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Contact: Richard H. Chapman, PhD(703.461.1827)
Release Date: 05/23/2005
Predictors of adherence with antihypertensive and lipid-lowering therapy.
Chicago, IL -- A study conducted by ValueMedics Research,
LLC, published this month in the Archives of Internal Medicine,
has found that adherence with concomitant antihypertensive
and lipid
lowering therapy
is poor, with only about 1 in 3 patients adherent with both medications
at 6 months. The results show that the percentage of patients adherent
with both
therapies declined sharply immediately following treatment initiation,
with only 44.7%, 35.9%, and 35.8% of patients adherent at 3, 6,
and 12 months, respectively.
However,
patients were more likely to be adherent if they were taking
fewer other medications, initiated
antihypertensive and lipid lowering therapy
together,
or had a history of coronary heart disease or congestive heart
failure. “These
findings demonstrate the value of simpler medication regimens
and simultaneous initiation of treatment when a patient
has both hypertension
and high cholesterol,” says
lead author Richard H. Chapman, PhD,
and Director of Health Economics at ValueMedics Research. “We believe
these are important findings because of the higher cardiovascular disease
risk faced by patients who have
both of these conditions,
which makes adherence with treatments especially imperative.”
This retrospective cohort study examined
8406 enrollees in a US managed care plan who initiated treatment
with antihypertensive and lipid lowering therapy
within a 90-day period. Adherence was measured as the proportion of days
covered in each 3-month interval following initiation of concomitant
therapy (mean follow-up
= 12.9 months). Patients were considered adherent if they had filled
prescriptions sufficient to cover at least 80% of days with both
classes of medications. A
multivariable regression model was used to evaluate potential predictors
of adherence. The study is available at www.archinternmed.com
“ValueMedics often works collaboratively with researchers from the study sponsor
as well as the best academic researchers to ensure that our studies achieve the
maximum scientific rigor, while at the same time answering questions that may
have important commercial implications,” says Josh Benner, PharmD, ScD, Principal
of ValueMedics Research and a co-author of the paper. ValueMedics Research
provides integrated and focused research in health outcomes, economics, pricing,
reimbursement,
and market access, from pre-launch through product maturity.
The study was supported by Pfizer, Inc.
The authors were: Richard H. Chapman, PhD; Joshua S. Benner,
PharmD, ScD; Allison A. Petrilla, BA; Jonothan C.
Tierce, CPhil; S. Robert Collins, BS; David S. Battleman, MD; J.
Sanford Schwartz,
MD.
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