Chronic intrathecal baclofen in severely disabling spasticity: selection, clinical assessment and long-term benefit.

Details

Serval ID
serval:BIB_3646E4A399C3
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Chronic intrathecal baclofen in severely disabling spasticity: selection, clinical assessment and long-term benefit.
Journal
Acta Neurologica Belgica
Author(s)
Pirotte B., Heilporn A., Joffroy A., Zegers de Beyl D., Wesel P., Brotchi J., Levivier M.
ISSN
0300-9009 (Print)
ISSN-L
0300-9009
Publication state
Published
Issued date
1995
Peer-reviewed
Oui
Volume
95
Number
4
Pages
216-225
Language
english
Notes
Publication types: Clinical Trial ; Controlled Clinical Trial ; Journal Article
Publication Status: ppublish
Abstract
Flexor and extensor spasms associated with severe spasticity frequently cause pain and suffering in neurologically impaired patients, and greatly interfere with comfort and activities. When high doses of oral medications are necessary to keep the symptoms under control and are poorly tolerated, the long-term spinal-selective intrathecal infusion of baclofen by means of implanted drug pump and catheter is a safe, efficient and reversible alternative to destructive surgical procedures. Between September 1991 and March 1995, intrathecal baclofen was infused in 18 selected patients out of a series of 42 severely disabled spastic cases. We report here our preliminary experience with the criteria of selection, the initial intrathecal bolus test and the long-term benefit of the selected patients. Our results confirm the dramatic immediate and long-term benefit reported in other series. After a period of treatment of 1 to 42 months, 13 patients had a complete disappearance of their spastic symptoms without any oral treatment, one patient kept unchanged clonus despite the use of low-dose oral treatment and another one a severe, not improved dysuria although in both of them hypertonia and spasms were abolished. Finally, 2 patients had important joint stiffness slightly impairing the benefit from the treatment. None of the 18 patients had central side-effects related to baclofen. With time, a slight increase in daily dose (inferior to 10%) was necessary in most patients.
Keywords
Adult, Aged, Baclofen/administration & dosage, Baclofen/therapeutic use, Disability Evaluation, Female, Humans, Infusion Pumps, Implantable, Injections, Spinal, Male, Middle Aged, Muscle Relaxants, Central/therapeutic use, Muscle Spasticity/drug therapy, Patient Selection
Pubmed
Web of science
Create date
20/01/2008 18:35
Last modification date
20/08/2019 14:24
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