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dc.contributor.author
Rey, María Verónica
dc.contributor.author
Perez Lloret, Santiago
dc.contributor.author
Pavy Le Traon, Anne
dc.contributor.author
Meissner, Wassilios G.
dc.contributor.author
Tison, Francois
dc.contributor.author
Rascol, Olivier
dc.date.available
2017-05-08T20:44:01Z
dc.date.issued
2014-03
dc.identifier.citation
Rey, María Verónica; Perez Lloret, Santiago; Pavy Le Traon, Anne; Meissner, Wassilios G.; Tison, Francois; et al.; A cross-sectional study on drug use in multiple system atrophy; Springer Verlag Berlín; Cns Drugs; 28; 5; 3-2014; 483-490
dc.identifier.issn
1172-7047
dc.identifier.uri
http://hdl.handle.net/11336/16095
dc.description.abstract
BACKGROUND: Drug use has rarely been studied in multiple system atrophy (MSA) while such patients receive many treatments based on weak evidence. OBJECTIVE: To analyze drug use from the database of the French MSA Reference Center, and to compare it with data from patients with Parkinson disease (PD). METHODS: Medication of 147 MSA and 180 age- and sex-matched PD patients was analyzed. Motor and autonomic symptoms were explored in MSA patients by the SCOPA-Autonomic and Unified MSA Rating Scale (UMSARS). RESULTS: MSA and PD patients received a mean of five different drugs. MSA patients were more frequently exposed to laxatives, antidiabetic medications, antihypotensives, muscarinic antagonists, alpha-adrenergic blockers, and antidepressants. Levodopa consumption was less in MSA-C (cerebellar) patients compared with MSA-P (parkinsonian) and PD patients. Dopamine agonists were more consumed by PD than MSA patients. MSA patients with more severe disability received more laxatives, anticoagulants, and antidepressants. MSA-P patients received more analgesics. “Probable” MSA patients received more antihypotensives and less alpha-adrenergic blockers. Patients with higher SCOPA-Autonomic scores were more frequently on antihypotensives or antidepressants. Drug associations leading to potential adverse interactions were uncommon (usually <5 %). CONCLUSIONS: Some differences in drug use between MSA and PD patients were observed and expected, including those used for the relief of parkinsonian motor symptoms, autonomic dysfunction, and depression. Many of these drugs are frequently used in MSA in the absence of well-established, positive, benefit-risk evaluations, thus calling for better assessments. The reason why other medications, including anti-diabetic medications, were more consumed by MSA patients remains unclear and deserves further exploration.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Springer Verlag Berlín
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Multiple System Atrophy
dc.subject
Medications Consumption
dc.subject
Drug Consumption
dc.subject.classification
Neurología Clínica
dc.subject.classification
Medicina Clínica
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
A cross-sectional study on drug use in multiple system atrophy
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2017-04-26T14:13:53Z
dc.identifier.eissn
1179-1934
dc.journal.volume
28
dc.journal.number
5
dc.journal.pagination
483-490
dc.journal.pais
Alemania
dc.journal.ciudad
Berlín
dc.description.fil
Fil: Rey, María Verónica. Inserm; Francia. University of Toulouse; Francia
dc.description.fil
Fil: Perez Lloret, Santiago. Inserm; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Toulouse; Francia
dc.description.fil
Fil: Pavy Le Traon, Anne. Inserm; Francia. University of Toulouse; Francia
dc.description.fil
Fil: Meissner, Wassilios G.. Universite de Bordeaux; Francia. Centre National de la Recherche Scientifique; Francia
dc.description.fil
Fil: Tison, Francois. Universite de Bordeaux; Francia. Centre National de la Recherche Scientifique; Francia
dc.description.fil
Fil: Rascol, Olivier. Inserm; Francia. University of Toulouse; Francia
dc.journal.title
Cns Drugs
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s40263-014-0159-1
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs40263-014-0159-1
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