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Label
Multiple Sclerosis (MS)

DefinitionEtiologyEpidemiologyPathophysiologyClinical Presentation
WorkupGoalsMed ChoicesClinical TrialsPipeline AgentsResourcesRefs
Definition:

Autoimmune inflammatory demyelinating disease that can affect any part of central nervous system.

 

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Etiology:

Unknown, but appears to be a compilation of several factors which includes: genetic susceptibility, viral or environmental factors, and autoimmune dysfunction.

  • Genetic susceptibility/predisposition
    • HLA linkage through HLA-DR2 and alleles of interleukin 2 (IL-2) and 7 (IL-7) receptor alpha gene
    • Other "hot spots" include genes for IL-7 and IL-20
  • Viral etiology:
    • Epstein bar virus (EBV) continues to be considered especially now in pediatric studies
  • Environmental factors:
    • Vitamin D deficiency, possibly secondary to reduced sun exposure
    • Cigarette smoking
  • Autoimmune dysfunction
    • Pathological lymphocytic infiltrates in acute plaques
    • Changes in peripheral blood lymphocytes similar to autoimmune patterns in animal models
    • Improvement or remission with drugs modulating or suppressing the immune system

 

Classification:

  • Primary progressive MS (PPMS)
    • Gradual progression with a changing slope
    • No apparent relapses
  • Progressive relapsing MS (PRMS)
    • Steady cumulative progression of clinical neurologic damage
    • Superimposed relapses with or without remissions
  • Relapsing remitting MS (RRMS)
    • Most common initial presentation
    • Periods of relapse during which time new symptoms can appear, followed by periods of complete or incomplete remission
  • Secondary progressive MS (SPMS)
    • Evolves from RRMS
    • SPMS is often typically preceded by a variable period (2-40 years) of RRMS
    • Steady progression of clinical neurologic damage in the absence of intervening relapses
    • Relapses, often with residual deficits may or may not ensue

 

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Epidemiology:
  • Typical age of onset: 20-40 years; range: 2-80 years
  • Mean age of onset 32 years
  • Female > Male
  • Worldwide incidence ~0.1%
  • Prevalence
    • Canada ~55,000-75,000
    • USA ~350,000-400,000
    • Worldwide ~2.5 million
  • Increased incidence observed when moving away from the equator in either direction
  • Economic impact: Cost of managing disease plus disability plus loss of manpower productivity for patient and care givers (the greatest cause of acquired non-traumatic neurological impairment in young people)
  • Death often results from medical complications (e.g. infections)

 

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Pathophysiology:
  • Demyelination: An immune mediated inflammation which denudes axons of their myelin
  • Demyelination is often followed by attempts of remyelination
  • The cycle of demyelination and remyelination, leads to inadequate and often ineffective myelination
  • In addition, axonal injury may eventually occur as "collateral" damage
  • Hence the initial relapsing remitting process may evolve into a secondary progression

 

The mechanism is as follows:

1-MS-Pathophysiology-Mechanism

 

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Clinical Presentation:

Variable neurological symptoms separated in space (depending on CNS areas involved) and time by months or years. There may well be a threshold beyond which progressive neurological decline may ensue.

Common eventual symptoms are:

  • Fatigue and generalized weakness
  • Abnormal reflexes: Absent or exaggerated
  • Vision disturbances: Impaired or double vision, nystagmus
  • Motor dysfunction: Focal weakness, tremor, incoordination
  • Sensory disturbances: Paraesthesias, impaired deep sensation, impaired vibratory and position sense
  • Impaired speech: Slurring, scanning (dysarthria)
  • Urinary dysfunction:
    • Hesitancy, frequency, urgency, retention, incontinence; urinary tract infections (UTI)
    • Urinary dysfunction affects about 90% of patients with MS and UTIs may exacerbate relapse of MS
  • Neurobehavioral syndromes: Depression, cognitive impairment, emotional liability

Symptoms of MS are often unpredictable, varying from person to person and from time to time in the same person.

 

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Investigation and Workup:

History:

  • History of previous transient neurological episodes, including duration of events and recurrence
  • Information of relapsing remitting phenomenon over time
  • Ocular history - including acuity, loss of color vision
  • History of depression or cognitive impairment

Other symptoms:

Bowel/bladder

  • Urinary urgency and frequency, may progress to incontinence and bladder atony
  • Urinary tract infections are common in MS (F > M), further contributes to bladder dysfunction
  • Constipation, fecal incontinence

Pain

  • Common complain
  • Approximately 43 % of patients report one or more painful symptoms such as trigeminal neuralgia, Lhermitte's phenomenon, dysesthesia, back pain, visceral pain, and pain due to muscle spasms

Sexual dysfunction

  • Men experience various degrees of erectile dysfunction
  • Women may experience lack of sensitivity and dyspareunia due to decreased vaginal lubrication

Uhthoff's phenomenon

  • Exposure to hot conditions (sun, sauna, hot-tubs etc.) transiently worsens neurological symptoms
  • Mechanism likely related to conduction block

