Incorporating the Newly Released ACC/AHA Guidelines into Practice - - PowerPoint PPT Presentation

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Incorporating the Newly Released ACC/AHA Guidelines into Practice - - PowerPoint PPT Presentation

Incorporating the Newly Released ACC/AHA Guidelines into Practice Dawn Mutchko, MSN, RN, NP-C, APN The Heart Institute AtlantiCare Regional Medical Center Brief review of prior guidelines New individualized risk calculator and its role


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Incorporating the Newly Released ACC/AHA Guidelines into Practice

Dawn Mutchko, MSN, RN, NP-C, APN The Heart Institute AtlantiCare Regional Medical Center

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 Brief review of prior guidelines  New individualized risk calculator and its role  Discuss the 2013 ACC/AHA recommendations

for risk reduction for MI & CVA through:

 Cholesterol level managment  Weight management  Lifestyle modications including diet & exercise

 Apply the 2013 guidelines for lipid

management in clinical practice

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 I have no disclosures for this presentation.

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 Who made them?

 ATP IV panel  Expert reviewers  Representatives of federal agencies

 How?

 Randomized controlled trials  Systematic reviews  Meta-analyses

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 Goal: treatment of blood cholesterol to reduce

atherosclerotic cardiovascular risk in adults, currently the leading cause of death and disability in America

 No Longer Appropriate To:

 Treat to target  Lower is better  Treat for lifetime risk

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 Statin eligibility could increase by 13 million  56 million Americans ages 40-75 are eligible

to consider a statin

 43 million under ATP III

 10.4 million of newly eligible would have NO

history of heart disease

 Ages 60-75 will have the largest effect

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 Individuals with clinical ASCVD  Individuals with LDL-C =/> 190mg/dL  Individuals 40-75 yo with DM and LDL-C 70-189

mg/dL without clinical ASCVD

 Individuals without clinical ASCVD or DM, who

are 40-75 yo with LDL-C 70-189 mg/dL and have 10 year risk of 7.5%+

using the Pooled Cohort Equations for ASCVD risk prediction

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HOW DO WE KNOW?

 Cardiac cath  Q waves on EKGs  TEE  cCTA  ACS  Coronary or other

arterial revascularization

 Non-invasive testing  Carotid duplex  UE/LE arterial duplex  Peripheral angiography  PVD presumed to be

atherosclerotic

 CVA/TIA

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 High intensity statin +/- another agent  If intolerant, ezetimibe or others with a > 50%

reduction goal

 FH often unable to reach previous goals even

with polypharmacy

 Goal reduction of LDL >50%

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 High intensity with 10 year risk > 7.5%  Moderate intensity with 10 year risk < 7.5%

INDICATED IN ALL PATIENTS WITH DIABETES

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 Moderate to high intensity statin indicated

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 Family history of premature ASCVD  LDL > 160  hsCRP > 2.0  Coronary calcium scores > 300  ABI < 0.9

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 Lifestyle modification  No more specific lipid targets  Pooled Cohort Equations  Those outside of 4 Statin Benefit Groups  Define high & moderate intensity statin

therapy

 Who should receive high vs. moderate therapy

A PARADIGM SHIFT

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 Risk assessments identify the likelihood of

heart disease, MI or CVA

 Calculated using age, gender, race,

cholesterol/BP levels, diabetes and smoking status as well as BP medications

 Calculate 10 year risk and lifetime  Family history and CRP  Repeat 4-6 years  Discuss

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 Continue to measure/treat cholesterol  Identify those who have OR are at risk of

having ASCVD

 Select most effective treatments in those most

likely to benefit

 Collect/Review history, lipid panel

 Coronary Artery Calcium score, hs-CRP, ABI  FH of hypercholesterolemia

 Healthy living discussions +/- medical therapy

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 Statins

 Very high LDL  DM Type II, age 40-75  >7.5%+ risk in 10 years, age 40-75  Others

 Other cholesterol-lowering medications

 Statin side-effects  Cannot tolerate ideal dose  Contradictions to statin use – labs, meds, etc  Additional therapy

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 Non-statin therapies alone and in combination

with statins, do not provide acceptable risk reduction given their side effect profiles

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 Consider confirming myalgias  Consider other conditions  Readdress:

 Lifestyle  Decrease dose  Change statin  Check serum vitamin D levels and replete

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 Healthy choices

 Diet, exercise, weight, smoking, drug therapy

 Side effects  Medication compliance  Laboratory compliance  Communicate

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 Diet rich in vegetables, fruits and whole grains  Regular exercise  Maintaining healthy weight  NOT smoking or cessation efforts  Compliance with health, risk factors and

medical orders

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 Dietary recommendations

 Lower cholesterol

 Saturated and trans-fats

 Lower blood pressure

 Sodium

 DASH Diet  USDA’s Choose My Plate/Food Pattern  AHA Diet

 Physical activity

 Recommendations

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 Definition  Benefits of weight loss (if needed)  Weight Loss Strategies  Bariatric surgery

