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
Since beginning her research into DNA markers for HOD and other Weimaraner inherited diseases, Dr. Noa Saffra has responded to numerous questions from Weimaraner Breeders. Noa would like to share with the membership the most often asked questions and her replies. Frequently Asked Questions About HOD By Noa Saffra DVM, PhD is a systemic disease that affects young include: depre
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