Key result
Disulfiram did not alter the QTc interval in cocaine-dependent patients, whereas recent cocaine use and possibly methadone treatment were identified as risk factors for QTc prolongation.
Why the study?
Does disulfiram alter the QTc interval in methadone-treated and non-opioid-dependent cocaine-dependent patients?
RCT (n=41)
Double-blind
Randomized
Does disulfiram alter the QTc interval in methadone-treated and non-opioid-dependent cocaine-dependent patients?
Disulfiram does not appear to exacerbate QTc prolongation in cocaine-dependent patients, whereas recent cocaine use and methadone treatment are associated with increased QTc.
Answers are grounded in this paper and cite their sources.
Supports disulfiram safety regarding QTc in cocaine dependence; extends QTc risk data to recent cocaine use and methadone.
OBJECTIVES: Methadone and cocaine are each known to prolong the QTc interval, a risk factor for developing potentially fatal cardiac arrhythmias. Disulfiram, often administered in the context of methadone maintenance to facilitate alcohol abstinence, has been shown to have some efficacy for cocaine dependence. Disulfiram has differential effects on cocaine and methadone metabolism, but its impact on methadone- or cocaine-induced changes in QTc interval is unclear. Thus, the effects of disulfiram on QTc interval in a subset of cocaine-dependent patients participating in a 14-week, randomized, double-blind, placebo-controlled clinical trial of disulfiram were prospectively determined. METHODS: Opioid-dependent participants were inducted onto methadone (weeks 1-2; MT) and both MT and non-opioid-dependent (UT) participants were randomized to receive disulfiram (weeks 3-14) at one of the following doses: 0, 250, 375, or 500 mg/d. Electrocardio-grams were obtained before study entry and during weeks 2 and 4. RESULTS: Complete QTc-interval data in 23 MT and 18 UT participants were analyzed. QTc interval tended to be higher in MT participants relative to UT participants, regardless of disulfiram dose and time point, but disulfiram did not differentially alter QTc interval. QTc interval was, however, significantly greater in participants with recent cocaine use than in those with no recent use. CONCLUSIONS: These results suggest that cocaine use and possibly MT status, but not disulfiram, are risk factors for QTc prolongation.
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Atkinson et al. (2013) conducted an RCT in Cocaine dependence (n=41). Disulfiram vs. Placebo (0 mg/d) was evaluated on QTc interval. Disulfiram did not alter the QTc interval in cocaine-dependent patients, whereas recent cocaine use and possibly methadone treatment were identified as risk factors for QTc prolongation.
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