by Food and Drug Administration (FDA) in near
future. Ephedra/caffeine combinations are already
banned by FDA. Subsequently sold in combination
with guaraná (the herbal and more potent form of
caffeine).
5.Conclusion: Ephedra products, especially ephedra/
guaraná combinations are banned substances, are
not safe, and have been demonstrated to cause
considerable harm. As negative publicity builds,
Ephedra-free versions of products appear, but
there is no evidence that these will be any safer
than the original formulations.
- Chromium picolinate (Fox and Sabovic, 1998;
McLeod, Gaynes, and Golden, 1999; Speetjens et al,
1999; Beutler and Jonas, 2004).- Primary use: Increase lean body mass, improve
glycemic control in diabetes.
2.Evidence: While earlier, design-flawed studies sug-
gested some beneficial effects, newer studies show
no ergogenic or fat-burning effects. Some studies
suggest slight, dose-dependant improvements in
diabetes control and lipid profiles. - Toxicity: Tremor, along with cognative, sleep, and
mood changes have been reported as side effects.
Concern exists for potential deoxyribonucleic acid
(DNA) mutations with long-term exposure to
chromium supplementation. - Regulated/Banned: No
- Conclusion: Though inexpensive and minimally
toxic with short-term use, real concern exists for
DNA mutations with long-term use or high
chromium levels. Since the reported benefits are
very small and the risk of long-term toxicity
potentially great, patients should avoid this sup-
plement.
- Primary use: Increase lean body mass, improve
- Pulsed electromagnetic field therapy(PEMF) (Bassett,
Payluk, and Pilla, 1974; Aaron, Ciombor, and Jolly,
1989; Hulme et al, 2002)
1 Primary use: Decrease pain and stiffness in
osteoarthritis
2. Evidence: The beneficial effect of PEMF therapy
in delayed union fractures is well established.
Similar magnetic fields have been found to stimu-
late proteoglycan production in vitrochondrocytes;
however, despite abundant anecdotal Internet
reports, a recent Cochrane review found only three
quality articles in the scientific literature. The
review found that PEMF produced statistically sig-
nificant, but clinically insignificant changes in
knee osteoarthritis(OA) pain and disability. The
optimum dosage and frequency of PEMF—as well
as acceptable technical standards for the PEMF
equipment—remain unknown. The cost of PEMF
can exceed $200 per day.
3. Toxicity: Unknown. The effects of pulsed electro-
magnetic fields on human tissues have not been
well-studied.
4. Regulated/Banned: No
5.Conclusion: Patients should be advised that
PEMF’s small benefits in OA pain and stiffness are
outweighed by uncertain side effects, incomplete
technical data, and tremendously high cost. Other
proven-effective, lower cost treatments for OA
exist; and are favored over PEMF therapy.
Permit
- Ginko leaf (Pittler and Ernst, 2000; van Dongen et al,
2000; Oken et al, 1998)- Primary use: Combat memory loss and slow pro-
gressive dementia. Also used to relieve vascular
claudication symptoms. - Evidence: Most studies suggest that ginko leaf can
slow dementia progression and increase cognitive
function in middle-aged adults without subjective
memory loss. In some countries, ginko is the stan-
dard of care (in place of cholinesterase inhibitors)
for Alzheimer’s dementia. More limited evidence
also suggests that ginko may improve walking dis-
tance in vascular claudication. - Toxicity: Mild gastrointestinal(GI) upset and con-
stipation are the most common side effects
reported; however, ginko has anticoagulant proper-
ties and lowers the seizure threshold. Ginko has
been linked to spontaneous bleeding. It should not
be used in patients taking other anticoagulants or
in those with a seizure disorder or in combination
with other drugs that lower seizure threshold. - Regulated/Banned: No
- Conclusion: In the appropriately selected patients,
ginko is a permissible alternative to conventional
drug treatments, especially if the patient prefers
ginko supplementation.
- Primary use: Combat memory loss and slow pro-
- St. John’s Wort (SJW) (Gaster, 2000; Woelk, 2000;
Brenner et al, 2000; Schrader, 2000; Beutler and
Jonas, 2004).
1.Primary use: Antidepressant, anxiolytic, anti-
insomnia, and adjunct to weight-loss uses are com-
monly described.
2. Evidence: Most evidence suggests SJW to be
effective for mild to moderate depression. SJW
may also be effective in obsessive-compulsive dis-
orders. Severe depression is not reliably treated by
SJW and higher dosages of SJW increase the risk
for severe skin reactions.
3. Toxicity: Insomnia, restlessness, and GI distress
are common. Hypericin doses over 5 mg/day
increase risk for severe photodermatitis. SJW has
fewer side effects than TCA or SSRI antidepressants;
456 SECTION 5 • PRINCIPLES OF REHABILITATION