Comparison key to lower drug costs, better outcomes

Patients can expect significant savings and better outcomes from their prescription medications when health care professionals use comparative effectiveness research, according to researchers at the University of Illinois at Chicago.

The American Recovery and Reinvestment Act signed by President Obama includes more than $1 billion over the next two years for comparative effectiveness research, a practice that evaluates different options for treating a medical condition among a certain group of patients.

"Despite having the highest per capita health care expenditures in the world, the United States does not always perform well on measures of health compared with other countries," said Glen Schumock, associate professor and director of the UIC Center for Pharmacoeconomic Research.

"With prescription drugs accounting for more than 10 percent -- $227.5 billion -- of the total amount Americans spent on health care in 2007, we need to know more about how drugs compare to one another in terms of effectiveness, safety, and value for money."

The analysis is published in the online version of American Journal of Health-Systems Pharmacy and is co-authored by A. Simon Pickard, UIC associate professor of pharmacy practice.

Comparative effectiveness is a relatively new concept, and it contains two important components, Schumock said. It provides information to help clinicians choose among alternative treatments, and it examines outcomes in actual practice.

Randomized control trials have long been the most widely accepted method to study the efficacy of innovative medical care interventions, and they are required by the U.S. Food and Drug Administration to market a new drug, Schumock said. However, such trials have drawbacks.

A traditional randomized control trial does not show how the drug works, Schumock said, "and it usually compares a new drug with a placebo or an inferior treatment option rather than the drug or drugs that might be legitimate therapeutic alternatives."

The patient populations are also narrowly selected, and are usually healthier than the patients who will eventually use the drug, he said.

Comparative effectiveness studies matches up comparable medications based on current choices available to health care professionals. The patients are those who actually use the drug once it is marketed. The outcomes, Schumock said, are more relevant to decisionmaking at the clinical or policy level.

Comparative effectiveness research may reduce spending on pharmaceuticals and lower overall health care costs, said Pickard. According to the Congressional Budget Office, direct spending by the federal government -- mostly for Medicare and Medicaid -- would be reduced by $100 million from 2008-2012 and $1.3 billion from 2008-2017.

Those figures could be much higher, as they were developed before the recent large investment in comparative effectiveness research, Pickard said.

"With the shared goal of improving decisionmaking at every level of the health care system, pharmacy and other professions can use comparative effectiveness research as an opportunity to be more efficient and more accountable," Pickard said.

Comments

  1. HARVEY GROVE HARVEY GROVE United States says:

    The idea is wishful thinking for many reasons. FDA regulations only require that a drug be safe and efficacious. There is no requirement to be more efficacious than another drug. No manufacturer wants to bring out a drug that is second best or third best because the cost of drug development is so high that they want to be sure there is a market for their product before they invest in it as there is no way to determine if this new entity they are investigating is better or not as good as the drug that dominates the market for this particular indication. NEWER DOES NOT MEAN BETTER. MANY TIMES IT IS BUT NOT FOR EVERYBODY.

    In addition, whenever a doctor prescribes ANY medication for you.... he is performing an EXPERIMENT as there is no guarantee you will respond in a manner similar to the reports in the literature that accompanies the drug (manufacturers package insert is the ONLY information allowed to be used for promotional purposes). More consideration.... what if a patient is allergic to any drug.... it is common for this patient to respond to a second drug for the same indication with no allergic reaction. Another consideration..... many patients have to take multiple medications at the same time for multiple problems, quite often when two or more drugs are taken simultaneously there is a drug INTERACTION or incompatibility that precludes taking a particular drug but another for the same indication will be safe and effective.  There is much more to this than you might know, however, if a manufacturer markets a drug it is because he expects the product to sell. On the other hand a good doctor will use only a few drugs he is familiar with so that he can learn to use them well.

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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