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May / June 2009

Health IT & Quality
Is It Time to Play NICE?
By Barry P. Chaiken, MD, FHIMSS
The American
Reinvestment and Recovery Act 2009 (ARRA) earmarks more than $800
million toward research on comparative effectiveness of medical
treatments. In addition, more than $700 million is directed to the
Agency for Healthcare Research and Quality, a research institution with
a long history of evaluating effectiveness of treatments. With
healthcare reform at the top of the agenda for the 111th Congress and
the Obama administration, will a NICE-like entity be part of the reform
package?
NICE, the National Institute for Health and
Clinical Excellence, makes recommendations on how care, treatments, and
medications are distributed through the United Kingdom's National
Health Service (NHS). In addition, other countries such as Brazil,
Columbia, Australia, and Thailand, follow NICE recommendations. Despite
initial opposition, pharmaceutical companies and device manufactures
routinely cut prices in Britain to obtain NICE approval. More than 95%
of the healthcare provided in Britain is through the NHS. Prior to
NICE, hospitals made decisions about care based upon financial
constraints, which led to great disparities in care. NICE's prior
approval of drugs and treatments guarantees that all institutions offer
the same care options.
Thrice as NICE
NICE is divide into three separate centers:
- The Center for Public Health Excellence
works to promote good health by providing public health guidance that
involves recommendations for "populations and individuals on
activities, policies, and strategies that can help prevent disease or
improve health."

- The Center for Clinical Practice develops clinical guidelines on appropriate treatment for specific diseases.

- The Center for Health Technology Evaluation
"develops technology appraisals and international procedures guidance."
The guidance, based on both clinical and economic research, focuses on
the appropriate use of mediations, medical devices, and diagnostic and
surgical procedures.
NICE has encountered much criticism due to its use
of economic research in establishing approved treatments and
medications. For example, NICE rarely approves treatments that offer
just six months of good-quality life and cost more than $23,000.
Perhaps this is why pharmaceutical and medical device manufacturers cut
prices so severely in Britain and not in other countries.
Oregon Déjà Vu
Although the use of cost-benefit analysis to
evaluate the appropriateness of medical treatments in the United States
may seem unique, the state of Oregon first used such an approach more
than 15 years ago. To address the rapidly expanding costs of Medicaid,
the state obtained a Medicaid waiver from then President Clinton and
established the Oregon Health Plan in 1993. The plan's administrators
assembled research panels that reviewed hundreds of treatments, ranked
them by benefit and cost, and produced an overall ranking of the
treatments for which Medicaid should pay. Estimating the expected
demand for each treatment, the administrators then applied the Medicaid
budget to the costs of the treatments as ranked, thereby producing a
list of approved treatments:
[Budget — (Treatment 1 Cost x Estimated Frequency) —
(Treatment 2 Cost x Estimated Frequency) — etc.]
The rejected treatments were those that ranked
where the budgeted Medicaid funds ran out. Since the list was developed
from both cost-benefit analysis and budgeted amounts, many critics of
the plan claimed it to be care rationing. Similar cries of foul
currently exist in Britain.
Much of the resistance to healthcare reform in
Congress and beyond is based on cost concerns. Even though the United
States spends more than 30% more per capita on healthcare than any
other country, healthcare policymakers struggle to find the sources of
revenue to enact reform. The ARRA offers a large sum of money to
research the same issues currently investigated by NICE. In addition,
the budget outline presented by the President early this year included
additional money for comparative effectiveness research as part of his
plan to reform healthcare. Perhaps the success of healthcare reform
depends on the ability of comparative effectiveness research to show
the way to cost savings that can fund the reform.
Wennberg Still Relevant
More than three decades ago Dr. Jack Wennberg
identified variation in care in communities in Vermont. Simple analysis
of his work showed that some of the care provided was inappropriate,
more expensive than alternatives, and offered worse outcomes. This work
continues today at Dartmouth College with repeated studies illuminating
similar findings across the country. Therefore, it is safe to assume
that large sums of money are being wasted on care that offers little
benefit and in some cases delivers harm.
How the Obama administration intends to apply
comparative effectiveness research in future forms of healthcare
delivery is unknown. Nevertheless, considering the large investment in
this area, it makes sense that at some point it will be offered up as a
source of revenue to pay for healthcare reform. Although this may be
good or bad policy to some, the reality is that in spite of all the
good care we offer to our patients, we spend an awful lot of money on
treatments that frankly do patients very little if any good. At the
same time, there are numerous treatments that patients never receive
due to our inability to effectively reach out to them. No matter what
form healthcare reform takes, comparative effectiveness research must
be included. It is time for us to apply the scientific method used in
our medical research, analysis of what is valuable and what is not, to
our appropriation of limited medical resources to the care of patients.
This is the only way we can expand access and improve quality without
bankrupting our economy and destroying American businesses.
Barry Chaiken is the chief medical officer of DocsNetwork, Ltd. and a member of the Editorial Advisory Board for Patient Safety & Quality Healthcare.
With more than 20 years of experience in medical research,
epidemiology, clinical information technology, and patient safety,
Chaiken is board certified in general preventive medicine and public
health and is a Fellow, Board Member, and Chair-Elect of HIMSS. As
founder of DocsNetwork, Ltd., he has worked on quality improvement
studies, health IT clinical transformation projects, and clinical
investigations for the National Institutes of Health, U.K. National
Health Service, and Boston University Medical School. Chaiken also
serves as an adjunct assistant professor in the Department of Public
Health and Family Medicine at Tufts University School of Medicine. He
may be contacted at
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