Please use this identifier to cite or link to this item: http://hdl.handle.net/10668/12020
Title: Continuous intestinal infusion of levodopa-carbidopa in patients with advanced Parkinson's disease in Spain: Subanalysis by autonomous community.
Other Titles: Uso de la infusión intestinal continua de levodopa-carbidopa en pacientes con enfermedad de Parkinson avanzada en España. Subanálisis por comunidades autónomas.
Authors: Santos-García, D
Catalán, M J
Puente, V
Valldeoriola, F
Regidor, I
Mir, P
Matías-Arbelo, J
Parra, J C
Grandas, F
Keywords: Carbidopa;Continuous infusion;Efectividad;Effectiveness;Enfermedad de Parkinson;Infusión continua;Levodopa;Motor symptoms;Parkinson's disease;Síntomas motores
metadata.dc.subject.mesh: Antiparkinson Agents
Carbidopa
Gels
Humans
Levodopa
Parkinson Disease
Retrospective Studies
Spain
Issue Date: 12-Jan-2018
Abstract: 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.
URI: http://hdl.handle.net/10668/12020
metadata.dc.identifier.doi: 10.1016/j.nrl.2017.11.006
Appears in Collections:Producción 2020

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