EFFECTIVENESS OF RETROSPECTIVE DRUG UTILIZATION REVIEW
EFFECTIVENESS OF RETROSPECTIVE DRUG UTILIZATION REVIEW
批准号:
2633353
负责人:
BRIAN LESLIE STROM
金额:
$28.84万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-03-15 至 1999-12-31
关键词:
angina pectoris antiinflammatory agents asthma behavioral /social science research tag chronic obstructive pulmonary disease clinical research drug adverse effect gastritis health care service evaluation health care service utilization hemorrhage hospital utilization human data myocardial infarction peptic ulcer pharmacy salicylate warfarin
中文摘要
处方不当是一个重要的公共卫生问题
英文摘要
Improper prescribing of medications is an important public health
problem. Because the aged are more likely to have concomitant
illnesses and medications, they are at greatest risk for adverse
outcomes. For example, one study conducted in the elderly found that
28% of hospital admissions were due to medication problems, and
showed that Medicaid recipients were at an especially increased
risk. Drug utilization review (DUR) is a procedure that seeks to
reduce the consequences of improper prescribing. In part because of
federal mandate, retrospective DUR is now being applied to millions
of older Americans, including all Medicaid enrollees and seventy-
five percent of all people with prescription insurance coverage.
This is despite the complete absence of rigorous evidence indicating
that DUR is effective in either altering drug therapy or improving
health outcomes. Given the existing federal mandate, an experimental
trial of DUR in the Medicaid population is infeasible. Therefore,
a timely, well-controlled observational trial of DUR's effectiveness
is badly needed.
The University of Pennsylvania has a unique opportunity to conduct
a rigorous observational trial of DUR's effects on prescribing
patterns and on clinical outcomes. Using a large, unique data
source, we intend to evaluate the effects of DUR on both process
measures and clinical outcome measures. The methodology that we
propose incorporates both pre-post intervention comparisons, and
concurrent controls. This will enable us to measure a number of
important effects of DUR, controlling for possible effects of
differences between state programs and causally unrelated secular
trends. We intend to employ three distinct, complementary sampling
frames from which to pose the study questions. The study questions
have been carefully selected, and address issues of practical and
theoretical importance.
The results of this study, whether positive or negative, will have
wide-ranging health policy and scientific implications, especially
with regard to the aged. The University of Pennsylvania has a great
deal of experience in pharmaceutical outcomes research projects such
as this, especially those using large claims databases. The
investigators will be able to provide clear, meaningful answers to
the study questions in a very short time-frame, and do so in a very
cost-efficient manner.
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