special forms of cardiomyopathy 762012

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3 Forms of Cardiomyopathy Dr Ihab Suliman Cardiology Morning Presentation 2 IM 7/6/2012

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Apical Ballooning ,HOCM, HTN

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Page 1: Special forms of cardiomyopathy 762012

3 Forms of Cardiomyopathy

Dr Ihab Suliman

Cardiology Morning Presentation

2 IM

7/6/2012

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• Sinus Tachycardia + LVH

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70 years old lady post operativefor CA Colon

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• Sinus Tachycardia, Low VoltaGE Limb Leads Lateral STEMI

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Sky High ST elevation with Minimal Rise in Cardaic Enzymes

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• Sky High ST Elevation

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• Cardiac Enzymes elevation is Much lower than expected with Sky High STEMI

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• Ballooned Apex

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• Apical Balloon

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Tako-tsubo Cardiomyopathy

• May account for up to 2% of suspected ACS• In-hospital mortality ranges 0-8%• Much more common in women (~90%),

especially postmenopausal women (>80% of cases)

• Mean age 58-75 years• Triggers: death of loved one, other catastrophic

news, devastating financial losses, natural disasters, physical illness/ICU, etc.

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Proposed Diagnostic Criteria

1. Transient a/dyskinesis of apical and midventricular segments in association with regional wall motion abnormalities that extend beyond the distribution of a single epicardial vessel

2. Absence on angiography of obstructive coronary artery disease or evidence of acute plaque rupture

3. New ST segment elevation or T wave inversions on ECG

4. Absence of recent significant head trauma, intracranial bleeding, pheochromocytoma, myocarditis, or hypertrophic cardiomyopathy

Proposed by Bybee, et al. 2004. Annals of Internal Medicine. 141: 858-865.

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The Second Form70 years old with Papitations

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• AF

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• NSR in contrast to AF

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• HTN , LVH

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The Third

• 37 years old lady with Familial type of Cardiomyopathy

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• HOCM Different echo views

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• AICD with atrial lead4 HOCM

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• Hypertrophic cardiomyopathy is a genetic disorder that is typically inherited in an autosomal dominant fashion with variable penetrance and variable expressivity.

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• HCM is the leading cause of sudden cardiac death in preadolescent and adolescent children.

• The hallmark of the disorder is myocardial hypertrophy that is inappropriate, often asymmetrical, and occurs in the absence of an obvious inciting hypertrophy stimulus. 

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Complications of HCM may include the following:

• Congestive heart failure or dilated eventually in 10 %

• Ventricular and supraventricular arrhythmias• Infective mitral endocarditis• Atrial fibrillation with mural thrombus

formation , AF worsen very much their status ,occur up to 25-30, ATC is important

• Sudden death

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Cardiology staff at NGHA ,Riyadh ,ksa