Long-term effects of dalfampridine in patients with multiple sclerosis

Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment par...

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Published in:Journal of the neurological sciences Vol. 337; no. 1-2; pp. 18 - 24
Main Authors: Ruck, T., Bittner, S., Simon, O.J., Göbel, K., Wiendl, H., Schilling, M., Meuth, S.G.
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 15.02.2014
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ISSN:0022-510X, 1878-5883, 1878-5883
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Abstract Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9–12months. Fifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2weeks and after 9–12months later. Thirty out of fifty-two patients (~60%) were still on treatment after 9–12months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9–12months. In contrast significant effects for velocity were observed only after 2weeks, for improvement in PASAT only after 9–12months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients. Dalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.
AbstractList Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9-12 months.BACKGROUND/OBJECTIVEDalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9-12 months.Fifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2 weeks and after 9-12 months later.METHODSFifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2 weeks and after 9-12 months later.Thirty out of fifty-two patients (~60%) were still on treatment after 9-12 months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9-12 months. In contrast significant effects for velocity were observed only after 2 weeks, for improvement in PASAT only after 9-12 months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients.RESULTSThirty out of fifty-two patients (~60%) were still on treatment after 9-12 months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9-12 months. In contrast significant effects for velocity were observed only after 2 weeks, for improvement in PASAT only after 9-12 months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients.Dalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.CONCLUSIONDalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.
Abstract Background/objective Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9–12 months. Methods Fifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2 weeks and after 9–12 months later. Results Thirty out of fifty-two patients (~ 60%) were still on treatment after 9–12 months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9–12 months. In contrast significant effects for velocity were observed only after 2 weeks, for improvement in PASAT only after 9–12 months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients. Conclusion Dalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.
Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9-12 months. Fifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2 weeks and after 9-12 months later. Thirty out of fifty-two patients (~60%) were still on treatment after 9-12 months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9-12 months. In contrast significant effects for velocity were observed only after 2 weeks, for improvement in PASAT only after 9-12 months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients. Dalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.
Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with multiple sclerosis. Our aim was to examine the short- and long-term effects of treatment with dalfampridine on motoric and cognitive assessment parameters of multiple sclerosis (MS) patients over 9–12months. Fifty-two patients with MS with an EDSS between 4.0 and 7.0 and impaired mobility were evaluated for parameters of walking ability, MSFC, cognitive and motor fatigue and evoked potentials at treatment initiation with dalfampridine as well as 2weeks and after 9–12months later. Thirty out of fifty-two patients (~60%) were still on treatment after 9–12months. Two weeks after treatment initiation, significant ameliorations could be found for T25FW, maximum walking distance as well as motoric and cognitive fatigue which still persisted after 9–12months. In contrast significant effects for velocity were observed only after 2weeks, for improvement in PASAT only after 9–12months. A tendency for improvement of somatosensory evoked potentials was found in a subset of patients. Dalfampridine shows positive short- and long-term effects on motoric and cognitive assessment parameters in an open-label observational study in a cohort of patients with MS.
Author Bittner, S.
Schilling, M.
Ruck, T.
Simon, O.J.
Wiendl, H.
Meuth, S.G.
Göbel, K.
