Cholesterol Management
Guidelines
Kerolus Shehata, MD
Lipoprotein Metabolism
Lipid lowering medications
Friedewald formula
Total cholesterol HDL + LDL + VLDL
VLDL TGs (mg/dL) / 5
LDL TC - HDL – (TGs/5)
**Not valid if TGs >400**
Example:
Total cholesterol: 230, TGs: 120, HDL: 25
• First calculate the VLDL: 120/5 = 24
• Then calculate LDL: 230 – (25+24) = 181 mg/dL
Causes of elevated LDL & TGs
Measurement of LDL
• Adult >20 YO and not on any lipid lowering medications  Measure lipid
panel (fasting or non-fasting) to estimate ASCVD
• If the non-fasting panel showed TGs >400 mg/dL  Repeat a fasting
panel.
• If LDL <70  May measure direct LDL or modified LDL estimate.
• If pt has a FHx of premature ASCVD or genetic HLD  may start with a
fasting panel.
Secondary ASCVD prevention
Cholesterol Management Guidelines
ASCVD Risk Estimator
Clinical ASCVD includes acute
coronary syndromes, or a history
of myocardial infarction, stable or
unstable angina, coronary or
other arterial revascularization,
stroke, transient ischemic attack,
or peripheral arterial disease
presumed to be of atherosclerotic
origin.
Who is at a very high risk for future ASCVD?
Severe Hypercholesterolemia (LDL ≥190)
ASCVD risk management for diabetics
Which diabetic patient is at a
very high risk to develop ASCVD?
Primary prevention of ASCVD
Statin use in
general risk
population
(without ASCVD events, LDL
>190mg/dl, or diabetes)
ASCVD risk enhancers
These can be used to refine risk assessment in certain
individuals at borderline or intermediate risk for ASCVD.
Statin therapy
Non-Statin therapy
Lifestyle and Lipids
Statin intolerant patients
• Myalgia that resolve with discontinuation of statin treatment and occur
with rechallenge
• Myalgia have been demonstrated with rechallenge on at least 2 or 3
statins, including those with different metabolic pathways, and at least
one statin at the lowest approved dose.
• Incidence: Ranges from 1-10%
• Risk factors: Impaired renal or hepatic function, ALT > 3X the upper limit of
normal, age >75, Asian ancestry, or on drugs that affect statin metabolism.
• Patients who develop myalgia on a statin should be tried on either a lower
dose of the same statin or a different statin, or even dosing the statin once
or twice weekly. >90 % will ultimately tolerate statin.
• When a high intensity statin is indicated but not tolerated and a moderate
intensity statin is used, further LDL lowering may be achieved with
ezetimibe or a bile acid sequestrant.
Statin use in pre-menopausal women
I C-LD
Women of childbearing age who are treated with statin therapy and
are sexually active should be counseled to use a reliable form of
contraception.
I C-LD
Women of childbearing age with hypercholesterolemia who plan to
become pregnant should stop the statin 1 to 2 months before
pregnancy is attempted, or if they become pregnant while on a
statin, should have the statin stopped as soon as the pregnancy is
discovered.
Statin use in CKD patients
• In patients with CKD (not treated with dialysis
or transplant) with LDL >70 and ASCVD risk of
≥ 7.5%  consider initiating moderate
intensity statin ± ezetimibe.
• In patients with CKD who require dialysis and
currently on statin May continue statin.
• In CKD patients who require dialysis  DON’T
start statin for primary prevention (Class III)
Statin use in chronic inflammatory
disorders & HIV
• Adults with these conditions and LDL >70 with
ASCVD risk of ≥ 7.5%  Consider starting
moderate or high intensity statin (Class I).
• Consider checking a fasting lipid profile before
starting therapy and 4-12 weeks after that.
When to use statin in patients 20 -39 Years old?
1) Severe hypercholesterolemia e.g. LDL ≥190
2) Those with LDL 160-189 plus a family history
of premature ASCVD (ASCVD event in men
less than 55 and women less than 65)
Statin use in patients ≥ 75 years old
• With clinical ASCVD  may initiate moderate
or high intensity statin after a thorough
discussion and evaluation.
• If patient tolerates high intensity statin 
May continue it.
Statin safety and side effects
• Need to have a discussion with your patient before starting statins regarding
potential side effects e.g. SAMS (Statin-associated muscle symptoms).
• SAMS include: Myalgia (normal CK), myositis, rhabdomyolysis and
autoimmune myopathy (HMG Coenzyme A Reductase AB)
• Mild or moderate SAMS  Reassess and Rechallenge.
• Severe SAMS on rechallenge  May start Non-statin therapy
