Use of levodopa-carbidopa intestinal gel to treat patients with multiple system atrophy.


Journal

Parkinsonism & related disorders
ISSN: 1873-5126
Titre abrégé: Parkinsonism Relat Disord
Pays: England
ID NLM: 9513583

Informations de publication

Date de publication:
07 2022
Historique:
received: 07 01 2022
revised: 14 05 2022
accepted: 19 05 2022
pubmed: 19 6 2022
medline: 29 6 2022
entrez: 18 6 2022
Statut: ppublish

Résumé

Levodopa-carbidopa intestinal gel (LCIG) is an effective treatment for late-stage Parkinson's disease (PD) but had not been evaluated in levodopa-responsive patients with the parkinsonian variant of multiple system atrophy (MSA-P) and motor fluctuations. We aimed to assess the safety of LCIG in MSA-P patients. In a retrospective, single-center study, we analyzed clinical and treatment-related data for all patients with MSA-P or PD treated with LCIG between December 2004 and November 2017. Adverse events (AEs) were classified into three classes: AEs related to gastrointestinal effects or to the PEG-J procedure, AEs related to the device, and AEs related to the pharmacological effect of LCIG. 7 MSA-P and 63 PD patients had been treated with LCIG for a median [interquartile range] period of 31 [16;43] and 19 [8;45] months, respectively. There were no significant intergroup differences in safety. Enteral nutrition was introduced at the same time as LCIG treatment in 4 (57%) MSA-P patients. In the MSA-P and PD groups, LCIG was associated with a better Global Clinical Impression score and discontinuation of oral anti-parkinsonian drugs (in 43% and 27% of cases, respectively). LCIG treatment is feasible in MSA-P patients with severe motor complications. The safety profile is similar to that seen in PD.

Sections du résumé

BACKGROUND
Levodopa-carbidopa intestinal gel (LCIG) is an effective treatment for late-stage Parkinson's disease (PD) but had not been evaluated in levodopa-responsive patients with the parkinsonian variant of multiple system atrophy (MSA-P) and motor fluctuations. We aimed to assess the safety of LCIG in MSA-P patients.
METHODS
In a retrospective, single-center study, we analyzed clinical and treatment-related data for all patients with MSA-P or PD treated with LCIG between December 2004 and November 2017. Adverse events (AEs) were classified into three classes: AEs related to gastrointestinal effects or to the PEG-J procedure, AEs related to the device, and AEs related to the pharmacological effect of LCIG.
RESULTS
7 MSA-P and 63 PD patients had been treated with LCIG for a median [interquartile range] period of 31 [16;43] and 19 [8;45] months, respectively. There were no significant intergroup differences in safety. Enteral nutrition was introduced at the same time as LCIG treatment in 4 (57%) MSA-P patients. In the MSA-P and PD groups, LCIG was associated with a better Global Clinical Impression score and discontinuation of oral anti-parkinsonian drugs (in 43% and 27% of cases, respectively).
CONCLUSIONS
LCIG treatment is feasible in MSA-P patients with severe motor complications. The safety profile is similar to that seen in PD.

Identifiants

pubmed: 35716627
pii: S1353-8020(22)00149-3
doi: 10.1016/j.parkreldis.2022.05.018
pii:
doi:

Substances chimiques

Antiparkinson Agents 0
Drug Combinations 0
Gels 0
Levodopa 46627O600J
Carbidopa MNX7R8C5VO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-44

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Auteurs

A S Blaise (AS)

CHU Lille, Neurology and Movement Disorders Department, F-59000, Lille, France. Electronic address: annesophie.blaise@chru-lille.fr.

E Cuvelier (E)

CHU Lille, Institut de Pharmacie, F-59000, Lille, France; Univ. Lille, CHU Lille, ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, F-59000, Lille, France.

N Carrière (N)

CHU Lille, Neurology and Movement Disorders Department, F-59000, Lille, France; Univ. Lille, INSERM, CHU Lille, UMR-S1172, Lille Neurosciences & Cognition, F-59000, Lille, France.

D Devos (D)

CHU Lille, Neurology and Movement Disorders Department, F-59000, Lille, France; Univ. Lille, INSERM, CHU Lille, UMR-S1172, Lille Neurosciences & Cognition, F-59000, Lille, France.

F Moreau (F)

CHU Lille, Institut de Pharmacie, F-59000, Lille, France.

L Defebvre (L)

CHU Lille, Neurology and Movement Disorders Department, F-59000, Lille, France; Univ. Lille, INSERM, CHU Lille, UMR-S1172, Lille Neurosciences & Cognition, F-59000, Lille, France.

E Mutez (E)

CHU Lille, Neurology and Movement Disorders Department, F-59000, Lille, France; Univ. Lille, INSERM, CHU Lille, UMR-S1172, Lille Neurosciences & Cognition, F-59000, Lille, France.

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Classifications MeSH