The prevalence of multiple sclerosis (MS) is now considered to be medium-to-high in the Middle East and is rising, particularly among women. While the characteristics of the disease and the response of patients to disease-modifying therapies are generally comparable between the Middle East and other areas, significant barriers to achieving optimal care for MS exist in these developing nations. A group of physicians involved in the management of MS in ten Middle Eastern countries met to consider the future of MS care in the region, using a structured process to reach a consensus. Six key priorities were identified: early diagnosis and management of MS, the provision of multidisciplinary MS centres, patient engagement and better communication with stakeholders, regulatory body education and reimbursement, a commitment to research, and more therapy options with better benefit-to-risk ratios. The experts distilled these priorities into a single vision statement: “Optimization of patient-centred multidisciplinary strategies to improve the quality of life of people with MS.” These core principles will contribute to the development of a broader consensus on the future of care for MS in the Middle East. 1. Introduction MS commonly appears in young adults and requires lifelong management, with significant potential for disability among people of working age. Indeed, the World Health Organisation and Multiple Sclerosis International Federation have estimated that about 60% of patients with MS will no longer have full ambulatory function twenty years following diagnosis of the disease [1]. There is a clear need to optimise the care of MS. A group of European experts in MS care recently used a structured process of information sharing and consensus building to define a new vision for optimal MS care in the 21st century [2]. As therapeutic practices and cultural influences vary between regions, it is important that such initiatives be conducted in other parts of the world where MS has a major impact on public health. Accordingly, a group of physicians involved in the care of MS patients from ten Middle Eastern countries recently considered the current and future management of MS within this region. 2. Methods The methodology used previously by a European expert group was adapted for use here [3]. The expert group are all coauthors of this paper and drawn from a panel of experts convened for this purpose (on the basis academic and research history in the field of MS and representation of countries across the Middle East and North Africa) at a closed meeting;
References
[1]
Multiple Sclerosis International Federation, “Atlas of MS,” 2013, http://www.msif.org/en/about_msif/what_we_do/atlas_of_ms.
[2]
P. Rieckmann, A. Boyko, D. Centonze, et al., “Future MS care: a consensus statement of the MS in the 21st Century Steering Group,” Journal of Neurology, vol. 260, no. 2, pp. 462–469, 2013.
[3]
A. H. Maghzi, H. Ghazavi, M. Ahsan et al., “Increasing female preponderance of multiple sclerosis in Isfahan, Iran: a population-based study,” Multiple Sclerosis, vol. 16, no. 3, pp. 359–361, 2010.
[4]
S. Bohlega, J. Inshasi, A. R. Al Tahan, A. B. Madani, H. Qahtani, and P. Rieckmann, “Multiple sclerosis in the Arabian Gulf countries: a consensus statement,” Journal of Neurology, 2013.
[5]
M. Etemadifar and S. H. Abtahi, “Multiple sclerosis in Isfahan, Iran: past, present and future,” International Journal of Preventive Medicine, vol. 3, no. 5, pp. 301–302, 2012.
[6]
J. Inshasi and M. Thakre, “Prevalence of multiple sclerosis in Dubai, United Arab Emirates,” International Journal of Neuroscience, vol. 121, no. 7, pp. 393–398, 2011.
[7]
J. Al-Hashel, A. D. Besterman, and C. Wolfson, “The prevalence of multiple sclerosis in the middle east,” Neuroepidemiology, vol. 31, no. 2, pp. 129–137, 2008.
[8]
D. Deleu, D. Mir, A. Al Tabouki, et al., “Prevalence, demographics and clinical characteristics of multiple sclerosis in Qatar,” Multiple Sclerosis, vol. 19, no. 6, pp. 816–819, 2013.
[9]
C. E. Markowitz, “The current landscape and unmet needs in multiple sclerosis,” The American Journal of Managed Care, vol. 16, no. 8, supplement, pp. S211–S218, 2010.
