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120 Zitate
Stichproben = 15 Pat.
Dauer6-9 Monate
EndpunktASD-Symptomkategorien
Verblindungn.a.
DesignBeobachtungsstudie (Compassionate Use)
Cannabinoidvollspektrum
THC:CBD75:1
Applikationoral
Kernaussage
CBD-angereicherter Cannabis-Extrakt verbesserte bei 14 von 15 ASD-Patienten mindestens eine Symptomkategorie, am stärksten Anfälle, ADHS, Schlaf und soziale Kommunikation.
Zusammenfassung
Beobachtungsstudie (n=15 adhärente ASD-Patienten, davon 10 nicht-epileptisch); CBD-reiches Cannabis-Extrakt (CBD:THC 75:1) über 6–9 Monate; 9 von 10 nicht-epileptischen Patienten zeigten Verbesserung ≥30% in mindestens einer von 8 Symptomkategorien; 6/10 Verbesserung ≥30% in ≥2 Kategorien; stärkste Verbesserungen bei Schlafstörungen, ADHS und sozialer Kommunikation.
P
PopulationAutismus-Spektrum-Störung (ASD), davon 10 nicht-epileptisch und 5 epileptisch, n=15 (Adhärenz-Kohorte aus n=18)
I
InterventionCBD-angereicherter Cannabis sativa-Extrakt (CBD:THC-Ratio 75:1), oral, Compassionate Use
O
OutcomeBei 14 von 15 adhärenten Patienten Verbesserung in mindestens einer von acht Symptomkategorien; stärkste Verbesserungen bei Anfällen, ADHS, Schlafstörungen und sozialer Kommunikation; bei 9 von 10 nicht-epileptischen Patienten ≥30% Verbesserung in mindestens einer Kategorie
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Abstract
Autism Spectrum Disorders comprise conditions that may affect cognitive development, motor skills, social interaction, communication, and behavior. This set of functional deficits often results in lack of independence for the diagnosed individuals, and severe distress for patients, families, and caregivers. There is a mounting body of evidence indicating the effectiveness of pure cannabidiol (CBD) and CBD-enriched Cannabis sativa extract (CE) for the treatment of autistic symptoms in refractory epilepsy patients. There is also increasing data support for the hypothesis that non-epileptic autism shares underlying etiological mechanisms with epilepsy. Here we report an observational study with a cohort of 18 autistic patients undergoing treatment with compassionate use of standardized CBD-enriched CE (with a CBD to THC ratio of 75/1). Among the 15 patients who adhered to the treatment (10 non-epileptic and five epileptic) only one patient showed lack of improvement in autistic symptoms. Due to adverse effects, three patients discontinued CE use before 1 month. After 6-9 months of treatment, most patients, including epileptic and non-epileptic, showed some level of improvement in more than one of the eight symptom categories evaluated: Attention Deficit/Hyperactivity Disorder; Behavioral Disorders; Motor Deficits; Autonomy Deficits; Communication and Social Interaction Deficits; Cognitive Deficits; Sleep Disorders and Seizures, with very infrequent and mild adverse effects. The strongest improvements were reported for Seizures, Attention Deficit/Hyperactivity Disorder, Sleep Disorders, and Communication and Social Interaction Deficits. This was especially true for the 10 non-epileptic patients, nine of which presented improvement equal to or above 30% in at least one of the eight categories, six presented improvement of 30% or more in at least two categories and four presented improvement equal to or above 30% in at least four symptom categories. Ten out of the 15 patients were using other medicines, and nine of these were able to keep the improvements even after reducing or withdrawing other medications. The results reported here are very promising and indicate that CBD-enriched CE may ameliorate multiple ASD symptoms even in non-epileptic patients, with substantial increase in life quality for both ASD patients and caretakers.
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