Pain Management in Myocardial Infarction
Morphine sulfate administered intravenously in doses of 2 to 4 mg with increments of 2 to 8 mg repeated at 5 to 15-minute intervals is the analgesic of choice for myocardial infarction. 1
Primary Analgesic: Morphine Sulfate
Morphine remains the definitive first-line analgesic for MI pain despite recent retrospective concerns about outcomes. 1 The drug works through multiple beneficial mechanisms beyond simple analgesia:
- Blocks sympathetic efferent discharge centrally, resulting in peripheral venous and arterial dilation that reduces both preload and afterload, thereby decreasing myocardial oxygen demand 1
- Reduces anxiety and circulating catecholamines, which may decrease associated arrhythmias 1
- Particularly beneficial in patients with acute pulmonary edema, as it alleviates work of breathing and favorably affects ventricular loading conditions 1
Dosing Protocol
Start with 2 to 4 mg IV, then titrate with increments of 2 to 8 mg repeated at 5 to 15-minute intervals based on pain relief and hemodynamic response. 1 Relatively large cumulative doses of 2 to 3 mg/kg are occasionally required. 1
Managing Morphine Side Effects
- For respiratory depression: Administer naloxone 0.1 to 0.2 mg IV every 15 minutes, though this will reverse pain relief as well 1
- For excessive bradycardia: Give atropine 0.5 to 1.5 mg IV 1
- For hypotension with inappropriate bradycardia (rare): Use leg elevation, fluids, and atropine 1
- Respiratory depression is rarely encountered in the setting of severe chest pain or pulmonary edema 1
Alternative Opioid Analgesics
If morphine is contraindicated due to documented hypersensitivity:
- Hydromorphone is an acceptable alternative 1
- Meperidine has been historically recommended for inferior wall infarction due to vagolytic properties, but when equipotent analgesic doses are given, it has no clear advantage over morphine 1
- Pentazocine should be avoided as it produces significant increases in systemic and pulmonary arterial pressures, left ventricular filling pressure, and systemic vascular resistance while decreasing ejection fraction—all deleterious in MI 2
Adjunctive Anti-Ischemic Therapy for Pain
Pain in acute MI results from continuing ischemia of living jeopardized myocardium rather than completed necrosis. 1 Therefore, anti-ischemic interventions can reduce pain:
- Intravenous nitroglycerin for ongoing chest pain: Start with 5 to 10 µg/min and increase by 5 to 10 µg/min every 5 to 10 minutes while monitoring blood pressure (never allow systolic BP <90 mm Hg) 1
- Oxygen for hypoxemic patients (oxygen saturation <90%), though routine oxygen in normoxemic patients may increase coronary vascular resistance 1
- Beta-adrenergic blocking agents reduce myocardial oxygen demand 1
Absolutely Contraindicated Analgesics
NSAIDs (both nonselective and COX-2 selective agents) are contraindicated and must be discontinued immediately. 1 These drugs are associated with:
- Increased risk of death 1
- Reinfarction 1
- Cardiac rupture 1
- Hypertension 1
- Heart failure 1
- Renal insufficiency 1
The ExTRACT TIMI-25 trial demonstrated increased risk of death, reinfarction, heart failure, or shock among patients taking NSAIDs within 7 days of enrollment. 1
Special Considerations for Inferior MI with Right Ventricular Involvement
In patients with right ventricular infarction (occurs in up to 50% of inferior MIs):
- Avoid nitrates entirely as they can cause profound hypotension by reducing preload 3, 4
- Morphine remains appropriate for analgesia but use cautiously with careful hemodynamic monitoring 4
- Maintain RV preload with IV normal saline for hypotension rather than relying solely on analgesics to reduce sympathetic drive 3, 4
Critical Timing Consideration
Effective analgesia should be promptly administered at the time of diagnosis and not unreasonably delayed to evaluate the results of anti-ischemic therapy or reperfusion. 1 While rapid pain relief often occurs after early reperfusion with thrombolytic therapy or PCI, waiting for reperfusion to relieve pain is inappropriate. 1
Addressing Recent Controversy
Recent retrospective analyses have raised concerns about morphine potentially delaying antiplatelet drug absorption and worsening outcomes. 5 However, the highest quality prospective data from the CIRCUS trial (969 patients with anterior STEMI followed for 1 year) found no significant difference in major adverse cardiovascular events between patients who received morphine versus those who did not (26.2% versus 22.0%, P=0.15), with similar all-cause mortality (5.3% versus 5.8%, P=0.89) and infarct size. 6 Given this prospective evidence and the continued Class I recommendation from ACC/AHA guidelines, morphine remains the standard of care. 1