Académique Documents
Professionnel Documents
Culture Documents
1.
Approach to Dyslipidemia
Based on the 2015 CPG for the Management of
Dyslipidemia in the Philippines
Fodor, G. Primary Prevention of CVD: Treating Dyslipidemia. Am Fam Physician. 2011 May 15;83(10):1207-1208.
TC = LDL + HDL + VLDL *(VLDL = TG/5, if TG < 400 mg/dL)
LDL-C “Bad Cholesterol” HDL “Good Cholesterol” Triglycerides
Smoking Cessation
Modified fat diet - aimed to include 30% or more energy from total fats and included higher levels of
mono-unsaturated or poly-unsaturated fats than the usual diet
The guidelines cited some studies that Asians may require a lesser dose and there is evidence that
high-dose statin used may lead to higher risk of ADR.
Obtain baseline measurement of hepatic transaminase levels (ALA, AST) before initiation of statin
therapy in patients at risk for developing liver injury.
In patients at risk for development of statin myopathies, baseline creatine phosphokinase and
subsequent monitoring should only be performed when symptoms are present.
Non-Statin Therapy
Fibrates are not recommended as an alternative to statins. It may be considered among men with high
baseline TG and low HDL-C once LDL-C target has been reached.
PUFA or Omega-3 fatty acid is not recommended as an alternative to statins for the secondary
prevention of CV events.
Combination therapy: non-statin (omega 3 FA, ezetimibe, fibrates) + statin - may allow for a greater
degree of LDL-C reduction and results in achievement of goal attainment for primary and secondary
prevention. It is recommended to attempt LDL-C reduction using statin therapy first. Other local
available therapies may be combined if the patient cannot attain the LDL-C goal with statin monotherapy.
Familial Hypercholesterolemia
FH is an autosomal dominant mutation of LDL-R resulting in elevated LDL C. An LDL-C above 190 mg/dL
should raise clinical suspicion. Affected individuals are at increased risk for CV events and premature
CAD. Early detection is deemed crucial for initiation of aggressive lipid-lowering therapy.
Dutch Lipid Network criteria is used for applicability in our setting with the exception of genetic testing.
Due to the high cardiovascular risk of these patients, the lipid profile should be carried out initially as
screening (patients with FH have LDL-C levels > 190 mg/dL) then subsequently for monitoring treatment
response since ALL patients with FH should be on aggressive LDL-C lowering therapy.