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Cites_doi 10.1016/S0306-4522(96)00477-0
10.1177/1352458510386998
10.1007/BF00810346
10.1097/01.wco.0000413319.87092.19
10.1016/j.pharmthera.2005.10.006
10.1016/j.acn.2005.07.006
10.1111/j.0953-816X.2004.03164.x
10.1038/283570a0
10.1177/1352458508088916
10.1016/j.expneurol.2013.05.016
10.1212/WNL.45.11.1956
10.1191/135248506ms1244oa
10.1006/exnr.1997.6706
10.1016/j.jns.2006.06.031
10.1002/ana.22240
10.1185/03007995.2011.583229
10.1007/s004150170222
10.1093/brain/123.1.171
10.1016/0006-8993(96)00667-1
10.1177/1352458509348519
10.1002/ana.20703
10.1056/NEJMra052130
10.1212/WNL.44.9.1701
10.1212/WNL.33.11.1444
10.1002/mus.880030202
10.1191/135245801701567050
10.1017/S0317167100048691
10.1016/S0140-6736(09)60442-6
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Issue 1-2
Keywords Mobility
Fatigue
Dalfampridine
Long-term treatment
MS
Walking ability
Language English
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References Heesen, Bohm, Reich, Kasper, Goebel, Gold (bb0015) 2008; 14
Dunn, Blight (bb0025) 2011; 27
Gobel, Wedell, Herrmann, Wachsmuth, Pankratz, Bittner (bb0120) 2013; 248C
Fisk, Pontefract, Ritvo, Archibald, Murray (bb0130) 1994; 21
Tombaugh (bb0135) 2006; 21
Meyer, Britton, Benecke, Bischoff, Machetanz, Conrad (bb0085) 1992; 239
Meuth, Bittner, Seiler, Gobel, Wiendl (bb0090) 2011; 17
Smith, Felts, John (bb0045) 2000; 123
Kurtzke (bb0095) 1983; 33
Shi, Kelly, Blight (bb0155) 1997; 148
Krupp, Coyle, Doscher, Miller, Cross, Jandorf (bb0105) 1995; 45
NHS Commisioning Board (bb0060)
Smits, Emmen, Bertelsmann, Kulig, van Loenen, Polman (bb0115) 1994; 44
Fehlings, Nashmi (bb0145) 1996; 736
Kallmann, Fackelmann, Toyka, Rieckmann, Reiners (bb0080) 2006; 12
Frohman, Racke, Raine (bb0005) 2006; 354
Comi, Leocani, Rossi, Colombo (bb0125) 2001; 248
Rossini, Pasqualetti, Pozzilli, Grasso, Millefiorini, Graceffa (bb0110) 2001; 7
Goodman, Brown, Krupp, Schapiro, Schwid, Cohen (bb0050) 2009; 373
Fischer, Jak, Kniker, Rudick, Cutter (bb0070) 2001
Judge, Bever (bb0140) 2006; 111
Daroff, Fenichel, Jankovic, Mazziota (bb0010) 2012
Goodman, Brown, Edwards, Krupp, Schapiro, Cohen (bb0055) 2010; 68
Sherratt, Bostock, Sears (bb0030) 1980; 283
Miller, Rhoades (bb0020) 2012
Karimi-Abdolrezaee, Eftekharpour, Fehlings (bb0150) 2004; 19
Kim, Goldner, Sanders (bb0040) 1980; 3
Amato, Portaccio (bb0100) 2007; 259
Penner, Raselli, Stocklin, Opwis, Kappos, Calabrese (bb0075) 2009; 15
Shi, Blight (bb0035) 1997; 77
Polman, Reingold, Edan, Filippi, Hartung, Kappos (bb0065) 2005; 58
Rossini (10.1016/j.jns.2013.11.011_bb0110) 2001; 7
Tombaugh (10.1016/j.jns.2013.11.011_bb0135) 2006; 21
Goodman (10.1016/j.jns.2013.11.011_bb0050) 2009; 373
Kallmann (10.1016/j.jns.2013.11.011_bb0080) 2006; 12
NHS Commisioning Board (10.1016/j.jns.2013.11.011_bb0060)
Shi (10.1016/j.jns.2013.11.011_bb0035) 1997; 77
Frohman (10.1016/j.jns.2013.11.011_bb0005) 2006; 354
Smith (10.1016/j.jns.2013.11.011_bb0045) 2000; 123
Judge (10.1016/j.jns.2013.11.011_bb0140) 2006; 111
Dunn (10.1016/j.jns.2013.11.011_bb0025) 2011; 27
Amato (10.1016/j.jns.2013.11.011_bb0100) 2007; 259
Meyer (10.1016/j.jns.2013.11.011_bb0085) 1992; 239
Comi (10.1016/j.jns.2013.11.011_bb0125) 2001; 248
Miller (10.1016/j.jns.2013.11.011_bb0020) 2012
Fisk (10.1016/j.jns.2013.11.011_bb0130) 1994; 21
Karimi-Abdolrezaee (10.1016/j.jns.2013.11.011_bb0150) 2004; 19
Fischer (10.1016/j.jns.2013.11.011_bb0070) 2001
Gobel (10.1016/j.jns.2013.11.011_bb0120) 2013; 248C
Daroff (10.1016/j.jns.2013.11.011_bb0010) 2012
Goodman (10.1016/j.jns.2013.11.011_bb0055) 2010; 68
Penner (10.1016/j.jns.2013.11.011_bb0075) 2009; 15
Krupp (10.1016/j.jns.2013.11.011_bb0105) 1995; 45
Fehlings (10.1016/j.jns.2013.11.011_bb0145) 1996; 736
Kim (10.1016/j.jns.2013.11.011_bb0040) 1980; 3
Shi (10.1016/j.jns.2013.11.011_bb0155) 1997; 148
Meuth (10.1016/j.jns.2013.11.011_bb0090) 2011; 17
Smits (10.1016/j.jns.2013.11.011_bb0115) 1994; 44
