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Potential Patient-Reported Toxicities With Disulfiram Treatment in Late Disseminated Lyme Disease.

Authors :
Trautmann A
Gascan H
Ghozzi R
Source :
Frontiers in medicine [Front Med (Lausanne)] 2020 Apr 20; Vol. 7, pp. 133. Date of Electronic Publication: 2020 Apr 20 (Print Publication: 2020).
Publication Year :
2020

Abstract

Recently, disulfiram has been proposed as a promising treatment for people suffering from persistent symptoms of Lyme Disease. Disulfiram has several distinct molecular targets. The most well-known is alcohol dehydrogenase, a key enzyme for detoxifying the organism after alcohol ingestion. Other targets and modes of action of disulfiram, that may present problematic side effects, are less commonly mentioned. The French Federation against Tick Borne Diseases (French acronym, FFMVT), which associates three main Lyme patient organizations, MDs and PhDs, has recently been alerted to severe and persistent toxic events in a patient suffering from a late disseminated form of Lyme Disease following disulfiram intake. FFMVT reacted by launching a national call to examine whether other patients in France following a similar treatment could be identified, and what benefits, or side effects could be reported. The statements of 16 patients taking disulfiram have been collected and are presented here. Thirteen out of 16 patients reported toxic events, and seven out of 16 reported benefits for at least part of their symptoms. Based on the collected observations, it seems too early to promote disulfiram as a promising new treatment until the reasons underlying the reported toxicities have been explored, and the results of a well-conducted double blind clinical trial published. The importance of taking into account patient-reported outcomes in Lyme Disease is underlined by the present study.<br /> (Copyright © 2020 Trautmann, Gascan and Ghozzi.)

Details

Language :
English
ISSN :
2296-858X
Volume :
7
Database :
MEDLINE
Journal :
Frontiers in medicine
Publication Type :
Academic Journal
Accession number :
32373619
Full Text :
https://doi.org/10.3389/fmed.2020.00133