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GRADE
Hoch
37 Zitate
Stichprobek = 6 Studien
n = 251 Pat.
n = 251 Pat.
Dauerunklar
KontrollePlacebo
EndpunktAgitation/Aggression
Verblindungdoppelblind
DesignMeta-Analyse
Kernaussage
Cannabinoide zeigten keinen signifikanten Effekt auf Agitation insgesamt (P = 0,10), wobei erhebliche Heterogenität vorlag; erhöhte Sedation wurde beobachtet.
Zusammenfassung
Meta-Analyse über k=6 doppelblinde, placebokontrollierte Studien (n=251) zu Cannabinoiden bei Agitation/Aggression in Alzheimer-Demenz; kein Gesamt-Effekt auf Agitation (SMD=-0.69, p=0.10), signifikante Heterogenität (I²=86%). Trend zu größerem Effekt synthetischer Cannabinoide vs. THC (χ²=3.05, p=0.08). Stärkerer Effekt bei höherer kognitiver Beeinträchtigung (B=0.27, p=0.03). Sedation signifikant häufiger als Placebo (RR=1.73, p=0.04).
P
PopulationAlzheimer-Patienten mit Agitation/Aggression, gepoolt n=251
I
InterventionNatürliche und synthetische Cannabinoide (verschiedene Substanzen)
C
KontrollePlacebo
O
OutcomeKein signifikanter Gesamteffekt auf Agitation (SMD: -0,69, p=0,10); Trend für synthetische Cannabinoide vs. THC (p=0,08); erhöhte Sedierung unter Cannabinoiden vs. Placebo (RR=1,73, p=0,04)
Vertrauen in die Evidenz
Hoch
Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Kein Nutzen
Zitate / Jahr
★★★★★
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Abstract
Objective: This meta-analysis investigated the efficacy of cannabinoids on agitation and aggression in patients with Alzheimer's disease (AD).
Data Sources: Electronic records up to August 2018 were searched from MEDLINE, EMBASE, and PsycINFO. Search terms included Alzheimer's disease, agitation, aggression, and cannabinoids.
Study Selection: Double-blind, placebo-controlled studies investigating the effect of cannabinoids on agitation in patients with AD were included. Of the 1,336 records returned, 123 were reviewed and 6 (N = 251 participants) were included.
Data Extraction: Data on demographics, study setting, trial length, intervention, outcomes, and dropouts were extracted.
Results: There was no effect of cannabinoids as a group on agitation (standard mean difference: -0.69, P = .10), though there was significant heterogeneity (chi(2)(6) = 43.53, P < .00001, I(2) = 86%). There was a trend for greater difference in agitation with synthetic cannabinoids over tetrahydrocannabinol (chi(2)(1) = 3.05, P = .08). Cannabinoids had a larger effect on agitation with greater cognitive impairment (B = 0.27, t(6) = 2.93, P = .03). Cannabinoids did not change overall neuropsychiatric symptoms or body mass index (BMI). However, there was a significant difference in patients with a lower BMI compared to patients with a higher BMI (chi(2)(1) = 4.63, P = .03). Sedation was significantly greater with cannabinoids compared to placebo (risk ratio = 1.73, P = .04), but there were no differences in the occurrence of adverse events or dropouts due to an adverse event between treatment groups.
Conclusions: The efficacy of cannabinoids on agitation and aggression in patients with AD remains inconclusive, though there may be a signal for a potential benefit of synthetic cannabinoids. Safety should be closely monitored as cannabinoid treatment was associated with increased sedation.
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