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Clinician Guide – Nov. 18, 2009
Treating Cholesterol With Combination Therapy: Clinician's Guide
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Table of Contents
- Introduction
- Clinical Bottom Line
- The Studies
- Lipid-Lowering Medications
- Resources for Patients
- Source
- For More Information
Introduction
This guide summarizes clinical evidence on using combinations of lipid-lowering medications for the treatment of high cholesterol. Most of the available evidence compares combination therapy with using a statin medication alone. This guide covers the major classes of lipid-lowering medications. It does not cover dietary and lifestyle changes.
Clinical Issue
High cholesterol is one of the most commonly treated medical conditions. There is general consensus that aggressive treatment is indicated for high-risk individuals. LDL levels are the primary target of treatment. Lowering LDL cholesterol reduces the risk of coronary heart disease and ischemic stroke.
After diet and exercise, a statin medication is the first line of treatment. Several other types of medications are available for lowering cholesterol. For people who do not achieve the desired treatment goal on statin monotherapy, combination therapy may permit using a lower dose of a statin and decrease the risk of side effects.
Much of the available evidence compares combination therapy to statin monotherapy using less than maximal statin dosages. For people who have not reached their cholesterol goal on lower doses of statins, the clinical options are either to raise the statin dose or to add a second lipid-lowering medication.
The systematic review on which this guide is based compared the following medication combinations with statin monotherapy:
- Statin plus a bile acid sequestrant,
- Statin plus ezetimibe,
- Statin plus a fibrate,
- Statin plus niacin, and
- Statin plus Omega-3 fatty acids.
Clinical Bottom Line
The evidence is insufficient to conclude that combination therapy leads to lower rates of clinical events and death (all cause mortality and vascular death) than statin monotherapy. In these studies, clinical events included myocardial infarctions, strokes, and the need for invasive vascular procedures.
The evidence is insufficient to assess whether any combination regimen provides greater reduction in LDL cholesterol than statin monotherapy. Evidence is also insufficient for other intermediate outcomes, including total cholesterol, HDL cholesterol, and coronary artery and carotid intima thickening.
The evidence is insufficient to draw conclusions about the rates of adverse events of combination therapy compared with statin monotherapy. The adverse events assessed in these studies included elevation of liver enzymes, myalgia, rhabdomyolysis, and cancer.
The Studies
While over 100 research studies were included in the systematic review, several characteristics of these studies made it difficult to draw firm conclusions.
- Small sample size – The trials generally were unable to detect end points that occurred infrequently.
- Short duration – On average, the trials were about 30 weeks long; some lasted as little as 4-6 weeks.
- Inconsistent results – When a trial showed superiority of a drug combination, other trials did not confirm this result.
- Lack of ethnic diversity – Most study participants were white males.
- Different definitions of treatment success – Trials used many different thresholds to classify participants as having improved cholesterol levels.
- Little analysis of non-LDL outcomes – The studies provided little data on other treatment effects, such as HDL and triglyceride levels.
Only 15 of the 102 studies compared combination therapy with higher dose statin therapy. Most used the same dose statin in both the monotherapy and combination therapy study arms. It is not possible to derive recommended doses from these studies.
Lipid-Lowering Medications
| Drug Name1 | Brand Name | Available as Generic? |
|---|---|---|
| Statins | ||
| Atorvastatin | Lipitor® | No |
| Fluvastatin | Lescol®, Lescol® XL2 | No |
| Lovastatin | Mevacor®, Altoprev®2 | Yes |
| Pravastatin | Pravachol® | Yes |
| Rosuvastatin | Crestor® | No |
| Simvastatin | Zocor® | Yes |
| Bile acid sequestrants | ||
| Cholestyramine | Questran® | Yes |
| Colesevelam | Welchol® | No |
| Colestipol | Colestid® | Yes |
| Cholesterol absorption inhibitors | ||
| Ezetimibe | Zetia® | No |
| Fibrates | ||
| Gemfibrozil | Lopid® | Yes |
| Fenofibrate | Lofibra®, TriCor® | Yes |
| Vitamins and supplements | ||
| Niacin | Niacor®, Niaspan®2 | Yes |
| Omega-3 fatty acids | Lovaza® | Yes |
| Combinations | ||
| Ezetimibe/simvastatin | Vytorin® | No |
| Niacin ER/lovastatin | Advicor® | No |
| Niacin ER/simvastatin | Simcor® | No |
1 These drugs were evaluated in the systematic review.
2 Extended release. Not available as generic.
XL/ER = extended release.
Resources for Patients
Treating High Cholesterol: A Guide for Adults is a companion to this Clinician’s Guide. It can help people talk with their health care professional about high cholesterol and the different types of lipid-lowering medications.
Source
The source material for this guide is a systematic review of 102 research studies. The review, Comparative Effectiveness of Lipid Modifying Agents (2009), was prepared by the University of Ottawa Evidence-based Practice Center. The Agency for Healthcare Research and Quality (AHRQ) funded the systematic review and this guide. The guide was developed using feedback from clinicians who reviewed preliminary drafts.
AHRQ created the John M. Eisenberg Center at Oregon Health & Science University to make research useful for decisionmakers. This guide was prepared by Bruin Rugge, M.D., Martha Schechtel, R.N., Rachelle Nicolai, B.A., Susan Severance, M.P.H., and David Hickam, M.D., of the Eisenberg Center.
For More Information
For free print copies call:
The AHRQ Publications Clearinghouse
(800) 358-9295
Consumer’s Guide,
AHRQ Pub. No. 09(10)-EHC024-A
Clinician’s Guide,
AHRQ Pub. No. 09(10)-EHC024-3

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