Chapter 14- Cardiomyopathies and Selected Non-Cardiac Heart Disease Flashcards
define cardiomyopathy
idiopathic heart muscle dysfunction
- can be primary (genetic) or secondary with known cause (HTN, Valvular disease)
What is dilated cariomyopathy (DCM)?
characterized by enlargement and muscle dysfunction of one or both ventricles.
When DCM is classifed as Idiopathic dilated cardiomyopathy ( IDC)
when complete evaluation does not identify a recognized cause.
What are the major causes of dilated cardiomyopathy?
- myocarditis - infectious including viral, bacterial and others
- ischemic heart diease- common, generally caused by severe three vessel disease can require CA
- peripartum- related to pregnancy, can also be called postpartum or peurperal cariomyothay- recovery is complete in most cases
- hypertensive - longstanding verdivle overload
- vulvular- severe aortic or mitral disease results eventually in severe LV,
- infectious-HIV, lyme disease
- systemic- sarcoidosis, connective tissue disease
- Toxic- alcohol, cocaine, amphetamines, colbar, chemo, radiation
- metabolic- thyroid hormone excess or deficiency, dM
- neuromuscular-
- familial- FDV
How is dilated cardiomyopathy diagnosed?
clinical CHF, or via transthoracic echocardiogram (TTE) s.t sxs of dyspnea or syncope.
ECG will show impaired global LV function demonstrated by decreased EF and LV dilatation on TTE
How is Dilated cardiomyopathy treated?
- tx underlying cause.
1. ACE inhibitors
2. beta blockers
3. diuretics
4. digoxin or newer vasopressin antagonists for heart failure.
5. antriarrhythmic drugs
6. anticoagulants - pace maker or implantable carioverter defibrillator or heart transplant
What should an UW consider with dilated cardiomyopathy?
TTE studies every 3 years.
* EF >40% has a better prognosis
What are some unfavourable features of dialted cardiomyopathy?
- significant LV enlargement
- Lower EF
- Left bundle branch block (LBBB)
- A fib, AV block and ventricular arrhythmias are less favourable.
What is Hypertrophic cardiomyopathy (HCM)
characterized by Myocardial hypertrophy
Autosomal dominant, associated with DNA mytations
Define hypertrophy
What is hypertrophic obstruction cardiomyopathy (HOCM)
what are examples of obstructive hypertrophy cardiomyopathy?
- HOCM
- IHSS (Idiopathic hypertrophic subaortic stenosis)
- Hypertrophic non-obstructive cardiomyopathy (HCM)
- asymmetric septal hypertrophy (ASK)
- Apical hypertrophic cariomyopathy.
When is HCM investigated?
FX or EKG changes
- heartmurmurs, and CV sxs are investigated for HCM.
How is HCM diagnosed?
With a TTE, and MRI when available.
-disorder is suspected when septal wall thickness is greater than 15mmm, or septal anterior motion of MV.
- SAM (systolic anterior motion) is the is confirmatory for HCXM. and LV cavity is small at early stages.
-
What is athletes heart
hypertrophy d/t athletic training, it seldome has a LV wall thickeness that exceeds 13mm.
- has a LV cavity dilation
What is Apical HCM?
when hypertrophy is localized to apex
- common in china and gene mutation
- dx by TEE, or CT or MRI
- no associted outflow tract obstruction but can inbvolve mid-ventricular obstruction.
- better prognosis, but higher rate of cardiac complications
How is hypertrophoc cardiomyopathy treated?
beta blockers
calcium channel blockers
to alleviate ischmia and heart failure
anticoagulants can be used in associated with A fib.
- possibla myocardial septum removal (septal myectomy)
- ablation to relive obstruction via alcohol.
- Implantavle cardioverter-defibrillator (ICD)
-
What must an underwriter consider when UW those with hx of HCM?
- Fx, EKG and full TTE study.
- Sudden death prior to 40 in Fx
- ## review: sxs, Fx, septal wall thickness, outflow gradient, arrhythmias and A fib, Ventricular tachycaria, Low exercise capacity
What are HCM favourable factors?
- age over 40
- no sign of progression over 5 ys on echo
- no sxs
- no Fx of suddent bdeath
- intravbentricular septum less than 16mm
- no outflow gradient or <10 mmHG
- no hx of arrythmias
- no strenuous exercise activities.
What is athletes heart?
myocardial hypertrophy (cardiac remodelling) due athletic training. - heart usually returns to high normal within two year of stopping serious training => Need to cypher from other enlarged heart disorders.