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      Patient and caregiver outcomes with levodopa-carbidopa intestinal gel in advanced Parkinson’s disease

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          Abstract

          Levodopa-carbidopa intestinal gel (LCIG) has shown to be efficacious in motor and non-motor symptoms (NMS). Nevertheless, studies with patient Quality of Life (QoL) as a primary endpoint are scarce. To assess the effect of LCIG on Advanced Parkinson’s Disease (APD) patients QoL. Secondarily, the impact on motor symptoms and NMS, emotional well-being, treatment satisfaction, and caregiver QoL, stress, disease burden, anxiety, depression, and work impairment were also investigated. In this prospective, 6-month multicenter postmarketing observational study, LCIG was administered to 59 patients with APD. Endpoints were assessed using validated scales and questionnaires. LCIG significantly improved patient QoL (PDQ-39 mean change ± standard deviation from baseline, −12.8 ± 14.6; P < 0.0001), motor symptoms (UPDRS-III in “On,” −6.5 ± 11.8; P = 0.0002), NMS (NMSS, −35.7 ± 31.1; P < 0.0001), mood (Norris/Bond-Lader VAS, −6.6 ± 21.1; P = 0.0297), fatigue (PFS-16, −0.6 ± 1.0; P = 0.0003), depression (BDI-II, −5.1 ± 9.4; P = 0.0002), anxiety (BAI, −6.2 ± 9.6; P < 0.0001), and patient treatment satisfaction (SATMED-Q, 16.1 ± 16.8; P < 0.0001). There were significant correlations between the change from baseline to 6 months between PDQ-39 and UPDRS-IV, NMSS, BAI, BDI-II, AS, and PFS-16 scores, and Norris/Bond-Lader alertness/sedation factor. Caregiver anxiety also improved (Goldberg anxiety scale, −1.1 ± 1.0; P = 0.0234), but the clinical relevance of this finding is questionable. The serious adverse events reported were similar to those previously described for LCIG. In patients with APD, LCIG improves QoL, motor symptoms and NMS, emotional well-being, and satisfaction with the treatment. Improvement in patient QoL is associated with improvements in motor complications, NMS, anxiety, depression, apathy and fatigue. Improvements in patients’ QoL does not correspond with improvements in caregivers’ QoL or burden.

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          Most cited references78

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          Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results.

          We present a clinimetric assessment of the Movement Disorder Society (MDS)-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS). The MDS-UDPRS Task Force revised and expanded the UPDRS using recommendations from a published critique. The MDS-UPDRS has four parts, namely, I: Non-motor Experiences of Daily Living; II: Motor Experiences of Daily Living; III: Motor Examination; IV: Motor Complications. Twenty questions are completed by the patient/caregiver. Item-specific instructions and an appendix of complementary additional scales are provided. Movement disorder specialists and study coordinators administered the UPDRS (55 items) and MDS-UPDRS (65 items) to 877 English speaking (78% non-Latino Caucasian) patients with Parkinson's disease from 39 sites. We compared the two scales using correlative techniques and factor analysis. The MDS-UPDRS showed high internal consistency (Cronbach's alpha = 0.79-0.93 across parts) and correlated with the original UPDRS (rho = 0.96). MDS-UPDRS across-part correlations ranged from 0.22 to 0.66. Reliable factor structures for each part were obtained (comparative fit index > 0.90 for each part), which support the use of sum scores for each part in preference to a total score of all parts. The combined clinimetric results of this study support the validity of the MDS-UPDRS for rating PD.
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            Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.

            Few detailed clinico-pathological correlations of Parkinson's disease have been published. The pathological findings in 100 patients diagnosed prospectively by a group of consultant neurologists as having idiopathic Parkinson's disease are reported. Seventy six had nigral Lewy bodies, and in all of these Lewy bodies were also found in the cerebral cortex. In 24 cases without Lewy bodies, diagnoses included progressive supranuclear palsy, multiple system atrophy, Alzheimer's disease, Alzheimer-type pathology, and basal ganglia vascular disease. The retrospective application of recommended diagnostic criteria improved the diagnostic accuracy to 82%. These observations call into question current concepts of Parkinson's disease as a single distinct morbid entity.
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              Systematic review of levodopa dose equivalency reporting in Parkinson's disease.

