canine myocardial disease Flashcards
Arrhythmogenic right ventricular cardiomyopathy (ARVC)
diseaes characterized by fatty or fibro-fatty replacement of the myocardium
predominately affects the right ventricle, +/- LV
results in myocardial dysfunction, ventricular arrhythmias, sudden death, CHF
etiology of ARVC
familial disease: autosomal dominant trait with incomplete penetrance
mutation within desmosmal protein-striatin (key component of gap junction)
other causes?
clinical presentation of ARVC
syncope
exercise intolerance
abdominal distension
respiratory distress
PE findings of patients with ARVC
often normal
arrhythmia-extrasystoles, tachycardia
murmur
signs of CHF
diagnosis of Arrhythmogenic right ventricular cardiomyopathy
histopathology
based on family hx of disease, evidence of cardiomyopathy, genotype, presence of ventricular arrhythmia (ventricular tachycardia, >1000 VPCs in 24 hours on holter), postmortem
ECG of Arrhythmogenic right ventricular cardiomyopathy
ventricular tachycardia
positive VPCs
starting in RV going to LV

treatment of Arrhythmogenic right ventricular cardiomyopathy
lidocaine-acute management
Sotalol-most commonly used, less side effects
amiodarone-hepatotoxic (patients usually on long term)
px of Arrhythmogenic right ventricular cardiomyopathy
many dogs die of sudden death
some will die within short time period regardless of therapy
many affected dogs can live for years with or without therapy
atrioventricular cardiomyopathy
progressive myocardial disease characterized by atrial fibrosis and enlargement, bradycardia, congestive heart failure, death
lose effects of SA node
atrioventricular cardiomyopathy affected dogs
springer spanials, english sheep dogs, <3 yo
atrioventricular cardiomyopathy presenting signs
weakness, synope, signs of heart failure
atrioventricular cardiomyopathy PE findings
bradycardia, CHF signs-ascites
atrioventricular cardiomyopathy ECG
atrial standstill

what chemotherapeutic agent causes cardiotoxicity
doxorubicin
anthracycline
myocarditis
focal or diffuse inflammatory process involving the myocardium
may result in arrhythmias, myocardial dysfunction, sudden death
myocarditis etiology
viral-parvo
protozoal-Chagas’ toxoplasma, neospora
mycotic-blastomycosis
bacterial-borreliosis
myocarditis pathophysiology
inflammation in myocardium disrupts normal electrical conduction-arrhythmias (VPC’s ventricular tachycardia)
myocardial dysfunction: inflammation induces myocardial necrosis, phenotypic change similar to DCM
myocarditis dx
difficult
presumptive if: arrhythmias (absent of other diseases), ECHO, hx of systemic illness
ECG, ECHO, myocardial bx, elevated myocardial biomarkers (cardiac troponin I)
troponin I
should be tightly bound to the thin filament
released with destruction of myocardial cell and thin filament-accumulate in plasma
following myocardial necrosis-detectable within 5-7 hours, peak: 12-48 hours, persist for 8 days, half life-2 hr
not specific for any one etiology
myocarditis tx
treat underlying cause
anti-arrhythmics
pacemarker
corticosteroids