MDS Virtual Congress 2020 » Quality Of Life/Caregiver Burden in Movement Disorders

Meeting: MDS Virtual Congress 2020

Care-giver Burden in Parkinson’s Disease and Atypical Parkinsonism in Indian Patients Using Zarit Burden Interview scale

D. Hoskere Sreenivasa, M. Philip, P. Kukkle (Bangalore, India)

Comparative analysis of the quality of life between healthy elderly people and those with Parkinson’s disease

L. Santos, A. Alonso, N. Luna, J. Greve (São Paulo, Brazil)

Concerns in patients with Parkinson’s disease in China: A content analysis of data from social listening

Y. Qian, X. Yang, S. Xu, X. He, Y. Zhang, C. Mo, Q. Xiao (Shanghai, China)

Determinants of quality of life in a large, online cohort of patients with Parkinson’s disease

M. Bock, E. Brown, C. Tanner (San Francisco, CA, USA)

Health care provision and health related quality of life in late stage Parkinson’s disease

K. Rosqvist, P. Odin, A. Schrag (Lund, Sweden)

Improvement in the handicap is maintained after 5 years of deep brain stimulation in Parkinson’s disease

D. Silva, M. Fabbri, L. Guedes, A. Caldas, P. Lobo, B. Cattoni, H. Carvalho, A. Ferreira, M. Rosa, J. Ferreira, M. Coelho (Lisbon, Portugal)

Loneliness/Social Isolation as a Risk Factor for Worsened Parkinson Disease Severity

I. Subramanian, L. Mischley, J. Farahnik (Los Angeles, CA, USA)

Longitudinal association between UPDRS and health-related quality of life in people with Parkinson´s disease

A. Reyes, L. Rutten-Jacobs, S. Roumpanis, S. Jauss, P. Coloma (Basel, Switzerland)

Nutrient patterns in Parkinson’s disease: A case-control study

S. Diaconu, A. Maceasa, B. Ciopleias, R. Zosin, C. Falup-Pecurariu (Braşov, Romania)

Patients’ perspectives on shared decision-making in Parkinson´s disease

E. Gülke, C. Wargel, A. Rahn, A. Solari, C. Buhmann, C. Gerloff, C. Heesen, M. Pötter-Nerger (Hamburg, Germany)

Perceived Stigma in Patients with Functional Movement Disorder: A Qualitative Study

L. Flaherty, C. Girgis, D. DiGasbarro, D. Mohanty, K. LaFaver (Louisville, KY, USA)

Predictors of quality of life in Machado-Joseph disease: A longitudinal observational study

I. Cunha, P. Silva, J. A Ribeiro, M. Santana, L. P Almeida, C. Januário (Coimbra, Portugal)

Quality of Life in Mexican Patients with Essential Tremor

S. Lopez-Alamillo, O. Esquivel-Zapata, C. Sarabia-Tapia, A. Cervantes-Arriaga, R. Abundes-Corona, F. Herrera-Rodriguez, E. Escobar, O. Cárdenas, Y. Ríos, I. González, M. Rodriguez-Violante (Mexico City, Mexico)

Quality of Life Study of Patients Living with Parkinson’s Disesae in Sub-Saharan Africa

M. Fall, T.M Sarr (Dakar, Senegal)

Quantifying the incremental burden of advancing Parkinson’s disease in patients meeting the “5-2-1” Criteria: Results from an international dataset from G7 countries

I. Malaty, M. Skorvanek, A. Alobaidi, K. Onuk, L. Bergmann, S. Femia, M. Lee, E. Jones, J. Pike, P. Martinez-Martin (Gainesville, FL, USA)

Resource patients involved in a program of therapeutic education of patients with Parkinson’s disease: contribution to patients’ recruitment

A.L Ramelli, M.L Fouquet, S. Vasa, P. Simoni, S. Stefanizzi, A. Petit, H. Salhi, G. Fénelon, P.h Remy (Creteil, France)