Safety and effectiveness of levodopa-carbidopa intestinal gel for advanced Parkinson's disease: A large single-center study.


Journal

Revue neurologique
ISSN: 0035-3787
Titre abrégé: Rev Neurol (Paris)
Pays: France
ID NLM: 2984779R

Informations de publication

Date de publication:
May 2020
Historique:
received: 13 05 2019
revised: 21 07 2019
accepted: 23 07 2019
pubmed: 2 11 2019
medline: 5 1 2021
entrez: 1 11 2019
Statut: ppublish

Résumé

Treatment with levodopa-carbidopa intestinal gel (LCIG) can effectively relieve motor and non-motor symptoms in advanced Parkinson's disease (PD). However, adverse events (AEs) are frequent. To describe AEs associated with LCIG treatment and the main reasons for treatment discontinuation. We also looked for factors that were potentially predictive of serious AEs and assessed the effectiveness of and satisfaction with LCIG. We retrospectively analyzed data on AEs in patients treated with LCIG at a French university medical center. For patients still receiving treatment at last follow-up, effectiveness was assessed according to the Clinical Global Impression (CGI) scale and the Movement Disorders Society - Unified Parkinson's Disease Rating Scale motor score. Of the 63 patients treated with LCIG for a mean (range) of 19 months (8-47), 57 (90%) experienced at least one AE (340 AEs in total). Most of the AEs (in 69.8% of the patients) were related to percutaneous endoscopic gastrostomy with a jejunal tube (PEG-J) or affected the gastrointestinal tract (granuloma, leakage, or a local infection). Device-related AEs (such as PEG-J removal and device occlusion) were frequent (in 63.5% of patients). Forty-three patients (68%) required at least one additional endoscopic procedure. Dopatherapy-related AEs occurred in 30 patients (48%). Most of the AEs occurred long after treatment initiations, and only a small proportion led to discontinuation. On the CGI scale, 53 patients (84.4%) considered that their condition had improved during LCIG treatment. Despite the high frequency of AEs, patients with advanced PD gain clinical benefit from treatment with LCIG. This treatment requires a competent, multidisciplinary team on site.

Sections du résumé

BACKGROUND BACKGROUND
Treatment with levodopa-carbidopa intestinal gel (LCIG) can effectively relieve motor and non-motor symptoms in advanced Parkinson's disease (PD). However, adverse events (AEs) are frequent.
OBJECTIVE OBJECTIVE
To describe AEs associated with LCIG treatment and the main reasons for treatment discontinuation. We also looked for factors that were potentially predictive of serious AEs and assessed the effectiveness of and satisfaction with LCIG.
METHOD METHODS
We retrospectively analyzed data on AEs in patients treated with LCIG at a French university medical center. For patients still receiving treatment at last follow-up, effectiveness was assessed according to the Clinical Global Impression (CGI) scale and the Movement Disorders Society - Unified Parkinson's Disease Rating Scale motor score.
RESULTS RESULTS
Of the 63 patients treated with LCIG for a mean (range) of 19 months (8-47), 57 (90%) experienced at least one AE (340 AEs in total). Most of the AEs (in 69.8% of the patients) were related to percutaneous endoscopic gastrostomy with a jejunal tube (PEG-J) or affected the gastrointestinal tract (granuloma, leakage, or a local infection). Device-related AEs (such as PEG-J removal and device occlusion) were frequent (in 63.5% of patients). Forty-three patients (68%) required at least one additional endoscopic procedure. Dopatherapy-related AEs occurred in 30 patients (48%). Most of the AEs occurred long after treatment initiations, and only a small proportion led to discontinuation. On the CGI scale, 53 patients (84.4%) considered that their condition had improved during LCIG treatment.
CONCLUSION CONCLUSIONS
Despite the high frequency of AEs, patients with advanced PD gain clinical benefit from treatment with LCIG. This treatment requires a competent, multidisciplinary team on site.

Identifiants

pubmed: 31668287
pii: S0035-3787(19)30655-1
doi: 10.1016/j.neurol.2019.07.024
pii:
doi:

Substances chimiques

Antiparkinson Agents 0
Drug Combinations 0
Gels 0
carbidopa, levodopa drug combination 0
Levodopa 46627O600J
Carbidopa MNX7R8C5VO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

268-276

Informations de copyright

Copyright © 2019 Elsevier Masson SAS. All rights reserved.

Auteurs

A-S Blaise (AS)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France. Electronic address: annesophie.blaise@outlook.fr.

G Baille (G)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

N Carrière (N)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

D Devos (D)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France; Pharmacology Department, Lille University, 59000 Lille, France.

K Dujardin (K)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

G Grolez (G)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

A Kreisler (A)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

M Kyheng (M)

Department of Biostatistics, University & EA 2694, Lille University, 59000 Lille, France.

C Moreau (C)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

E Mutez (E)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

D Seguy (D)

Nutrition department, Lille University, 59000 Lille, France.

L Defebvre (L)

Neurology and Movement Disorders Department, Lille University, 59000 Lille, France; U1171, INSERM, Lille University, 59000 Lille, France.

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Classifications MeSH