
Psychiatr News October 21, 2005
Volume 40, Number 20, page 24
© 2005 American Psychiatric Association
APA Concerned About Formulary Restrictions
Widespread misinterpretation of the results of the National Institute of
Mental Health's Clinical Antipsychotic Trials of Intervention Effectiveness
(CATIE) has led to concern that the study results could be used to restrict
the availability of antipsychotic medications in Medicare or Medicaid
formularies.
Data from the first phase of CATIE, which compared the effectiveness of
four newer, more expensive second-generation antipsychotic drugs and an older,
first-generation medication available in cheaper, generic formulations, were
published in the September 22 New England Journal of Medicine (see
story beginning on page
1).
Reports in major daily newspapers across the country noted that the four
newer medications compared with the first-generation antipsychotic,
perphenazine, were found to be "no more effective or better
tolerated." In fact, the study found significant differences in efficacy
of one drug in particular, as well as differences in the tolerability of the
five drugs studied.
The issue of restricted formularies in entitlement programs is particularly
timely because the new Medicare Part D prescription drug benefit begins on
January 1, 2006. Currently, Part D will pay for all of the newer, more
expensive antipsychotics (Psychiatric News, July 15), and most state
Medicaid programs have included open access to all antipsychotics. However,
cost-control mechanisms have increasingly been used in the last three
years.
"From a public policy perspective, it would be a dire mistake to
conclude that restricting access to any of the currently available
antipsychotic medications, either by formulary limitations or by other means
such as tiered pricing and `must fail' policies, is in the best interest of
patients," said APA Medical Director James H. Scully Jr., M.D., in a
letter to Mark McClellan, M.D., Ph.D., administrator of the Centers for
Medicare and Medicaid Services (CMS).
"APA is concerned that some of CATIE's early findings have been
erroneously interpreted and reported in the press as grounds for a restrictive
formulary and utilization-review policy of medications based on cost rather
than medical judgment," Scully wrote.
"Critical facts have been lost," he continued. "The study
demonstrated that all of these medications have substantial benefit, but none
is without side effects."
The study also showed, he added, that four times as many patients on the
older, cheaper drug discontinued their medication because of extrapyramidal
symptoms, compared with those taking newer medications.
Indeed, Scully told McClellan, CATIE validated "clinicians' belief
that to offer the greatest benefit and the least-adverse side effects for the
individual patient, it is often necessary to try two or more
medications."
He concluded, "APA strongly urges CMS to continue to allow physicians
and patients to work together to select a treatment plan that is most
beneficial for the individual patient and not restrict access to the full
range of medications based on arbitrary concerns and questionable reporting of
data."
Related Article:
-
Government Antipsychotic Study Finds No Clear Winner in `Horse Race'
- Jim Rosack
Psychiatr News 2005 40: 1-25.
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