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HMG-CoA Reductase Inhibitors Joanne Ong California State University, San Marcos School of Nursing Pharmacology and Pathophysiology NURS 312 Gary Veale, RN, MSN, Ed. July 16, 2015

Pharmacology teaching project final

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Page 1: Pharmacology teaching project final

HMG-CoA Reductase Inhibitors

Joanne Ong

California State University, San Marcos

School of Nursing

Pharmacology and Pathophysiology

NURS 312

Gary Veale, RN, MSN, Ed.

July 16, 2015

Page 2: Pharmacology teaching project final

HMG-CoA Reductase Inhibitors

Prototype drug: Atorvastatin

Page 3: Pharmacology teaching project final

Pharmacologic class: HMG-CoA reductase inhibitors

Therapeutic class: Lipid-lowering agents/statin

Pregnancy risk: Pregnancy Category X

Contraindicated with pregnancy and lactation due to its potential for adverse reactions on the

fetus or neonate (Karch, 2013, p. 789)

Page 4: Pharmacology teaching project final

Examples include:Atorvastatin (Lipitor) (Prototype)

Fluvastatin (Lescol)

Lovastatin (Mevacor)

Pitavastatin (Livalo)

Pravastatin (Pravachol)

Rosuvastatin (Crestor)

Simvastatin (Zocor)

HMG-CoA Reductase Inhibitors

Page 5: Pharmacology teaching project final

HMG-CoA reductase is an enzyme responsible for cholesterol synthesis. Inhibiting this enzyme will lower the levels of serum cholesterol and LDL levels, an important element of developing atherosclerosis, and slightly increase HDL levels, the “good cholesterol,” due to the fat metabolism shift (Karch, 2013, p. 788).

This drug class is typically used for treatment of hyperlipidemia/hypercholesterolemia and to slow progression of CAD (Karch, 2013, p. 789)

Page 6: Pharmacology teaching project final

According to the literature search of Thomas et al. (2010) in the PubMed database from January 1984-April 2009, they found that “from large, randomized, controlled trials show that statin therapy lowers both all-cause and coronary heart disease mortality and reduces myocardial infarction, stroke and the need for revascularization in individuals aged ≥65 years who have a history of coronary heart disease… there is substantial potential for statin treatment to provide benefits in this population.”

Page 7: Pharmacology teaching project final

Statin, the drug of choice for lowering cholesterol levels…

New guidelines on November 2013, jointly issued by the American College of Cardiology (ACC) and the American Heart Association (AHA) will greatly impact the treatment of hyperlipidemia… 25% increase of overall population that is treated with statins

over the next 3 years, increasing from 3,909,407 (27.7%) patients to 4,892,668 (34.7%) patients (Tran et al., 2013).

Statins will be utilized as a primary prevention medication for patients aged 40 to 75 years who were not on any anti-cholesterol medications at baseline (Tran et al., 2013).

“…increase the overall number of statin prescriptions by 25% and will decrease the number of non-statin cholesterol-lowering medication prescriptions by 68% during the next 3 years” (Tran et al., 2013).

Page 8: Pharmacology teaching project final

PathophysiologyHyperlipidemia lipids are cholesterol and triglycerides elevated levels of serum cholesterol and triglycerides increased level of the lipoprotein LDL (“bad cholesterol”) and

low level of HDL (“good cholesterol”) high lipids will increase risk of atherosclerosis and CAD

Atherosclerosis type of arteriosclerosis (hardening of arteries). fatty, fibrous plaque formed in the lining of the arteries (aorta

and its branches, coronary and cerebral) (Porth, 2011, p. 411) leading cause of coronary artery disease, stroke and peripheral

artery disease (Porth, 2011, p. 411)

Page 9: Pharmacology teaching project final
Page 10: Pharmacology teaching project final

Therapeutic Goals

Treatment for hyperlipidemia/hypercholesterolemia/dyslipidemia

Increase HDL levels “the good cholesterol”

Help to slow progression of CAD Prevent MI (in patients with CAD or

high risk from developing CAD) Reduction of the risk of undergoing

revascularization procedures Statins adjunct with proper diet (low-

fat, low-cholesterol) and exercise

(Karch, 2013, p. 786-789)

Page 11: Pharmacology teaching project final

Adverse Effects

Most common (GI): flatulence, abdominal pain, cramps, N/V, constipation

(CNS):

headache, dizziness, blurred vision, insomnia, fatigue,

cataract development

More serious: Rhabdomyolysis (rovustatin), increased liver enzymes and

acute liver failure (atorvastatin and fluvastatin) Rhabdomyolysis

Page 12: Pharmacology teaching project final

Nursing Management and Interventions

Monitor lipid blood level Administer medication at bedtime (atorvastatin may be given

anytime of the day) Monitor LFTs (liver damage) Lifestyle changes to decrease risk for CAD Cholesterol lowering diet Contraceptives for women of childbearing age (Pregnancy

category X) Monitor for side effects Assess for compliance with treatment regimen

(Karch, 2013, p. 791-792)

Page 13: Pharmacology teaching project final

Lipid Blood Level

Total cholesterol = Normal <200, Borderline High 200-239, High ≥240

Low-density lipoprotein cholesterol (LDL) = Optimal <100, Normal 100-129, Borderline High 130-159, High 160-189, Very High ≥190

High-density lipoprotein cholesterol (HDL) “the good cholesterol” = Low <40, high ≥60

high level is good, low level is bad.

Triglycerides = Normal <150, Borderline High 150-199, High 200-499, Very High ≥500(Karch, 2013, p. 782)

Page 14: Pharmacology teaching project final

Drug-herbal interaction: St. John’s Wort may decrease levels and

effectiveness of lovastatin and simvastatin (Deglin & Vallerand, 2009).

Drug-food interaction: Large quantities of grapefruit juice increase

blood levels and increase risk of rhabdomyolysis (Deglin & Vallerand, 2009).

Hyperlipidemia: herbal therapyGarlic – decrease total cholesterol and

triglyceride levels and to

Increase HDL levels.

Olive (oil and leaf) – when part of a diet high in monounsaturated fats, may

lower cholesterol levels.

Onion – used as raw herb for hypercholesterolemia

(Springhouse, 2009)

Page 15: Pharmacology teaching project final

ReferenceDeglin, J. H., & Vallerand, A. H. (2009). Davis's drug guide for nurses. Philadelphia, PA: F.A. Davis.

Karch, A.M. (2013). Focus on nursing pharmacology. (6th ed.). Philadelphia: Lippincott, Williams & Wilkins. ISBN: 978-1-4511-2834-5

Porth, C.M. (2011). Essentials of Physiology (3rd ed.). Philadelphia: Lippincott, Williams & Wilkins. ISBN: 9781582557243

Springhouse (2009) Nursing Herbal Medicine Handbook (3rd ed.). Lippincott, Williams and Wilkins ISBN-13 9781582554174

Thomas, J. E., Tershakovec, A. M., Jones-Burton, C., Sayeed, R. A., & Foody, J. M. (2010). Lipid Lowering for Secondary Prevention of Cardiovascular Disease in Older Adults. Drugs & Aging, 27(12), 959-972. doi:10.2165/11539550-000000000-00000

Tran, J. N., Caglar, T., Stockl, K. M., Lew, H. C., Solow, B. K., & Chan, P. S. (2014). Impact of the New ACC/AHA Guidelines on the Treatment of High Blood Cholesterol in a Managed Care Setting. American Health & Drug Benefits, 7(8), 430-441.