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Published in: Current Treatment Options in Neurology 4/2015

01-04-2015 | Multiple Sclerosis and Related Disorders (P Villoslada, Section Editor)

Therapeutic Management of Severe Relapses in Multiple Sclerosis

Authors: Carolyn Bevan, MD, MS, Jeffrey M. Gelfand, MD, MAS

Published in: Current Treatment Options in Neurology | Issue 4/2015

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Opinion statement

While not all multiple sclerosis (MS) relapses require treatment, relapses that are bothersome or that impair function should prompt consideration of timely treatment to restore function and minimize disability. Patients with suspected MS relapses should be evaluated to confirm the diagnosis, exclude other causes of neurological dysfunction, and identify potential triggers for relapse or pseudo-relapse, such as urinary tract infections, fever, or metabolic derangements. The diagnosis of an MS relapse is clinical, but MRI may be useful for confirmation and to evaluate for multifocal disease activity. High-dose oral or intravenous glucocorticoids, with or without an oral taper, are first-line therapy for MS relapses. Adrenocorticotropic hormone (ACTH) provides an alternative to glucocorticoid treatment but is currently much more expensive and does not have proven superiority. If the acute neurological deficits remain severe after steroid treatment, and particularly if there is persistent abnormal contrast-enhancement of the symptomatic lesion on repeat MRI, plasma exchange (PLEX) should be considered as an acute rescue therapy for relapse. In exceptional cases, particularly fulminant or tumefactive disease that fails to improve following treatment with steroids and PLEX, cytoxic agents such as cyclophosphamide or B cell-depleting regimens such as rituximab may be considered, although risk must be carefully weighed and the kinetics of such regimens indicate that they probably serve more to accelerate remission of disease activity than as an immediate relapse remedy. A single dose of natalizumab given as acute therapy for MS relapse was shown not to improve clinical outcomes in a randomized controlled trial. Attention to symptom management and promotion of neurorehabilitation are important aspects of MS relapse care. Neuroprotective and neuroreparative therapies remain under investigation, but are likely to become important complementary elements of relapse therapy in the future. Relapses serve as important indicators of MS disease activity. In the context of the emerging treatment paradigm of targeting freedom from evidence of MS disease activity, relapses should prompt consideration of transitioning to a disease-modifying treatment that may offer better efficacy.
Literature
1.
go back to reference Gelfand JM. Multiple sclerosis: diagnosis, differential diagnosis, and clinical presentation. Handb Clin Neurol. 2014;122:269–90.CrossRefPubMed Gelfand JM. Multiple sclerosis: diagnosis, differential diagnosis, and clinical presentation. Handb Clin Neurol. 2014;122:269–90.CrossRefPubMed
2.
go back to reference Weinshenker BG et al. The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course. Brain. 1989;112(Pt 6):1419–28.CrossRefPubMed Weinshenker BG et al. The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course. Brain. 1989;112(Pt 6):1419–28.CrossRefPubMed
4.
go back to reference Scalfari A et al. The natural history of multiple sclerosis: a geographically based study 10: relapses and long-term disability. Brain. 2010;133(Pt 7):1914–29.CrossRefPubMedCentralPubMed Scalfari A et al. The natural history of multiple sclerosis: a geographically based study 10: relapses and long-term disability. Brain. 2010;133(Pt 7):1914–29.CrossRefPubMedCentralPubMed
5.
go back to reference Confavreux C, Vukusic S, Adeleine P. Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process. Brain. 2003;126(Pt 4):770–82.CrossRefPubMed Confavreux C, Vukusic S, Adeleine P. Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process. Brain. 2003;126(Pt 4):770–82.CrossRefPubMed
8.
go back to reference Horsfield MA et al. Diffusion magnetic resonance imaging in multiple sclerosis. J Neurol Neurosurg Psychiatry. 1998;64 Suppl 1:S80–4.PubMed Horsfield MA et al. Diffusion magnetic resonance imaging in multiple sclerosis. J Neurol Neurosurg Psychiatry. 1998;64 Suppl 1:S80–4.PubMed
9.
