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Antipsychotic drugs and risks of myocardial infarction: a self-controlled case series study
Ruth Brauer1, Liam Smeeth2, Karim Anaya-Izquierdo3
1Department of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK ruth.brauer@lshtm.ac.uk.
Insights
Antipsychotic medications are linked to a higher risk of myocardial infarction, especially within 30 days of starting treatment. This study used a self-controlled design to confirm this association, controlling for individual patient differences.
Area of Science:
- Cardiology
- Psychopharmacology
- Epidemiology
Background:
- Antipsychotics are associated with increased stroke risk.
- The impact of antipsychotics on myocardial infarction (MI) risk is unclear due to confounding vascular risk factors.
- Self-controlled case series (SCCS) design can mitigate between-person confounding.
Purpose of the Study:
- To investigate the association between antipsychotic use and myocardial infarction risk.
- To utilize the SCCS design to eliminate confounding by indication and other between-person differences.
- To compare findings with a classical case-control study.
Main Methods:
- Employed a self-controlled case series design using UK Clinical Practice Research Datalink data.
- Identified patients with first MI and antipsychotic prescription.
- Estimated incidence rate ratios (IRR) for MI during exposure periods versus unexposed periods within individuals.
- Conducted a comparative classical case-control study.
Main Results:
- An increased risk of MI was observed within 30 days of initiating antipsychotic therapy.
- First-generation agents showed an IRR of 2.82 (95% CI: 2.0-3.99).
- Second-generation agents showed an IRR of 2.5 (95% CI: 1.18-5.32).
- Case-control analysis yielded similar results for new users of both agent types.
Conclusions:
- Initiation of antipsychotic medication is associated with an increased risk of myocardial infarction.
- This elevated risk is evident shortly after prescription and is not due to pre-existing differences between patients.
- Findings highlight the need for cardiovascular risk monitoring in patients starting antipsychotic treatment.
Aim:
Antipsychotics increase the risk of stroke. Their effect on myocardial infarction remains uncertain because people prescribed and not prescribed antipsychotic drugs differ in their underlying vascular risk making between-person comparisons difficult to interpret. The aim of our study was to investigate this association using the self-controlled case series design that eliminates between-person confounding effects.
Methods And Results:
All the patients with a first recorded myocardial infarction and prescription for an antipsychotic identified in the Clinical Practice Research Datalink linked to the Myocardial Ischaemia National Audit Project were selected for the self-controlled case series. The incidence ratio of myocardial infarction during risk periods following the initiation of antipsychotic use relative to unexposed periods was estimated within individuals. A classical case-control study was undertaken for comparative purposes comparing antipsychotic exposure among cases and matched controls. We identified 1546 exposed cases for the self-controlled case series and found evidence of an association during the first 30 days after the first prescription of an antipsychotic, for first-generation agents [incidence rate ratio (IRR) 2.82, 95% confidence interval (CI) 2.0-3.99] and second-generation agents (IRR: 2.5, 95% CI: 1.18-5.32). Similar results were found for the case-control study for new users of first- (OR: 3.19, 95% CI: 1.9-5.37) and second-generation agents (OR: 2.55, 95% CI: 0.93-7.01) within 30 days of their myocardial infarction.
Conclusion:
We found an increased risk of myocardial infarction in the period following the initiation of antipsychotics that was not attributable to differences between people prescribed and not prescribed antipsychotics.
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