Cardiovascular Disease Clinical Trial
Official title:
Multisite Randomized Controlled Trial of Continuing vs. Discontinuing Statins
The purpose of this study is to determine if there is a difference in survival rate at 60 days after enrollment between patients with advanced life-limiting illness for whom statins are discontinued vs. for patients with advanced life-limiting illness who are maintained on the medication. Secondary outcomes of this study will determine the effects of medication cessation on overall survival, important cardiovascular events, quality of life (QOL), symptoms, performance status, polypharmacy issues, satisfaction with care, and costs.
Currently, over 80% of the population is expected to die of chronic life-limiting illnesses,
predominant among which are the various manifestations of cardiovascular disease, cancer,
dementia, and chronic lung disease. Patients with high cholesterol and those potentially at
risk for atherosclerotic heart disease and stroke are often treated preventively with HMG
Co-A reductase inhibitors (a.k.a., statins). Clinical trial evidence supports the use of
statins for patients with hyperlipidemia and established ischemic heart disease to reduce
risk of future cardiovascular events and mortality, and to reduce risk of future
cardiovascular events in patients with multiple cardiac risk factors. Beneficial outcomes are
evident in these trials after 3-6 years of treatment. Hence, statins are among the most
prescribed medications in the world. In the United States, over 25% of Medicare beneficiaries
take a statin medication. Statin medications are frequently continued until the patient can
no longer eat or swallow at the end of life, because there are no evidence-based guidelines
regarding when or how to discontinue medications for co-morbidities. The risks and costs vs.
benefits of statins for palliative care patients, for whom prognosis is limited, remains a
genuine clinical uncertainty. Meanwhile, medications for symptoms and other concerns
accumulate as illness progresses, and therefore polypharmacy and compounding medication side
effects are troublesome problems in the setting of advanced life-limiting illness. While
multiple studies have demonstrated the benefit of long-term preventive statin use for
patients at cardiovascular risk, other studies have supported the discontinuation of
medications (specifically statins) in end-stage disease. A rational approach to medication
discontinuation, specifically statin discontinuation, therefore has the potential to reduce
patient burden, polypharmacy, and side effects, while also preserving healthcare resources
for more beneficial interventions.
This study is a multi-site randomized controlled trial of discontinuing vs. continuing statin
medications in patients with advanced life-limiting illness. Eligible participants are adults
with advanced life-limiting illness with an estimated prognosis of 1-6 months who are on
statins for primary or secondary prevention of cardiovascular events. The primary outcome is
survival rate at 60 days; secondary outcomes address cardiovascular events, polypharmacy,
medication adverse effects, quality of life (QOL), and measures of the patient's
health-related experience. The primary hypothesis is that discontinuing statins will not
influence survival. Secondary hypotheses are that discontinuation of statins will not
adversely affect cardiovascular events or overall QOL, but will improve statin-related
symptoms and decrease polypharmacy.
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