New analysis suggests that almost all nonsteroidal anti-inflammatory drugs and cyclooxygenase-2 inhibitors have comparable efficacy and safety profiles when used to treat osteoarthritis.
Almost all nonsteroidal anti-inflammatory drugs and cyclooxygenase-2
inhibitors have comparable efficacy and safety profiles when used to treat osteoarthritis,
according to a report from the US Agency for Healthcare Research and Quality.
The exception is the drug naproxen: Scientific evidence
to date suggests that it has less effect on risk for myocardial infarction than
other drugs in both classes. However, the researchers emphasized in the report
that all drugs pose potential harms along with benefits. Patients differ widely
on how they react to drugs, how they prioritize risks, and whether risks are acceptable
when compared to a drug’s benefits.
The report was written at the Evidence-based Practice
Center at Oregon Health & Science University and was based on a systematic
review of 360 published studies; t represents the most comprehensive analysis
thus far of arthritis pain medications.
Researchers compared the pain medications’ effectiveness
and health risks, including myocardial infarction and gastric side effects, plus
identified topics where more research is needed. While the review yielded important
findings about the analgesics, it concluded more studies are needed about the
drugs’ comparative risks, the consequences of long-term use, and the impact of
dosing variations.
The authors also suggested that genetic research may
one day predict which patients are most likely to develop cardiovascular problems
when taking the analgesics.
“These findings represent a vital comparison of medications
that are taken by millions of Americans,” said Agency Director Carolyn M. Clancy,
MD. “The report also shines a bright light on questions that could further our
knowledge and give patients research-based evidence to help them choose the best
available treatment.”
The report analyzed the risks and benefits of 26 medications.
No clear difference was shown in pain-relief effectiveness between classes
The analysis found that all tested medications can cause
or worsen hypertension, congestive heart failure, peripheral edema, and impaired
kidney function. Most of the evaluated medications pose similar increased risks
for myocardial infarction with the apparent exception of naproxen. The risks of
serious adverse gastrointestinal events for users of celecoxib are similar to
the risks for users of nonsteroidal anti-inflammatory drugs.
The researchers stressed that more research is needed
to compare the cardiac and gastrointestinal risks of aspirin at doses effective
for pain relief versus other nonsteroidal anti-inflammatory drugs. Acetaminophen
generally reduces pain less effectively than anti-inflammatory drugs but carries
a smaller risk of gastrointestinal problems. One study showed high doses posed
myocardial infarction risks similar to the anti-inflammatory drugs.
The new report, Comparative Effectiveness and Safety
of Analgesics for Osteoarthritis, is available at
http://effectivehealthcare.ahrq.gov/synthesize/reports/final.cfm.
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