Acute mi treatment Davidson

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I have enough context to provide a comprehensive answer on Acute MI treatment in the style of Davidson's (Harrison's + Braunwald's cover the same curriculum). The read also captured Harrison's block 30 with the treatment tables. Let me now compile a thorough, well-structured answer based on what I've gathered from these authoritative sources plus my medical knowledge.

Note: Davidson's Principles and Practice of Medicine is not in this textbook library. The answer below is based on Harrison's Principles of Internal Medicine 22e (2025) and Braunwald's Heart Disease, which cover the same content as Davidson's for AMI management.

Acute Myocardial Infarction - Treatment

Classification for Management Purposes

TypeDefinitionStrategy
STEMIST elevation or new LBBBEmergency reperfusion (primary PCI preferred)
NSTEMINo ST elevation, troponin positiveEarly invasive or conservative strategy
UANo ST elevation, troponin negativeMedical management + risk stratification

Immediate / General Measures ("MONA" + more)

1. Oxygen

  • Supplemental O2 only if SpO2 <94% - routine O2 in normoxic patients is NOT recommended (may increase infarct size).

2. Analgesia

  • Morphine IV (2-4 mg, titrated) for unrelieved chest pain - but use with caution; associated with delayed P2Y12 absorption and worse outcomes in some studies.
  • IV nitrates for pain relief if no hypotension (SBP >90 mmHg), no RV infarct, no PDE5 inhibitor use.

3. Antiplatelets (Dual Antiplatelet Therapy - DAPT)

  • Aspirin 300 mg loading dose (crushed/chewed), then 75 mg daily indefinitely.
  • P2Y12 inhibitor (choose one):
    • Ticagrelor 180 mg load, then 90 mg BD (preferred - PLATO trial; irreversible, faster onset)
    • Prasugrel 60 mg load, then 10 mg OD (preferred in STEMI if no prior stroke/TIA, age <75, weight >60 kg)
    • Clopidogrel 600 mg load, then 75 mg OD (less potent; used if others contraindicated or thrombolysis given)

4. Anticoagulation

  • Unfractionated heparin (UFH): IV bolus 60 units/kg (max 4000 units), infusion 12 units/kg/hr - used with PCI or thrombolysis.
  • LMWH (Enoxaparin): 1 mg/kg SC BD (preferred over UFH in NSTEMI if no renal failure).
  • Fondaparinux: 2.5 mg SC OD - preferred in NSTEMI managed conservatively (OASIS-5 trial).
  • Bivalirudin: Direct thrombin inhibitor; preferred option for primary PCI (lower bleeding risk).

5. Beta-blockers

  • Oral beta-blocker (e.g., metoprolol 25-50 mg BD) within 24 hours if no contraindications.
  • Contraindications: cardiogenic shock, acute decompensated HF, PR >0.24s, 2nd/3rd degree AV block, bronchospasm.
  • IV beta-blockers only for ongoing ischaemia/tachyarrhythmia without contraindications.

6. ACE Inhibitors / ARBs

  • Start within 24 hours in STEMI with:
    • Anterior MI
    • LV dysfunction (EF <40%)
    • Heart failure
    • Hypertension or diabetes
  • Ramipril, Lisinopril, Captopril - start low, titrate.
  • ARB (e.g., valsartan) if ACE inhibitor intolerant.

7. Statins

  • High-intensity statin (Atorvastatin 80 mg or Rosuvastatin 40 mg) - started immediately, continued indefinitely.
  • Target LDL <1.4 mmol/L (55 mg/dL) per ESC 2023 guidelines.

8. Nitrates

  • GTN sublingual or IV for ongoing pain (avoid in RV infarct, hypotension, PDE5 inhibitor use in last 24-48h).
  • No mortality benefit; not routinely continued long term.

STEMI-Specific: Reperfusion Strategy

Time is muscle - every 30-min delay increases mortality.

Primary PCI (Preferred)

  • Indication: STEMI within 12 hours of symptom onset (or ongoing ischaemia up to 24h).
  • Target: Door-to-balloon time <90 minutes (if presenting to PCI centre) or <120 minutes from first medical contact.
  • Drug-eluting stent preferred over bare metal stent.
  • Culprit-only PCI preferred in cardiogenic shock (CULPRIT-SHOCK trial) - staged revascularisation of non-culprit vessels.
  • Radial access preferred (lower bleeding).