go back to reference Simon JH. MRI outcomes in the diagnosis and disease course of multiple sclerosis. Handb Clin Neurol. 2014;122:405–25.CrossRefPubMed Simon JH. MRI outcomes in the diagnosis and disease course of multiple sclerosis. Handb Clin Neurol. 2014;122:405–25.CrossRefPubMed
10.
go back to reference Isaac C et al. Multiple sclerosis: a serial study using MRI in relapsing patients. Neurology. 1988;38(10):1511–5.CrossRefPubMed Isaac C et al. Multiple sclerosis: a serial study using MRI in relapsing patients. Neurology. 1988;38(10):1511–5.CrossRefPubMed
11.
go back to reference Green AJ. Understanding pseudo: the symptoms are real, the cause is unclear. Neurology. 2009;72(19):1626–7.CrossRefPubMed Green AJ. Understanding pseudo: the symptoms are real, the cause is unclear. Neurology. 2009;72(19):1626–7.CrossRefPubMed
13.
go back to reference Panitch HS. Influence of infection on exacerbations of multiple sclerosis. Ann Neurol. 1994;36(Suppl):S25–8.CrossRefPubMed Panitch HS. Influence of infection on exacerbations of multiple sclerosis. Ann Neurol. 1994;36(Suppl):S25–8.CrossRefPubMed
14.
go back to reference Trapp BD et al. Axonal transection in the lesions of multiple sclerosis. N Engl J Med. 1998;338(5):278–85.CrossRefPubMed Trapp BD et al. Axonal transection in the lesions of multiple sclerosis. N Engl J Med. 1998;338(5):278–85.CrossRefPubMed
15.
go back to reference Ramo-Tello C et al. A randomized clinical trial of oral versus intravenous methylprednisolone for relapse of MS. Mult Scler. 2014;20(6):717–25.CrossRefPubMed Ramo-Tello C et al. A randomized clinical trial of oral versus intravenous methylprednisolone for relapse of MS. Mult Scler. 2014;20(6):717–25.CrossRefPubMed
16.
go back to reference Filippini G et al. Corticosteroids or ACTH for acute exacerbations in multiple sclerosis. Cochrane Database Syst Rev. 2000;4, CD001331.PubMed Filippini G et al. Corticosteroids or ACTH for acute exacerbations in multiple sclerosis. Cochrane Database Syst Rev. 2000;4, CD001331.PubMed
18.
go back to reference Ross AP, Halper J, Harris CJ. Assessing relapses and response to relapse treatment in patients with multiple sclerosis: a nursing perspective. Int J MS Care. 2012;14(3):148–59.CrossRefPubMedCentralPubMed Ross AP, Halper J, Harris CJ. Assessing relapses and response to relapse treatment in patients with multiple sclerosis: a nursing perspective. Int J MS Care. 2012;14(3):148–59.CrossRefPubMedCentralPubMed
19.
go back to reference Thompson AJ et al. Relative efficacy of intravenous methylprednisolone and ACTH in the treatment of acute relapse in MS. Neurology. 1989;39(7):969–71.CrossRefPubMed Thompson AJ et al. Relative efficacy of intravenous methylprednisolone and ACTH in the treatment of acute relapse in MS. Neurology. 1989;39(7):969–71.CrossRefPubMed
20.
go back to reference Glaser GH, Merritt HH. Effects of ACTH and cortisone in multiple sclerosis. Trans Am Neurol Assoc. 1951;56:130–3.PubMed Glaser GH, Merritt HH. Effects of ACTH and cortisone in multiple sclerosis. Trans Am Neurol Assoc. 1951;56:130–3.PubMed
21.
