Article Text
Carphology
Carphology
Statistics from Altmetric.com
Weed out the seizures
Just when you thought there was little new in epilepsy therapeutics, there comes a double-blind, placebo-controlled trial of a novel compound in 120 people with Dravet syndrome. The fact that this also provides the first class I evidence for the use of cannabidiol in epilepsy, and that the trial participants had an epileptic encephalopathy (defined by multiple seizures types that are pharmacoresistant), makes this all the more astonishing. Convulsive seizures decreased from 12.4 to 5.9 per month with treatment (14.9–14.1 with placebo), p=0.01. As expected, there were more adverse events in the cannabidiol group, such as gastrointestinal symptoms fatigue, fever, somnolence and abnormal liver function tests; these …
Other content recommended for you
- Evidence for cannabis and cannabinoids for epilepsy: a systematic review of controlled and observational evidence
- Cannabidiol reduced frequency of convulsive seizures in drug resistant Dravet syndrome
- Cannabis and epilepsy
- Perioperative considerations for adult patients with Dravet syndrome in regional centres
- Fifteen-minute consultation: When medicines don’t work—the child with poorly controlled seizures
- Medical cannabis for severe treatment resistant epilepsy in children: a case-series of 10 patients
- Balancing risks and benefits of cannabis use: umbrella review of meta-analyses of randomised controlled trials and observational studies
- The case for medical cannabis—an essay by M P Barnes
- FDA approves its first cannabis based medicine
- NICE guideline review: Epilepsies in children, young people and adults NG217