CMOP

(redirected from cardiomyopathy)
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Related to cardiomyopathy: hypertrophic cardiomyopathy, Dilated cardiomyopathy
AcronymDefinition
CMOPConsolidated Mail Outpatient Pharmacy (US VA)
CMOPCoalbed Methane Outreach Program (US EPA)
CMOPCanadian Model of Occupational Performance
CMOPCenter for Coastal Margin Observation & Prediction (Beaverton, OR)
CMOPConsolidated Mail Out Pharmacy (DVA)
CMOPCardiomyopathy (heart disease)
CMOPConfiguration Management Operating Plan
References in periodicals archive ?
One, in reviewing a Dutch cohort of 90 proven dilated cardiomyopathy families, she and her coinvestigators discovered five families, or 6%, had members with peripartum cardiomyopathy.
The diagnosis of peripartum cardiomyopathy was made and the patient was treated for congestive heart failure with diuretics, digitalis and angiotensin converting enzyme inhibitors (ACE-I).
The presence of at least one of the following criteria classified the cardiomyopathy as mild: mild electrocardiographic changes in ventricular repolarization or sinus bradycardia; as moderate: left anterior fascicular block, incomplete left bundle branch block, right bundle branch block, second-degree atrioventricular block-Mobitz type I, or atrial fibrillation in patients older than 50 years; and as severe: cardiomegaly, dilatative cardiomyopathy, complete left bundle branch block, atrioventricular block-Mobitz type II, complete atrioventricular block, or atrial fibrillation in patients younger than 50 years.
Conclusion: We have shown that patients with idiopathic dilated cardiomyopathy and angiographically normal coronary arteries have higher TIMI frame counts for all three coronary vessels, indicating impaired coronary blood flow, compared to control subjects without dilated cardiomyopathy.
For one family research into all types of cardiomyopathy is very much welcomed.
Hypertrophic cardiomyopathy (HCM) is a primary disorder of the cardiac sarcomere due to inherited mutations in contractile proteins, and characterized by left- and sometimes right-ventricular myocardial hypertrophy.
I was told I had cardiomyopathy and that the walls of my heart had thickened and that caused me to black out.
Many people live with cardiomyopathy with few complications but, depending on the severity of the disease, in some cases the only treatment is a heart transplant.
A post-mortem examination revealed he died from hypertrophic cardiomyopathy, a condition that causes the heart muscle to thicken.
Cardiomyopathy affects all ages and is the biggest medical cause of sudden death in young people.
This report describes a 70-year-old woman who presented with syncope, severe diastolic heart failure, features of hypertrophic cardiomyopathy and severe symptomatic conduction system disease requiring a pacemaker.
The mother-of-three, who has a 28-year-old daughter, Nicola, said: "The coroner phoned me to say it is the same cause of death, hypertrophic cardiomyopathy.
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