22.
go back to reference Weinshenker BG et al. A randomized trial of plasma exchange in acute central nervous system inflammatory demyelinating disease. Ann Neurol. 1999;46(6):878–86.CrossRefPubMed Weinshenker BG et al. A randomized trial of plasma exchange in acute central nervous system inflammatory demyelinating disease. Ann Neurol. 1999;46(6):878–86.CrossRefPubMed
23.
go back to reference Weiner HL et al. Double-blind study of true vs. sham plasma exchange in patients treated with immunosuppression for acute attacks of multiple sclerosis. Neurology. 1989;39(9):1143–9.CrossRefPubMed Weiner HL et al. Double-blind study of true vs. sham plasma exchange in patients treated with immunosuppression for acute attacks of multiple sclerosis. Neurology. 1989;39(9):1143–9.CrossRefPubMed
24.
go back to reference O’Connor PW et al. Randomized multicenter trial of natalizumab in acute MS relapses: clinical and MRI effects. Neurology. 2004;62(11):2038–43.CrossRefPubMed O’Connor PW et al. Randomized multicenter trial of natalizumab in acute MS relapses: clinical and MRI effects. Neurology. 2004;62(11):2038–43.CrossRefPubMed
25.
26.
go back to reference Edan G et al. Mitoxantrone prior to interferon beta-1b in aggressive relapsing multiple sclerosis: a 3-year randomised trial. J Neurol Neurosurg Psychiatry. 2011;82(12):1344–50.CrossRefPubMed Edan G et al. Mitoxantrone prior to interferon beta-1b in aggressive relapsing multiple sclerosis: a 3-year randomised trial. J Neurol Neurosurg Psychiatry. 2011;82(12):1344–50.CrossRefPubMed
27.
28.
go back to reference Pfender N, Saccardi R, Martin R. Autologous hematopoietic stem cell transplantation as a treatment option for aggressive multiple sclerosis. Curr Treat Options Neurol. 2013;15(3):270–80.CrossRefPubMed Pfender N, Saccardi R, Martin R. Autologous hematopoietic stem cell transplantation as a treatment option for aggressive multiple sclerosis. Curr Treat Options Neurol. 2013;15(3):270–80.CrossRefPubMed
29.
go back to reference Burman J et al. Autologous haematopoietic stem cell transplantation for aggressive multiple sclerosis: the Swedish experience. J Neurol Neurosurg Psychiatry. 2014;85(10):1116–21.CrossRefPubMed Burman J et al. Autologous haematopoietic stem cell transplantation for aggressive multiple sclerosis: the Swedish experience. J Neurol Neurosurg Psychiatry. 2014;85(10):1116–21.CrossRefPubMed
30.
31.
go back to reference Sorensen PS. New management algorithms in multiple sclerosis. Curr Opin Neurol. 2014;27(3):246–59.CrossRefPubMed Sorensen PS. New management algorithms in multiple sclerosis. Curr Opin Neurol. 2014;27(3):246–59.CrossRefPubMed
32.
go back to reference Okuda DT. Immunosuppressive treatments in multiple sclerosis. Handb Clin Neurol. 2014;122:503–11.CrossRefPubMed Okuda DT. Immunosuppressive treatments in multiple sclerosis. Handb Clin Neurol. 2014;122:503–11.CrossRefPubMed
33.
go back to reference O’Connor PW, Oh J. Disease-modifying agents in multiple sclerosis. Handb Clin Neurol. 2014;122:465–501.CrossRefPubMed O’Connor PW, Oh J. Disease-modifying agents in multiple sclerosis. Handb Clin Neurol. 2014;122:465–501.CrossRefPubMed
34.
go back to reference Beck RW et al. A randomized, controlled trial of corticosteroids in the treatment of acute optic neuritis. The Optic Neuritis Study Group. N Engl J Med. 1992;326(9):581–8.CrossRefPubMed Beck RW et al. A randomized, controlled trial of corticosteroids in the treatment of acute optic neuritis. The Optic Neuritis Study Group. N Engl J Med. 1992;326(9):581–8.CrossRefPubMed
35.
go back to reference Goodin DS. Perils and pitfalls in the interpretation of clinical trials: a reflection on the recent experience in multiple sclerosis. Neuroepidemiology. 1999;18(2):53–63.CrossRefPubMed Goodin DS. Perils and pitfalls in the interpretation of clinical trials: a reflection on the recent experience in multiple sclerosis. Neuroepidemiology. 1999;18(2):53–63.CrossRefPubMed
36.
