Studienlage · Detail
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GRADE
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43 Zitate
Stichproben = 38 Pat.
Dauer8 Tage stationär, Follow-up bis…
KontrollePlacebo oral zweimal täglich
EndpunktCWS
Verblindungdoppelblind
DesignRCT (doppelblind, Parallel-Gruppe)
Kernaussage
Lithiumcarbonat reduzierte den Gesamt-Entzugsscore nicht signifikant gegenüber Placebo.
Zusammenfassung
RCT (n=38 cannabis-abhängige Erwachsene, stationäre Entzugsbehandlung 8 Tage); Lithiumcarbonat 500 mg 2×/Tag vs. Placebo. Primäres Outcome (Cannabis Withdrawal Scale Gesamtscore): kein signifikanter Gruppenunterschied (p nicht signifikant). Individuelle Symptome 'Alpträume/seltsame Träume', 'Appetitlosigkeit' und 'Magenschmerzen' unter Lithium signifikant reduziert. Negativstudie mit relevanter Entzugspopulation (n<60).
P
PopulationCannabisabhängige Erwachsene (Treatment-seeking), n=38, stationäre Entzugsbehandlung
I
InterventionLithiumcarbonat oral 500 mg zweimal täglich für 8 Tage
C
KontrollePlacebo oral zweimal täglich
O
OutcomeKein signifikanter Unterschied im Gesamt-CWS-Score zwischen Lithium und Placebo; einzelne Symptome (Appetitverlust, Magenschmerzen, Albträume) signifikant reduziert unter Lithium
Vertrauen in die Evidenz
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Zweite von vier GRADE-Stufen, die Effektschätzung ist begrenzt verlässlich.
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VerzerrungsrisikoUngenauigkeit
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Kein Nutzen
Zitate / Jahr
★★★★★
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Abstract
<h4>Rationale</h4>Preclinical studies suggest that lithium carbonate (lithium) can reduce precipitated cannabinoid withdrawal in rats by stimulating release of the neuropeptide oxytocin, while two open-label studies indicate lithium may ameliorate cannabis withdrawal symptoms in humans.<h4>Objectives</h4>This study was conducted to examine the efficacy and safety of lithium in the inpatient management of cannabis withdrawal and to determine whether lithium affects plasma oxytocin and the rate of elimination of plasma cannabinoids during abstinence.<h4>Methods</h4>Treatment-seeking cannabis-dependent adults (n = 38) were admitted for 8 days to an inpatient withdrawal unit and randomized to either oral lithium (500 mg) or placebo given twice a day under double-blind randomized controlled trial (RCT) conditions. Primary outcomes included withdrawal severity [cannabis withdrawal scale (CWS)], rates of detoxification completion, and adverse events. Plasma cannabinoids, plasma oxytocin and serum lithium levels were measured repeatedly over admission. Follow-up research interviews were conducted at 14, 30, and 90 days postdischarge.<h4>Results</h4>Lithium did not significantly affect total CWS scores relative to placebo, although it significantly reduced individual symptoms of "loss of appetite," "stomach aches," and "nightmares/strange dreams." No significant group differences were found in treatment retention or adverse events. Lithium did not increase plasma oxytocin levels nor influence the rate of elimination of cannabinoids. Both placebo- and lithium-treated participants showed reduced levels of cannabis use (verified by urinalysis) and improved health and psychosocial outcomes at 30- and 90-day follow-up relative to pretreatment baselines.<h4>Conclusions</h4>Despite the strong rationale for the present study, the efficacy of lithium over placebo in the management of cannabis withdrawal was not demonstrated.
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