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Praween Lolekha 2 Articles
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Validation of the Thai Version of the Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale
Priya Jagota, Prachaya Srivanitchapoom, Sitthi Petchrutchatachart, Surat Singmaneesakulchai, Apichart Pisarnpong, Praween Lolekha, Suwanna Setthawatcharawanich, Parnsiri Chairangsaris, Natlada Limotai, Pawut Mekawichai, Pattamon Panyakaew, Onanong Phokaewvarangkul, Jirada Sringean, Yuvadee Pitakpatapee, Nancy LaPelle, Pablo Martinez-Martin, Xuehan Ren, Sheng Luo, Glenn T. Stebbins, Christopher G. Goetz, Roongroj Bhidayasiri
J Mov Disord. 2022;15(2):151-155.   Published online March 16, 2022
DOI: https://doi.org/10.14802/jmd.21104
  • 4,419 View
  • 166 Download
  • 5 Web of Science
  • 5 Crossref
AbstractAbstract PDFSupplementary Material
Objective
This study aims to validate the Thai translation of the Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS).
Methods
The English version was translated into Thai and then back-translated into English. The translated version underwent 2 rounds of cognitive pretesting to assess the ease of comprehension, ease of use and comfort with the scale. Then, it underwent large clinimetric testing.
Results
The Thai version was validated in 354 PD patients. The comparative fit index (CFI) for all four parts of the Thai version of the MDS-UPDRS was 0.93 or greater. Exploratory factor analysis identified isolated item differences in factor structure between the Thai and English versions.
Conclusion
The overall factor structure of the Thai version was consistent with that of the English version based on the high CFIs (all CFI ≥ 0.90). Hence, it can be designated the official Thai version of the MDS-UPDRS.

Citations

Citations to this article as recorded by  
  • Validation of the Kazakh Version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale
    Saltanat Abdraimova, Zhanybek Myrzayev, Altynay Karimova, Altynay Talgatkyzy, Talgat Khaibullin, Gulnaz Kaishibayeva, Sandugash Elubaeva, Karlygash Esembekova, Dongrak Choi, Pablo Martinez-Martin, Christopher G. Goetz, Glenn T. Stebbins, Sheng Luo, Chingi
    Clinical Parkinsonism & Related Disorders.2024; 10: 100232.     CrossRef
  • Residual effects of combined vibratory and plantar stimulation while seated influences plantar pressure and spatiotemporal gait measures in individuals with Parkinson’s disease exhibiting freezing of gait
    Warongporn Phuenpathom, Pattamon Panyakaew, Peerapon Vateekul, Decho Surangsrirat, Roongroj Bhidayasiri
    Frontiers in Aging Neuroscience.2024;[Epub]     CrossRef
  • User-centred design, validation and clinical testing of an anti-choking mug for people with Parkinson’s disease
    Roongroj Bhidayasiri, Araya Chaisongkram, Chanawat Anan, Warongporn Phuenpathom
    Scientific Reports.2024;[Epub]     CrossRef
  • Global Epidemiology of Movement Disorders: Rare or Underdiagnosed?
    Sarah A. O'Shea, Ludy C. Shih
    Seminars in Neurology.2023; 43(01): 004.     CrossRef
  • Vibratory and plantar pressure stimulation: Steps to improve freezing of gait in Parkinson's disease
    Warongporn Phuenpathom, Pattamon Panyakaew, Peerapon Vateekul, Decho Surangsrirat, Akarin Hiransuthikul, Roongroj Bhidayasiri
    Parkinsonism & Related Disorders.2022; 105: 43.     CrossRef
Creutzfeldt-Jakob Disease in a Tertiary Care Hospital in Thailand: A Case Series and Review of the Literature
Praween Lolekha, Ahmed Rasheed, Chutanat Yotsarawat
J Mov Disord. 2015;8(3):136-140.   Published online September 10, 2015
DOI: https://doi.org/10.14802/jmd.15014
  • 19,234 View
  • 86 Download
  • 9 Web of Science
  • 8 Crossref
AbstractAbstract PDF
Creutzfeldt-Jakob Disease (CJD) is an incurable and inevitably fatal neurodegenerative disorder. Although CJD has a worldwide distribution, there are no official statistics on CJD in Thailand. A diagnosis of CJD is suspected when a patient develops rapidly progressive dementia with myoclonus. However, CJD may be mistaken for a variety of illnesses because its initial presentation frequently consists of non-specific symptoms. Here, we examined cases of sporadic CJD (sCJD) from Thammasat University Hospital (a tertiary care hospital in Thailand) between January 1, 2012 and December 31, 2014. Three cases of probable and possible sCJD were collected. All cases presented with rapidly progressive cognitive dysfunction accompanied by spontaneous myoclonus. Classical electroencehalography changes and typical abnormal MRI features were observed. All of the cases died within a period of 8 months. None of the patients underwent brain biopsy. Our findings raise questions about the prevalence of CJD in Thailand, which needs further study.