go back to reference Miller H, Newell DJ, Ridley A. Multiple sclerosis. Treatment of acute exacerbations with corticotrophin (A.C.T.H.). Lancet. 1961;2(7212):1120–2.CrossRefPubMed Miller H, Newell DJ, Ridley A. Multiple sclerosis. Treatment of acute exacerbations with corticotrophin (A.C.T.H.). Lancet. 1961;2(7212):1120–2.CrossRefPubMed
37.
go back to reference Rose AS et al. Cooperative study in the evaluation of therapy in multiple sclerosis. ACTH vs. placebo—final report. Neurology. 1970;20(5):1–59.PubMed Rose AS et al. Cooperative study in the evaluation of therapy in multiple sclerosis. ACTH vs. placebo—final report. Neurology. 1970;20(5):1–59.PubMed
38.
go back to reference Sellebjerg F et al. Randomized controlled trial of high-dose peroral methylprednisolone in attacks of multiple sclerosis. Ugeskr Laeger. 1999;161(48):6625–9.PubMed Sellebjerg F et al. Randomized controlled trial of high-dose peroral methylprednisolone in attacks of multiple sclerosis. Ugeskr Laeger. 1999;161(48):6625–9.PubMed
39.
go back to reference Sellebjerg F et al. Double-blind, randomized, placebo-controlled study of oral, high-dose methylprednisolone in attacks of MS. Neurology. 1998;51(2):529–34.CrossRefPubMed Sellebjerg F et al. Double-blind, randomized, placebo-controlled study of oral, high-dose methylprednisolone in attacks of MS. Neurology. 1998;51(2):529–34.CrossRefPubMed
40.
go back to reference Filipovic SR et al. The effects of high-dose intravenous methylprednisolone on event-related potentials in patients with multiple sclerosis. J Neurol Sci. 1997;152(2):147–53.CrossRefPubMed Filipovic SR et al. The effects of high-dose intravenous methylprednisolone on event-related potentials in patients with multiple sclerosis. J Neurol Sci. 1997;152(2):147–53.CrossRefPubMed
41.
go back to reference Milligan NM, Newcombe R, Compston DA. A double-blind controlled trial of high dose methylprednisolone in patients with multiple sclerosis: 1. Clinical effects. J Neurol Neurosurg Psychiatry. 1987;50(5):511–6.CrossRefPubMedCentralPubMed Milligan NM, Newcombe R, Compston DA. A double-blind controlled trial of high dose methylprednisolone in patients with multiple sclerosis: 1. Clinical effects. J Neurol Neurosurg Psychiatry. 1987;50(5):511–6.CrossRefPubMedCentralPubMed
42.
go back to reference Durelli L et al. High-dose intravenous methylprednisolone in the treatment of multiple sclerosis: clinical-immunologic correlations. Neurology. 1986;36(2):238–43.CrossRefPubMed Durelli L et al. High-dose intravenous methylprednisolone in the treatment of multiple sclerosis: clinical-immunologic correlations. Neurology. 1986;36(2):238–43.CrossRefPubMed
43.
go back to reference Morrow SA et al. The bioavailability of IV methylprednisolone and oral prednisone in multiple sclerosis. Neurology. 2004;63(6):1079–80.CrossRefPubMed Morrow SA et al. The bioavailability of IV methylprednisolone and oral prednisone in multiple sclerosis. Neurology. 2004;63(6):1079–80.CrossRefPubMed
44.
go back to reference Martinelli V et al. A short-term randomized MRI study of high-dose oral vs intravenous methylprednisolone in MS. Neurology. 2009;73(22):1842–8.CrossRefPubMed Martinelli V et al. A short-term randomized MRI study of high-dose oral vs intravenous methylprednisolone in MS. Neurology. 2009;73(22):1842–8.CrossRefPubMed
45.
