Concomitant Medication Usage with Levodopa-Carbidopa Intestinal Gel: Results from the COSMOS Study
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, pozorovací studie, práce podpořená grantem
PubMed
33908647
PubMed Central
PMC8453961
DOI
10.1002/mds.28596
Knihovny.cz E-zdroje
- Klíčová slova
- levodopa-carbidopa intestinal gel; monotherapy; Parkinson's disease; drug polytherapy; observational studies,
- MeSH
- antiparkinsonika MeSH
- fixní kombinace léků MeSH
- gely MeSH
- karbidopa * MeSH
- levodopa MeSH
- lidé MeSH
- Parkinsonova nemoc * farmakoterapie MeSH
- retrospektivní studie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiparkinsonika MeSH
- fixní kombinace léků MeSH
- gely MeSH
- karbidopa * MeSH
- levodopa MeSH
BACKGROUND: Levodopa-carbidopa intestinal gel (LCIG) is administered directly to the small intestine of patients with advanced Parkinson's disease (APD) to help maintain stable plasma levodopa levels. OBJECTIVE: The objective of this study was to investigate the effect of LCIG in reducing polypharmacy for the treatment of APD. METHODS: The COmedication Study assessing Mono- and cOmbination therapy with levodopa-carbidopa inteStinal gel (COSMOS) is a large, real-world, multinational observational study investigating comedication use with LCIG. All enrolled patients had used LCIG for ≥12 months and data were collected cross-sectionally (study visit) and retrospectively. The primary endpoint was the percentage of patients using LCIG as monotherapy (without add-on PD medications) at initiation and at 3, 6, 9, and 12 months thereafter. RESULTS: Overall, 409 patients were enrolled from 14 countries and were treated with LCIG for a mean of 35.8 ± 23.2 months. A total of 15.2% of patients initiated LCIG as monotherapy and 31.7% were receiving monotherapy at 12 months after initiation. The mean duration of LCIG monotherapy was 39.3 ± 25.6 months. Use of add-on medications decreased over time with all LCIG regimens. From LCIG initiation to the patient visit, mean off time decreased by 3.8, 4.6, and 3.9 hours/day for LCIG monotherapy, LCIG daytime monotherapy, and LCIG polytherapy groups, respectively, while duration of dyskinesia decreased by 1.7, 2.0, and 1.9 hours/day, respectively. Adverse events likely related to study treatment occurred in 112 patients (27.4%) during LCIG treatment. CONCLUSIONS: LCIG is an effective long-term monotherapy option with a positive risk-benefit profile and contributes to reduced polypharmacy for patients with APD. © 2021 The AbbVie Inc. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
AbbVie Inc North Chicago Illinois USA
Department of Clinical Neuroscience Section for Neurology Karolinska Institutet Stockholm Sweden
Department of Neurology Hospital Universitario Fundación Alcorcón Madrid Spain
Zobrazit více v PubMed
Wang L, Li J, Chen J. Levodopa‐carbidopa intestinal gel in Parkinson's disease: a systematic review and meta‐analysis. Front Neurol 2018;9:620. PubMed PMC
Hauser RA. Levodopa: past, present, and future. Eur Neurol 2009;62:1–8. PubMed
Morin L, Johnell K, Laroche ML, Fastbom J, Wastesson JW. The epidemiology of polypharmacy in older adults: register‐based prospective cohort study. Clin Epidemiol 2018;10:289–298. PubMed PMC
Daley DJ, Myint PK, Gray RJ, Deane KH. Systematic review on factors associated with medication non‐adherence in Parkinson's disease. Parkinsonism Relat Disord 2012;18:1053–1061. PubMed
Suttrup I, Warnecke T. Dysphagia in Parkinson's disease. Dysphagia 2016;31:24–32. PubMed
Davis KL, Edin HM, Allen JK. Prevalence and cost of medication nonadherence in Parkinson's disease: evidence from administrative claims data. Mov Disord 2010;25:474–480. PubMed
Malek N, Grosset DG. Medication adherence in patients with Parkinson's disease. CNS Drugs 2015;29:47–53. PubMed
Wirdefeldt K, Odin P, Nyholm D. Levodopa‐carbidopa intestinal gel in patients with Parkinson's disease: a systematic review. CNS Drugs 2016;30:381–404. PubMed
Nyholm D, Nilsson Remahl AI, Dizdar N, Constantinescu R, Holmberg B, Jansson R, et al. Duodenal levodopa infusion monotherapy vs oral polypharmacy in advanced Parkinson disease. Neurology 2005;64:216–223. PubMed
