Pharmacotherapy of Dyslipidemia KHOI NGUYEN LAM Disease State Definition
• Premature CAD • Typically with first degree relative
Epidemiology - 65 million quality for lifestyle changes
- 1/67 Ashkenazi Jews - 1/100 Afrikaners, South African Indians
- Susceptible genotype (no gene discovered)
physiology
- Aggravated by excessive saturated fat, trans
- Decreased LDL cellular uptake - Diet high in fat/cholesterol decrease LDL
Clinical Presentation
- Premature Coronary artery disease (CAD)
o Abdominal obesity (♂ > 40”; ♀ > 35”)
Risk Factors
o Cigarette Smoking o HTN (>140/90) o HDL (< 40) o Family Hx o Age (♂ > 45; ♀ > 55)
Diagnosis Therapeutic Outcomes* *Reference of Guidelines Used (ATP 3)
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
Treatment Options**
o Eat Plant Stanols / Sterols (additive to margarines, salad dressin, mayonnaise) and Fiber
(Non-drug Therapy – include all therapeutic classes/agents available and preferences per treatment guidelines) **See Treatment Options Table
o Gemfibrozile (Lopid) o Clofibrate (d/c)
o Cholestyramine o Colestipol (Colestid) o Colesevelam (Welchol)
o Lovastatin + Niacin (Advicor) o Atorvastatin + Amlodipine (Caduet) o Pravastatin + ASA (Pravigard Pac) o Simvastatin + Ezetimibe (Vytorin) o
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
Pharmacological Treatment Options for Dyslipidemia KHOI NGUYEN LAM
Statins Fibric
Lovastation (Mevacor, Altocor/Altoprave)
Availability Generic (Brand)
Cerivastatin (Baycol)***d/c 2001 Rosuvastatin (Crestor)
Fluvastatin (Lescol) Pravastatin (Pravachol)
Mechanism
• Analogue for cholesterol precursor (HMG CoA)
of Action
• Binds to HMG CoA Reductase and destroys it
• By lowering LDL, increase LDL receptor on Liver
• Breaks down and remove chylomicron, VLDL
EFFICACY (Indication/Use, Clinical Data
• Antiproliferation effects on smooth muscle cells
Support)
o Dyspepsia 20%, ab pain 10%, diarrhea 7%,
(Major Drug
o Constipation, flatulence, dyspepsia, ab pain
Interactions,
o Similar to Placebo, abnormal LFT (FENO)
Pre-cautions,
o Hepatitis, cholestasis, jaundice, cirrhosis, hep
indications,
o Antidiabetic agents, hypoglycemia, incr insulin
Adverse Effects,
o Infection, rhinitis, sinusitis, steve-johnson
Pregnancy Risk
o GEM, Bile Acid Seq, take two hours apart
Category)
o 3A4 substrate (amiodarone, barbiturates, St.
John’s Wort, phenytoin, anti-retroviral protease
o Ezetimibe, (w/GEM, ?, cause cholelithiasis)
o 2C9 substrate for Fluvastatin (amiodarone,
fluoxetine, zafirlukast, STI-571”Imatinib”,
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
Statins Fibric
o Digoxin toxicity (80mg/QD strength) o Erythomycin, Clarithromycin (Myopathy) o Exenatide (AUC, Cmax decr, clinical relevance
o Fibric Acid (Myopathy) o Other Statins o Oral Contraceptives (Lipitor, Crestor) o Glitazone (Lipitor) o Repaglinide “Prandin” (Zocor) incr Prandin SE o Warfarin (Lovastatin, Fluvastatin, Crestor,
o EtOH o Asians (Crestor) – 2X plasma o DM (renal dx) o Elderly o Renal defficient o Hepatic deficient
o Alcoholism o Hepatic Disease o Manitol hypersensitivity (Baycol)
Dosage & Administration (Include renal and/or hepatic adjustments) Monitoring
• Toxicity :: CPK (creatine phoshokinase,
• Tell your dr other medications you’re taking
Education
• Cause blurred vision, dizziness (careful
Lovastatin 40mg = $62.90 Pravachol 40mg = $147.03 Crestor 40mg = $116.57 Zocor Simvastatin
References
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
Pharmacological Treatment Options for Dyslipidemia KHOI NGUYEN LAM 2-azetidinone compound Nicotinic Acid Bile Acid Sequesterates Availability Generic (Brand) Mechanism of Action EFFICACY (Indication/Use, Clinical Data Support)
• Not absorbed, safer toxicity profile
(Major Drug Interactions, Pre-cautions, indications, Adverse Effects, Pregnancy Risk Category) Dosage & Administration
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
2-azetidinone compound Nicotinic Acid Bile Acid Sequesterates Monitoring (Efficacy and Toxicity Parameters)
• Take ezetimibe >2 hrs before or 4
Education References
Pharmacotherapy Presentation – Pharmaceutical Care Rotation
University of Maryland School of Pharmacy
Happy Harry’s Pharmacy Patient Care Center, Perryville, MD
Table B1. Estimate of 10-Year Risk for Men (Framingham Point Scores) Total Cholesterol Age 20-39 Age 40-49 Age 50-59 Age 60-69 Age 70-79 Age 20-39 Age 40-49 Age 50-59 Age 60-69 Age 70-79 Nonsmoker HDL (mg/dL) Systolic BP (mmHg) If Untreated If Treated Point Total 10-Year Risk % Table B2. Estimate of 10-Year Risk for Women (Framingham Point Scores) Total Cholesterol Age 20-39 Age 40-49 Age 50-59 Age 60-69 Age 70-79 Age 20-39 Age 40-49 Age 50-59 Age 60-69 Age 70-79 Nonsmoker HDL (mg/dL) Systolic BP (mmHg) If Untreated If Treated Point Total 10-Year Risk %
LDL Cholesterol: The Primary Target of Therapy
Risk Assessment: First Step in Risk Management
Method of risk assessment: counting major risk factors and estimating 10-year CHD risk
Role of other risk factors in risk assessment
The link between risk assessment and cost effectiveness
Primary Prevention With LDL-Lowering Therapy
Secondary Prevention With LDL-Lowering Therapy
LDL-Lowering Therapy in Three Risk Categories
Multiple (2+) risk factors and 10-year risk •20%
Therapeutic Lifestyle Changes in LDL-Lowering Therapy
Drug Therapy to Achieve LDL Cholesterol Goals
Secondary prevention: drug therapy for CHD and CHD risk equivalents
LDL-lowering drug therapy for primary prevention
Benefit Beyond LDL Lowering: The Metabolic Syndrome as a Secondary Target of Therapy
Management of underlying causes of the metabolic syndrome
Specific Treatment of Lipid and Non-Lipid Risk Factors
Management of Specific Dyslipidemias
Special Considerations for Different Population Groups
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