• Even in patients with increased risk for DM  Continue statin (Class I)
• Severe SAMS  Measure CK and LFTs
• Transaminases elevation > 3x upper normal limit is infrequent
• Patient with chronic stable liver disease who has high ASCVD risk  get a
baseline LFTs and OK to start statin with close follow up (Class I).
• Coenzyme Q10 is NOT recommended for routine use or in treatment of SAMS.
• Don’t routinely check CK or transaminases in every patient on Statins.
Management of SAMS
Management of Hypertriglyceridemia
• Adult with moderate hyperTGs (177-499)Address obesity and metabolic
syndrome. Treat the secondary factors (DM, CKD, Nephrotic syndrome, chronic
liver disease, hypothyroidism and medications that increase TGs
• Adult with moderate or severe hyperTGs with ASCVD risk of ≥ 7.5% consider
initiating statin therapy.
• Adult with fasting TGs ≥1000 Consider adding Fibrate therapy and omega-3 FAs
Coronary Artery Calcium (CAC) score
• Use to refine risk in individuals with borderline to intermediate risk.
• Use in patients with intermediate ASCVD risk, but reluctant to start a statin.
• Patients ≥55 Years of age who have a CAC of Zero may consider withholding a
statin and reassessing in 5-10 years, however statin should be initiated if CAC is
more than zero.
CAC score Action
Zero Treatment with statin therapy may be withheld
or delayed, except in cigarette smokers, those
with diabetes mellitus, and those with a strong
family history of premature ASCVD
1 – 99 Favors statin therapy, especially in those ≥55
years of age.
> 100 Statin therapy is indicated
Miscellaneous
• Individuals from South Asia have increased ASCVD risk.
• ASCVD risk is higher among individuals from Puerto Rico than those from Mexico.
• Native American/Alaskan populations have high rates of risk factors for ASCVD.
• In Asians, Start low dose (5 mg) of rosuvastatin versus 10 mg in whites.
• Baseline serum CK values are higher in blacks than in whites.
• In adults of East Asian descent, other statins should be used preferentially over
simvastatin.
• Resistance exercise training will reduce LDL.
• Fenofibrate (not gemfibrozil) can be combined with statins if indicated.
• Goal LDL in patients with severe hypercholesterolemia (LDL-C>19) is greater than
50% reduction in LDL and resultant LDL<100mg/dl.
• Bile acid sequestrants are contraindicated when serum triglycerides >300mg/dl.
• All patients with diabetes who are 40 and older should be treated with a statin.
• PCSK9 inhibitors have no role in lipid management in patients with DM (unless
have established ASCVD or LDL>190mg/dL).
• Use high intensity statin if ASCVD risk >20%.
Take Home Messages - I
• In all individuals, emphasize a heart-healthy lifestyle across the life course.
• CAC scores can be used in patients up to age 80
• In patients with clinical ASCVD, reduce LDL with high-intensity statins or
maximally tolerated statin therapy.
• In very high-risk ASCVD, use a LDL threshold of 70 to consider the addition
of non-statins to statin therapy.
• In patients with LDL ≥ 190, start high intensity statins without calculating 10-
year ASCVD risk.
• In patients 40 to 75 years of age with DM and LDL>70 mg/dl, start
moderate-intensity statin (High intensity if with multiple risk factors) without
calculating 10-year ASCVD risk.
• In patient 40 to 75 years of age evaluated for primary ASCVD prevention,
have a clinician–patient risk discussion before starting statin therapy.
Take Home Messages - II
• In patients 40 to 75 years of age without DM, but with LDL≥70 and ASCVD
risk of ≥7.5%, start a moderate-intensity statin if patient agrees.
• In patients 40 to 75 years of age without DM, but with ASCVD risk of 7.5%
to 19.9% (intermediate risk), risk-enhancing factors favor initiation of
statins.
• In patients 40 to 75 years of age without DM, but with LDL ≥70, at a 10-
year ASCVD risk of 7.5% to 19.9% (intermediate risk), if a decision about
statin therapy is uncertain, consider measuring CAC
• Assess adherence and percentage response to LDL lowering medications
and lifestyle changes with repeat lipid panel in 1-3 months after statin
initiation or dose adjustment, repeated every 3 to 12 months as needed.
• In patients who smoke, a CAC score of zero does not exclude coronary artery
disease. The CAC score is also limited in those with diabetes and those with
a family history of early CAD.
Summary
Thank You