go back to reference Barnes D et al. Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis. Lancet. 1997;349(9056):902–6.CrossRefPubMed Barnes D et al. Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis. Lancet. 1997;349(9056):902–6.CrossRefPubMed
46.
go back to reference Piper JM et al. Corticosteroid use and peptic ulcer disease: role of nonsteroidal anti-inflammatory drugs. Ann Intern Med. 1991;114(9):735–40.CrossRefPubMed Piper JM et al. Corticosteroid use and peptic ulcer disease: role of nonsteroidal anti-inflammatory drugs. Ann Intern Med. 1991;114(9):735–40.CrossRefPubMed
47.
go back to reference Arvin AM et al. Varicella-zoster virus infections in patients treated with fingolimod: risk assessment and consensus recommendations for management. JAMA Neurol. 2015;72(1):31–9.CrossRefPubMed Arvin AM et al. Varicella-zoster virus infections in patients treated with fingolimod: risk assessment and consensus recommendations for management. JAMA Neurol. 2015;72(1):31–9.CrossRefPubMed
48.
go back to reference Arnason BG et al. Mechanisms of action of adrenocorticotropic hormone and other melanocortins relevant to the clinical management of patients with multiple sclerosis. Mult Scler. 2013;19(2):130–6.CrossRefPubMedCentralPubMed Arnason BG et al. Mechanisms of action of adrenocorticotropic hormone and other melanocortins relevant to the clinical management of patients with multiple sclerosis. Mult Scler. 2013;19(2):130–6.CrossRefPubMedCentralPubMed
51.
go back to reference Keegan M et al. Plasma exchange for severe attacks of CNS demyelination: predictors of response. Neurology. 2002;58(1):143–6.CrossRefPubMed Keegan M et al. Plasma exchange for severe attacks of CNS demyelination: predictors of response. Neurology. 2002;58(1):143–6.CrossRefPubMed
52.
go back to reference Llufriu S et al. Plasma exchange for acute attacks of CNS demyelination: predictors of improvement at 6 months. Neurology. 2009;73(12):949–53.CrossRefPubMed Llufriu S et al. Plasma exchange for acute attacks of CNS demyelination: predictors of improvement at 6 months. Neurology. 2009;73(12):949–53.CrossRefPubMed
53.
go back to reference Sorensen PS et al. IV immunoglobulins as add-on treatment to methylprednisolone for acute relapses in MS. Neurology. 2004;63(11):2028–33.CrossRefPubMed Sorensen PS et al. IV immunoglobulins as add-on treatment to methylprednisolone for acute relapses in MS. Neurology. 2004;63(11):2028–33.CrossRefPubMed
54.
go back to reference Visser LH et al. A randomized, double-blind, placebo-controlled pilot study of i.v. immune globulins in combination with i.v. methylprednisolone in the treatment of relapses in patients with MS. Mult Scler. 2004;10(1):89–91.CrossRefPubMed Visser LH et al. A randomized, double-blind, placebo-controlled pilot study of i.v. immune globulins in combination with i.v. methylprednisolone in the treatment of relapses in patients with MS. Mult Scler. 2004;10(1):89–91.CrossRefPubMed
55.
go back to reference Roed HG et al. A double-blind, randomized trial of IV immunoglobulin treatment in acute optic neuritis. Neurology. 2005;64(5):804–10.CrossRefPubMed Roed HG et al. A double-blind, randomized trial of IV immunoglobulin treatment in acute optic neuritis. Neurology. 2005;64(5):804–10.CrossRefPubMed
56.
go back to reference Haas J, Hommes OR. A dose comparison study of IVIG in postpartum relapsing-remitting multiple sclerosis. Mult Scler. 2007;13(7):900–8.CrossRefPubMed Haas J, Hommes OR. A dose comparison study of IVIG in postpartum relapsing-remitting multiple sclerosis. Mult Scler. 2007;13(7):900–8.CrossRefPubMed
57.
