Colchicine in The Treatment of Acute Low Back Pain
Resistant Disc Disorders
Over the past
30 years, Rask has treated thousands of patients with resistant disc disorders
with oral and intravenous colchicine and has noted a 90-95% improvement rate.
Since 1979, he has published the results of his uncontrolled studies, some involving
up to 500 patients, who have suggested significant therapeutic benefits from colchicine
therapy with fewer adverse effects than typically associated with the use of aspirin.
In a 1985 double blind study of 39 patients with low back pain of at least two months duration, Meek compared combined intravenous and oral colchicine treatment with placebo. Patients in the treatment group received colchicine .6-mg orally b.i.d. (twice a day) for 14 days and one-mg IV (intravenous) on days one, four and eight of the 14 day study period.
Adverse Effects
While no real effect from
placebo administration was observed, the treatment group demonstrated significant
improvements in pain, weakness, leg raising limitations, and muscle spasm. Adverse
effects from colchicine administration were documented in only one patient in
the form of a burn at the IV site. In a double blind study of oral colchicine
in the treatment of low back pain, Schnebel and Simmons compared oral colchicine
with placebo in 34 patients with low back symptoms of less than three months duration.
Over the 12-week study period, both groups of patients continued in a comprehensive
physical therapy program and were administered NSAIDs and muscle relaxants. No
significant differences in therapeutic response were noted between the treatment
and placebo groups, but an increased number of adverse effects, mainly diarrhea
and vomiting, were observed in the colchicine group. This study has several limitations,
including a small sample size, multiple etiologies of low back pain, poor patient
compliance, and the use of concomitant treatments.
Contraindications
Colchicine
use is contraindicated those patients with serious gastrointestinal, renal, hepatic
or cardiac disease. Colchicine can also harm the fetus when used during pregnancy.
When administered intravenously for the treatment of an acute gouty attack, the
total dosage over the first 24-hours should not exceed four milligrams, as greater
cumulative dosages have been associated with multiple organ failure and death.
Abdominal pain, nausea, vomiting, and diarrhea, are typically the earliest and most common adverse effects associated with colchicine over dosage. These gastrointestinal side effects can be almost entirely avoided with intravenous use. Colchicine has also been noted to cause a transient leukopenia (abnormal decrease in the number of white blood cells), which is soon replaced with a leukocytosis (abnormal increase in the number of white blood cells). Myopathy and neuropathy have been noted in patients with impaired renal function receiving colchicine treatment.
Colchicine
and Low Back Pain
The use of colchicine in the treatment of the acute low back
pain patient is not commonly practiced. While some practitioners have found colchicine
effective in this patient population, others have not. Further investigation in
this area is needed before colchicine use can be recommended for the low back
pain patient. These studies may be helpful in further defining colchicine's place
among other available anti-inflammatory and analgesic agents.
Reference:
Malanga
GA, et al. Pharmacologic Treatment of Low Back Pain. In Physical Medicine and
Rehabilitation State of the Art Reviews, Philadelphia, Hanley and Belfus Vol.13,
No.3, October, 1999
Find A Professional in Your Area


