Affiliations 

  • 1 Department of Neurology, Kuala Lumpur Hospital, Kuala Lumpur, Malaysia
  • 2 University of Medicine 1, Yangon, Myanmar
  • 3 Brunei Neuroscience Stroke and Rehabilitation Centre, Pantai Jerudong Specialist Centre, Brunei Darussalam
  • 4 Department of Neurology, National Neuroscience Institute, Singapore, Singapore
  • 5 Division of Neurology, Faculty of Medicine, Siriraj Hospital, Bumrungrad International Hospital, Bangkok, Thailand
  • 6 Asia Royal Hospital, Yangon, Myanmar
  • 7 Department of Neurology, Cipto Mangunkusumo Hospital/Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia
  • 8 Jerudong Park Medical Centre, Jerudong, Brunei Darussalam
  • 9 Philippine General Hospital, Metro Manila, Philippines
  • 10 Neurology Department, Mittaphab Hospital, Vientiane, Lao PDR
  • 11 Department of Neurology, Military Hospital 175, Ho Chi Minh, Vietnam
  • 12 Laboratory Sciences and Services Division (LSSD), The International Centre for Diarrhoeal Disease, Dhaka, Bangladesh
  • 13 Terumo BCT Asia Pte Ltd, Singapore, Singapore
J Cent Nerv Syst Dis, 2021;13:11795735211057314.
PMID: 35173510 DOI: 10.1177/11795735211057314

Abstract

Therapeutic plasma exchange (TPE) is an effective and affordable treatment option in most parts of Southeast Asia (SEA). In 2018, the SEA TPE Consortium (SEATPEC) was established, consisting of regional neurologists working to improve outcome of various autoimmune neurological diseases. We proposed an immunotherapeutic guideline prioritizing TPE for this region. We reviewed disease burden, evidence-based treatment options, and major guidelines for common autoimmune neurological disorders seen in SEA. A modified treatment algorithm based on consensus agreement by key-opinion leaders was proposed. Autoimmune antibody diagnostic testing through collaboration with accredited laboratories was established. Choice of first-line immunotherapies (IVIg/corticosteroid/TPE) is based on available evidence, clinicians' experience, contraindications, local availability, and affordability. TPE could be chosen as first-line therapy for GBS, CIDP, MG (acute/short term), IgG, A paraproteinemic neuropathy, and NMDAR encephalitis. Treatment is stopped for acute monophasic conditions such as GBS and ADEM following satisfactory outcome. For chronic immune disorders, a therapy taper or long-term maintenance therapy is recommended depending on the defined clinical state. TPE as second-line treatment is indicated for IVIg or corticosteroids refractory cases of ADEM, NMOSD (acute), MG, and NMDAR/LGI1/CASPR2/Hashimoto's encephalitis. With better diagnosis, treatment initiation with TPE is a sustainable and effective immunotherapy for autoimmune neurological diseases in SEA.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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