Sherratt (10.1016/j.jns.2013.11.011_bb0030) 1980; 283
Kurtzke (10.1016/j.jns.2013.11.011_bb0095) 1983; 33
Polman (10.1016/j.jns.2013.11.011_bb0065) 2005; 58
Heesen (10.1016/j.jns.2013.11.011_bb0015) 2008; 14
References_xml – volume: 123
  start-page: 171
  year: 2000
  end-page: 184
  ident: bb0045
  article-title: Effects of 4-aminopyridine on demyelinated axons, synapses and muscle tension
  publication-title: Brain
– volume: 248C
  start-page: 62
  year: 2013
  end-page: 71
  ident: bb0120
  article-title: 4-Aminopyridine ameliorates mobility but not disease course in an animal model of multiple sclerosis
  publication-title: Exp Neurol
– volume: 259
  start-page: 118
  year: 2007
  end-page: 122
  ident: bb0100
  article-title: Clinical outcome measures in multiple sclerosis
  publication-title: J Neurol Sci
– volume: 111
  start-page: 224
  year: 2006
  end-page: 259
  ident: bb0140
  article-title: Potassium channel blockers in multiple sclerosis: neuronal Kv channels and effects of symptomatic treatment
  publication-title: Pharmacol Ther
– volume: 68
  start-page: 494
  year: 2010
  end-page: 502
  ident: bb0055
  article-title: A phase 3 trial of extended release oral dalfampridine in multiple sclerosis
  publication-title: Ann Neurol
– volume: 7
  start-page: 354
  year: 2001
  end-page: 358
  ident: bb0110
  article-title: Fatigue in progressive multiple sclerosis: results of a randomized, double-blind, placebo-controlled, crossover trial of oral 4-aminopyridine
  publication-title: Mult Scler
– volume: 77
  start-page: 553
  year: 1997
  end-page: 562
  ident: bb0035
  article-title: Differential effects of low and high concentrations of 4-aminopyridine on axonal conduction in normal and injured spinal cord
  publication-title: Neuroscience
– volume: 373
  start-page: 732
  year: 2009
  end-page: 738
  ident: bb0050
  article-title: Sustained-release oral fampridine in multiple sclerosis: a randomised, double-blind, controlled trial
  publication-title: Lancet
– volume: 3
  start-page: 105
  year: 1980
  end-page: 111
  ident: bb0040
  article-title: Facilitatory effects of 4-aminopyridine on normal neuromuscular transmission
  publication-title: Muscle Nerve
– volume: 736
  start-page: 135
  year: 1996
  end-page: 145
  ident: bb0145
  article-title: Changes in pharmacological sensitivity of the spinal cord to potassium channel blockers following acute spinal cord injury
  publication-title: Brain Res
– volume: 248
  start-page: 174
  year: 2001
  end-page: 179
  ident: bb0125
  article-title: Physiopathology and treatment of fatigue in multiple sclerosis
  publication-title: J Neurol
– volume: 44
  start-page: 1701
  year: 1994
  end-page: 1705
  ident: bb0115
  article-title: The effects of 4-aminopyridine on cognitive function in patients with multiple sclerosis: a pilot study
  publication-title: Neurology
– ident: bb0060
  article-title: Clinical commissioning policy statement: Fampridine for, multiple sclerosis
– volume: 21
  start-page: 9
  year: 1994
  end-page: 14
  ident: bb0130
  article-title: The impact of fatigue on patients with multiple sclerosis
  publication-title: Can J Neurol Sci
– year: 2001
  ident: bb0070
  article-title: Multiple Sclerosis Functional Composite (MSFC): administration and scoring manual
– volume: 354
  start-page: 942
  year: 2006
  end-page: 955
  ident: bb0005
  article-title: Multiple sclerosis — the plaque and its pathogenesis
  publication-title: N Engl J Med
– volume: 21
  start-page: 53
  year: 2006
  end-page: 76
  ident: bb0135
  article-title: A comprehensive review of the Paced Auditory Serial Addition Test (PASAT)
  publication-title: Arch Clin Neuropsychol
– volume: 19
  start-page: 577
  year: 2004
  end-page: 589
  ident: bb0150
  article-title: Temporal and spatial patterns of Kv1.1 and Kv1.2 protein and gene expression in spinal cord white matter after acute and chronic spinal cord injury in rats: implications for axonal pathophysiology after neurotrauma
