, August 4, 2013

Cardiomyopathy

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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