Epilepsy
Study register · detail Klinische Studie · Epilepsy · 2021

Effect of Cannabidiol on Interictal Epileptiform Activity and Sleep Architecture in Children with Intractable Epilepsy: A Prospective Open-Label Study.

Clear benefit GRADE Low 31 citations
Samplen = 35 Pat.
Duration3 months
EndpointIED rate per minute
Blindingeinfachblind
DesignKlinische Studie
Cannabinoidcbd
Routeoral
Key finding

Cannabidiol significantly reduced the frequency of interictal epileptic discharges and improved sleep microstructure in children with treatment-refractory epilepsy.

Summary

Prospective open-label study on CBD (20–50 mg/kg/d) in treatment-refractory epilepsy in childhood; n=35 (age 10,1±0,86 years). Interictal epileptiform discharges (IEDs) significantly reduced after 3 months (19,6±19,5 vs. 36,8±27,2 discharges/min at baseline, p<0,0001). Moderate correlation between IED reduction and seizure reduction (r=0,39, p=0,02). Sleep architecture abnormal in 56,5% initially, improved under CBD in 84,6% of these cases.

P
PopulationChildren with pharmacoresistant epilepsy (including Dravet syndrome, Lennox-Gastaut syndrome), n=35, mean age 10,1 years
I
InterventionCannabidiol oral 20 mg/kg/day (up to max. 50 mg/kg/day), open-label, add-on to stable concomitant medication
O
OutcomeIED rate significantly reduced after 3 months (19,6 ± 19,5 vs. 36,8 ± 27,2 per minute; p<0,0001); sleep microstructure improved in 84,6% of initially pathological cases
Confidence in the evidence
Low

The second of four GRADE levels, the effect estimate is of limited reliability.

Downgraded for
Risk of biasImprecision
Quality profile
Sample size
Blinding Single-blind
Effect size Clear benefit
Citations / year
Authors
Klotz KA, Grob D, Schonberger J, Nakamura L, Metternich B, Schulze-Bonhage A, Jacobs J
DOI 10.1007/s40263-021-00867-0
Design: Klinische Studie
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Abstract
Background: Cannabidiol has been shown to be effective in seizure reduction in patients with Dravet syndrome, Lennox-Gastaut syndrome, and tuberous sclerosis. However, very little is known about its potential to reduce interictal epileptiform activity and improve sleep architecture. Objective: The objective of this prospective study was to evaluate the influence of cannabidiol therapy on the frequency of interictal epileptiform discharges (IEDs) and sleep microstructure in a cohort of children with drug-resistant epilepsy. Methods: Children with drug-resistant epilepsy were prospectively followed from November 2019 to January 2021 during an open-label trial of cannabidiol at a dose of 20 mg/kg/day (to a maximum of 50 mg/kg/day) and stable concomitant medication. Electroencephalograms were recorded at baseline (T0) and after 3 months (T1). Two independent raters, blinded to clinical outcome, evaluated 5-min segments of sleep stage 2 or low-noise awake state. IEDs were visually identified and rates per minute calculated. Sleep microstructure was considered improved if sleep structures were seen at T1 that were not present at T0. IED rates at T0 and T1 were compared and correlated with seizure outcome, cannabidiol dose, initial IED rate, and disease duration. Results: In total, 35 children (mean +/- standard deviation age 10.1 +/- 0.86) were included. The IED rate at T1 was significantly lower than at T0 (19.6 +/- 19.5 vs. 36.8 +/- 27.2, respectively; p < 0.0001). We found a moderate correlation between IED reduction and percentage of seizure reduction compared with baseline (Pearson's r = 0.39; p = 0.02), a moderate negative correlation between IED reduction and IED rate at T0 (r = - 0.34; p = 0.04), and a trend towards a moderate negative correlation between IED reduction and disease duration (r = - 0.32; p = 0.06). Sleep was recorded in 23 patients. Sleep microstructure was initially abnormal in 56.5% of sleep recordings and improved in 84.6% of those cases. Conclusion: Our results strongly suggest the utility of cannabidiol in reducing IEDs and improving sleep microstructure in children with drug-resistant epilepsy. Larger controlled studies are needed to evaluate the clinical relevance of this effect in different epilepsy types. Trial Registration: DRKS00013177; 25 June 2019.

The impediment to action advances action. — Marcus Aurelius