Olanow CW, Kieburtz K, Odin P, Espay AJ, Standaert DG, Fernandez HH, et al. Continuous intrajejunal infusion of levodopa‐carbidopa intestinal gel for patients with advanced Parkinson's disease: a randomised, controlled, double‐blind, double‐dummy study. Lancet Neurol 2014;13:141–149. PubMed PMC
Fernandez HH, Standaert DG, Hauser RA, Lang AE, Fung VS, Klostermann F, et al. Levodopa‐carbidopa intestinal gel in advanced Parkinson's disease: final 12‐month, open‐label results. Mov Disord 2015;30:500–509. PubMed PMC
Slevin JT, Fernandez HH, Zadikoff C, Hall C, Eaton S, Dubow J, et al. Long‐term safety and maintenance of efficacy of levodopa‐carbidopa intestinal gel: an open‐label extension of the double‐blind pivotal study in advanced Parkinson's disease patients. J Parkinsons Dis 2015;5:165–174. PubMed
Standaert DG, Rodriguez RL, Slevin JT, Lobatz M, Eaton S, Chatamra K, et al. Effect of levodopa‐carbidopa intestinal gel on non‐motor symptoms in patients with advanced Parkinson's disease. Mov Disord Clin Pract 2017;4:829–837. PubMed PMC
Buhmann C, Hilker R, Lingor P, Schrader C, Schwarz J, Wolz M, et al. Levodopa/carbidopa intestinal gel (LCIG) infusion as mono‐ or combination therapy. J Neural Transm (Vienna) 2017;124:1005–1013. PubMed
Antonini A, Poewe W, Chaudhuri KR, Jech R, Pickut B, Pirtosek Z, et al. Levodopa‐carbidopa intestinal gel in advanced Parkinson's: final results of the GLORIA registry. Parkinsonism Relat Disord 2017;45:13–20. PubMed
Poewe W, Bergmann L, Kukreja P, Robieson WZ, Antonini A. Levodopa‐carbidopa intestinal gel monotherapy: GLORIA registry demographics, efficacy and safety. J Parkinsons Dis 2019;9:531–554. PubMed PMC
Katzenschlager R, Hughes A, Evans A, Manson AJ, Hoffman M, Swinn L, et al. Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: a prospective study using single‐dose challenges. Mov Disord 2005;20:151–157. PubMed
Deuschl G, Schade‐Brittinger C, Krack P, Volkmann J, Schäfer H, Bötzel K, et al. A randomized trial of deep‐brain stimulation for Parkinson's disease. N Engl J Med 2006;355:896–908. PubMed
Kimber TE, Fang J, Huddy LJ, Thompson PD. Long‐term adherence to apomorphine infusion in patients with Parkinson disease: a 10‐year observational study. Intern Med J 2017;47:570–573. PubMed
Antonini A, Isaias IU, Rodolfi G, Landi A, Natuzzi F, Siri C, et al. A 5‐year prospective assessment of advanced Parkinson disease patients treated with subcutaneous apomorphine infusion or deep brain stimulation. J Neurol 2011;258:579–585. PubMed
Hardoff R, Sula M, Tamir A, Soil A, Front A, Badarna S, et al. Gastric emptying time and gastric motility in patients with Parkinson's disease. Mov Disord 2001;16:1041–1047. PubMed
Straka I, Minár M, Škorvánek M, Grofik M, Danterová K, Benetin J, et al. Adherence to pharmacotherapy in patients with Parkinson's disease taking three and more daily doses of medication. Front Neurol 2019;10:799. PubMed PMC
Grosset D, Antonini A, Canesi M, Pezzoli G, Lees A, Shaw K, et al. Adherence to antiparkinson medication in a multicenter European study. Mov Disord 2009;24:826–832. PubMed
Cenci MA, Ohlin KE, Odin P. Current options and future possibilities for the treatment of dyskinesia and motor fluctuations in Parkinson's disease. CNS Neurol Disord Drug Targets 2011;10:670–684. PubMed
Grandas F. Subcutaneous infusions of apomorphine: a reappraisal of its therapeutic efficacy in advanced Parkinson's disease. Expert Rev Neurother 2013;13:1343–1353. PubMed
Anderson VC, Burchiel KJ, Hogarth P, Favre J, Hammerstad JP. Pallidal vs subthalamic nucleus deep brain stimulation in Parkinson disease. Arch Neurol 2005;62:554–560. PubMed
Moro E, Lozano AM, Pollak P, Agid Y, Rehncrona S, Volkmann J, et al. Long‐term results of a multicenter study on subthalamic and pallidal stimulation in Parkinson's disease. Mov Disord 2010;25:578–586. PubMed
Zadikoff C, Poewe W, Boyd JT, Bergmann L, Ijacu H, Kukreja P, et al. Safety of levodopa‐carbidopa intestinal gel treatment in patients with advanced Parkinson's disease receiving ≥2000 mg daily dose of levodopa. Parkinsons Dis 2020;2020:9716317. PubMed PMC
Levodopa-carbidopa intestinal gel in advanced Parkinson's disease: long-term results from COSMOS