  publication-title: Eur J Neurosci
– volume: 27
  start-page: 1415
  year: 2011
  end-page: 1423
  ident: bb0025
  article-title: Dalfampridine: a brief review of its mechanism of action and efficacy as a treatment to improve walking in patients with multiple sclerosis
  publication-title: Curr Med Res Opin
– volume: 45
  start-page: 1956
  year: 1995
  end-page: 1961
  ident: bb0105
  article-title: Fatigue therapy in multiple sclerosis: results of a double-blind, randomized, parallel trial of amantadine, pemoline, and placebo
  publication-title: Neurology
– volume: 15
  start-page: 1509
  year: 2009
  end-page: 1517
  ident: bb0075
  article-title: The Fatigue Scale for Motor and Cognitive Functions (FSMC): validation of a new instrument to assess multiple sclerosis-related fatigue
  publication-title: Mult Scler
– volume: 33
  start-page: 1444
  year: 1983
  end-page: 1452
  ident: bb0095
  article-title: Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS)
  publication-title: Neurology
– volume: 58
  start-page: 840
  year: 2005
  end-page: 846
  ident: bb0065
  article-title: Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”
  publication-title: Ann Neurol
– start-page: 92
  year: 2012
  end-page: 116
  ident: bb0010
  article-title: Bradley's neurology in clinical practice
– volume: 239
  start-page: 251
  year: 1992
  end-page: 255
  ident: bb0085
  article-title: Motor responses evoked by magnetic brain stimulation in psychogenic limb weakness: diagnostic value and limitations
  publication-title: J Neurol
– volume: 17
  start-page: 198
  year: 2011
  end-page: 203
  ident: bb0090
  article-title: Natalizumab restores evoked potential abnormalities in patients with relapsing–remitting multiple sclerosis
  publication-title: Mult Scler
– volume: 12
  start-page: 58
  year: 2006
  end-page: 65
  ident: bb0080
  article-title: Early abnormalities of evoked potentials and future disability in patients with multiple sclerosis
  publication-title: Mult Scler
– volume: 148
  start-page: 495
  year: 1997
  end-page: 501
  ident: bb0155
  article-title: Conduction block in acute and chronic spinal cord injury: different dose–response characteristics for reversal by 4-aminopyridine
  publication-title: Exp Neurol
– start-page: S4
  year: 2012
  end-page: S10
  ident: bb0020
  article-title: Treatment of relapsing–remitting multiple sclerosis: current approaches and unmet needs
  publication-title: Curr Opin Neurol
– volume: 283
  start-page: 570
  year: 1980
  end-page: 572
  ident: bb0030
  article-title: Effects of 4-aminopyridine on normal and demyelinated mammalian nerve fibres
  publication-title: Nature
– volume: 14
  start-page: 988
  year: 2008
  end-page: 991
  ident: bb0015
  article-title: Patient perception of bodily functions in multiple sclerosis: gait and visual function are the most valuable
  publication-title: Mult Scler
– volume: 77
  start-page: 553
  year: 1997
  ident: 10.1016/j.jns.2013.11.011_bb0035
  article-title: Differential effects of low and high concentrations of 4-aminopyridine on axonal conduction in normal and injured spinal cord
  publication-title: Neuroscience
  doi: 10.1016/S0306-4522(96)00477-0
– volume: 17
  start-page: 198
  year: 2011
  ident: 10.1016/j.jns.2013.11.011_bb0090
  article-title: Natalizumab restores evoked potential abnormalities in patients with relapsing–remitting multiple sclerosis
  publication-title: Mult Scler
  doi: 10.1177/1352458510386998
– ident: 10.1016/j.jns.2013.11.011_bb0060
– volume: 239
  start-page: 251
  year: 1992
  ident: 10.1016/j.jns.2013.11.011_bb0085
  article-title: Motor responses evoked by magnetic brain stimulation in psychogenic limb weakness: diagnostic value and limitations
  publication-title: J Neurol
  doi: 10.1007/BF00810346
– start-page: S4
  issue: 25 Suppl.
