Abstract
Background: In 2018 multiple sclerosis (MS) care unit (MSCU) recommendations were defined. Nevertheless, the information on MS care, and whether MS centres fulfil the international recommendation is limited. Thus our objectives were to assess whether centres meet the MSCU recommendations and gain a comprehensive overview of MS care in Central-Eastern European countries. Methods: A self-report questionnaire assessing aspects of the MSCU recommendations, disease-modifying therapy (DMT) and registry use and the patient number was assembled and sent to nine Central-Eastern European countries. Furthermore, one Danish and one German centre were contacted as a reference. Results: In 9/9 countries, MS care was pursued in centres by MS neurologists and MS nurses. In Austria and the Czech Republic, management of MS was conducted under strict regulations displaying a referral centre system, fundamentally similar to but independent of the MSCU criteria. Several centres fulfilled all aspects of the MSCU criteria, while others had similar insufficiencies consisting of a speech therapist, continence, pain and spasticity specialist, neuro-ophthalmologist, and oto-neurologist. In 9/9 countries, DMTs were reimbursed. However, some centres did not provide every available DMT. A national registry was available in 4/9 countries with mandatory registry use only in Austria and the Czech Republic. Conclusion: In countries where MSCU recommendations are not fulfilled, a strictly regulated centre system similar to the Austrian and Czech model with a registry-based quality control might ensure appropriate care for people with MS.
| Originalsprog | Engelsk |
|---|---|
| Artikelnummer | 104406 |
| Tidsskrift | Multiple Sclerosis and Related Disorders |
| Vol/bind | 69 |
| Antal sider | 13 |
| ISSN | 2211-0348 |
| DOI | |
| Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:The authors thank the Danube Symposium for Neurological Sciences for collaboration. In addition, the authors would like to thank the following colleagues for their contribution to the data acquisition on the management of MS in participating MS centres:, Austria: Harald Hegen, Croatia: Mario Habek, Marija Ratković, Spomenka Kidemet-Piskac, Tea Mirosevic Zubonja, Czech Republic: Jan Kolčava, Eva Meluzínová, Marek Peterka, Eva Recmanova, Jana Adamkova, Marta Vachová, Radek Ampapa, Ivana Stetkarová, Hungary: Ágnes Köves, Ferenc Fazekas, Adrienne Jóri Birkás, Gabriella Katona, Krisztina Kovács, Dániel Milanovich, Enikő Dobos, István Kapás, Gábor Jakab, Tünde Csépány, Erzsébet Bense, Klotild Mátyás, Gábor Rum, Zoltán Szolnoki, István Deme, Zita Jobbágy, Dávid Kriston, Zsuzsanna Gerócs, Péter Diószeghy, László Bors, Adrián Varga, Levente Kerényi, Gabriella Molnár, Piroska Kristóf, Zsuzsanna Ágnes Nagy, Mária Sátori, Piroska Imre, Szilvia Péntek, Poland: Stanisław Rusek, Marcin Wnuk, Izabela Domitrz, Anna Pokryszko-Dragan, Slawomir Budrewicz, Andrzej Glabinski, Elzbieta Jasinska, Mariusz Stasiołek, Beata Zakrzewska-Pniewska, Slawomir Wawrzyniak, Jacek Zaborski, Waldemar Brola, Robert Bonek, Iwona Kurkowska-Jastrzebska, Ewa Krzystanek, Marcin P. Mycko, Anna Karbicka, Adam Stepien, Alicja Kalinowska, Karolina Piasecka-Stryczynska, Monika Adamczyk-Sowa, Anetta Lasek-Bal, Alina Kułakowska, Romania: Delia Stanca, Tudor Lupescu, Ignat Emilian-Bogdan, Roman-Filip Corina, Cristina Aura Panea, Anabella Cioabla, Adriana Dulamea, Eugenia Irene Davidescu, Rodica Bălașa, Carmen Burloiu, Albu Valeria Carmen, Monica Sabău, Simu Mihaela Adriana, Cristina Florentina Plesa, Slovakia: Darina Slezáková, Peter Valkovič, Jarmila Szilasiová, Egon Kurča, Georgi Krastev, Viera Hančinová, Slavomira Kovacova, Andrea Cimprichová, Peter Koleda, Slovenia: Jožef Magdič, Serbia: Evica Dincic, Gordana Tončev, Slobodan Vojinovic, Lorand Sakalas
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