[10]
R. Gold, J. S. Wolinsky, M. P. Amato, and G. Comi, “Evolving expectations around early management of multiple sclerosis,” Therapeutic Advances in Neurological Disorders, vol. 3, no. 6, pp. 351–367, 2010.
[11]
K. Noyes, A. Bajorska, A. Chappel et al., “Cost-effectiveness of disease-modifying therapy for multiple sclerosis: a population-based study,” Neurology, vol. 77, no. 4, pp. 355–363, 2011.
[12]
National institute for Health and Clinical Excellence, “Multiple sclerosis: CG 8. Management of multiple sclerosis in primary and secondary care,” 2013, http://publications.nice.org.uk/multiple-sclerosis-cg8.
[13]
A. Jain, “NICE recommends faster, easier access to care for MS patients,” Bitish Medical Journal, vol. 327, no. 7426, article 1247, 2003.
[14]
B. I. Yamout, M. Dahdaleh, M. A. A. Jumah et al., “Adherence to disease-modifying drugs in patients with multiple sclerosis: a consensus statement from the middle east MS advisory group,” International Journal of Neuroscience, vol. 120, no. 4, pp. 273–279, 2010.
[15]
A. Ri?on, M. Buch, D. Holley, and E. Verdun, “The MS Choices Survey: findings of a study assessing physician and patient perspectives on living with and managing multiple sclerosis,” Patient Preference and Adherence, vol. 5, pp. 629–643, 2011.
[16]
R. L. Askew, D. Amtmann, V. G. Weir, and K. Johnson, “Exploring unmet needs in multiple sclerosis: who needs what?” International Journal of MS Care, vol. 14, supplement 2, p. 86, 2012.
[17]
J. Wollin, H. Dale, N. Spenser, and N. Walsh, “What people with newly diagnosed MS (and their families and friends) need to know,” International Journal of MS Care, vol. 2, no. 3, pp. 29–39, 2000.
[18]
I. Juraskova, J. Chapman, P. N. Butow, et al., “Challenges, needs, rewards, and psychological well-being of multiple sclerosis support-group facilitators,” International Journal of MS Care, vol. 10, no. 3, pp. 85–93, 2008.
[19]
M. Plow, M. Finlayson, and C. Cho, “Correlates of nutritional behavior in individuals with multiple sclerosis,” Disability and Health Journal, vol. 5, no. 4, pp. 284–291, 2012.
[20]
M. Edlin and P. Sonnenreich, “Trends in managing multiple sclerosis,” P & T, vol. 33, no. 10, pp. 611–614, 2008.
[21]
P. McCrone, M. Heslin, M. Knapp, P. Bull, and A. Thompson, “Multiple sclerosis in the UK: service use, costs, quality of life and disability,” PharmacoEconomics, vol. 26, no. 10, pp. 847–860, 2008.
[22]
F. Ashtari and M. R. Savoj, “Effects of low dose Methotrexate on relapsing-remitting multiple sclerosis in comparison to Interferon β-1α: a randomized controlled trial,” Journal of Research in Medical Sciences, vol. 16, no. 4, pp. 457–462, 2011.
[23]
M. Etemadifar, M. Janghorbani, and V. Shaygannejad, “Comparison of Betaferon, Avonex, and Rebif in treatment of relapsing-remitting multiple sclerosis,” Acta Neurologica Scandinavica, vol. 113, no. 5, pp. 283–287, 2006.
[24]
M. Mazdeh, S. Afzali, and M. R. Jaafari, “The therapeutic effect of avonex, rebif and betaferon on EDSS and relapse in multiple sclerosis: a comparative study,” Acta Medica Iranica, vol. 48, no. 2, pp. 83–88, 2010.
[25]
M. Etemadifar, M. Janghorbani, and V. Shaygannejad, “Comparison of interferon beta products and azathioprine in the treatment of relapsing-remitting multiple sclerosis,” Journal of Neurology, vol. 254, no. 12, pp. 1723–1728, 2007.
