| Frequently Asked Questions About CHAMP |
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Q.
Are lipid panels obtained in the hospital accurate? |
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A.
Studies have shown that lipid panels obtained in the first 6-12 hours
after the onset of acute myocardial infarction are reflective of the
patient’s baseline steady state lipid levels.
At that time frame an acute phase response occurs, with a fall in
total cholesterol levels and LDL cholesterol levels.
This can decrease LDL levels by as much as 50% below baseline
values. It can take 4 to 6
weeks for the levels to return to baseline.
Studies have shown that despite the fall in absolute levels of
LDL, the acute phase response make LDL more prone to oxidation and HDL
“proinflammatory”. Patients
are thus not protected from atherosclerosis during this time frame. A
nonfasting lipid panel obtained on or shortly after admission can be
used to assess the patients’ baseline lipid levels, diagnose
lipoprotein disorders, and guide the statin starting dose.
Lipid profiles obtained 24 hours to 6 weeks after myocardial
infarction onset or after CABG, should be interpreted know the LDL level
may be as much as twice the measured value. |
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Q. If patients with coronary artery disease and low or normal LDL levels benefit from statin treatment, why bother to check a baseline lipid level? |
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A.
Studies have shown that patients with LDL cholesterols even in the range
of 70 –130 mg/dl have a nonfatal cardiovascular event and mortality
reduction with statin treatment. Some
have argued that knowing the patient has atherosclerosis is evidence
enough for starting statin treatment.
One option is to initiate statin treatment in all patients
without checking baseline levels. At
6 weeks, when a lipid panel is obtained the dose of statin can be
adjusted to achieve an LDL < 100 mg/dl.
Drawing an admission lipid panel dose have certain advantages.
Patients often like to know what their baseline lipid levels were
before starting on treatment. The
baseline lipid level can help guide the dose of statin needed to reduce
the LDL to < 100 mg/dl. Patients
with complex lipid disorders and be identified early so appropriate
follow-up can be arranged. |
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Q.
Are there benefits to the hospital if treatments rate improve? |
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A.
There are a number of quality indicators that are in place or are being
phased in that use of appropriate cardiac therapies.
The Joint Commission assesses measures such as use of aspirin,
beta blockers, and ACE inhibitors in patients with acute myocardial
infarction. In addition
NCQA measures are used by health plans and employer groups to see what
medical groups and hospitals they want to contract with.
The measurement, evaluation and treatment of LDL after a cardiac
hospitalization is one of the NCQA measures.
With the CHAMP program, length of stay and inpatient medical
costs were reduced. In
addition UCLA Medical Center was noted to have one of the lowest risk
adjusted mortality rates for acute myocardial infarction rates in the
State of California after starting this program.
The Pacific Business Group on Health awarded UCLA Medical Center
a Blue Ribbon Award for Excellence in 2000 for providing preventive care
services for patients with high blood pressure and high cholesterol.
This award was given to only 7 hospitals in the state, which UCLA being
the only teaching hospital to be so commended. There are thus many
benefits to the hospital to have a treatment program in place, beyond
the knowledge that quality of care is being improved and long term
mortality rates reduced. |
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Q. How can we get a program going when the physicians at my hospital cannot seem to agree on anything? |
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A.
Getting a team together to review the baseline treatment rates in your
hospital can help to make everyone aware that there are opportunities to
improve care for cardiac patients. The treatments recommended as part of
this program have all been proven to work in prospective randomized
placebo controlled trials. The
American Heart Association and American College of Cardiology guidelines
recommend their use in appropriate patients.
National organizations that assess the quality of health care
include the frequency of use of these treatments as quality indicators.
It may be easier than you think to have physicians agree when all the
evidence supporting treatment is reviewed.
Providing examples of the improved treatment rates that have been
accomplished at other medical centers can also help. |
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Q. Will primary care physicians get upset if patients are started on lipid lowering medications prior to hospital discharge? |
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A.
In the 7 years that CHAMP has been in place at the UCLA Medical Center,
there have been no significant complaints.
Having the physicians and nurses that care for patients with
cardiovascular disease work together to implement the treatment program
can help address any of these concerns. Initiation of lipid lowering
treatment prior to hospital discharge can improve patient understanding
and compliance with treatment. Often
patients assume that because the physician that treated them during
their cardiac hospitalization did not start them on treatment, it is not
essential. Many physicians appreciate that when the first outpatient
lipid panel is obtained at 6 weeks after hospital discharge in a patient
that was started on lipid lowering therapy, the patient will be much. |
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Q.
Should ACE
inhibitors be used for only 6 weeks after myocardial infarction or only
in patients with low ejection fraction? |
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A. While initial studies were done in low ejection fractions or used ACE inhibitors for only 6 weeks after myocardial infarction, new trials clearly demonstrate that all patients with atherosclerosis have reduced risk of myocardial infarction, stroke, cardiac mortality and total mortality with ACE inhibitor treatment. ACE inhibitors benefit patients with normal or reduced ejection fraction, normal or elevated blood pressure, early or late after myocardial infarction, diabetes or no diabetes. Thus similar to aspirin, a diagnosis of coronary, cerebral, or peripheral vascular disease, is indication for ACE inhibitor treatment.
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| For other questions please contact: Gregg C. Fonarow, M.D. |
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