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 BMI

 Overweight BMI >25.0-29.9 kg/m2  Obesity BMI > or = 30 kg/m2

 Class I 30-34.99  Class II 35-39.99  Morbid Obesity 40+

 Waist circumference

 Men >40 inches/102 cm  Women >35 inches/88 cm

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 78 million Americans  Five critical questions related to CV risk

reduction

 Weight loss  BMI/waist circumference  Different diets  Comprehensive lifestyle intervention  Bariatric surgery

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 Weight loss >5%  Caloric intake  Men 1500-1800 kcal/day  Women 1200-1500 kcal/day  Evidence based diet  Comprehensive Lifestyle Program (6+ months)  Medically monitored diets  Long-term comprehensive weight loss maintenance  Bariatric surgery

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 Risk Assessment

 Long-Term Risk Assessment  Implementation  Lifetime Risk

 Lifestyle Management

 Blood Pressure  Lipids  Diet – sodium, potassium

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 NYHA Class 2-4  Dialysis patients  HIV + patients  Solid organ transplant recipients

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 Will additional GLs come out for groups when

RCT are available to review?

 Hypertriglyceridemia?  Relevance of treatment markers such as Lp(a), LDL

particles, ApoB?

 What non-invasive studies should we run?  How should lifetime risk be used?  What is the optimal age to start a statin?  Role of pharmocogenomics?  Long term effects of statin- associated new onset

diabetes and management?

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 Calculator overestimates/doesn’t make sense

 Dr. Nissen sites examples

 47 yo AA male - TC 160, HDL 44, SBP 130 on HCTZ

25mg, -DM, - tobacco; 10 year risk  7.6%

 60yo AA male – TC 150, SBP 125 w/o meds, - DM, -

tobacco (no risk factors); 10 year risk  7.5%

 44 yo Caucasian male – strong FH of MI, TC 250, HDL

28, LDL 182, SBP 120 w/o meds, - DM, - tobacco; 10 year risk  5.0%

 Similar for healthy Caucasian male age 58

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 No targets  Identify patients

 4 high risk groups

 Use statins  Healthy lifestyle

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63 yo male, 2 weeks post STEMI

Former smoker with HTN

He was discharged on atorvastatin 80mg daily, dual anti-platelet therapy, long-acting metoprolol, and an ACE inhibitor.

One year before the acute MI, he was prescribed simvastatin 40mg which was then increased to simvastatin 80 mg. He stopped the simvastatin 80mg 2 weeks later after developing muscle cramps in his legs. At that time he was also on a calcium channel blocker for his hypertension. Although he has no muscle symptoms since he started the atorvastatin 80 mg, he is concerned about having had muscle cramps in the past on a statin and would like to decrease the atorvastatin to 20 mg daily.

Systematic meta-analyses of randomized clinical trials support using an intensive statin dose such as atorvastatin 80 mg/day over a moderate intensity statin. He should stay on atorvastatin 80 mg.

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After 2 years of treatment with atorvastatin 80mg daily free of muscle symptoms, the patient developed progressive muscle pains in both lower legs. He stopped the statin 2 weeks prior to his clinic visit but the muscle pain and weakness did not noticeably

  • improve. He now wants to know if he can be switched to red rice

yeast.

On examination, he has mild difficulty getting out of a chair and also has weakness after doing 3 squats. He remembers he felt fine doing squats at the gym about 6 months ago.

He should stay off the statin until he is evaluated for possible causes of his muscle problems. A useful approach is to look for exogenous causes, systemic causes, and primary muscle disorders.

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44 yo female has a 10-year history of type 2 diabetes.

She is a nonsmoker with well-controlled hypertension and microalbuminuria.

She is on dietary management, metformin, and takes one omega-3 fatty acid capsule.

She takes lisinopril/HCTZ for HTN.

She has a family history of diabetes, but not premature ASCVD.

She has a BP 134/78 and a BMI of 36.0.

Her fasting lipid panel reveals an LDL–C 95, triglycerides 350 and HDL–C 38. Her hemoglobin A1c is 7.5%.

Her 10-year ASCVD risk should be calculated to determine if she needs a high- or moderate-intensity statin.

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26 yo female has an LDL–C of 260, HDL–C of 51 and triglycerides of 102.

She reports having elevated LDL–C levels of over 200 since her teens and has tried various diets without success but has never taken a drug to lower her cholesterol.

She is worried because her father died suddenly at age 38 and her father's brother had a myocardial infarction at age 32. Both were smokers. She is currently on a 2nd generation oral contraceptive and wonders if she should get off the contraceptive pill since she is engaged to be married in 6 months.

