3.8 Article

Levodopa-carbidopa intestinal gel in a subgroup of patients with dyskinesia a baseline from the GLORIA Registry

Journal

NEURODEGENERATIVE DISEASE MANAGEMENT
Volume 9, Issue 1, Pages 39-46

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/nmt-2018-0034

Keywords

dyskinesia; levodopa; Parkinson's disease; quality of life

Funding

  1. AbbVie Inc., North Chicago, IL, USA
  2. National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
  3. Parkinson's UK
  4. PDNMG
  5. EU Horizon 2020
  6. IMI initiative
  7. UCB
  8. Britannia
  9. AbbVie
  10. GSK Pharmaceuticals
  11. Boehringer Ingelheim
  12. Neuronova
  13. Mundipharma

Ask authors/readers for more resources

Aim: To evaluate long-term effects of levodopa-carbidopa intestinal gel on dyskinesia burden. Patients & methods: Post hoc analysis of the GLORIA registry assessed subgroups of advanced Parkinson's disease patients with <4 and >= 4 h/day of levodopa-induced dyskinesia at baseline. Results & conclusions: Mean dyskinesia duration significantly (p < 0.0001) decreased by 3.5 h in patients with >= 4 h baseline dyskinesia; conversely, dyskinesia duration increased by 1.6 h in patients with <4 h baseline dyskinesia. Quality of life improved in both subgroups. Adverse drug reactions occurred at similar rates in both subgroups. Despite increases in levodopa dose, levodopa-carbidopa intestinal gel treatment led to significant and sustained reductions in dyskinesia time, severity and associated pain in advanced Parkinson's disease patients with high baseline dyskinesia burden.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available