Elsevier eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 135 - 145
Published: Jan. 1, 2023
Language: Английский
Elsevier eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 135 - 145
Published: Jan. 1, 2023
Language: Английский
Paediatrics & Child Health, Journal Year: 2024, Volume and Issue: 29(2), P. 104 - 112
Published: April 5, 2024
Abstract Interest in using cannabis products for a medical purpose children under the age of 18 years is increasing. There are many available that can include cannabidiol (CBD) or delta-9-tetrahydrocannabinol (THC), both. Despite therapeutic claims, there few rigorous studies to inform dosing, safety, and efficacy paediatric clinical practice. This statement reviews current evidence provides recommendations children. Longer-term (2-year) reports support sustained tolerability therapy patients with Lennox-Gastaut Dravet syndromes. CBD-enriched extracts containing small amounts THC have been evaluated number patients, further research needed practice guidelines. Given widespread use Canada, paediatricians should be prepared engage open, ongoing discussions families about its potential benefits risks, develop individualized plans monitor efficacy, reduce harms, mitigate drug–drug interactions.
Language: Английский
Citations
5Therapeutic Advances in Neurological Disorders, Journal Year: 2023, Volume and Issue: 16
Published: Jan. 1, 2023
Background: Epilepsy is one of the most common chronic brain diseases. Almost one-third patients have drug-resistant epilepsy (DRE). Cannabidiol being considered as a potential novel drug for treating DRE. Objectives: To investigate long-term efficacy and safety cannabidiol in treatment DRE differences among with different characteristics. Design: Systematic review meta-analysis. Data sources methods: Medline, Embase, CENTRAL were searched literature. RevMan5.4 was used The Intention-to-treat set random effect main analysis. Subgroup analyses performed according to age, dose, concomitant antiseizure medications (ASMs), syndromes, study designs. Results: Fifty studies included this systematic review. A total 4791 participants collected. responder rates (seizure frequency reduced at least 50%) 12-, 24-, 48-, 72-, 96-, 144-week 0.40 [0.36, 0.45], 0.39 [0.34, 0.44], 0.37 [0.30, 0.27 [0.17, 0.37], 0.22 [0.14, 0.30], 0.38 [0.23, 0.53]. Seizure-free 0.04 [0.03, 0.06], 0.05], 0.03 [0.02, 0.03], 0.02 [0.01, 0.06]. Proportion adverse events 0.72 [0.61, 0.83], 0.62 [0.42, 0.81], 0.60 [0.41, 0.79], 0.35 0.56], 0.83 [0.75, 0.90], 0.96 [0.94, 0.99]. pooled proportion serious 0.15 [0.09, 0.21], 0.23 0.31], 0.10 [0.06, 0.15], 0.31 [0.24, 0.38], [0.35, 0.45]. showed that there no significant difference on age subgroups syndromes subgroups. For periods, dose ASMs. However, higher doses more ASMs associated events. Conclusion: has stable fewer early period. Long-term use may decreased increased Dose escalation not increase efficacy, but Furthermore, reduce dosage other without reducing thereby effects. similar effects various syndromes. Trial registration: PROSPERO (CRD42022351250).
Language: Английский
Citations
12Journal of Ethnopharmacology, Journal Year: 2023, Volume and Issue: 320, P. 117386 - 117386
Published: Nov. 11, 2023
Language: Английский
Citations
10Epilepsia, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 13, 2025
Abstract Objective Identifying factors influencing cannabidiol (CBD) exposure can optimize treatment efficacy and safety. We aimed to describe the population pharmacokinetics of CBD in children with drug‐resistant developmental epileptic encephalopathies (DEEs) assess influence environmental, pharmacological, clinical characteristics on systemic exposure. Methods Data from two pharmacokinetic studies patients aged 2–18 years DEEs were included ( N = 48 patients). Serial blood samples collected during maintenance treatment, before after morning dose, up 6 h a dose purified oil formulation, or without normocaloric breakfast. plasma concentrations also available following administration CBD‐enriched formulation. Samples quantified using validated liquid chromatography/tandem mass spectrometry assay. A model was developed nonlinear mixed‐effects modeling. The effects concomitant food intake, demographic, clinical, pharmacological evaluated. Simulated maximum concentration (C max ) area under concentration–time curve between 0 12 (AUC 0‐12 calculated. Results one‐compartment transit compartments first‐order elimination best described pharmacokinetics. Mean values for apparent clearance (CL/F) volume distribution (V/F) 143.5 L/h 1892.4 L, respectively. Weight allometrically scaled V/F CL/F, sex associated V/F, both formulation condition F (relative bioavailability). C increased by 41% AUC 45% when administered compared fasting. Dose‐normalized approximately 50% lower CBD. Significance In present study, we DEEs. Increased intake significant changes drug switching formulations should be considered patient management.
Language: Английский
Citations
0Integrative Medicine Reports, Journal Year: 2025, Volume and Issue: 4(1), P. 9 - 43
Published: Jan. 1, 2025
Language: Английский
Citations
0Epilepsy & Behavior, Journal Year: 2023, Volume and Issue: 144, P. 109210 - 109210
Published: May 15, 2023
Language: Английский
Citations
9Neurological Sciences, Journal Year: 2022, Volume and Issue: 44(1), P. 297 - 304
Published: Sept. 21, 2022
Language: Английский
Citations
13Epilepsy Research, Journal Year: 2023, Volume and Issue: 190, P. 107098 - 107098
Published: Jan. 25, 2023
Language: Английский
Citations
8Epileptic Disorders, Journal Year: 2023, Volume and Issue: 25(1), P. 18 - 27
Published: Feb. 1, 2023
Abstract Ketogenic diet therapy (KDT) is a nonpharmacological treatment that has been demonstrated to be effective in reducing seizures patients with drug‐resistant epilepsy. As the majority of on KDT are also receiving anti‐seizure medications (ASMs), questions about their combination often arise. typically implemented as an add‐on, and not substitute for ASMs. Drug monitoring specific laboratory studies may helpful cases cotherapy. Valproate, topiramate, zonisamide, lamotrigine potentially problematic KDT, but evidence this conclusive. ASM reduction usually attempted after 1 month if child showing seizure (but weaning ASMs does require freedom). Failure wean mean failed adding new beneficial those several months fine‐tuning. The purpose review was discuss possible negative (or positive) pharmacodynamic interactions between In addition, practical suggestions or provided.
Language: Английский
Citations
8Epilepsy & Behavior, Journal Year: 2023, Volume and Issue: 143, P. 109245 - 109245
Published: May 12, 2023
Language: Английский
Citations
8