She has an occasional cigarette and says that it is "social smoking."

On exam, BP is 110/60 and BMI is 24. Her cardiovascular examination is normal.

She likely has heterozygous familial hypercholesterolemia and should start a high-intensity statin.

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60 yo AA female has asked whether she should be taking a statin to reduce her risk of stroke, but is worried about the statin causing diabetes.

Her mother had diabetes and had a stroke at age 62.

She is a nonsmoker.

Blood pressure is 142/88 on dual antihypertensives and BMI is 31.

Her fasting lipid panel reveals a total cholesterol 200, HDL–C 55, triglyceride 100, and LDL–C 125.

Her fasting blood sugar is 109 mm/dL and hemoglobin A1c is 5.9%.

According to the Pooled Cohort Equation for African-American Women, her estimated 10-year ASCVD risk is 8.7%.

She should start a moderate or high intensity statin.

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35 yo male has a strong family history of premature coronary disease, with both father and brother having an MI before age 55.

He is a nonsmoker, nondiabetic and exercises for 150 minutes/week. He has gained 10 lbs since age 18.

His BP is 140/90, weight is 170 pounds, height is 70 inches, and BMI is 24.4.

On a fasting lipid panel, his LDL–C is 160, HDL–C 45 and triglyceride 100.

His fasting blood glucose is 92 mg/dL.

He is on a heart-healthy diet and exercises 150 minutes a week. He and his wife would like to discuss statin therapy given his strong family history.

Should consider:

Strong family history of premature ASCVD

Lifetime risk of ASCVD of 46%

LDL-C ≥160 mg/dL

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32 yo male has gained 35 pounds since he graduated from college and started working as computer programmer.

He never smoked.

He has treated hypertension.

He has tried several popular diets to lose weight and lost about 20 pounds each time, but he always regains the weight lost within one year.

He bowls once a week.

He weighs 220 lbs and his BMI is 32.5, and the highest it has ever been.

His BP is 138/92.

TC 218, triglycerides 188, HDL–C 40, LDL–C 138 and non HDL–C 178.

His fasting glucose is 101 mg/dL. His father died of an MI at age 73.

Refer to a program providing a series of group counseling comprehensive lifestyle change sessions.

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55 yo male developed exertional chest pain. He had a positive stress exercise test and a coronary angiogram that revealed 2-vessel nonobstructive coronary disease.

His risk profile indicates he is a nonsmoker with treated hypertension, and a low HDL– C.

His father had an MI at age 67. His mother had type 2 diabetes diagnosed at age 60.

He is on a low dose aspirin, long-acting beta blocker, a high-intensity statin, and an ACE inhibitor.

His BP 135/86, pulse 58, weight 183 lbs and BMI 26.3.

His LDL–C is 95, HDL–C 39 and triglycerides are 145.

His fasting glucose is 109 mg/dL.

He wants to know what dietary change recommendations you would make.

His cardiologist has given him physical activity recommendations.

He should consume a dietary pattern that emphasizes vegetables, fruits, and whole grains; includes low-fat dairy products, poultry, fish, legumes, nontropical vegetable oils and nuts; and limits intake of sweets, sugar-sweetened beverages and red meats.

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48 yo male man with FH and history of 3-vessel coronary artery bypass surgery 7 years ago sees you now for statin intolerance.

The maximum dose of statin that he can tolerate is rosuvastatin 10 mg twice a week.

On more frequent dosing, he developed shoulder, low back, and thigh aching without weakness and a normal CK level.

He had similar symptoms on low doses of simvastatin, atorvastatin and pravastatin.

On rosuvastatin 10 mg twice a week, his most recent LDL–C was 168, triglycerides were 138 and HDL–C was 46.

Bile acid sequestrants have been shown to reduce ASCVD events when used as monotherapy in men with primary

  • hypercholesterolemia. He should continue the rosuvastatin and

cholestyramine 4g packet BID should be added.

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Two months ago, a 63yo Hispanic male had a MI followed by an angioplasty and DES.

He was discharged on 80 mg atorvastatin, low-dose aspirin, clopidogrel, a long-acting beta blocker, and lisinopril 5 mg.

One year ago his LDL–C was 140. He was prescribed a low dose of pravastatin 10 mg/day at that time but never returned for a follow-up lipid panel.

He reported stopping the pravastatin about 6 months before his MI. He returns now for a follow-up visit. He reports adhering to a heart healthy diet and taking atorvastatin 80 mg/day for the first month after discharge.

He had no musculoskeletal or other symptoms during this period but did not refill the prescription. He thought he was already taking too many pills and did not understand why he was taking a pill for cholesterol. His fasting lipid panel returns with an LDL-C of 125.

Nonadherence to statin therapy is associated with an increased risk of stroke, MI and death.

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