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3 Forms of Cardiomyopathy
         Dr Ihab Suliman
 Cardiology Morning Presentation
                2 IM
             7/6/2012
• Sinus Tachycardia + LVH
70 years old lady post operative
         for CA Colon
• Sinus Tachycardia, Low VoltaGE Limb
  Leads Lateral STEMI
Sky High ST elevation with
Minimal Rise in Cardaic
Enzymes
• Sky High ST Elevation
• Cardiac Enzymes elevation is Much lower
  than expected with Sky High STEMI
• Ballooned Apex
• Apical Balloon
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.
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.
The Second Form
70 years old with Papitations
• AF
• NSR in contrast to AF
• HTN , LVH
The Third
• 37 years old lady with Familial type of
  Cardiomyopathy
• HOCM Different echo views
• AICD with atrial lead4 HOCM
• Hypertrophic cardiomyopathy is a genetic
  disorder that is typically inherited in an
  autosomal dominant fashion with variable
  penetrance and variable expressivity.
• 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.
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
Cardiology staff at NGHA ,Riyadh ,ksa

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Special forms of cardiomyopathy 762012

  • 1. 3 Forms of Cardiomyopathy Dr Ihab Suliman Cardiology Morning Presentation 2 IM 7/6/2012
  • 2.
  • 4. 70 years old lady post operative for CA Colon
  • 5. • Sinus Tachycardia, Low VoltaGE Limb Leads Lateral STEMI
  • 6.
  • 7. Sky High ST elevation with Minimal Rise in Cardaic Enzymes
  • 8. • Sky High ST Elevation
  • 9.
  • 10.
  • 11.
  • 12. • Cardiac Enzymes elevation is Much lower than expected with Sky High STEMI
  • 13.
  • 14.
  • 15.
  • 17.
  • 19.
  • 20.
  • 21. 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.
  • 22. 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.
  • 23.
  • 24.
  • 25. The Second Form 70 years old with Papitations
  • 27.
  • 28. • NSR in contrast to AF
  • 29.
  • 30.
  • 31.
  • 32.
  • 33. • HTN , LVH
  • 34. The Third • 37 years old lady with Familial type of Cardiomyopathy
  • 35.
  • 36.
  • 37.
  • 38.
  • 39.
  • 40. • HOCM Different echo views
  • 41.
  • 42. • AICD with atrial lead4 HOCM
  • 43. • Hypertrophic cardiomyopathy is a genetic disorder that is typically inherited in an autosomal dominant fashion with variable penetrance and variable expressivity.
  • 44. • 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.
  • 45. 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
  • 46. Cardiology staff at NGHA ,Riyadh ,ksa