Besides its other effects, MMT (methadone maintenance treatment) reduces the high
mortality of intravenous heroin addicts to about 30 % of controls. On the other hand,
deaths of patients and non-patients have been attributed to methadone. Here, we will
report on the major reasons for deaths attributed to methadone and discuss suggestions
for their prevention. 69 % of deaths attributed to methadone occurred in subjects
not on MMT at the time of their death. 51 % of deaths attributed to methadone in subjects
in MMT occurred during the dose-finding period of MMT. Further apparent risk situations
are methadone intake in addition to that received for MMT, discharge from prison and
intravenous injection of methadone. Intake of methadone in non-patients is almost
entirely due to abuse of diverted take-home methadone. Not giving methadone as take-home
should reduce methadone deaths most effectively. Replacing take-home methadone by
substances acting longer than one day, such as LAAM (levacetylmethadol) or buprenorphine,
should also be effective. Restriction of take-home prescriptions to substances with
a slow onset of action, such as LAAM, or to partial agonists with an extended safety
margin such as buprenorphine should be partly effective. Meticulous evaluation of
substance history, slow dose increases and strict supervision of the patient by experienced
personal should prevent methadone overdose during the dose-finding period. Discharge
from prison closely corresponds to this situation; informing addicts shortly before
discharge and psychosocial help during the first months out of prison may reduce this
risk. Naloxone as an adjunct to oral agonist preparations should effectively prevent
high-risk intravenous injection, for example of methadone syrup. This has been the
case with tilidine plus naloxone in Germany. Reducing deaths attributable to methadone
increases the net benefit of MMT. Also, reducing deaths attributable to methadone
avoids decreases in the public acceptance of MMT.
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Dr. med. Stefan Viktor Vormfelde
Department of Clinical Pharmacology
University Hospital
Robert-Koch-Straße 40
37075 Göttingen
Telefon: + 49-551-39-9651
Fax: + 49-551-39-12767
eMail: stefan.vormfelde@med.uni-goettingen.de