Description

Overproduction of growth hormone in acromegaly can result in a cardiomyopathy. Control of the underlying disease results in control of the heart disease. Failure to control progression of the cardiac disease increases morbidity and mortality.


 

Risk factors for cardiomyopathy:

(1) long duration of disease

(2) active, uncontrolled disease

 

Clinical features:

(1) tachycardia

(2) hypertension

(3) left ventricular hypertrophy followed by biventricular dilatation (dilated cardiomyopathy)

(4) heart failure

Structural Changes

Cardiac Output

Functional Status

Stage

none apparent

high (increased contractility, low vascular resistance)

asymptomatic

early hyperkinetic

myocardial hypertrophy, interstitial fibrosis, mucin deposits

diastolic dysfunction

dyspnea on exertion

intermediate

ventricular dilatation

low with systolic dysfunction and heart failure

dyspnea at rest

late and end-stage

 

Additional cardiac disorders in acromegaly:

(1) valvular disease

(2) cardiac arrhythmias

(3) coronary artery disease with myocardial ischemia or infarction

 


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