[26]
S. Nafissi, A. Azimi, A. Amini-Harandi, S. Salami, M. A. Shahkarami, and R. Heshmat, “Comparing efficacy and side effects of a weekly intramuscular biogeneric/biosimilar interferon beta-1a with Avonex in relapsing remitting multiple sclerosis: a double blind randomized clinical trial,” Clinical Neurology and Neurosurgery, vol. 114, no. 7, pp. 986–989, 2012.
[27]
H. Pakdaman, M. A. Sahraian, A. Fallah et al., “Effect of early interferon beta-1a therapy on conversion to multiple sclerosis in Iranian patients with a first demyelinating event,” Acta Neurologica Scandinavica, vol. 115, no. 6, pp. 429–431, 2007.
[28]
M. R. Motamed, N. Najimi, and S.-M. Fereshtehnejad, “The effect of interferon-beta1a on relapses and progression of disability in patients with clinically isolated syndromes (CIS) suggestive of multiple sclerosis,” Clinical Neurology and Neurosurgery, vol. 109, no. 4, pp. 344–349, 2007.
[29]
I. Kister, E. Chamot, J. H. Bacon, G. Cutter, and J. Herbert, “Trend for decreasing Multiple Sclerosis Severity Scores (MSSS) with increasing calendar year of enrollment into the New York State Multiple Sclerosis Consortium,” Multiple Sclerosis, vol. 17, no. 6, pp. 725–733, 2011.
[30]
D. S. Goodin, A. T. Reder, and G. C. Ebers, “Survival in MS: a randomized cohort study 21 years after the start of the pivotal IFNβ-1b trial,” Neurology, vol. 78, no. 17, pp. 1315–1322, 2012.
[31]
L. Ottoboni, B. T. Keenan, P. Tamayo, et al., “An RNA profile identifies two subsets of multiple sclerosis patients differing in disease activity,” Science Translational Medicine, vol. 4, no. 153, p. 153ra131, 2012.
[32]
National Institutes of Health, “Estimates of Funding for Various Research, Condition, and Disease Categories (RCDC),” 2013, http://report.nih.gov/categorical_spending.aspx.
[33]
W. H. Stuart, “Clinical management of multiple sclerosis: the treatment paradigm and issues of patient management,” Journal of Managed Care Pharmacy, vol. 10, no. 3, pp. S19–S25, 2004.
[34]
N. S. Roskell, E. A. Zimovetz, C. E. Rycroft, B. J. EckertJ, and D. A. Tyas, “Annualized relapse rate of first-line treatments for multiple sclerosis: a meta-analysis, including indirect comparisons versus fingolimod,” Current Medical Research and Opinion, vol. 28, no. 5, pp. 767–780, 2012.
[35]
L. La Mantia, L. Vacchi, C. Di Pietrantonj, et al., “Interferon beta for secondary progressive multiple sclerosis,” Cochrane Database of Systematic Reviews, vol. 1, Article ID CD005181, 2012.
[36]
H. Tedeholm, J. Lycke, B. Skoog, et al., “Time to secondary progression in patients with multiple sclerosis who were treated with first generation immunomodulating drugs,” Multiple Sclerosis, vol. 19, no. 6, pp. 765–774, 2013.
[37]
G. L. Plosker, “Interferon-β-1b: a review of its use in multiple sclerosis,” CNS Drugs, vol. 25, no. 1, pp. 67–88, 2011.
[38]
N. Girouard and N. Soucy, “Patient considerations in the management of multiple sclerosis: development and clinical utility of oral agents,” Patient Preference and Adherence, vol. 5, pp. 101–108, 2011.
[39]
K. K. Daugherty, J. S. Butler, M. Mattingly, and M. Ryan, “Factors leading patients to discontinue multiple sclerosis therapies,” Journal of the American Pharmacists Association, vol. 45, no. 3, pp. 371–375, 2005.