Citations

Citations to this article as recorded by  
  • Sporadic Creutzfeldt-Jakob disease: Brain MRI lesion features from 2 cases reports
    Hoang Dinh Au, Nguyen Thu Lan, Nguyen Thai Binh, Le Tuan Linh, Ma Mai Hien, Nguyen Minh Duc
    Radiology Case Reports.2024; 19(3): 939.     CrossRef
  • A systemic analysis of Creutzfeldt Jakob disease cases in Asia
    Urwah Rasheed, Sana Khan, Minahil Khalid, Aneeqa Noor, Saima Zafar
    Prion.2024; 18(1): 11.     CrossRef
  • Updated global epidemiology atlas of human prion diseases
    Li-Ping Gao, Ting-Ting Tian, Kang Xiao, Cao Chen, Wei Zhou, Dong-Lin Liang, Run-Dong Cao, Qi Shi, Xiao-Ping Dong
    Frontiers in Public Health.2024;[Epub]     CrossRef
  • Characteristics of Creutzfeldt-Jakob disease at Siriraj Hospital, Thailand: Case series and literature review
    Chaisak Dumrikarnlert, Nuttapong Kanokkawinwong, Chatchawan Rattanabannakit, Vorapun Senanarong
    Clinical Parkinsonism & Related Disorders.2024; : 100281.     CrossRef
  • The importance of ongoing international surveillance for Creutzfeldt–Jakob disease
    Neil Watson, Jean-Philippe Brandel, Alison Green, Peter Hermann, Anna Ladogana, Terri Lindsay, Janet Mackenzie, Maurizio Pocchiari, Colin Smith, Inga Zerr, Suvankar Pal
    Nature Reviews Neurology.2021; 17(6): 362.     CrossRef
  • Case series of Creutzfeldt-Jakob disease in a third-level hospital in Quito
    Germaine Eleanor Torres Herrán, Andrés Damián Ortega Herrera, Braulio Martinez Burbano, Marcos Serrano-Dueñas, María Angélica Ortiz Yepez, Raúl Alberto Barrera Madera, Luis Alfredo Masabanda Campaña, Guillermo David Baño Jiménez, Denny Maritza Santos Salt
    BMC Neurology.2018;[Epub]     CrossRef
  • An Evaluation of Rapidly Progressive Dementia Culminating in a Diagnosis of Creutzfeldt–Jakob Disease
    Parmvir Parmar, Curtis L. Cooper, Daniel Kobewka
    Case Reports in Infectious Diseases.2018; 2018: 1.     CrossRef
  • Diffusion-weighted MRI abnormalities antedate the onset of sporadic Creutzfeldt-Jakob disease
    Keisuke Suzuki, Akiko Kawasaki, Takahide Nagashima, Koichi Hirata
    Neurology.2016; 87(8): 843.     CrossRef

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