More Related Content

PPTX
Dyslipdemia Guidelines Head to Head
PDF
Management of dyslipidemia
PDF
Risk assessment for cardiovascular disease prevention
PPTX
Management of dyslipidemia
PDF
2019 ESC/EAS Guidelines on Dyslipidaemias
PPTX
Diabetic Kidney Disease 2022 Update
PPT
Anti mullerian hormone
PPTX
Guide Extension Catheter
Dyslipdemia Guidelines Head to Head
Management of dyslipidemia
Risk assessment for cardiovascular disease prevention
Management of dyslipidemia
2019 ESC/EAS Guidelines on Dyslipidaemias
Diabetic Kidney Disease 2022 Update
Anti mullerian hormone
Guide Extension Catheter

What's hot (20)

PPTX
DYSLIPIDEMIA GUIDELINES
PPTX
What’s new in Lipidology, Lessons from “recent guidelines“
PPTX
Vymada - Sacubitril & Valsartan (ARNI) For Heart Failure
PDF
[2015] the treatment of diabetes mellitus of patients with chronic liver disease
PPTX
Management of dyslipidemia
PPT
Rosuvastatin
PPT
Diabetic Dyslipidemia- Dr Shahjada Selim
PDF
Dyslipidemia lecture
PPT
Diabetes mellitus and hypertension
PPTX
Diabetes management in ramadan
PPT
Dyslipidemia approach
PPTX
Management of dyslipidemia 2019 update
PPTX
CARDIOVASCULAR DISEASE AND DIABETES
PPTX
Sodium glucose co transporter( SGLT2) Inhibitors
PPT
Updates of Diabetes Management by Dr Selim
PPTX
Dyslipidemia
PDF
Acc 2018 guidelines on lipids
PPTX
Diabetic dyslipidemia
PPTX
Current management of dyslipidemia final
PPTX
Lipid lowering trials ppt
DYSLIPIDEMIA GUIDELINES
What’s new in Lipidology, Lessons from “recent guidelines“
Vymada - Sacubitril & Valsartan (ARNI) For Heart Failure
[2015] the treatment of diabetes mellitus of patients with chronic liver disease
Management of dyslipidemia
Rosuvastatin
Diabetic Dyslipidemia- Dr Shahjada Selim
Dyslipidemia lecture
Diabetes mellitus and hypertension
Diabetes management in ramadan
Dyslipidemia approach
Management of dyslipidemia 2019 update
CARDIOVASCULAR DISEASE AND DIABETES
Sodium glucose co transporter( SGLT2) Inhibitors
Updates of Diabetes Management by Dr Selim
Dyslipidemia
Acc 2018 guidelines on lipids
Diabetic dyslipidemia
Current management of dyslipidemia final
Lipid lowering trials ppt
Ad

Similar to Cholesterol Management Guidelines (20)

PPTX
Dyslipedemia management according to risk stratification
PPT
Evaluation & management of dyslipidemia
PPTX
Dyslipidemia aha acc 2013
PPTX
Dyslipidaemia presentation
PDF
dyslipidaemiappt-1612191hbbbnnnnbbbbbbbh
PPT
Dyslipidemia in diabetes
PPTX
Statins
PPTX
Dyslipidemia presentation.pptx
PPTX
statin.pptx
PPTX
dyslipidemia latest PPT.pptx Disorders of lipid metabolism
PPTX
Statin Therapy.pptx
PPTX
Guidelinesonlipidmanagement 131214232350-phpapp01
PDF
Dyslipedemia
PDF
Hypertension
PPTX
Hyperlipidemia/ Dyslipidemia Pharmacotherapy
PPT
Lipid management 2013 acc-aha guidelines
PDF
cuando, porque y como disminuir el colesterol en mis pacientes?
PPTX
Latest updated hyperlipidemia guidelines.pptx
PPTX
Dyslipidemia in a high risk patient
PPTX
lipid guidelines.pptx
Dyslipedemia management according to risk stratification
Evaluation & management of dyslipidemia
Dyslipidemia aha acc 2013
Dyslipidaemia presentation
dyslipidaemiappt-1612191hbbbnnnnbbbbbbbh
Dyslipidemia in diabetes
Statins
Dyslipidemia presentation.pptx
statin.pptx
dyslipidemia latest PPT.pptx Disorders of lipid metabolism
Statin Therapy.pptx
Guidelinesonlipidmanagement 131214232350-phpapp01
Dyslipedemia
Hypertension
Hyperlipidemia/ Dyslipidemia Pharmacotherapy
Lipid management 2013 acc-aha guidelines
cuando, porque y como disminuir el colesterol en mis pacientes?
Latest updated hyperlipidemia guidelines.pptx
Dyslipidemia in a high risk patient
lipid guidelines.pptx
Ad

