A subgroup of self-injuring patients responds positively to the opiate-bloc
king agent naltrexone in acute, double-blind studies. In this study we exam
ined the effects of naltrexone after acute treatment and the long-term effe
cts of naltrexone on SIE. Rates of SIE were collected from pretreatment bas
eline; a second baseline a year after the acute trial; and a subsequent 12-
month double-blind, placebo-controlled treatment. A subgroup of patients de
creased SIE for a year without treatment after acute exposure to naltrexone
. Five participants who decreased SIE by 70% after acute treatment increase
d SIE to the long-term treatment with naltrexone. In contrast, those for wh
om SIE increased over the one-year treatment hiatus decreased their SIE aft
er the first long-term treatment. Discussion of these complex effects consi
dered the role of background opioid levels, dosing, and treatment regimen o
f naltrexone and other factors limiting receptor adaptation among patients
who exhibit SIE.