Acute coronary syndrome Flashcards

1
Q

Describe : MYOCARDIAL INFARCTION (MI)

A

Myocardial cell death caused by ischemia,
evidenced by a rise and fall in cardiac biomarkers.

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2
Q

Describe : ACUTE CORONARY SYNDROME (ACS (3)

A
  • An ischemic chest pain syndrome usually associated with coronary artery plaque rupture and occlusion.
  • ACS entities : include STEMI, NSTEMI, and Unstable Angina.
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3
Q

Describe : UNSTABLE ANGINA (UA) (3)

A
  • A type of ACS in which biomarkers are not elevated
  • and chest pain is of new onset, is changing in frequency or severity, or occurs at rest. Interestingly
  • the advent of high-sensitivity troponin assays has led to greater detection of subtly elevated cardiac biomarkers; as a result, the diagnosis of UA is being made less frequently.
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4
Q

Describe : NON-ST ELEVATION MYOCARDIAL INFARCTION (NSTEMI) (2)

A
  • A type of ACS that lacks new ST elevation on ECG
  • and in which cardiac biomarkers are eventually elevated.
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5
Q

Describe : ST-ELEVATION MYOCARDIAL INFARCTION (STEMI) (35)

A
  • A type of ACS in which significant ST elevation is found in two or more contiguous ECG leads.
  • It is typically associated with epicardial coronary artery occlusion and transmural infarction, resulting in myocardial cell death.
  • Q waves will manifest on the ECG if perfusion is not restored quickly.
  • STEMI occurs when the affected coronary artery is completely occluded.
  • It is treated with immediate reperfusion therapy, such as thrombolysis or PCI.
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6
Q

What’s the difference between NSTEMI and Unstable Angina? (1)

A

Elevation in cardiac
markers eventually distinguishes NSTEMI from UA.

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7
Q

Name the leads for each territory

A
  • Lateral : I, aVL, V5, V6
  • Inferior : II, III, aVF
  • Septal : V1,V2
  • Anterior : V3,V4
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8
Q

Name : RISK FACTORS FOR CORONARY HEART DISEASE (7)

A
  • DB
  • Hypercholesterolemia; high-density lipoprotein (HDL) cholesterol less than 40 mg/dL
  • Current tobacco use
  • HTA
  • Age (45 or older if male; 55 or older if female, or premature menopause)
  • Family history of premature CHD (MI or sudden death before age 55 years in male first-degree relative; before 65 years in female first-degree relative)
  • Sympathomimetic use (cocaine and amphetamines)
  • Rheumatologic conditions (rheumatoid arthritis and systemic lupus erythematosus)
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9
Q

What (HEART) score have been developed to help risk-stratify patients with undifferentiated chest pain?

A

HEART score
(History, ECG, Age, Risk factor, and Troponin)

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10
Q

Traitements à débuter en cas de SCA

A
  • À DISCUTER AVEC LE SÉNIOR/PATRON
  • Double antiplaquettaire :
  • 1er antiplaquettaire : ASA 360mg PO x1, puis 80 mg PO die
  • 2e antiplaquettaire :
    Ticagrelor 180mg PO x1, puis 90mg PO bid
    (Le premier choix la majorité du temps en SCA)
    C-I si atcd de saignement intracrânien

Plavix 300-600mg PO x1, puis 75mg PO die
(À choisir si patient anticoagulé ou thrombolysé)
* Anticoagulant
Héparine IV (le plus souvent utilisé; il y a un protocole à remplir)

Héparine de bas poids moléculaire : Fragmin 120 unités/kg (max 10 000
unités/dose) s/c bid

Fondaparinux : si on peut pas donner d’héparine (ex. atcd de HIT)

  • Statines
    Lipitor 80 mg PO die
    Crestor 40 mg PO die
  • Éventuellement B-bloqueurs (peut être débuté d’emblée si patient stable) et IECA (après coro)
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11
Q

Describe : Pour soulager DRS si persiste/récidive (4)

A
  • Nitro spray PRN +/- Timbre de Nitro +/- Nitro IV (nécessite une unité monitorisée et des pressions adéquates)
  • Opioïdes (fentanyl/morphine/dilaudid)
  • B-bloqueurs
  • Si DRS persiste malgré traitement adéquat et/ou TA trop basse pour optimiser traitement Possible indication de coro urgente = À DISCUTER AVEC LE SÉNIOR/PATRON
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12
Q

When the ECG reveals STEMI and symptoms have been present for less than 12 hours, what to do?

A

immediate reperfusion therapy is indicated. Optimally, total ischemic time should be limited to less than 120 minutes.

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13
Q

There are two ways to achieve
reperfusion. Name them.

A
  • primary PCI (angioplasty or stent placement)
  • thrombolysis.
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14
Q
A
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15
Q

The standard “door-to-balloon time” goal is what?

A

is 90 minutes, although benefit extends to 12 hours from the time of pain onset.

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16
Q

Recent studies suggest that if a patient presents to a hospital that does not offer PCI, transfer to a neighboring facility for primary PCI is superior to thrombolysis if what?

A

if transfer can be accomplished within 120 minutes.

17
Q

Thrombolysis should be done within what time frame?

A

Though the benefit of thrombolysis extends out to 12 hours, it is greatest when begun within four hours and approaches that of primary PCI when started within 30 minutes.

18
Q

Should PCI still be done after thrombolytic therapy?

A

Even if there is evidence of successful reperfusion, PCI is indicated and should be performed within 24 hours of thrombolytic therapy.

19
Q

Describe tx : UA and NSTEMI (5)

A
  • based on ECG findings, cardiac marker results, TIMI risk score, and whether the patient is likely to undergo early angiography and PCI.
  • Aspirin and nitroglycerin = minimum therapy.
  • Morphine is added when chest discomfort continues despite nitroglycerin therapy.
  • Beta-blockers, such as IV metoprolol, may be added in cases presenting with hypertension or tachycardia; however, they should be used with caution (risk of caridogenic shock).
  • In high-risk patients, such as those with ischemic ECG changes, elevated cardiac
    markers, and TIMI risk score of 3 or greater, adding an anticoagulant agent, such as unfractionated heparin or LMWH, may work to halt the thrombotic process.
  • IV glycoprotein IIB/IA inhibitors, such as abciximab, or direct thrombin inhibitors, such as bivalirudin, are sometimes used in patients undergoing early angiography and PCI.
20
Q

Name complications : acute MI (6)

A
  • ventricular tachycardia and ventricular fibrillation (sudden death) are the most frequently encountered complications in the ED and prehospital setting, occurring in approximately 10% of cases.
  • Bradyarrhythmias : heart block from irreversible damage to the His-Purkinje system after an anterior MI or arteriovenous (AV) node dysfunction from an inferior MI. Emergent pacemaker placement may be necessary.
  • Left ventricular dysfunction that occurs with anterior MI usually causes** pulmonary edema** or cardiogenic shock.
  • Right ventricular infarction
21
Q
A
21
Q

Name late complications of MI (5)

A

that tend to occur several hours to days after presentation include left ventricular free wall rupture causing
* tamponade
* ventricular septal defect
* pericarditis
* left ventricular aneurysm
* thromboembolism.

21
Q
A
22
Q

Name iatrogenic complications of MI therapy (3)

A
  • Heparin and antiplatelet therapies lead to significant bleeding in up to 10% of patients.
  • Intracranial hemorrhage occurs in 0.5% to 0.7% of patients who receive thrombolytics for STEMI.
  • These bleeds are often fatal.