TREATMENT FOR OVERDOSE
AND ADDICTION
In case of overdose,
the opiate antagonist naloxone (Narcan) almost immediately reverses the life-threatening suppression of breathing. Treating opiate addiction is another matter. As with
other addictions, there is no easy
solution. People have tried many of the strategies used for alcoholics. A number of groups, such as Narcotics
Anonymous, emphasize abstention, attendance at meetings, and so forth.
In addition, two drugs
have proved to be very effective in treating narcotic addiction. Methadone is a long-acting opiate that can be given on
an outpatient basis to patients in
treatment programs. The idea of this strategy is to allow the addict to avoid withdrawal and the constant need to procure the drug. The other advantages of methadone
are that the drug is given orally,
without the risks of IV administration, and that the dose is controlled and can gradually be worked down.
Although some complain that this
method just substitutes one addiction for another without addressing the social and psychological reasons for
the addiction, patients' lifestyles
do improve. The bottom line is that methadone works—it helps users abstain and get back to productive lives and
decreases mortality compared to users
receiving non-drug-based therapy. Recently, buprenorphine, another opiate
drug, has been approved for the treatment of opiate addiction in the form of a pill that you place
under the tongue, or an implant
placed under the skin to provide the drug constantly It is somewhat different from methadone. It also
stimulates opiate receptors and provides
a "substitution" strategy. But when an addict takes buprenorphine, it keeps effective agonists like heroin
from getting to the receptors. So it
has just enough activity to stave off withdrawal. The addict doesn't get high on buprenorphine and can't get high on
heroin. Some formulations of
buprenorphine are combined with naloxone, so if users inject it rather than
taking it as a pill, he or she cannot get high and likely will experience withdrawal symptoms. The goal of this
formulation is to decrease potential
abuse. The reason for this formulation is that buprenorphine, unlike methadone, can be prescribed by a
doctor. Methadone can only be used in
conjunction with a clinic visit: this is a real turnoff to long-term
clients who complain that the only' time they are around the old drug-taking environment is when they are
forced to visit the clinic to receive their medication.
Pellets containing
long-term-release preparations of the opioid antagonist naltrexone are also available. Like
buprenorphine, they are implanted under
the skin and provide the drug continuously In this case, they keep the user from getting high as long as they last—and
that's the problem. The pellets wear
out, and the user simply goes back to getting high. The success of this strategy is less than those using
methadone or buprenorphine. Another
strategy that received some (undeserved) attention was the idea of putting a patient to sleep with a
general anesthetic fin' the first eighteen
to twenty-four hours of withdrawal along with an opioid antagonist to help speed the normalization of opioid
receptor function. Again, this was
based on valid pharmacology—the opioid antagonist would help remove any remaining opioid from sites where it was active. However, it is extremely
dangerous to put someone under anesthesia for so long. Furthermore, these programs typically offered little follow-up,
and people were just as likely to
start using opiates again after this program as if they had not been
treated. Most reputable physicians have rejected these treatments. Finally, scientists are studying ibogaine,
a chemical contained in an African shrub, after some sensationalistic
reports in the addiction underworld
that one ibogaine experience led them to give up opioids forever. Ibogaine is a hallucinogen, and although
research is progressing, it seems unlikely that it will pan out to be a
mainstream treatment for opioid addiction.
While there are numerous clinics around the world, the National Institute on Drug Abuse decided that it
has too many side effects to commit
resources to studying its potential, and so there is little about it in
the scientific literature.