go back to reference Achiron A et al. Effect of intravenous immunoglobulin treatment on pregnancy and postpartum-related relapses in multiple sclerosis. J Neurol. 2004;251(9):1133–7.CrossRefPubMed Achiron A et al. Effect of intravenous immunoglobulin treatment on pregnancy and postpartum-related relapses in multiple sclerosis. J Neurol. 2004;251(9):1133–7.CrossRefPubMed
58.
go back to reference Achiron A et al. Intravenous immunoglobulin treatment in multiple sclerosis and experimental autoimmune encephalomyelitis—the Israeli experience. MS Study Group. Mult Scler. 1997;3(2):142–4.CrossRefPubMed Achiron A et al. Intravenous immunoglobulin treatment in multiple sclerosis and experimental autoimmune encephalomyelitis—the Israeli experience. MS Study Group. Mult Scler. 1997;3(2):142–4.CrossRefPubMed
59.
go back to reference Fazekas F et al. Randomised placebo-controlled trial of monthly intravenous immunoglobulin therapy in relapsing-remitting multiple sclerosis. Austrian Immunoglobulin in Multiple Sclerosis Study Group. Lancet. 1997;349(9052):589–93.CrossRefPubMed Fazekas F et al. Randomised placebo-controlled trial of monthly intravenous immunoglobulin therapy in relapsing-remitting multiple sclerosis. Austrian Immunoglobulin in Multiple Sclerosis Study Group. Lancet. 1997;349(9052):589–93.CrossRefPubMed
60.
go back to reference Elovaara I et al. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases: EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases. Eur J Neurol. 2008;15(9):893–908.CrossRefPubMed Elovaara I et al. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases: EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases. Eur J Neurol. 2008;15(9):893–908.CrossRefPubMed
61.
go back to reference Goodin DS et al. Disease modifying therapies in multiple sclerosis: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines. Neurology. 2002;58(2):169–78.CrossRefPubMed Goodin DS et al. Disease modifying therapies in multiple sclerosis: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines. Neurology. 2002;58(2):169–78.CrossRefPubMed
62.
go back to reference Fazekas F et al. Intravenous immunoglobulin in relapsing-remitting multiple sclerosis: a dose-finding trial. Neurology. 2008;71(4):265–71.CrossRefPubMed Fazekas F et al. Intravenous immunoglobulin in relapsing-remitting multiple sclerosis: a dose-finding trial. Neurology. 2008;71(4):265–71.CrossRefPubMed
63.
64.
go back to reference Sempere AP et al. Neurological picture. Rituximab for tumefactive demyelination refractory to corticosteroids and plasma exchange. J Neurol Neurosurg Psychiatry. 2013;84(12):1338–9.CrossRefPubMed Sempere AP et al. Neurological picture. Rituximab for tumefactive demyelination refractory to corticosteroids and plasma exchange. J Neurol Neurosurg Psychiatry. 2013;84(12):1338–9.CrossRefPubMed
65.
go back to reference Fan X et al. Rituximab for tumefactive inflammatory demyelination: a case report. Clin Neurol Neurosurg. 2012;114(10):1326–8.CrossRefPubMed Fan X et al. Rituximab for tumefactive inflammatory demyelination: a case report. Clin Neurol Neurosurg. 2012;114(10):1326–8.CrossRefPubMed
66.
go back to reference Hardy TA, Chataway J. Tumefactive demyelination: an approach to diagnosis and management. J Neurol Neurosurg Psychiatry. 2013;84(9):1047–53.CrossRefPubMed Hardy TA, Chataway J. Tumefactive demyelination: an approach to diagnosis and management. J Neurol Neurosurg Psychiatry. 2013;84(9):1047–53.CrossRefPubMed
67.
go back to reference Harrison DM et al. Treatment of relapsing-remitting multiple sclerosis with high-dose cyclophosphamide induction followed by glatiramer acetate maintenance. Mult Scler. 2012;18(2):202–9.CrossRefPubMedCentralPubMed Harrison DM et al. Treatment of relapsing-remitting multiple sclerosis with high-dose cyclophosphamide induction followed by glatiramer acetate maintenance. Mult Scler. 2012;18(2):202–9.CrossRefPubMedCentralPubMed
68.
