Oxygen delivered by a high flow concentrator for the treatment of medication-overuse headache

Treatment of medication-overuse headache (MOH) relies on detoxification, during which patients face rebound headache without alternative to painkiller. As oxygen has been proven effective for cluster and other headache subtypes, we sought to evaluate use of normobaric oxygen delivered by a high flow...

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Main Authors: Jerome Mawet (Author), Dominique Valade (Author), Marie Vigan (Author), Cedric Laouenan (Author), Caroline Roos (Author)
Format: Book
Published: SAGE Publishing, 2018-11-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jerome Mawet  |e author 
700 1 0 |a Dominique Valade  |e author 
700 1 0 |a Marie Vigan  |e author 
700 1 0 |a Cedric Laouenan  |e author 
700 1 0 |a Caroline Roos  |e author 
245 0 0 |a Oxygen delivered by a high flow concentrator for the treatment of medication-overuse headache 
260 |b SAGE Publishing,   |c 2018-11-01T00:00:00Z. 
500 |a 2515-8163 
500 |a 10.1177/2515816318810196 
520 |a Treatment of medication-overuse headache (MOH) relies on detoxification, during which patients face rebound headache without alternative to painkiller. As oxygen has been proven effective for cluster and other headache subtypes, we sought to evaluate use of normobaric oxygen delivered by a high flow concentrator (HFC) in patients suffering MOH. For this purpose, twenty patients with MOH were included in this prospective monocentric open-labeled feasibility study. All patients received standard care with detoxification in addition to HFC delivering normobaric oxygen at 9 l/min, used to their discretion to treat rebound headache. Primary endpoint was acceptance of HFC and secondary endpoints evaluated its efficacy. Four patients were lost of follow-up after inclusion, one was excluded. HFC was accepted by 14/15 (93.3%). At M6 of follow-up, 15/15 (100%) reverted to episodic headache. In conclusion, normobaric oxygen delivered by HFC appears to be safe, feasible, and probably efficient to help patient with MOH who undergo withdrawal therapy. A larger double-blind, sham-controlled prospective study is needed. Trial registration : Clinical trials: NCT02302027. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Neurosciences. Biological psychiatry. Neuropsychiatry 
690 |a RC321-571 
655 7 |a article  |2 local 
786 0 |n Cephalalgia Reports, Vol 1 (2018) 
787 0 |n https://doi.org/10.1177/2515816318810196 
787 0 |n https://doaj.org/toc/2515-8163 
856 4 1 |u https://doaj.org/article/332a80a87c7f4b6f9a8d1392f7f97ad7  |z Connect to this object online.