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Sökning: WFRF:(Lindemans Jan W) > (2024) > Inventory of curren...

Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries

Schoenmakers, Daphne H. (författare)
Amsterdam Neuroscience,University of Amsterdam,Vrije Universiteit Amsterdam
Mochel, Fanny (författare)
Brain and Spine Institute (ICM)
Adang, Laura A. (författare)
The Children's Hospital of Philadelphia
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Boelens, Jaap Jan (författare)
Memorial Sloan-Kettering Cancer Center
Calbi, Valeria (författare)
San Raffaele Hospital
Eklund, Erik A. (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital
Grønborg, Sabine W. (författare)
Copenhagen University Hospital
Fumagalli, Francesca (författare)
Groeschel, Samuel (författare)
University Hospital of Tubingen
Lindemans, Caroline (författare)
Princess Maxima Center for Pediatric Oncology/Hematology,Wilhelmina Children’s Hospital
Sevin, Caroline (författare)
Assistance Publique des Hôpitaux de Paris
Schöls, Ludger (författare)
University of Tübingen,German Center for Neurodegenerative Diseases (DZNE), Bonn
Ram, Dipak (författare)
Royal Manchester Children's Hospital
Zerem, Ayelet (författare)
Tel-Aviv University
Graessner, Holm (författare)
University of Tübingen
Wolf, Nicole I. (författare)
Amsterdam Neuroscience,Vrije Universiteit Amsterdam
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 (creator_code:org_t)
2024
2024
Engelska.
Ingår i: Orphanet Journal of Rare Diseases. - 1750-1172. ; 19:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: For decades, early allogeneic stem cell transplantation (HSCT) has been used to slow neurological decline in metachromatic leukodystrophy (MLD). There is lack of consensus regarding who may benefit, and guidelines are lacking. Clinical practice relies on limited literature and expert opinions. The European Reference Network for Rare Neurological Diseases (ERN-RND) and the MLD initiative facilitate expert panels for treatment advice, but some countries are underrepresented. This study explores organizational and clinical HSCT practices for MLD in Europe and neighboring countries to enhance optimization and harmonization of cross-border MLD care. Methods: A web-based EUSurvey was distributed through the ERN-RND and the European Society for Blood and Marrow Transplantation Inborn Errors Working Party. Personal invitations were sent to 89 physicians (43 countries) with neurological/metabolic/hematological expertise. The results were analyzed and visualized using Microsoft Excel and IBM SPSS statistics. Results: Of the 30 countries represented by 42 respondents, 23 countries offer HSCT for MLD. The treatment is usually available in 1–3 centers per country (18/23, 78%). Most countries have no or very few MLD patients transplanted during the past 1–5 years. The eligibility criteria regarding MLD subtype, motor function, IQ, and MRI largely differ across countries. Conclusion: HSCT for MLD is available in most European countries, but uncertainties exist in Eastern and South-Eastern Europe. Applied eligibility criteria and management vary and may not align with the latest scientific insights, indicating physicians’ struggle in providing evidence-based care. Interaction between local physicians and international experts is crucial for adequate treatment decision-making and cross-border care in the rapidly changing MLD field.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Health Care Service and Management, Health Policy and Services and Health Economy (hsv//eng)

Nyckelord

Europe
Healthcare disparities
Hematopoietic stem cell transplantation
Leukodystrophy, Metachromatic
Rare diseases

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