              Interpretation of clinical trials comparing different drug regimens for Parkinson's disease (PD) is complicated by the different dose intensities used: higher doses of levodopa and, possibly, other drugs produce better symptomatic control but more late complications. To address this problem, conversion factors have been calculated for antiparkinsonian drugs that yield a total daily levodopa equivalent dose (LED). LED estimates vary, so we undertook a systematic review of studies reporting LEDs to provide standardized formulae. Electronic database and hand searching of references identified 56 primary reports of LED estimates. Data were extracted and the mean and modal LEDs calculated. This yielded a standardized LED for each drug, providing a useful tool to express dose intensity of different antiparkinsonian drug regimens on a single scale. Using these conversion formulae to report LEDs would improve the consistency of reporting and assist the interpretation of clinical trials comparing different PD medications. © 2010 Movement Disorder Society.
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                Author and article information

                Contributors
                fvallde@clinic.cat
                Journal
                NPJ Parkinsons Dis
                NPJ Parkinsons Dis
                NPJ Parkinson's Disease
                Nature Publishing Group UK (London )
                2373-8057
                30 November 2021
                30 November 2021
                2021
                : 7
                : 108
                Affiliations
                [1 ]Movement Disorders Unit, Neurology Service, Clínic Hospital, 170, Villarroel St., 08036 Barcelona, Spain
                [2 ]Neurology Service, Clínico San Carlos Hospital, Profesor Martín Lagos St., 28040 Madrid, Spain
                [3 ]GRID grid.411380.f, ISNI 0000 0000 8771 3783, Movement Disorders Unit. Neurology Service, , Virgen de las Nieves University Hospital, “Biohealth Investigation Institute. Ibs, ; Granada, Spain
                [4 ]GRID grid.411089.5, ISNI 0000 0004 1768 5165, Neurology Service, Elche University General Hospital, ; 11, Camino Almazara St., 03203 Elche, Alicante Spain
                [5 ]GRID grid.413486.c, ISNI 0000 0000 9832 1443, Neurology Service, Torrecárdenas Hospital Center, ; Hermandad de Donantes de Sangre St., 04009 Almería, Spain
                [6 ]GRID grid.23520.36, ISNI 0000 0000 8569 1592, Neurology Service, , Burgos University Hospital, ; 3, Islas Baleares Av., 09006 Burgos, Spain
                [7 ]GRID grid.411066.4, ISNI 0000 0004 1771 0279, Department of Neurology, , A Coruña University Hospital Center (CHUAC), ; A Coruña, Spain
                [8 ]GRID grid.411129.e, ISNI 0000 0000 8836 0780, Neurology Service, , Bellvitge University Hospital, ; Feixa Llarga St., 08907L’Hospitalet de Llobregat, Barcelona, Spain
                [9 ]GRID grid.413448.e, ISNI 0000 0000 9314 1427, National Center of Epidemiology and Center for Networked Biomedical Research in Neurodegenerative Diseases (CIBERNED), ; Carlos III Institute of Health, 5, Monforte de Lemos Av., 28029 Madrid, Spain
                [10 ]AbbVie Spain, S.L.U., 91, De Burgos Av., 28050 Madrid, Spain
                [11 ]Neurology Service, Insular of Gran Canaria University Hospital, Marítima del Sur Av., 35016 Las Palmas, de Gran Canaria Spain
                Author information
                http://orcid.org/0000-0002-8680-4274
                http://orcid.org/0000-0003-2149-2668
                http://orcid.org/0000-0002-3126-5111
                Article
                246
                10.1038/s41531-021-00246-y
                8633325
                34848716
                5f516621-da27-4794-8a7f-6fead7c6a894
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 7 April 2020
                : 7 June 2021
                Funding
                Funded by: FundRef https://doi.org/10.13039/100006483, AbbVie (AbbVie Inc.);
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                parkinson's disease,outcomes research
                parkinson's disease, outcomes research

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