More from Kerolus Shehata (20)

PDF
Cardiology Pearls for Primary Care Providers
PDF
Spontaneous Coronary Artery Dissection (SCAD)
PDF
Invasive Hemodynamics: Assessment and interpretation
PDF
Infective Endocarditis
PDF
Stress Echocardiography
PPTX
Exercise ECG Testing
PPTX
Guideline‐Directed Medical Therapy in HFrEF
PPTX
Atrial Fibrillation
PDF
Preoperative evaluation
PPTX
ASPREE Trial
PPTX
Complete EKG Interpretation Course
PPTX
Evaluation of Chest Pain in the Ambulatory Setting
PPTX
Management of hypertension
PPTX
Anticoagulation in venous thromboembolism
PPTX
Hyperglycemic crises and hypoglycemia
PPTX
Left Bundle Branch Block (LBBB)
PPTX
Non-Astherosclerotic Spontaneous Coronary Dissection
PPTX
Make your life worth living
PPTX
First Aid, illustrated & simplified
PPTX
Get inspired and motivated
Cardiology Pearls for Primary Care Providers
Spontaneous Coronary Artery Dissection (SCAD)
Invasive Hemodynamics: Assessment and interpretation
Infective Endocarditis
Stress Echocardiography
Exercise ECG Testing
Guideline‐Directed Medical Therapy in HFrEF
Atrial Fibrillation
Preoperative evaluation
ASPREE Trial
Complete EKG Interpretation Course
Evaluation of Chest Pain in the Ambulatory Setting
Management of hypertension
Anticoagulation in venous thromboembolism
Hyperglycemic crises and hypoglycemia
Left Bundle Branch Block (LBBB)
Non-Astherosclerotic Spontaneous Coronary Dissection
Make your life worth living
First Aid, illustrated & simplified
Get inspired and motivated

Recently uploaded (20)

PPT
ANTI-HYPERTENSIVE PHARMACOLOGY Department.ppt
PPTX
Genetics and health: study of genes and their roles in inheritance
PDF
Integrating Traditional Medicine with Modern Engineering Solutions (www.kiu....
PPTX
Introduction to CDC (1).pptx for health science students
PPTX
Approach to Abdominal trauma Gemme(COMMENT).pptx
PPTX
Hypertensive disorders in pregnancy.pptx
PPTX
المحاضرة الثالثة Urosurgery (Inflammation).pptx
PPTX
Tuberculosis : NTEP and recent updates (2024)
PPT
intrduction to nephrologDDDDDDDDDy lec1.ppt
PPTX
Surgical anatomy, physiology and procedures of esophagus.pptx
PPTX
Peripheral Arterial Diseases PAD-WPS Office.pptx
PPTX
CASE PRESENTATION CLUB FOOT management.pptx
PPTX
Biostatistics Lecture Notes_Dadason.pptx
PPTX
sexual offense(1).pptx download pptx ...
PPTX
Pharynx and larynx -4.............pptx
PDF
Nematodes - by Sanjan PV 20-52.pdf based on all aspects
PPTX
SEMINAR 6 DRUGS .pptxgeneral pharmacology
PDF
Gonadotropin-releasing hormone agonist versus HCG for oocyte triggering in an...
PDF
neonatology-for-nurses.pdfggghjjkkkkkkjhhg
PDF
NCM-107-LEC-REVIEWER.pdf 555555555555555
ANTI-HYPERTENSIVE PHARMACOLOGY Department.ppt
Genetics and health: study of genes and their roles in inheritance
Integrating Traditional Medicine with Modern Engineering Solutions (www.kiu....
Introduction to CDC (1).pptx for health science students
Approach to Abdominal trauma Gemme(COMMENT).pptx
Hypertensive disorders in pregnancy.pptx
المحاضرة الثالثة Urosurgery (Inflammation).pptx
Tuberculosis : NTEP and recent updates (2024)
intrduction to nephrologDDDDDDDDDy lec1.ppt
Surgical anatomy, physiology and procedures of esophagus.pptx
Peripheral Arterial Diseases PAD-WPS Office.pptx
CASE PRESENTATION CLUB FOOT management.pptx
Biostatistics Lecture Notes_Dadason.pptx
sexual offense(1).pptx download pptx ...
Pharynx and larynx -4.............pptx
Nematodes - by Sanjan PV 20-52.pdf based on all aspects
SEMINAR 6 DRUGS .pptxgeneral pharmacology
Gonadotropin-releasing hormone agonist versus HCG for oocyte triggering in an...
neonatology-for-nurses.pdfggghjjkkkkkkjhhg
NCM-107-LEC-REVIEWER.pdf 555555555555555

