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Doctor... Does Ultram Help With Arthritis?
By Nathan Wei
Non-steroidal
anti-inflammatory drugs (NSAIDS) have been the mainstay of treatment for
arthritis symptoms. Physicians often advise patients to use over-the-counter
preparations... or also use prescription NSAIDS for more severe problems.
Unfortunately, NSAIDS do have many potential side-effects including the
potential for creating stomach and small bowel ulceration, kidney dysfunction,
liver damage, fluid retention and a small but real increased incidence of
cardiovascular events.
So... a real dilemma for many clinicians is how to control arthritis pain in
patients for whom NSAIDS have already caused problems or for patients who have
the potential for developing problems.
One drug that has been used primarily for pain control is tramadol (Ultram).
This is a drug that is a mild centrally acting narcotic drug with little
addictive potential.
Tramadol is increasingly used for the treatment of osteoarthritis (OA)
because it does not produce gastrointestinal bleeding or kidney problems and
does not adversely affect cartilage, a controversial but possible side effect
associated with NSAIDS.
A recent study sought to determine the analgesic effectiveness, the effect
on physical function, the duration of benefit, and the safety of oral tramadol
in patients with OA.
(Cepeda MS, et al. J Rheumatol. 2007; 34:543-545)
The scientists searched the Cochrane Central Register of Controlled Trials
(Central), Medline, Embase, and Lilacs databases up to August 2005.
They included randomized controlled trials (RCT) that evaluated the effect
of tramadol or tramadol plus paracetamol (equivalent to acetaminophen) on pain
levels and/or physical function.
The researchers included 11 RCT with a total of 1019 participants who
received tramadol or tramadol/paracetamol and 920 participants who received
placebo or active control. Participants who received tramadol reported (1) less
pain, a 12% relative decrease in pain intensity; (2) higher degree of global
improvement: one of every 6 individuals taking tramadol or tramadol/paracetamol
exhibited at least moderate global improvement; and (3) improvement in stiffness
and function, than patients who received placebo. In terms of adverse events,
one of every 5 participants who received tramadol or tramadol/paracetamol
experienced minor adverse events and one of every eight stopped taking the
medication because of adverse events compared to participants who received
placebo.
Their conclusion was that tramadol or tramadol/paracetamol decreased pain
intensity, produced symptom relief, and improved function in patients with OA,
but these benefits were small.
In actual practice, tramadol is a drug that is often added to an NSAID for
better pain control or used instead of an NSAID in high risk patients. As with
most therapies, a patient’s response is often dependent on the expectations of
the physician.
Caution must be exercised when using tramadol.
First, particularly in older patients dosing must start at a low level,
probably 25 mgs per day with a gradual increase as tolerated.
Second, there have been sporadic reports of increased risk of seizures in
patients taking anti-depressant medicines such as selective serotonin reuptake
inhibitors (SSRIs).
Tramadol should also be tapered when discontinued.
There are some potential drug interactions and these need to be evaluated.
A sustained release form of tramadol (Ultram ER) is now available in the U.S
and appears to have a good tolerability profile.
About the Author: Nathan Wei, MD FACP FACR is a rheumatologist and Director
of the Arthritis and Osteoporosis Center of Maryland. He is a Clinical Assistant
Professor of Medicine at the University of Maryland School of Medicine. For more
info:
Arthritis Treatment
Source: www.isnare.com
Permanent Link:
http://www.isnare.com/?aid=216503&ca=Medicines+and+Remedies
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