Conditions associated with sudden cardiac death Flashcards

(17 cards)

1
Q

Long QT Syndrome - symptoms

A
  • Syncope
  • Exercise induced syncope
  • Often people don’t know they have this condition until they
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2
Q

Long QT Syndrome - causes

A
  • It is often inherited: genetic cardiac ion channel mutation (Na+, K+)
  • Drugs: amiodarone, TCA’s, many antibiotics, fluconazole, erythromycin, metoclopramide, quinidine, haloperidol, droperidol, methadone, ondansetron, SSRI’s
  • Myocardial disease: MI, RF (rheumatic fever) , 3rd degree HB, cardiomyopathy
  • Electrolytes: low Ca2+, low K+, low Mg2+
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3
Q

Long QT Syndrome - ECG features

A
  • QTc duration of >440 in men
  • QTc duration of >460 in women
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4
Q

Brugada Syndrome - symptoms

A
  • Two-thirds of people are asymptomatic
  • Syncope
  • Unexplained cardiac arrest (usually during sleep or rest)
  • Nocturnal agonal respirations
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5
Q

Brugada Syndrome - causes

A
  • Autosomal-dominant inherited cardiac sodium channelopathy
  • More common in males
  • More common in people of Southeast Asian descent
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6
Q

Brugada Syndrome - ECG features

A

There are three ECG findings associated with Brugada:
- Type 1 (diagnostic) with coved-type ST elevation of >2mm and negative T waves in V1-V3 (along with at least one of the clinical criteria)
- Type 2 with saddle-back ST elevation of >2mm and positive or biphasic T wave
- Type 3 with morphology of either type 1 or type 2 but with <2mm of ST elivation
- Atrial fibrillation / flutter may also be present

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7
Q

Brugada syndrome - clinical criteria

A
  • Documented polymorphic VT or VF
  • Family history of sudden cardiac death at <45 years old
  • Coved-type ECGs in family members
  • Inducibility of VT with programmed electrical stimulation
  • Syncope
  • Nocturnal agonal respiration
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8
Q

Hypertrophic Cardiomyopathy (HCM) - symptoms

A
  • Dyspnoea
  • Syncope/presyncope
  • Chest pain
  • Angina
  • Palpitations
  • Symptoms of HF: orthopnoea, paroxysmal nocturnal dyspnoea
  • Sudden cardiac death
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9
Q

Hypertrophic Cardiomyopathy (HCM) - causes

A

Genetic condition affecting sarcomeric proteins causing left ventricular wall thickness - not explained by abnormal loading conditions

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10
Q

Hypertrophic Cardiomyopathy (HCM) - ECG features

A
  • Left ventricular hypertrophy (voltage + non-voltage) criteria
  • Deep anterior lateral T wave inversions
  • Dagger like Q waves in inferior lateral leads
    (Inferior lateral leads - II, III, aVF, V5 and V6)
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11
Q

Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia (ARVC/D) - symptoms

A
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12
Q

Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia (ARVC/D) - ECG features

A
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13
Q

Dilated Cardiomyopathy - symptoms

A
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14
Q

Dilated Cardiomyopathy - ECG features

A
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15
Q

Wolf-Parkinson White Syndrome - symptoms

A
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16
Q

Wolf-Parkinson White Syndrome - ECG features

17
Q

Myocarditis - symptoms