Cholesterol Management Guidelines

  • 4. Friedewald formula Total cholesterol HDL + LDL + VLDL VLDL TGs (mg/dL) / 5 LDL TC - HDL – (TGs/5) **Not valid if TGs >400** Example: Total cholesterol: 230, TGs: 120, HDL: 25 • First calculate the VLDL: 120/5 = 24 • Then calculate LDL: 230 – (25+24) = 181 mg/dL
  • 5. Causes of elevated LDL & TGs
  • 6. Measurement of LDL • Adult >20 YO and not on any lipid lowering medications  Measure lipid panel (fasting or non-fasting) to estimate ASCVD • If the non-fasting panel showed TGs >400 mg/dL  Repeat a fasting panel. • If LDL <70  May measure direct LDL or modified LDL estimate. • If pt has a FHx of premature ASCVD or genetic HLD  may start with a fasting panel.
  • 9. ASCVD Risk Estimator Clinical ASCVD includes acute coronary syndromes, or a history of myocardial infarction, stable or unstable angina, coronary or other arterial revascularization, stroke, transient ischemic attack, or peripheral arterial disease presumed to be of atherosclerotic origin.
  • 10. Who is at a very high risk for future ASCVD?
  • 12. ASCVD risk management for diabetics
  • 13. Which diabetic patient is at a very high risk to develop ASCVD?
  • 15. Statin use in general risk population (without ASCVD events, LDL >190mg/dl, or diabetes)
  • 16. ASCVD risk enhancers These can be used to refine risk assessment in certain individuals at borderline or intermediate risk for ASCVD.
  • 20. Statin intolerant patients • Myalgia that resolve with discontinuation of statin treatment and occur with rechallenge • Myalgia have been demonstrated with rechallenge on at least 2 or 3 statins, including those with different metabolic pathways, and at least one statin at the lowest approved dose. • Incidence: Ranges from 1-10% • Risk factors: Impaired renal or hepatic function, ALT > 3X the upper limit of normal, age >75, Asian ancestry, or on drugs that affect statin metabolism. • Patients who develop myalgia on a statin should be tried on either a lower dose of the same statin or a different statin, or even dosing the statin once or twice weekly. >90 % will ultimately tolerate statin. • When a high intensity statin is indicated but not tolerated and a moderate intensity statin is used, further LDL lowering may be achieved with ezetimibe or a bile acid sequestrant.
  • 21. Statin use in pre-menopausal women I C-LD Women of childbearing age who are treated with statin therapy and are sexually active should be counseled to use a reliable form of contraception. I C-LD Women of childbearing age with hypercholesterolemia who plan to become pregnant should stop the statin 1 to 2 months before pregnancy is attempted, or if they become pregnant while on a statin, should have the statin stopped as soon as the pregnancy is discovered.
  • 22. Statin use in CKD patients • In patients with CKD (not treated with dialysis or transplant) with LDL >70 and ASCVD risk of ≥ 7.5%  consider initiating moderate intensity statin ± ezetimibe. • In patients with CKD who require dialysis and currently on statin May continue statin. • In CKD patients who require dialysis  DON’T start statin for primary prevention (Class III)
  • 23. Statin use in chronic inflammatory disorders & HIV • Adults with these conditions and LDL >70 with ASCVD risk of ≥ 7.5%  Consider starting moderate or high intensity statin (Class I). • Consider checking a fasting lipid profile before starting therapy and 4-12 weeks after that.
  • 24. When to use statin in patients 20 -39 Years old? 1) Severe hypercholesterolemia e.g. LDL ≥190 2) Those with LDL 160-189 plus a family history of premature ASCVD (ASCVD event in men less than 55 and women less than 65)
  • 25. Statin use in patients ≥ 75 years old • With clinical ASCVD  may initiate moderate or high intensity statin after a thorough discussion and evaluation. • If patient tolerates high intensity statin  May continue it.
  • 26. Statin safety and side effects • Need to have a discussion with your patient before starting statins regarding potential side effects e.g. SAMS (Statin-associated muscle symptoms). • SAMS include: Myalgia (normal CK), myositis, rhabdomyolysis and autoimmune myopathy (HMG Coenzyme A Reductase AB) • Mild or moderate SAMS  Reassess and Rechallenge. • Severe SAMS on rechallenge  May start Non-statin therapy • Even in patients with increased risk for DM  Continue statin (Class I) • Severe SAMS  Measure CK and LFTs • Transaminases elevation > 3x upper normal limit is infrequent • Patient with chronic stable liver disease who has high ASCVD risk  get a baseline LFTs and OK to start statin with close follow up (Class I). • Coenzyme Q10 is NOT recommended for routine use or in treatment of SAMS. • Don’t routinely check CK or transaminases in every patient on Statins.
