Related Experiment Video
Updated: Aug 24, 2026

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Cardiovascular risk assessment and triptans
1Hypertension Research Center, Georgetown University, Wasington, DC 20422, USA.
Insights
Triptan prescribing requires careful cardiovascular risk assessment. Patients with low risk can take triptans, while those with established heart disease or intermediate risk need further evaluation.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Triptans are effective migraine treatments but carry cardiovascular risks.
- Assessing cardiovascular risk in patients without diagnosed disease is challenging.
- A structured framework for risk assessment is needed for safe triptan prescription.
Purpose of the Study:
- To discuss coronary heart disease pathophysiology and cardiovascular risk assessment.
- To provide a framework for evaluating patients for triptan therapy.
- To guide decisions on prescribing triptans based on cardiovascular risk.
Main Methods:
- Review of coronary heart disease pathophysiology.
- Application of current cardiovascular risk assessment guidelines.
- Stratification of patients into low, intermediate, and high cardiovascular risk categories.
Main Results:
- Low-risk patients (0-1 risk factor) may receive triptans without intensive evaluation.
- High-risk patients (established cardiovascular disease) should not receive triptans.
- Intermediate-risk patients (≥2 risk factors) require cardiovascular evaluation before triptan use.
Conclusions:
- Cardiovascular risk assessment is crucial for safe triptan prescribing.
- Existing risk models have limitations in predicting acute coronary events.
- Guidelines should be applied considering the inability to accurately quantify plaque burden.
Abstract:
Identifying the patient for whom triptans are contraindicated because of recognized, diagnosed cardiovascular disease is relatively straightforward. Determining whether a patient with potential unrecognized cardiovascular disease is an appropriate candidate for triptan therapy, however, constitutes a difficult challenge, especially in the absence of a framework for workup of patients. This article discusses the pathophysiology of coronary heart disease and issues involved in assessing cardiovascular risk, and it attempts to provide a framework for cardiovascular risk assessment that can be applied to decisions for prescribing triptans. Current guidelines for cardiovascular risk assessment allow stratification of patients to low, intermediate, or high risk of coronary heart disease events. This framework for risk assessment can be applied to decisions for prescribing triptans. Cardiovascular risk-assessment algorithms discussed elsewhere in this supplement suggest that patients at low risk (1 or no risk factors) of coronary heart disease can be prescribed triptans without the need for a more intensive cardiovascular evaluation. Conversely, patients with established coronary heart disease or coronary heart disease risk equivalents should not be prescribed triptans according to the current prescribing recommendations. Patients at intermediate risk (2 or more risk factors) of coronary heart disease require cardiovascular evaluation before triptans can be prescribed. Current understanding suggests that the risk of future acute coronary events is a function of the absolute number of vulnerable plaques present, a variable that cannot be accurately determined using available technology or risk-prediction models. Cardiovascular risk-assessment guidelines should be evaluated in the context of this limitation.
Related Concept Videos
Imaging Studies for Cardiovascular System VI: Calcium -Scoring CT
Venous Thrombosis III: Interprofessional Care
Atherosclerosis III: Management
Angina IV: Management
Transient Ischemic Attack l: Introduction
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...