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STATIN THERAPY
STATIN THERAPY
Primary
Prevention
0
1
Secondar
y
Preventio
n
0
2
Adverse
Effects
0
3
Non-Statin
Therapy
0
4
TABLE OF CONTENTS
HMG-CoA
Reductase
Inhibitors LDL-C Plasma
levels
Hepatic LDL receptor activity
Circulating LDL clearance
STATINS
Primary
Prevention
01
In specific populations with disease
entities
Screening and
Treatment
Algorithm for
the
Management of
Dyslipidemia
≥ 2 risk
factors
≥45 years
with LDL
≥130 mg/dL
02
01
Prevention in: Individuals with
no ASCVD Male sex
Postmenopausal
Smoker
HPN
Obesity (>25kg/m2)
Family history of CHD
LVH
Proteinuria
Screening and
Treatment
Algorithm for
the
Management of
Dyslipidemia
Diabetic only
With > 1 risk factor
(based on Risk Factor Counting
method)
Recurrent CV
(stroke, unstable angina, MI)
LDL Levels
Prevention in: Individuals with
Diabetes Mellitus
< 100mg/dL
< 70mg/dL
< 55mg/dL
Screening and
Treatment
Algorithm for
the
Management of
Dyslipidemia
Without target organ damage
With target organ damage
LDL Levels
Prevention in: Individuals with FH
< 70mg/dL
< 55mg/dL
Screening and
Treatment
Algorithm for
the
Management of
Dyslipidemia
Secondary
Prevention
02
Dyslipidemia Management on Acute Coronary
Syndrome
Among individuals with acute
coronary syndrome (ACS),
should statins be given?
• For individuals with ACS, early high-
intensity statin that is maximally-tolerated
is RECOMMENDED and should not be
discontinued.
• Statins should be given to ACS patients
immediately
Statin Treatment Intensity
Cholesterol target for different
patient groups
Adverse Effects
03
Among individuals taking statin
therapy, what is the
risk of developing adverse
effects?
a. Statin-associated Muscle Symptoms
b. New-onset Diabetes
c. Dementia / cognitive dysfunction / intracerebral
hemorrhage
• Treatment with statins is associated
with a low risk of developing statin-
associated muscle symptoms (SAMS),
but the benefits of cardiovascular risk
reduction outweigh the risk
Algorithm for Statin Induced
Myopathy
• Treatment with statins is associated
with an increased risk of new-onset
diabetes mellitus, but the benefits of
statin treatment for cardiovascular
risk reduction outweigh the risk.
• Treatment with statins is not
associated with the development of
dementia and cognitive dysfunction
• Treatment with statins is not
associated with an increased risk of
intracerebral hemorrhage
Non-Statin
Therapy
04
Brief Details on the use of Ezetimibe,
Fenofibrates, and Omega Fatty Acids
Among individuals with ASCVD,
should ezetimibe be given on top
of statin therapy?
Ezetimibe
A cholesterol absorption inhibitor that
targets uptake at the jejunal enterocyte
brush border
Inhibits intestinal cholesterol
absorption by selectively blocking the
NPC1L1 protein in the jejunal brush
border, integral to the uptake of
intestinal lumen micelles into the
enterocyte
• For individuals with documented
ACS, and target LDL-C has not been
reached despite maximally tolerated
high-intensity statin therapy,
ezetimibe may be added on top of
statin therapy to get to goal LDL-C.
Among individuals with
ASCVD, should fibrates be given
on top of statin therapy once
LDL-C goal is achieved?
• Among individuals not at goal LDL-
C, routinely adding fibrates on top of
statin therapy is NOT
RECOMMENDED for primary or
secondary prevention of
cardiovascular disease.
However, adding fibrates to statins may
be considered among MEN with
controlled diabetes, low HDL-C (200
mg/dl) for prevention of CV disease.
Fibrates
Good efficacy in
lowering fasting
TG levels
≤20% reduction
of the LDL-C
level
50% reduction of
the TG level
increase of the
HDL-C level of
≤20%
Among individuals with ASCVD,
should omega fatty acids be
given on top of statin therapy
once LDL-C goal is achieved
• Among individuals with ASCVD,
omega fatty acids (EPA+DHA) given
on top of statin therapy is NOT
RECOMMENDED.
• Among individuals with ASCVD on
statin therapy at goal LDL-C, but
with persistently high triglyceride
levels of 150-499 mg/dl, omega fatty
acids (pure EPA) MAY be given
Monitoring of
Lipids and
Enzymes
05
How often should
lipids be tested?