Fatigue

  • The degree of fatigue is discordant with the level of activity. May precede focal neurological symptoms

Depression

  • More than 50% of patients may have some degree of depression
  • Multifactorial, related to psychological aspect of acquiring a potentially debilitating chronic progressive disorder ±co-morbidities

Cognitive dysfunction

  • Cognitive impairment occurs in 34-65% of patients
  • May be present at time of detection of MS

Epilepsy

  • 2-3% of patients may develop epilepsy

 

Neurological Examination

Eye examination

  • Fundoscopy (optic nerve assessment for optic neuritis)
  • Nystagmus
  • Assessment of loss of vision

Motor symptoms

  • Face, limb or trunk weakness ±associated in-coordination

Sensory Symptoms

  • Numbness, tingling, pins-and-needles, coldness
  • Band-like tightness around limbs or torso
  • Decreased sensitivity to light touch
  • Paraesthesia, impaired deep, vibratory and positional sensations

Vertigo

  • Sense of the movement (often rotational) of a person or to an external environment. May be due to brain stem plaques
  • May also occur in conjunction with other brain stem findings including nystagmus, diplopia, facial weakness or dysesthesia, hyper- or hypoacusis, and long track signs (hemi-sensory or hemi-motor deficits)

Lhermitte's phenomenon

  • Transient sensory disturbance with the sensation of an electric-like shock radiating down the spine into the limbs and triggered by neck flexion
  • Occurs with other lesions of the upper cervical cord including tumors, cervical disc herniation, and trauma

Coordination and balance

  • Incoordination of limbs (including finger dexterity), trunk and gait
  • Impact on ADLs such as writing, eating, dressing, walking etc.

 

Laboratory:

  • CBC
  • Electrolytes, calcium
  • B12, folate
  • ESR
  • ANA/rheumatoid factor
  • Antiphospholipid/anticardiolipin antibodies
  • Thyroid studies (freeT4, TSH)
  • NMO-IgG [if neuromyelitis optica (Devic's disease) suspected]
  • Lyme serology (if in endemic area)
  • Serology for HTLV I/HTLV II (if tropical spastic paraparesis suspected)
  • HIV (if PML suspected)

 

CNS Imaging

MRI

  • 95% sensitive in patients with established disease, detects white matter lesions with brain and spinal cord

2010 McDonald criteria for the diagnosis of multiple sclerosis

The revised McDonald criteria replaced the previously used terms such as "clinically definite" and "probable MS" with following:

  • The diagnosis of "MS" is given if diagnostic criteria are fulfilled
  • The diagnosis of "possible MS" is given if the criteria are not completely met
  • The diagnosis of "not MS" is given if the criteria are fully explored and not met

 

CSF Analysis

  • Oligoclonal bands: Distinct electrophoretic patterns reflecting elevation of IgG, present in >95% of patients with established disease but can be non-specific, as can the MRI imaging, and may be seen in other neurodegenerative conditions and CNS infections
  • Elevated IgG index in <90% of patients (values reported as > 0.7)
  • Mild pleocytosis (unusual to have WBC >50)
  • Mildly elevated protein is not unusual

 

Evoked potentials

  • A measure of electrical conductance along the neuroaxis
  • Electrodes placed at different points over peripheral nerves, spinal cord and cortex can be used to detect conduction delays in an induced electrical potential
  • Delays in conduction may help to localize lesions
  • Types of evoked potentials:
    • Somatosensory evoked potential (SSEP)
    • Brain stem auditory evoked potential (BAER)
    • Motor evoked potentials via magnetic stimulation
    • Visual evoked potentials (VEP)-(the most useful of all)

 

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Treatment Goals:
  • Decrease the number of relapses and minimize new lesions
  • Prevent and manage disability
  • Optimize quality of life, by improving functionality
  • Treat acute attacks quickly and adequately
  • Symptomatic management

Factors contributing to achieve the goals are:

  • Early diagnosis and intervention (as required)
  • Use of disease modifying agents
  • Commitment and compliance to the treatment
  • Patient's knowledge and participation in treatment

 

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Therapeutic Choices:

Goal is to:

  • Shorten the acute exacerbation
  • Decrease the frequency of acute attacks and delay disease progression
  • Relieve the symptoms to maintain the quality of life

 

Treatment strategies:

  • a) Treatment of acute exacerbation
  • b) Disease modifying therapy
  • c) Symptomatic treatment
  • d) Non-pharmacological treatment

 

A) Acute exacerbations:

For patients presenting with functional impairment, in acute phase, the recommended first line treatment is glucocorticoids.