go back to reference Krishnan C et al. Reduction of disease activity and disability with high-dose cyclophosphamide in patients with aggressive multiple sclerosis. Arch Neurol. 2008;65(8):1044–51.PubMedCentralPubMed Krishnan C et al. Reduction of disease activity and disability with high-dose cyclophosphamide in patients with aggressive multiple sclerosis. Arch Neurol. 2008;65(8):1044–51.PubMedCentralPubMed
70.
go back to reference Smith DR et al. A randomized blinded trial of combination therapy with cyclophosphamide in patients-with active multiple sclerosis on interferon beta. Mult Scler. 2005;11(5):573–82.CrossRefPubMed Smith DR et al. A randomized blinded trial of combination therapy with cyclophosphamide in patients-with active multiple sclerosis on interferon beta. Mult Scler. 2005;11(5):573–82.CrossRefPubMed
71.
go back to reference Le Page E et al. Long-term safety profile of mitoxantrone in a French cohort of 802 multiple sclerosis patients: a 5-year prospective study. Mult Scler. 2011;17(7):867–75.CrossRefPubMed Le Page E et al. Long-term safety profile of mitoxantrone in a French cohort of 802 multiple sclerosis patients: a 5-year prospective study. Mult Scler. 2011;17(7):867–75.CrossRefPubMed
72.
go back to reference Azzopardi L et al. Predicting autoimmunity after alemtuzumab treatment of multiple sclerosis. J Neurol Neurosurg Psychiatry. 2014;85(7):795–8.CrossRefPubMed Azzopardi L et al. Predicting autoimmunity after alemtuzumab treatment of multiple sclerosis. J Neurol Neurosurg Psychiatry. 2014;85(7):795–8.CrossRefPubMed
73.
go back to reference Bevan CJ, Cree BA. Disease activity free status: a new end point for a new era in multiple sclerosis clinical research? JAMA Neurol. 2014;71(3):269–70.CrossRefPubMed Bevan CJ, Cree BA. Disease activity free status: a new end point for a new era in multiple sclerosis clinical research? JAMA Neurol. 2014;71(3):269–70.CrossRefPubMed
74.
go back to reference Havrdova E et al. Disease-activity-free status in patients with relapsing-remitting multiple sclerosis treated with daclizumab high-yield process in the SELECT study. Mult Scler. 2014;20(4):464–70.CrossRefPubMed Havrdova E et al. Disease-activity-free status in patients with relapsing-remitting multiple sclerosis treated with daclizumab high-yield process in the SELECT study. Mult Scler. 2014;20(4):464–70.CrossRefPubMed
75.
go back to reference Giovannoni G et al. Sustained disease-activity-free status in patients with relapsing-remitting multiple sclerosis treated with cladribine tablets in the CLARITY study: a post-hoc and subgroup analysis. Lancet Neurol. 2011;10(4):329–37.CrossRefPubMed Giovannoni G et al. Sustained disease-activity-free status in patients with relapsing-remitting multiple sclerosis treated with cladribine tablets in the CLARITY study: a post-hoc and subgroup analysis. Lancet Neurol. 2011;10(4):329–37.CrossRefPubMed
76.
go back to reference Vercellino M et al. Multiple sclerosis relapses: a multivariable analysis of residual disability determinants. Acta Neurol Scand. 2009;119(2):126–30.CrossRefPubMed Vercellino M et al. Multiple sclerosis relapses: a multivariable analysis of residual disability determinants. Acta Neurol Scand. 2009;119(2):126–30.CrossRefPubMed
78.
go back to reference van Winsen LM et al. Outcome measurement in multiple sclerosis: detection of clinically relevant improvement. Mult Scler. 2010;16(5):604–10.CrossRefPubMed van Winsen LM et al. Outcome measurement in multiple sclerosis: detection of clinically relevant improvement. Mult Scler. 2010;16(5):604–10.CrossRefPubMed
79.
