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<mods:namePart>Chaudhuri, K. Ray</mods:namePart>
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<mods:namePart>Kovács, Norbert</mods:namePart>
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<mods:namePart>Pontieri, Francesco E.</mods:namePart>
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<mods:namePart>Aldred, Jason</mods:namePart>
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<mods:namePart>Bourgeois, Paul</mods:namePart>
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<mods:namePart>Davis, Thomas L.</mods:namePart>
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<mods:namePart>Cubo Delgado, Esther</mods:namePart>
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<mods:namePart>Siddiqui, Mustafa S.</mods:namePart>
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<mods:namePart>Simu, Mihaela</mods:namePart>
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<mods:namePart>Kukreja, Pavnit</mods:namePart>
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<mods:namePart>Ladhani, Omar</mods:namePart>
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<mods:namePart>Jia, Jia</mods:namePart>
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<mods:namePart>Standaert, David G.</mods:namePart>
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<mods:dateAccessioned encoding="iso8601">2024-03-15T09:40:13Z</mods:dateAccessioned>
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<mods:dateIssued encoding="iso8601">2023-07</mods:dateIssued>
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<mods:identifier type="issn">1877-7171</mods:identifier>
<mods:identifier type="uri">http://hdl.handle.net/10259/8834</mods:identifier>
<mods:identifier type="doi">10.3233/JPD-225105</mods:identifier>
<mods:identifier type="essn">1877-718X</mods:identifier>
<mods:abstract>Background:&#xd;
Levodopa-carbidopa intestinal gel (LCIG) improves motor and non-motor symptoms in patients with advanced Parkinson’s disease (aPD).&#xd;
&#xd;
Objective:&#xd;
To present the final 36-month efficacy and safety results from DUOGLOBE (DUOdopa/Duopa in Patients with Advanced Parkinson’s Disease – a GLobal OBservational Study Evaluating Long-Term Effectiveness; NCT02611713).&#xd;
&#xd;
Methods:&#xd;
DUOGLOBE was an international, prospective, long-term, real-world, observational study of patients with aPD initiating LCIG in routine clinical care. The primary endpoint was change in patient-reported “Off” time to Month 36. Safety was assessed by monitoring serious adverse events (SAEs).&#xd;
&#xd;
Results:&#xd;
Significant improvements in “Off” time were maintained over 3 years (mean [SD]: –3.3 hours [3.7]; p &lt; 0.001). There were significant improvements to Month 36 in total scores of the Unified Dyskinesia Rating Scale (–5.9 [23.7]; p = 0.044), Non-Motor Symptoms Scale (–14.3 [40.5]; p = 0.002), Parkinson’s Disease Sleep Scale-2 (–5.8 [12.9]; p &lt; 0.001), and Epworth Sleepiness Scale (–1.8 [6.0]; p = 0.008). Health-related quality of life and caregiver burden significantly improved through Months 24 and 30, respectively (Month 24, 8-item Parkinson’s Disease Questionnaire Summary Index, –6.0 [22.5]; p = 0.006; Month 30, Modified Caregiver Strain Index, –2.3 [7.6]; p = 0.026). Safety was consistent with the well-established LCIG profile (SAEs: 54.9% of patients; discontinuations: 54.4%; discontinuations due to an adverse event: 27.2%). Of 106 study discontinuations, 32 patients (30.2%) continued LCIG outside the study.&#xd;
&#xd;
Conclusion:&#xd;
DUOGLOBE demonstrates real-world, long-term, reductions in motor and non-motor symptoms in patients with aPD treated with LCIG.</mods:abstract>
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<mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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<mods:accessCondition type="useAndReproduction">Atribución 4.0 Internacional</mods:accessCondition>
<mods:subject>
<mods:topic>DUOGLOBE</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Parkinson’s disease</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Levodopa-carbidopa intestinal gel</mods:topic>
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<mods:subject>
<mods:topic>Dyskinesia</mods:topic>
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<mods:subject>
<mods:topic>Real-world data</mods:topic>
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<mods:titleInfo>
<mods:title>Levodopa Carbidopa Intestinal Gel in Advanced Parkinson’s Disease: DUOGLOBE Final 3-Year Results</mods:title>
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