  • 28. Management of Hypertriglyceridemia • Adult with moderate hyperTGs (177-499)Address obesity and metabolic syndrome. Treat the secondary factors (DM, CKD, Nephrotic syndrome, chronic liver disease, hypothyroidism and medications that increase TGs • Adult with moderate or severe hyperTGs with ASCVD risk of ≥ 7.5% consider initiating statin therapy. • Adult with fasting TGs ≥1000 Consider adding Fibrate therapy and omega-3 FAs
  • 29. Coronary Artery Calcium (CAC) score • Use to refine risk in individuals with borderline to intermediate risk. • Use in patients with intermediate ASCVD risk, but reluctant to start a statin. • Patients ≥55 Years of age who have a CAC of Zero may consider withholding a statin and reassessing in 5-10 years, however statin should be initiated if CAC is more than zero. CAC score Action Zero Treatment with statin therapy may be withheld or delayed, except in cigarette smokers, those with diabetes mellitus, and those with a strong family history of premature ASCVD 1 – 99 Favors statin therapy, especially in those ≥55 years of age. > 100 Statin therapy is indicated
  • 30. Miscellaneous • Individuals from South Asia have increased ASCVD risk. • ASCVD risk is higher among individuals from Puerto Rico than those from Mexico. • Native American/Alaskan populations have high rates of risk factors for ASCVD. • In Asians, Start low dose (5 mg) of rosuvastatin versus 10 mg in whites. • Baseline serum CK values are higher in blacks than in whites. • In adults of East Asian descent, other statins should be used preferentially over simvastatin. • Resistance exercise training will reduce LDL. • Fenofibrate (not gemfibrozil) can be combined with statins if indicated. • Goal LDL in patients with severe hypercholesterolemia (LDL-C>19) is greater than 50% reduction in LDL and resultant LDL<100mg/dl. • Bile acid sequestrants are contraindicated when serum triglycerides >300mg/dl. • All patients with diabetes who are 40 and older should be treated with a statin. • PCSK9 inhibitors have no role in lipid management in patients with DM (unless have established ASCVD or LDL>190mg/dL). • Use high intensity statin if ASCVD risk >20%.
  • 31. Take Home Messages - I • In all individuals, emphasize a heart-healthy lifestyle across the life course. • CAC scores can be used in patients up to age 80 • In patients with clinical ASCVD, reduce LDL with high-intensity statins or maximally tolerated statin therapy. • In very high-risk ASCVD, use a LDL threshold of 70 to consider the addition of non-statins to statin therapy. • In patients with LDL ≥ 190, start high intensity statins without calculating 10- year ASCVD risk. • In patients 40 to 75 years of age with DM and LDL>70 mg/dl, start moderate-intensity statin (High intensity if with multiple risk factors) without calculating 10-year ASCVD risk. • In patient 40 to 75 years of age evaluated for primary ASCVD prevention, have a clinician–patient risk discussion before starting statin therapy.
  • 32. Take Home Messages - II • In patients 40 to 75 years of age without DM, but with LDL≥70 and ASCVD risk of ≥7.5%, start a moderate-intensity statin if patient agrees. • In patients 40 to 75 years of age without DM, but with ASCVD risk of 7.5% to 19.9% (intermediate risk), risk-enhancing factors favor initiation of statins. • In patients 40 to 75 years of age without DM, but with LDL ≥70, at a 10- year ASCVD risk of 7.5% to 19.9% (intermediate risk), if a decision about statin therapy is uncertain, consider measuring CAC • Assess adherence and percentage response to LDL lowering medications and lifestyle changes with repeat lipid panel in 1-3 months after statin initiation or dose adjustment, repeated every 3 to 12 months as needed. • In patients who smoke, a CAC score of zero does not exclude coronary artery disease. The CAC score is also limited in those with diabetes and those with a family history of early CAD.