Polypills for the secondary prevention of cardiovascular disease: effective in improving adherence but are they safe?
Vanessa SelakRuth WebsterPublished in: Therapeutic advances in drug safety (2017)
International guidelines recommend blood pressure-lowering therapy, statins and aspirin for people who have had a cardiovascular event but use of these medications is low, particularly for lower income countries. Clinical trials have demonstrated that combining these medications into a single pill or capsule (a 'polypill') improves adherence, systolic blood pressure and low density lipoprotein cholesterol compared with usual care in secondary prevention. Uptake of polypill-based care has been underwhelming, possibly due to safety concerns. Overall, results from the clinical trials of polypill use among people who have had a cardiovascular event show no immediate safety concerns. Increased use and adherence to medications will always be associated with side effects however use within a combination medication has not been shown to be any less safe than individual component medications. Research investigating the relative consequences of nonadherence to a polypill compared with individual components would be useful.
Keyphrases
- blood pressure
- clinical trial
- cardiovascular disease
- healthcare
- hypertensive patients
- palliative care
- heart rate
- quality improvement
- low dose
- heart failure
- pain management
- phase ii
- type diabetes
- mental health
- stem cells
- left ventricular
- physical activity
- clinical practice
- mesenchymal stem cells
- randomized controlled trial
- coronary artery disease
- atrial fibrillation
- antiplatelet therapy
- blood glucose
- drug induced
- percutaneous coronary intervention
- adverse drug