Continuous intestinal infusion of levodopa-carbidopa in patients with advanced Parkinson's disease in Spain: Subanalysis by autonomous community.

Uso de la infusión intestinal continua de levodopa-carbidopa en pacientes con enfermedad de Parkinson avanzada en España. Subanálisis por comunidades autónomas.
Carbidopa Continuous infusion Efectividad Effectiveness Enfermedad de Parkinson Infusión continua Levodopa Motor symptoms Parkinson's disease Síntomas motores

Journal

Neurologia
ISSN: 2173-5808
Titre abrégé: Neurologia (Engl Ed)
Pays: Spain
ID NLM: 101778590

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 09 08 2017
revised: 07 11 2017
accepted: 07 11 2017
pubmed: 18 1 2018
medline: 9 9 2021
entrez: 18 1 2018
Statut: ppublish

Résumé

To compare the characteristics of patients undergoing treatment with continuous intestinal infusion of levodopa-carbidopa (CIILC) for advanced Parkinson's disease and the data on the effectiveness and safety of CIILC in the different autonomous communities (AC) of Spain. A retrospective, longitudinal, observational study was carried out into 177 patients from 11 CAs who underwent CIILC between January 2006 and December 2011. We analysed data on patients' clinical and demographic characteristics, variables related to effectiveness (changes in off time/on time with or without disabling dyskinesia; changes in Hoehn and Yahr scale and Unified Parkinson's Disease Rating Scale scores; non-motor symptoms; and Clinical Global Impression scale scores) and safety (adverse events), and the rate of CIILC discontinuation. Significant differences were observed between CAs for several baseline variables: duration of disease progression prior to CIILC onset, off time (34.9-59.7%) and on time (2.6-48.0%; with or without disabling dyskinesia), Hoehn and Yahr score during on time, Unified Parkinson's Disease Rating Scale-III score during both on and off time, presence of≥ 4 motor symptoms, and CIILC dose. Significant differences were observed during follow-up (> 24 months in 9 of the 11 CAs studied) for the percentage of off time and on time without disabling dyskinesia, adverse events frequency, and Clinical Global Impression scores. The rate of CIILC discontinuation was between 20-40% in 9 CAs (78 and 80% in remaining 2 CAs). This study reveals a marked variability between CAs in terms of patient selection and CIILC safety and effectiveness. These results may have been influenced by patients' baseline characteristics, the availability of multidisciplinary teams, and clinical experience.

Identifiants

pubmed: 29338936
pii: S0213-4853(17)30374-2
doi: 10.1016/j.nrl.2017.11.006
pii:
doi:

Substances chimiques

Antiparkinson Agents 0
Gels 0
Levodopa 46627O600J
Carbidopa MNX7R8C5VO

Types de publication

Journal Article Observational Study

Langues

eng spa

Sous-ensembles de citation

IM

Pagination

101-111

Informations de copyright

Copyright © 2017 Sociedad Española de Neurología. Publicado por Elsevier España, S.L.U. All rights reserved.

Auteurs

D Santos-García (D)

Sección de Neurología, Hospital Arquitecto Marcide, Complejo Hospitalario Universitario de Ferrol (CHUF), Ferrol, A Coruña España. Electronic address: diegosangar@yahoo.es.

M J Catalán (MJ)

Servicio de Neurología, Hospital Clínico San Carlos, Madrid, España.

V Puente (V)

Unidad de Trastornos del Movimiento, Servicio de Neurología, Parc de Salut Mar, Institut Municipal d'Investigació Medica Hospital del Mar, Universitat Autònoma de Barcelona, Barcelona, España.

F Valldeoriola (F)

Unidad de Trastornos del Movimiento, Servicio de Neurología, Hospital Clínic, Barcelona, España.

I Regidor (I)

Unidad de Neurocirugía Funcional, Hospital Universitario Ramón y Cajal, Madrid, España.

P Mir (P)

Unidad de Trastornos del Movimiento, Servicio de Neurología, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío, Consejo Superior de Investigaciones Científicas, Universidad de Sevilla, Sevilla, España; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, España.

J Matías-Arbelo (J)

Servicio de Neurología, Hospital Universitario Insular de Gran Canaria, Las Palmas de Gran Canaria, Las Palmas, España.

J C Parra (JC)

AbbVie Spain, S. L. U., Madrid, España.

F Grandas (F)

Servicio de Neurología, Hospital General Universitario Gregorio Marañón, Madrid, España.

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Classifications MeSH