  year: 2012
  ident: 10.1016/j.jns.2013.11.011_bb0020
  article-title: Treatment of relapsing–remitting multiple sclerosis: current approaches and unmet needs
  publication-title: Curr Opin Neurol
  doi: 10.1097/01.wco.0000413319.87092.19
– volume: 111
  start-page: 224
  year: 2006
  ident: 10.1016/j.jns.2013.11.011_bb0140
  article-title: Potassium channel blockers in multiple sclerosis: neuronal Kv channels and effects of symptomatic treatment
  publication-title: Pharmacol Ther
  doi: 10.1016/j.pharmthera.2005.10.006
– volume: 21
  start-page: 53
  year: 2006
  ident: 10.1016/j.jns.2013.11.011_bb0135
  article-title: A comprehensive review of the Paced Auditory Serial Addition Test (PASAT)
  publication-title: Arch Clin Neuropsychol
  doi: 10.1016/j.acn.2005.07.006
– volume: 19
  start-page: 577
  year: 2004
  ident: 10.1016/j.jns.2013.11.011_bb0150
  article-title: Temporal and spatial patterns of Kv1.1 and Kv1.2 protein and gene expression in spinal cord white matter after acute and chronic spinal cord injury in rats: implications for axonal pathophysiology after neurotrauma
  publication-title: Eur J Neurosci
  doi: 10.1111/j.0953-816X.2004.03164.x
– volume: 283
  start-page: 570
  year: 1980
  ident: 10.1016/j.jns.2013.11.011_bb0030
  article-title: Effects of 4-aminopyridine on normal and demyelinated mammalian nerve fibres
  publication-title: Nature
  doi: 10.1038/283570a0
– volume: 14
  start-page: 988
  year: 2008
  ident: 10.1016/j.jns.2013.11.011_bb0015
  article-title: Patient perception of bodily functions in multiple sclerosis: gait and visual function are the most valuable
  publication-title: Mult Scler
  doi: 10.1177/1352458508088916
– volume: 248C
  start-page: 62
  year: 2013
  ident: 10.1016/j.jns.2013.11.011_bb0120
  article-title: 4-Aminopyridine ameliorates mobility but not disease course in an animal model of multiple sclerosis
  publication-title: Exp Neurol
  doi: 10.1016/j.expneurol.2013.05.016
– volume: 45
  start-page: 1956
  year: 1995
  ident: 10.1016/j.jns.2013.11.011_bb0105
  article-title: Fatigue therapy in multiple sclerosis: results of a double-blind, randomized, parallel trial of amantadine, pemoline, and placebo
  publication-title: Neurology
  doi: 10.1212/WNL.45.11.1956
– start-page: 92
  year: 2012
  ident: 10.1016/j.jns.2013.11.011_bb0010
– volume: 12
  start-page: 58
  year: 2006
  ident: 10.1016/j.jns.2013.11.011_bb0080
  article-title: Early abnormalities of evoked potentials and future disability in patients with multiple sclerosis
  publication-title: Mult Scler
  doi: 10.1191/135248506ms1244oa
– volume: 148
  start-page: 495
  year: 1997
  ident: 10.1016/j.jns.2013.11.011_bb0155
  article-title: Conduction block in acute and chronic spinal cord injury: different dose–response characteristics for reversal by 4-aminopyridine
  publication-title: Exp Neurol
  doi: 10.1006/exnr.1997.6706
– volume: 259
  start-page: 118
  year: 2007
  ident: 10.1016/j.jns.2013.11.011_bb0100
  article-title: Clinical outcome measures in multiple sclerosis
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2006.06.031
– volume: 68
  start-page: 494
  year: 2010
  ident: 10.1016/j.jns.2013.11.011_bb0055
  article-title: A phase 3 trial of extended release oral dalfampridine in multiple sclerosis
  publication-title: Ann Neurol
  doi: 10.1002/ana.22240
– volume: 27
  start-page: 1415
  year: 2011
  ident: 10.1016/j.jns.2013.11.011_bb0025
  article-title: Dalfampridine: a brief review of its mechanism of action and efficacy as a treatment to improve walking in patients with multiple sclerosis
  publication-title: Curr Med Res Opin
  doi: 10.1185/03007995.2011.583229
– volume: 248
  start-page: 174
  year: 2001
  ident: 10.1016/j.jns.2013.11.011_bb0125
  article-title: Physiopathology and treatment of fatigue in multiple sclerosis
  publication-title: J Neurol
  doi: 10.1007/s004150170222
– volume: 123
  start-page: 171
  issue: Pt 1
  year: 2000
  ident: 10.1016/j.jns.2013.11.011_bb0045
