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Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience

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<b><i>Background:</i></b> Levodopa therapy in Parkinson's disease (PD) is often associated with disabling motor and non-motor complications in patients with advanced disease due to the variable absorption of levodopa because of an irregular or erratic emptying of the gastric content. <b><i>Methods:</i></b> Prospective single movement disorder center study using pre-set selection criteria, unified PD scale (UPDRS III), non-motor symptoms scale (NMSS), and PD questionnaire-8 (PDQ-8) to evaluate the efficacy, safety, and long-term treatment outcomes using levodopa-carbidopa intestinal gel (LCIG) infusion in patients with advanced PD, who were followed up every 6 months. <b><i>Results:</i></b> Twenty patients were recruited over a period of 6 years. Disease duration prior to LCIG infusion ranged from 5 to 18 years (mean 11.4 ± 4.2). The mean follow-up time on LCIG therapy was 48.5 ± 23.2 months (range 11-83 months). Mean ‘off' time, UPDRS III, NMSS, and PDQ-8 improvement were statistically significant. Two patients dropped out and 66.7% of patients required tube replacement. <b><i>Conclusion:</i></b> LCIG infusion monotherapy demonstrated significant improvement in reducing the ‘off' time, reducing levodopa-induced dyskinesia, and improving non-motor symptoms and quality of life. This therapy is recommended for patients in whom motor fluctuations are inadequately treated with traditional oral PD therapy.
Title: Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience
Description:
<b><i>Background:</i></b> Levodopa therapy in Parkinson's disease (PD) is often associated with disabling motor and non-motor complications in patients with advanced disease due to the variable absorption of levodopa because of an irregular or erratic emptying of the gastric content.
<b><i>Methods:</i></b> Prospective single movement disorder center study using pre-set selection criteria, unified PD scale (UPDRS III), non-motor symptoms scale (NMSS), and PD questionnaire-8 (PDQ-8) to evaluate the efficacy, safety, and long-term treatment outcomes using levodopa-carbidopa intestinal gel (LCIG) infusion in patients with advanced PD, who were followed up every 6 months.
<b><i>Results:</i></b> Twenty patients were recruited over a period of 6 years.
Disease duration prior to LCIG infusion ranged from 5 to 18 years (mean 11.
4 ± 4.
2).
The mean follow-up time on LCIG therapy was 48.
5 ± 23.
2 months (range 11-83 months).
Mean ‘off' time, UPDRS III, NMSS, and PDQ-8 improvement were statistically significant.
Two patients dropped out and 66.
7% of patients required tube replacement.
<b><i>Conclusion:</i></b> LCIG infusion monotherapy demonstrated significant improvement in reducing the ‘off' time, reducing levodopa-induced dyskinesia, and improving non-motor symptoms and quality of life.
This therapy is recommended for patients in whom motor fluctuations are inadequately treated with traditional oral PD therapy.

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