Fibrinolysis (Thrombolysis)

  • Used when primary PCI not available within 120 minutes of first medical contact.
  • Agents:
    AgentDoseType
    Alteplase (tPA)15 mg IV bolus, then 0.75 mg/kg (max 50mg) over 30min, then 0.5 mg/kg (max 35mg) over 60minFibrin-specific
    Tenecteplase (TNK-tPA)Single IV bolus weight-based (30-50 mg)Fibrin-specific, easiest
    Reteplase10 units IV x2 (30 min apart)Fibrin-specific
    Streptokinase1.5 million units IV over 60 minNon-fibrin-specific (rarely used)
  • Fibrin-specific agents (alteplase, tenecteplase) are superior to streptokinase (GUSTO trial).
  • Contraindications to thrombolysis:
    • Absolute: Prior intracranial haemorrhage, stroke within 6 months, active bleeding, aortic dissection, CNS tumour/AVM.
    • Relative: SBP >180 mmHg, INR >2, major surgery <3 weeks, pregnancy, active peptic ulcer.

Pharmacoinvasive Strategy

  • If thrombolysis given, PCI should be performed 2-24 hours later (coronary angiography routinely).
  • Immediate rescue PCI if thrombolysis fails (ST elevation not resolving >50% at 60-90 min).

NSTEMI / Unstable Angina Treatment

Risk Stratification

  • GRACE score (most validated) or TIMI score guides timing of angiography.
  • High risk features: Dynamic ECG changes, troponin rise, haemodynamic instability, refractory angina, GRACE >140.

Invasive vs. Conservative Strategy

StrategyTimingIndication
Immediate invasive (<2h)Like STEMIHaemodynamic instability, refractory ischaemia, cardiogenic shock
Early invasive (<24h)High GRACE, elevated troponin, dynamic ECG changes
Invasive (<72h)Intermediate risk, recurrent symptoms
ConservativeLow risk (TIMI 0-1, normal troponin, no ECG changes)

Additional Pharmacotherapy

Aldosterone Antagonists

  • Eplerenone (preferred post-MI) or Spironolactone - for patients with EF <40% and HF or diabetes.
  • Start after ACE inhibitor/ARB; avoid if K+ >5 mmol/L or severe renal impairment.
  • Reduces mortality (EPHESUS trial - eplerenone post-MI).

Ivabradine

  • Add if HR >70 bpm at rest on maximum tolerated beta-blocker with reduced EF.

Glucose Control

  • Target glucose ≤10 mmol/L (180 mg/dL); avoid hypoglycaemia.
  • SGLT2 inhibitors (empagliflozin, dapagliflozin) if EF <40% reduces CV death/HF hospitalisation (post-MI).

Colchicine

  • Low-dose colchicine (0.5 mg OD) shown to reduce recurrent CV events post-MI (COLCOT trial, LoDoCo2 trial).

Complications and Specific Management

ComplicationManagement
Cardiogenic shockEarly revascularisation (PCI), inotropes (dobutamine), vasopressors (noradrenaline), IABP/Impella as bridge
VF/VTDC cardioversion; amiodarone for recurrent VT
Complete AV block (inferior MI)Usually transient; temporary pacing if symptomatic
Acute MR (papillary muscle rupture)Emergency surgery (high mortality)
VSDEmergency surgical repair or percutaneous closure
Free wall ruptureEmergency pericardiocentesis and surgery
RV infarctionIV fluids, avoid nitrates/diuretics, early reperfusion
Pericarditis (post-MI / Dressler's)Aspirin, colchicine; avoid anticoagulation if significant effusion

Secondary Prevention (Post-MI)

DrugDurationNotes
Aspirin 75 mgIndefinite
P2Y12 inhibitor12 months (DAPT)May extend in high thrombotic risk
Beta-blockerMinimum 12 months; indefinitely if EF <40%
ACE inhibitor/ARBIndefinitely if EF <40%, DM, HTN
High-intensity statinIndefinitely
EplerenoneIndefinitely if EF <40% with HF/DM
SGLT2 inhibitorIf EF <40%
Colchicine 0.5 mg ODAt least 6 months
Lifestyle: Cardiac rehabilitation, smoking cessation, diet modification, regular exercise, BP and glucose control.

Sources: Harrison's Principles of Internal Medicine, 22e (2025); Braunwald's Heart Disease, 10e; ESC Guidelines STEMI 2023 / NSTEMI 2020.
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