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Multiple treatment comparison in narcolepsy: a network meta-analysis

STUDY OBJECTIVES: Randomized controlled trials (RCTs) that compared the safety and efficacy of medical treatments for narcolepsy were analyzed using network meta-analysis. METHODS: The RCTs in narcolepsy were searched. Network meta-analysis compared efficacy and safety of multiple treatments, multi-...

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Autores principales: Lehert, Philippe, Falissard, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289237/
https://www.ncbi.nlm.nih.gov/pubmed/30239930
http://dx.doi.org/10.1093/sleep/zsy185
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author Lehert, Philippe
Falissard, Bruno
author_facet Lehert, Philippe
Falissard, Bruno
author_sort Lehert, Philippe
collection PubMed
description STUDY OBJECTIVES: Randomized controlled trials (RCTs) that compared the safety and efficacy of medical treatments for narcolepsy were analyzed using network meta-analysis. METHODS: The RCTs in narcolepsy were searched. Network meta-analysis compared efficacy and safety of multiple treatments, multi-arm studies, and multi-criteria treatment decisions, based on a random model that assumed heterogeneity between studies, with corrections for multi-arm studies. RESULTS: Fourteen RCTs, three drug treatments, and six doses were identified: sodium oxybate (6 and 9 g/d), modafinil (between 200 and 400 mg/d), and pitolisant (up to 20 and up to 40 mg/d). Significant heterogeneity (>50%) between studies was found in 12/14 studies for almost all endpoints, but between-design consistency was present. For ESS and MWT, sodium oxybate 9 g/d, modafinil, and pitolisant up to 40 mg/d had similar efficacy. Pitolisant 40 mg/d and sodium oxybate 9 g/d in two nightly doses had similar efficacy in reducing cataplexy. A good safety profile characterized by a TEAE incidence risk ratio (IRR) <1.5 was found for all the compared treatments, except for sodium oxybate 9 g/d. Although no significant difference was found, Pitolisant 40 mg was shown with the best P scores for the benefit/risk (BR) ratio. CONCLUSIONS: Modafinil (200–400 mg/d), sodium oxybate 9 g/d, and pitolisant up to 40 mg/d had similar efficacy in reducing excessive day time sleepiness. Only sodium oxybate 9 g/d and pitolisant up to 40 mg/d were shown with a comparable beneficial effect on cataplexy. Overall, Pitolisant was found with the best P score on the BR ratio CLINICAL TRIAL REGISTRATION: PROSPERO 2017 CRD42017054686. Efficacy, safety, and benefit-risk comparison of alternative treatments in narcolepsy: a network multiple comparisons of treatment meta-analysis. http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017054686.
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spelling pubmed-62892372018-12-14 Multiple treatment comparison in narcolepsy: a network meta-analysis Lehert, Philippe Falissard, Bruno Sleep Neurological Disorders STUDY OBJECTIVES: Randomized controlled trials (RCTs) that compared the safety and efficacy of medical treatments for narcolepsy were analyzed using network meta-analysis. METHODS: The RCTs in narcolepsy were searched. Network meta-analysis compared efficacy and safety of multiple treatments, multi-arm studies, and multi-criteria treatment decisions, based on a random model that assumed heterogeneity between studies, with corrections for multi-arm studies. RESULTS: Fourteen RCTs, three drug treatments, and six doses were identified: sodium oxybate (6 and 9 g/d), modafinil (between 200 and 400 mg/d), and pitolisant (up to 20 and up to 40 mg/d). Significant heterogeneity (>50%) between studies was found in 12/14 studies for almost all endpoints, but between-design consistency was present. For ESS and MWT, sodium oxybate 9 g/d, modafinil, and pitolisant up to 40 mg/d had similar efficacy. Pitolisant 40 mg/d and sodium oxybate 9 g/d in two nightly doses had similar efficacy in reducing cataplexy. A good safety profile characterized by a TEAE incidence risk ratio (IRR) <1.5 was found for all the compared treatments, except for sodium oxybate 9 g/d. Although no significant difference was found, Pitolisant 40 mg was shown with the best P scores for the benefit/risk (BR) ratio. CONCLUSIONS: Modafinil (200–400 mg/d), sodium oxybate 9 g/d, and pitolisant up to 40 mg/d had similar efficacy in reducing excessive day time sleepiness. Only sodium oxybate 9 g/d and pitolisant up to 40 mg/d were shown with a comparable beneficial effect on cataplexy. Overall, Pitolisant was found with the best P score on the BR ratio CLINICAL TRIAL REGISTRATION: PROSPERO 2017 CRD42017054686. Efficacy, safety, and benefit-risk comparison of alternative treatments in narcolepsy: a network multiple comparisons of treatment meta-analysis. http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017054686. Oxford University Press 2018-09-19 /pmc/articles/PMC6289237/ /pubmed/30239930 http://dx.doi.org/10.1093/sleep/zsy185 Text en © Sleep Research Society 2018. Published by Oxford University Press [on behalf of the Sleep Research Society]. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neurological Disorders
Lehert, Philippe
Falissard, Bruno
Multiple treatment comparison in narcolepsy: a network meta-analysis
title Multiple treatment comparison in narcolepsy: a network meta-analysis
title_full Multiple treatment comparison in narcolepsy: a network meta-analysis
title_fullStr Multiple treatment comparison in narcolepsy: a network meta-analysis
title_full_unstemmed Multiple treatment comparison in narcolepsy: a network meta-analysis
title_short Multiple treatment comparison in narcolepsy: a network meta-analysis
title_sort multiple treatment comparison in narcolepsy: a network meta-analysis
topic Neurological Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289237/
https://www.ncbi.nlm.nih.gov/pubmed/30239930
http://dx.doi.org/10.1093/sleep/zsy185
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