Statin Discontinuation in Advanced Illness
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Purpose
The purpose of this study is to determine if there is a difference in survival time 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 polypharmacy issues, quality of life (QOL) and cardiovascular events.
| Condition | Intervention |
|---|---|
|
Palliative Medicine Cardiovascular Disease |
Other: discontinue statins |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Multisite Randomized Controlled Trial of Continuing vs. Discontinuing Statins |
- Survival Time [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]Objective is to determine if there is a difference in survival time 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.
| Estimated Enrollment: | 1200 |
| Study Start Date: | May 2011 |
| Estimated Study Completion Date: | May 2015 |
| Estimated Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
No Intervention: Continue Statins
Participant will continue on statins as per usual
|
Other: discontinue statins
patients will be randomized to either continue taking statins or discontinue.
|
|
Experimental: Discontinue statins
Participant will stop taking their statin drugs
|
Other: discontinue statins
patients will be randomized to either continue taking statins or discontinue.
|
Detailed Description:
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 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 (i.e. time to death); 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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- age >18 years old;
- have an advanced life-limiting illness;
- have a life expectancy of >1 month, AND patient exhibits declining functional status, defined as a reduction in Australia-modified Karnofsky Performance Status (AKPS)22 score to <80% in the previous 3 months;
- be on a statin medication for primary or secondary prevention of cardiovascular disease for ≥3 months;
- have adequately intact cognitive status to provide informed consent and complete the baseline assessment, as evidenced by a Short Portable Mental Status Questionnaire (SPMSQ)23 score of ≥6;
- provide informed consent; and,
- speak and read English at or above a grade 5 level (per patient or caregiver report).
Exclusion Criteria:
- primary treating physician/care provider estimates their life expectancy as < 1 month;
- under the care of a primary treating physician/primary care provider who is unwilling to have the patient enrolled;
- not consenting;
- having known active cardiovascular disease or sufficient risk of active cardiovascular disease to require ongoing therapy with statin drugs, in the opinion of the treating physician; OR,
- exhibiting obvious symptoms of myositis, known liver function test (LFT) abnormalities of >2.5x the upper limit of normal (ULN), known creatine kinase (CK) abnormalities of >2.5x ULN, or other contraindications to continuing statins, in the opinion of the treating physician.
Contacts and Locations| United States, Alabama | |
| University of Alabama, Birmingham | Recruiting |
| Birmingham, Alabama, United States, 35294 | |
| Contact: Patty Goode, MD 205-934-3259 | |
| United States, California | |
| San Diego Hospice and the Institute for Palliative Medicine | Recruiting |
| San Diego, California, United States, 92103 | |
| Contact: Charles von Gunten, MD 619-278-6225 | |
| United States, Colorado | |
| University of Colorado, Denver | Recruiting |
| Denver, Colorado, United States, 80217 | |
| Contact: Jean Kutner, MD 303-724-2240 | |
| United States, Illinois | |
| Northwestern University | Recruiting |
| Chicago, Illinois, United States, 60611 | |
| Contact: Adeboye Ogunseitan, MD 312-926-0259 | |
| United States, Minnesota | |
| Mayo Clinic | Not yet recruiting |
| Rochester, Minnesota, United States, 55905 | |
| Contact: Keith Swetz, MD Swetz.Keith@mayo.edu | |
| United States, New York | |
| Beth Israel Medical Center | Recruiting |
| New York, New York, United States, 10003 | |
| Contact: Russell Portenoy, MD 917-285-0438 | |
| Mount Sinai School of Medicine | Recruiting |
| New York, New York, United States, 10029 | |
| Contact: Sean Morrison, MD 212-824-8300 | |
| United States, North Carolina | |
| University of North Carolina, Chapel Hill | Recruiting |
| Chapel Hill, North Carolina, United States, 27599 | |
| Contact: Laura Hanson, MD 919-966-2939 | |
| Duke University Medical Center | Recruiting |
| Durham, North Carolina, United States, 27710 | |
| Contact: Amy Abernethy, MD 919-668-0647 | |
| Four Seasons Hospice and Palliative Care | Recruiting |
| Flat Rock, North Carolina, United States, 28731 | |
| Contact: Janet Bull, MD 828-692-6178 | |
| United States, Wisconsin | |
| University of Wisconsin Hospital and Clinics | Recruiting |
| Madison, Wisconsin, United States, 53792 | |
| Contact: James Cleary, MD 608-265-2789 | |
| Principal Investigator: | Amy Abernethy, MD | Duke University |
| Principal Investigator: | Jean Kutner, MD | University of Colorado, Denver |
More Information
No publications provided
| Responsible Party: | Amy Abernethy, MD, Palliative Care Research Cooperative Group |
| ClinicalTrials.gov Identifier: | NCT01415934 History of Changes |
| Other Study ID Numbers: | PCRC-001.1, UC4NR012584 |
| Study First Received: | May 10, 2011 |
| Last Updated: | March 30, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Cardiovascular Diseases Hydroxymethylglutaryl-CoA Reductase Inhibitors Anticholesteremic Agents Hypolipidemic Agents Antimetabolites |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Enzyme Inhibitors Lipid Regulating Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 23, 2013