Geriatrische Patienten
Studienlage · Detail RCT · Geriatrische Patienten · 2023

Examining the use of cannabidiol and delta-9-tetrahydrocannabinol-based medicine among individuals diagnosed with dementia living within residential aged care facilities: Results of a double-blind randomised crossover trial.

Gemischt GRADE Moderat 7 Zitate
Stichproben = 21 Pat.
Dauer18 Wochen
KontrollePlacebo
EndpunktNPI
Verblindungdoppelblind
DesignRCT
Cannabinoidkombination
THC:CBD3:2
Applikationoral
Kernaussage

Keine signifikanten Unterschiede zwischen Placebo und Cannabinoid-Medikament bei Verhalten, Lebensqualität oder Schmerz, außer einer Abnahme von Agitation am Ende der Behandlung zugunsten des Cannabinoid-Medikaments.

Zusammenfassung

n=21 Demenz-Patienten in Pflegeheimen (77% weiblich, Ø85 Jahre), 18-Wochen-RCT THC:CBD 3:2 vs. Placebo; keine signifikanten Unterschiede in BPSD, QoL oder Schmerz außer Agitations-Reduktion am Behandlungsende zugunsten CBM. Qualitative Daten: verbesserte Entspannung/Schlaf bei einigen Individuen. Post-hoc-Schätzung: n=50 erforderlich für NPI-Sensitivität. Minimal Nebenwirkungen, Medikation erschien sicher.

P
PopulationÄltere Erwachsene mit Demenz in stationären Pflegeeinrichtungen (RACF), n=21, Durchschnittsalter 85 Jahre, 77% weiblich
I
InterventionTHC:CBD-basierte Medizin (3:2-Verhältnis Delta-9-THC:CBD), orale Gabe, titriert auf tolerierbare Dosis, 18-wöchige Crossover-Periode
C
KontrollePlacebo
O
OutcomeKeine signifikanten Unterschiede zwischen CBM und Placebo für Verhalten, Lebensqualität oder Schmerz; signifikante Reduktion von Agitation am Behandlungsende zugunsten von CBM
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
Verblindung Doppelblind
Effektstärke Gemischt
Zitate / Jahr
Autoren
Timler A, Bulsara C, Bulsara M, Vickery A, Jacques A, Codde J
DOI 10.1111/ajag.13224
Design: RCT
Teilen
Abstract
Objective: Dementia affects individuals older than 65 years. Currently, residential aged care facilities (RACF) use psychotropic medications to manage behavioural and neuropsychiatric symptoms of dementia (BPSD), which are recommended for short-term use and have substantial side effects, including increased mortality. Cannabinoid-based medicines (CBM) have some benefits that inhibit BPSD and cause minimal adverse effects (AEs), yet limited research has been considered with this population. The study aimed to determine a tolerable CBM dose (3:2 delta-9-tetrahydrocannabinol:cannabidiol), and assessed its effect on BPSD, quality of life (QoL) and perceived pain. Methods: An 18-week randomised, double-blinded, crossover trial was conducted. Four surveys, collected on seven occasions, were used to measure changes in BPSD, QoL and pain. Qualitative data helped to understand attitudes towards CBM. General linear mixed models were used in the analysis, and the qualitative data were synthesised. Results: Twenty-one participants (77% female participants, mean age 85) took part in the trial. No significant differences were seen between the placebo and CBM for behaviour, QOL or pain, except a decrease in agitation at the end of treatment in favour of CBM. The qualitative findings suggested improved relaxation and sleep among some individuals. Post hoc estimates on the data collected suggested that 50 cases would draw stronger conclusions on the Neuropsychiatric Inventory. Conclusions: The study design was robust, rigorous and informed by RACF. The medication appeared safe, with minimal AEs experienced with CBM. Further studies incorporating larger samples when considering CBM would allow researchers to investigate the sensitivity of detecting BPSD changes within the complexity of the disease and concomitant with medications.

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