• Before starting lipid-
lowering drug
treatment, at least
two measurements
should be made, with
an interval of 1–12
weeks, with the
exception of
conditions where
prompt drug treatment
is suggested, such as
ACS and very high-
risk patients.
• After starting
treatment: 8 (±4)
weeks.
• After adjustment of
treatment: 8 (±4)
weeks until the goal is
achieved.
How often should lipids be
tested?
How often should lipids be tested
once a patient has achieved the
target or optimal lipid level?
Annually
How often should
liver enzymes (ALT)
be routinely
measured in patients
on lipid-lowering
drugs?
• Before treatment
• Once, 8–12 weeks
after starting a drug
treatment or after
dose increase.
• Routine control of
ALT thereafter is not
recommended during
statin treatment,
unless symptoms
suggesting liver
disease evolve.
• During treatment with
fibrates, control of
ALT is still
recommended.
How often should lipids be
tested?
What if liver enzymes
become elevated in a
person taking lipid-
lowering drugs?
Elevated ALT
ALT ≥3×
ULN
ALT <3× ULN
≥3×
<3×
• Continue therapy.
• Recheck liver enzymes in 4–6 weeks.
• Stop lipid-lowering therapy or reduce dose and
recheck liver enzymes within 4–6 weeks.
• Cautious reintroduction of therapy may be
considered after ALT has returned to normal.
• If ALT remains elevated check for the other
How often should CK be
measured in patients taking
lipid-lowering drugs?
Pre-treatment
• Before starting
therapy
• If baseline CK is
>4× ULN, do not
start drug therapy;
recheck
Monitoring
• Routine
monitoring of CK
is not necessary
• Check CK if
patient develops
myalgia
How often should CK be
measured in patients taking
lipid-lowering drugs?
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Statin Therapy.pptx

Editor's Notes

  1. Before we proceed to discussing the clinical practice guidelines, let’s quickly review statins and their mechanism of action Statins are also called HMG-CoA reductase inhibitors. These drugs [click] increase hepatic LDL receptor activity [click] leading to increased circulating LDL clearance and [click] thereby, decrease the circulating levels of LDL in our plasma. Statins also have side effects as all other drugs have and these will be discussed in the later parts of the report as part of the CPG.
  2. We have this diagram that shows the [read title] [click ] First and foremost, lifestyle modification would be our recommendation for patients who are at risk of developing atherosclerosis based on their history and physical exam. However, there is a specific criteria with which we could add or start statin therapy to these patients.
  3. In the primary prevention in individuals with no atherosclerotic cardiovascular diseases, the following criteria were given which could be bases to initiate statin therapy in Filipino patients In the 2015 CPG, the authors have identified a Risk Factor Counting as the method in identifying the risks for developing cardiovascular problems in Filipino individuals This method is being continuously recommended by the physicians for identification of CVD risk, as well as those needing medical therapy for primary prevention [press] So, if these criteria or risk factors have been identified in patients, we could initiate statin therapy as early, on top of recommendations for lifestyle modification
  4. Even without the presence of ASCVD or presence of risks for such, statin therapy must be initiated in patients with Diabetes Mellitus. However, in the event of concomitant CV diseases in these individuals, there are target LDL levels that must be met for maintenance.
  5. Statin doses given for patients with DM should be optimized to maintain the following LDL levels [click]. Maintaining these levels would be very useful for secondary prevention that which will be discussed later.
  6. Familial hypercholesterolemia is a dominantly inherited gene disorder wherein mutations in the LDL-receptor pathway causes markedly elevated LDL levels from birth. Untreated FH leads to premature death due to the early development of coronary artery disease in these patients secondary to accelerated atherosclerosis. It is vital, therefore, that these patients should be identified early on and be started on statin therapy.
  7. Since patient with FH are considered high-risk populations, they are started with high-dose intensity statins to maintain the following levels of LDL
  8. Statins can be safely started on patients with CKD but those who are not on RRT or dialysis Those who are on hemodialysis or those who have undergone kidney transplants, guidelines recommend referral to nephrologists for lipid management.
  9. After the initiation of statins and after patient’s have been identified based on their CV risks, they can be re-assessed after 6-8 weeks. LDL levels can be evaluated after this given period of time to see if recommended LDL levels are maintained especially for those who are in high-risk groups.