  article-title: Effects of 4-aminopyridine on demyelinated axons, synapses and muscle tension
  publication-title: Brain
  doi: 10.1093/brain/123.1.171
– volume: 736
  start-page: 135
  year: 1996
  ident: 10.1016/j.jns.2013.11.011_bb0145
  article-title: Changes in pharmacological sensitivity of the spinal cord to potassium channel blockers following acute spinal cord injury
  publication-title: Brain Res
  doi: 10.1016/0006-8993(96)00667-1
– year: 2001
  ident: 10.1016/j.jns.2013.11.011_bb0070
– volume: 15
  start-page: 1509
  year: 2009
  ident: 10.1016/j.jns.2013.11.011_bb0075
  article-title: The Fatigue Scale for Motor and Cognitive Functions (FSMC): validation of a new instrument to assess multiple sclerosis-related fatigue
  publication-title: Mult Scler
  doi: 10.1177/1352458509348519
– volume: 58
  start-page: 840
  year: 2005
  ident: 10.1016/j.jns.2013.11.011_bb0065
  article-title: Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”
  publication-title: Ann Neurol
  doi: 10.1002/ana.20703
– volume: 354
  start-page: 942
  year: 2006
  ident: 10.1016/j.jns.2013.11.011_bb0005
  article-title: Multiple sclerosis — the plaque and its pathogenesis
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra052130
– volume: 44
  start-page: 1701
  year: 1994
  ident: 10.1016/j.jns.2013.11.011_bb0115
  article-title: The effects of 4-aminopyridine on cognitive function in patients with multiple sclerosis: a pilot study
  publication-title: Neurology
  doi: 10.1212/WNL.44.9.1701
– volume: 33
  start-page: 1444
  year: 1983
  ident: 10.1016/j.jns.2013.11.011_bb0095
  article-title: Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS)
  publication-title: Neurology
  doi: 10.1212/WNL.33.11.1444
– volume: 3
  start-page: 105
  year: 1980
  ident: 10.1016/j.jns.2013.11.011_bb0040
  article-title: Facilitatory effects of 4-aminopyridine on normal neuromuscular transmission
  publication-title: Muscle Nerve
  doi: 10.1002/mus.880030202
– volume: 7
  start-page: 354
  year: 2001
  ident: 10.1016/j.jns.2013.11.011_bb0110
  article-title: Fatigue in progressive multiple sclerosis: results of a randomized, double-blind, placebo-controlled, crossover trial of oral 4-aminopyridine
  publication-title: Mult Scler
  doi: 10.1191/135245801701567050
– volume: 21
  start-page: 9
  year: 1994
  ident: 10.1016/j.jns.2013.11.011_bb0130
  article-title: The impact of fatigue on patients with multiple sclerosis
  publication-title: Can J Neurol Sci
  doi: 10.1017/S0317167100048691
– volume: 373
  start-page: 732
  year: 2009
  ident: 10.1016/j.jns.2013.11.011_bb0050
  article-title: Sustained-release oral fampridine in multiple sclerosis: a randomised, double-blind, controlled trial
  publication-title: Lancet
  doi: 10.1016/S0140-6736(09)60442-6
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Snippet Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired mobility in patients with...
Abstract Background/objective Dalfampridine is the extended-release formulation of 4-aminopyridine and is approved for the symptomatic treatment of impaired...
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SubjectTerms 4-Aminopyridine - therapeutic use
Cognition Disorders - drug therapy
Cognition Disorders - etiology
Dalfampridine
Disability Evaluation
Drug Delivery Systems
Electroencephalography
Evoked Potentials - drug effects
Evoked Potentials - physiology
Fatigue
Female
Follow-Up Studies
Humans
Long-term treatment
Male
Middle Aged
Mobility
Multiple Sclerosis - complications
Multiple Sclerosis - drug therapy
Neurology
Potassium Channel Blockers - therapeutic use
Severity of Illness Index
Statistics, Nonparametric
Time Factors
Walking - physiology
Walking ability
Title Long-term effects of dalfampridine in patients with multiple sclerosis
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https://www.ncbi.nlm.nih.gov/pubmed/24290498
https://www.proquest.com/docview/1500698161
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