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Published on: May 28, 2019
Prehospital opioid dose and myocardial injury in patients with ST elevation myocardial infarction
Himawan Fernando1,2,3, Ziad Nehme4,5, Karlheinz Peter1,3
1Department of Cardiology, Alfred Hospital, Melbourne, Victoria, Australia.
Insights
Higher opioid doses in ST-elevation myocardial infarction (STEMI) patients did not show benefits and may increase heart attack size. Further research is needed to confirm this link and explore alternative pain management strategies.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Opioid use is common in ST-elevation myocardial infarction (STEMI) patients for pain management.
- The relationship between opioid dosage and myocardial infarct size requires further clarification.
Purpose of the Study:
- To investigate the association between opioid dose and myocardial infarct size in STEMI patients.
- To determine if higher opioid doses correlate with larger infarcts.
Main Methods:
- Retrospective analysis of 422 STEMI patients from the Air versus Oxygen in Myocardial Infarction (AVOID) study.
- Patients were categorized by opioid dose: low (≤8.75 mg), intermediate (8.76-15 mg), and high (>15 mg) of intravenous morphine equivalent.
- Infarct size was assessed using cardiac biomarkers; cardiogenic shock patients were excluded.
Main Results:
- A higher proportion of patients in the high-dose opioid group had poor coronary blood flow (TIMI 0-1) before percutaneous coronary intervention (PCI).
- Increased thrombus aspiration catheter use was observed in the high-dose group.
- A dose-dependent association was found between opioid dose and increased peak creatine kinase, a marker of myocardial injury, though this was not significant after adjusting for TIMI flow.
Conclusions:
- The study suggests no benefit from higher opioid doses and indicates a potential dose-dependent increase in myocardial infarct size.
- Causality requires confirmation through prospective randomized controlled trials, as greater ischemic burden might necessitate higher opioid doses for pain.
- Future research should address opioid-P2Y12 inhibitor interactions and non-opioid analgesia for ischemic chest pain.
Objective:
To characterise the relationship between opioid dose and myocardial infarct size in patients with ST elevation myocardial infarction (STEMI).
Methods:
Patients given opioid treatment by emergency medical services with confirmed STEMI were included in this secondary, retrospective cohort analysis of the Air versus Oxygen in Myocardial Infarction (AVOID) study. Patients with cardiogenic shock were excluded. The primary endpoint was comparison of cardiac biomarkers as a measure of infarct size based on opioid dose (low ≤8.75 mg, intermediate 8.76-15 mg and high >15 mg of intravenous morphine equivalent dose).
Results:
422 patients were included in the analysis. There was a significantly higher proportion of patients with Thrombolysis in Myocardial Infarction (TIMI) 0 or 1 flow pre-percutaneous coronary intervention (PCI) (94% vs 81%, p=0.005) and greater use of thrombus aspiration catheters (59% vs 30%, p<0.001) in the high compared with low-dose opioid group. After adjustment for potential confounders, every 1 mg of intravenous morphine equivalent dose was associated with a 1.4% (95% CI 0.2%, 2.7%, p=0.028) increase in peak creatine kinase; however, this was no longer significant after adjustment for TIMI flow pre-PCI.
Conclusions:
Our study suggests no benefit of higher opioid dose and a dose-dependent signal between opioid dose and increased myocardial infarct size. Prospective randomised controlled trials are required to establish causality given that this may also be explained by patients with a greater ischaemic burden requiring higher opioid doses due to more severe pain. Future research also needs to focus on strategies to mitigate the opioid-P2Y12 inhibitor interaction and non-opioid analgesia to treat ischaemic chest pain.
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