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PHARMAC and lack of funding for clopidogrel
1Green Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand. harveyw@adhb.govt.nz
Insights
Clopidogrel effectively reduces cardiovascular events compared to aspirin for patients with atherosclerotic vascular disease. New Zealand
Area of Science:
- Cardiology
- Pharmacology
Background:
- Clopidogrel is a proven antiplatelet medication reducing cardiovascular death, stroke, and myocardial infarction.
- Evidence supporting clopidogrel's benefits has been available for 5-10 years.
- Aspirin allergy affects approximately 5% of patients.
Purpose of the Study:
- To highlight the delayed access of New Zealand patients to funded clopidogrel.
- To advocate for a more efficient drug funding process in New Zealand.
Main Methods:
- Review of clinical trial data on clopidogrel efficacy.
- Analysis of current New Zealand pharmaceutical funding policies and timelines.
- Comparison of international guidelines with New Zealand's access to clopidogrel.
Main Results:
- Clopidogrel demonstrates significant clinical event reduction versus aspirin in atherosclerotic vascular disease.
- Clopidogrel addition to aspirin reduces events by 20% in unstable angina and post-coronary stenting.
- New Zealand patients have limited funded access to clopidogrel (typically 3 weeks post-stenting) despite strong evidence.
Conclusions:
- New Zealanders have been denied timely access to evidence-based treatments like clopidogrel due to funding delays.
- PHARMAC's drug approval process needs improvement for faster patient access to new medications.
- A streamlined process is crucial for New Zealanders to rapidly benefit from new pharmaceutical advancements.
Abstract:
Clopidogrel is an antiplatelet drug that has been shown in several trials to reduce clinical events such as cardiovascular death, stroke, and myocardial infarction when compared to aspirin in a broad range of patients with atherosclerotic vascular disease. Clopidogrel has also been shown to reduce the same events by 20% when added to aspirin in patients with unstable angina and also in patients undergoing coronary artery stenting. Despite this information being available for 5 to 10 years, guideline recommendations, and the knowledge that 5% of patients have major allergy to aspirin, New Zealand patients have only been able to receive funded clopidogrel for a short period, typically 3 weeks, after coronary artery stenting. We believe this is an example where New Zealanders have been denied treatments, despite a strong evidence-base, by PHARMAC's actions of delaying the funding of new drugs. We need to have a better process whereby New Zealanders can rapidly access new treatments.
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