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Jesse Elliott

Researcher at University of Ottawa

Publications -  23
Citations -  368

Jesse Elliott is an academic researcher from University of Ottawa. The author has contributed to research in topics: Randomized controlled trial & Percutaneous coronary intervention. The author has an hindex of 8, co-authored 22 publications receiving 210 citations.

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Journal ArticleDOI

Testosterone therapy in hypogonadal men: a systematic review and network meta-analysis.

TL;DR: Despite a class effect of improving quality of life, depression, erectile function and libido, major improvements were not observed with the use of any individual product and longer-term high-quality trials are needed to fully assess the risk of harm.
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Cannabis-based products for pediatric epilepsy: A systematic review.

TL;DR: To assess the benefits and harms of cannabis‐based products for pediatric epilepsy, a large number of patients with epilepsy have received treatment with these products through a combination of conventional and cannabinoid‐based methods.
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ALK inhibitors for non-small cell lung cancer: A systematic review and network meta-analysis.

TL;DR: Treatment-related deaths were infrequent among ALK-positive NSCLC and PFS may be improved by alectinib and brigatinib relative to other ALK inhibitors; however, the assessment of OS is likely confounded by treatment crossover and should be interpreted with caution.
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Pharmacologic treatment of attention deficit hyperactivity disorder in adults: A systematic review and network meta-analysis.

TL;DR: There were few differences among individual medications, although atomoxetine was associated with improved patient-reported clinical response and quality of life compared with placebo, and the choice between ADHD pharmacotherapies may depend on individual patient considerations.
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Cannabis-based products for pediatric epilepsy: An updated systematic review.

TL;DR: Newly available evidence supports earlier findings that cannabidiol probably reduces the frequency of seizures among children with drug-resistant epilepsy; however, there is an increased risk of gastrointestinal adverse events.