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<dc:title>Application of the ‘5-2-1’ screening criteria in advanced Parkinson’s disease: interim analysis of DUOGLOBE</dc:title>
<dc:creator>Aldred, Jason</dc:creator>
<dc:creator>Anca-Herschkovitsch, Marieta</dc:creator>
<dc:creator>Antonini, Angelo</dc:creator>
<dc:creator>Bajenaru, Ovidiu</dc:creator>
<dc:creator>Bourgeois, Paul</dc:creator>
<dc:creator>Cubo Delgado, Esther</dc:creator>
<dc:creator>Davis, Thomas L.</dc:creator>
<dc:creator>Iansek, Robert</dc:creator>
<dc:creator>Kovács, Norbert</dc:creator>
<dc:creator>Kukreja, Pavnit</dc:creator>
<dc:creator>Onuk, Koray</dc:creator>
<dc:creator>Pontieri, Francesco E.</dc:creator>
<dc:creator>Robieson, Weining</dc:creator>
<dc:creator>Siddiqui, Mustafa S.</dc:creator>
<dc:creator>Simu, Mihaela</dc:creator>
<dc:creator>Standaert, David G.</dc:creator>
<dc:creator>Chaudhuri, K. Ray</dc:creator>
<dc:subject>5-2-1</dc:subject>
<dc:subject>Criteria for advanced PD</dc:subject>
<dc:subject>Dyskinesia</dc:subject>
<dc:subject>LCIG</dc:subject>
<dc:subject>Levodopa</dc:subject>
<dc:subject>Levodopa-carbidopa intestinal gel</dc:subject>
<dc:subject>Off time</dc:subject>
<dc:subject>Parkinson’s disease</dc:subject>
<dc:description>Aim: A Delphi expert consensus panel proposed that fulfilling ≥1 of the ‘5-2-1 criteria’ (≥five-times daily oral levodopa use, ≥two daily hours with ‘Off’ symptoms or ≥one daily hour with troublesome dyskinesia) suggests advanced Parkinson’s disease (PD). Patients &amp; methods: DUOdopa/Duopa in Patients with Advanced PD – a GLobal OBservational Study Evaluating Long-Term Effectiveness (DUOGLOBE) – is a single-arm, postmarketing, observational, long-term effectiveness study of levodopa–carbidopa intestinal gel (LCIG) for advanced PD. Results: This 6-month interim analysis (n = 139) affirms that most (98%) enrolled patients fulfill ≥1 of the 5-2-1 criteria. These patients responded favorably to LCIG treatment. Safety was consistent with other LCIG studies. Conclusion: In advanced PD patients, the 5-2-1 criteria generally aligns with clinician assessment.</dc:description>
<dc:date>2024-03-11T11:15:23Z</dc:date>
<dc:date>2024-03-11T11:15:23Z</dc:date>
<dc:date>2020-09</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1758-2024</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/8797</dc:identifier>
<dc:identifier>10.2217/nmt-2020-0021</dc:identifier>
<dc:identifier>1758-2032</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Neurodegenerative Disease Management. 2020, V. 10, n. 5, p. 309-323</dc:relation>
<dc:relation>https://doi.org/10.2217/nmt-2020-0021</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>Future Medicine</dc:publisher>
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