go back to reference Solaro C, Uccelli MM. Management of pain in multiple sclerosis: a pharmacological approach. Nat Rev Neurol. 2011;7(9):519–27.CrossRefPubMed Solaro C, Uccelli MM. Management of pain in multiple sclerosis: a pharmacological approach. Nat Rev Neurol. 2011;7(9):519–27.CrossRefPubMed
80.
go back to reference Hadjimichael O et al. Persistent pain and uncomfortable sensations in persons with multiple sclerosis. Pain. 2007;127(1–2):35–41.CrossRefPubMed Hadjimichael O et al. Persistent pain and uncomfortable sensations in persons with multiple sclerosis. Pain. 2007;127(1–2):35–41.CrossRefPubMed
81.
go back to reference Tang DH et al. Impact of urinary incontinence on health-related quality of life, daily activities, and healthcare resource utilization in patients with neurogenic detrusor overactivity. BMC Neurol. 2014;14:74.CrossRefPubMedCentralPubMed Tang DH et al. Impact of urinary incontinence on health-related quality of life, daily activities, and healthcare resource utilization in patients with neurogenic detrusor overactivity. BMC Neurol. 2014;14:74.CrossRefPubMedCentralPubMed
82.
go back to reference Rizzo MA et al. Prevalence and treatment of spasticity reported by multiple sclerosis patients. Mult Scler. 2004;10(5):589–95.CrossRefPubMed Rizzo MA et al. Prevalence and treatment of spasticity reported by multiple sclerosis patients. Mult Scler. 2004;10(5):589–95.CrossRefPubMed
83.
go back to reference Zwibel HL, Smrtka J. Improving quality of life in multiple sclerosis: an unmet need. Am J Manag Care. 2011;17(Suppl 5 Improving):S139–45.PubMed Zwibel HL, Smrtka J. Improving quality of life in multiple sclerosis: an unmet need. Am J Manag Care. 2011;17(Suppl 5 Improving):S139–45.PubMed
85.
go back to reference Courtney AM et al. Functional treatments in multiple sclerosis. Curr Opin Neurol. 2011;24(3):250–4.CrossRefPubMed Courtney AM et al. Functional treatments in multiple sclerosis. Curr Opin Neurol. 2011;24(3):250–4.CrossRefPubMed
86.
go back to reference Craig J et al. A randomised controlled trial comparing rehabilitation against standard therapy in multiple sclerosis patients receiving intravenous steroid treatment. J Neurol Neurosurg Psychiatry. 2003;74(9):1225–30.CrossRefPubMedCentralPubMed Craig J et al. A randomised controlled trial comparing rehabilitation against standard therapy in multiple sclerosis patients receiving intravenous steroid treatment. J Neurol Neurosurg Psychiatry. 2003;74(9):1225–30.CrossRefPubMedCentralPubMed
87.
go back to reference Hauser SL, Chan JR, Oksenberg JR. Multiple sclerosis: prospects and promise. Ann Neurol. 2013;74(3):317–27.CrossRefPubMed Hauser SL, Chan JR, Oksenberg JR. Multiple sclerosis: prospects and promise. Ann Neurol. 2013;74(3):317–27.CrossRefPubMed
88.
go back to reference Suhs KW et al. A randomized, double-blind, phase 2 study of erythropoietin in optic neuritis. Ann Neurol. 2012;72(2):199–210.CrossRefPubMed Suhs KW et al. A randomized, double-blind, phase 2 study of erythropoietin in optic neuritis. Ann Neurol. 2012;72(2):199–210.CrossRefPubMed
Metadata
Title
Therapeutic Management of Severe Relapses in Multiple Sclerosis
Authors
Carolyn Bevan, MD, MS
Jeffrey M. Gelfand, MD, MAS
Publication date
01-04-2015
Publisher
Springer US
Published in
Current Treatment Options in Neurology / Issue 4/2015
Print ISSN: 1092-8480
Electronic ISSN: 1534-3138
DOI
https://doi.org/10.1007/s11940-015-0345-6

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