Study register · detailRetrospektive Kohortenstudie · PTSD · 2014
Use of a Synthetic Cannabinoid in a Correctional Population for Posttraumatic Stress Disorder–Related Insomnia and Nightmares, Chronic Pain, Harm Reduction, and Other Indications
Cameron et al.·Journal of Clinical PsychopharmacologyImpact 1.6
Clear benefitGRADELow172 citations
Samplen = 104 Pat.
Durationunclear
EndpointPTSD-associated…
Blindingn.a.
DesignRetrospektive Kohortenstudie
Cannabinoidthc
Max. dose4.0 mg
Routeoral
”Key finding
Nabilone showed significant improvements in PTSD-associated insomnia, nightmares, PTSD symptoms and Global Assessment of Functioning as well as subjective pain improvement; enabled reduction of riskier medications without abuse evidence in the prison population.
Summary
Retrospective analysis of n=104 male prisoners with severe mental illnesses and PTSD under nabilone (mean 4,0 mg/day). Significant improvements in PTSD-associated insomnia, nightmares, PTSD symptoms and Global Assessment of Functioning (p-values not reported). Nabilone targeted on average 3,5 indications per patient. No evidence of abuse in this high-risk population.
P
PopulationMale prisoners with severe mental illnesses under nabilone prescription, n=104
I
InterventionNabilone (synthetic cannabinoid), mean final dose 4,0 mg, oral (capsule or powder in water)
O
OutcomeSignificant improvement in PTSD-associated insomnia, nightmares, PTSD symptoms and Global Assessment of Functioning; subjective improvement of chronic pain; no evidence of abuse
Confidence in the evidence
Very lowLowModerateHigh
Low
The second of four GRADE levels, the effect estimate is of limited reliability.
Nabilone is a synthetic cannabinoid that has shown promise for the treatment of posttraumatic stress disorder (PTSD)-related insomnia and nightmares as well as efficacy in the management of chronic pain. It has also been proposed for harm reduction in cannabis dependence. Its effectiveness for management of concurrent disorders in seriously mentally ill correctional populations has not been evaluated. This retrospective study of 104 male inmates with serious mental illness prescribed nabilone analyzes the indications, efficacy, and safety of its use. Medications discontinued with the initiation of nabilone were also reviewed. The results showed nabilone targeting a mean of 3.5 indications per patient, thus likely reducing polypharmacy risk. The mean final dosage was 4.0 mg. Results indicated significant improvement in PTSD-associated insomnia, nightmares, PTSD symptoms, and Global Assessment of Functioning and subjective improvement in chronic pain. Medications associated with greater risk for adverse effects or abuse than nabilone were often able to be discontinued with the initiation of nabilone, most often antipsychotics and sedative/hypnotics. There was no evidence of abuse within this high-risk population or reduction of efficacy when nabilone was given in powder form with water rather than as a capsule. This study supports the promise of nabilone as a safe, effective treatment for concurrent disorders in seriously mentally ill correctional populations. Prospective, randomized controlled trials are required to confirm our preliminary results. Follow-up in the community will be required to confirm effectiveness in harm reduction.