  • Methylprednisolone: 1-2 g/day IV usually for 3-5 days (but can be used up to 10 days). May be followed by tapering dose of oral prednisone (e.g. 100 mg x 1 dose then decrease by 10 mg daily until finished)
  • Prednisone: 500-1 g PO daily for 3-5 days. May be followed by tapering dose of oral prednisone

 

B) Disease modifying therapy:

Indications:

  • Relapsing remitting (RRMS) phase
  • Secondary progressive multiple sclerosis (SPMS)
  • There is no FDA approved treatment for primary progressive; trials with IFN beta, glatiramer acetate and mitoxantrone have shown no benefits

Drug options with proven benefit:

Interferon Beta 1a:

  • Intramuscular: 30 µg every week
  • Subcutaneous: 22−44 µg three times per week

Interferon Beta 1b:

  • Dose: 250 µg SC daily

Glatiramer acetate:

  • Dose: 20 mg SC daily

Fingolimod:

  • Dose: 0.5 mg (500 µg) PO daily

Teriflunomide:

  • Dose: 7-14mg PO daily

Natalizumab:

  • Dose: 300 mg IV once in 4 weeks
  • Indicated for refractory and aggressive RRMS
  • Associated with risk of progressive multifocal leukoencephalopathy

Mitoxantrone:

  • Dose: 5-12 mg/m2 IV every 3 months for 2 years, with a lifetime cumulative dose of 140 mg/m2
  • Indicated for refractory MS
  • Potentially cardio-toxic; baseline LV function is required. Risk of leukemia is lifelong and a yearly CBC is recommended

Plasma exchange

  • For steroid resistant exacerbation

 

Other agents which have been tried but without proven benefit include:

Cyclophosphamide:

  • Dose: 700 mg/m2 IV; every month along with 1 g of methylprednisolone
  • Highly myelosuppressive; monitor absolute neutrophils count for dose adjustment

Other experimental modalities include:

  • Hematopoietic stem cell transplantation

Intravenous immunoglobulin (IVIG):

  • In the partum or immediate post-partum period
    • Induction with 0.4 g/kg daily for 5 days followed by monthly 1 g/kg

 

C) Symptomatic treatment:

  • Inevitable as disease advances
  • Complex due to the widespread compromise of CNS function

 

Symptoms often requiring attention include:

1) Spasticity:

Pain and constipation may trigger spasticity. Assess and treat before using antispasmodics.

Treatment:

Baclofen:

  • Dose: 5-10 mg PO TID
  • Maximum dose: 80 mg/day

Tizanidine:

  • Dose: 2-4 mg PO TID
  • Maximum dose: 36 mg/day

Gabapentin:

  • Dose: Begin at 100 to 300 mg TID
  • Effective dose range: 900-1800 mg/daily in 3 divided doses
  • Maximum dose: 2400 mg-3,600 mg/day

Diazepam:

  • Dose: 5-10 mg PO TID PRN

Cannabinoids(delta-9-tetrahydrocannabinol & cannabidiol)

  • Dose: Buccal 1 spray every 4 hr, 4-5 sprays/day for MS
  • May start initially with 1 spray/day; increase every 1-2d; Max. ~12 sprays/day

Caution: Abrupt discontinuation of the above agents may cause seizures and withdrawal symptoms.

Botulinum toxin:

  • Dose dependent on site of administration and severity of disease

 

2) Fatigue:

May be characterized as:

  • Neuromuscular fatigue
  • Daytime drowsiness secondary to insomnia
  • Fatigue associated with depression

Treatment:

Amantadine:

  • Dose: 100 mg PO BID; may improve MS associated lassitude

Modafinil:

  • Dose: 100 mg PO BID

Antidepressant:

  • For fatigue associated with depression(e.g. fluoxetine)

Fampridine (4 amino pyridine):

  • Dose: 10 mg PO daily

 

3) Pain:

  • Acute or chronic pain is a frequent complaint in MS patients affecting the quality of life
  • Chronic pain description include burning, squeezing, lancinating or gritty
  • Neuropathic pain does not respond to NSAIDs

Treatment:

Gabapentin:

  • Dose: Begin at 100 to 300 mg PO TID
  • Effective dose range: 900-1800 mg/daily in 3-4 divided doses
  • Maximum dose: 2400mg-3,600 mg/day

Carbamazepine:

  • Dose: 100-200 mg PO daily
  • Increase up to a total daily dosage of 600-1,600 mg (divided) as tolerated
  • Monitor drug levels, CBC,LFTs

Tramadol:

  • Dose: 50-400 mg PO daily as tolerated

Pregabalin:

  • Dose: May begin with 25-75 mg PO daily and increase to 150 mg PO BID
  • Effective dose range: 900-1800 mg/daily in 3-4 divided doses
  • Maximum dose: 600 mg daily in divided doses

Cannabinoids(delta-9-tetrahydrocannabinol & cannabidiol)

  • Dose: Buccal 1 spray every 4 hr, 4-5 sprays/day for MS
  • May start initially with 1 spray/day; increase every 1-2 d; Max. ~12 sprays/day

 

4) Paroxysmal symptoms:

  • Lhermitte sign or barber chair phenomenon (an electrical sensation that radiates down the vertebra on flexion or extension of neck)
  • Intermittent vertigo

Treatment:

  • Carbamazepine
  • Gabapentin

 

5) Bladder dysfunction:

Bladder spasticity:

  • Oxybutynin: 5 mg PO TID or QID
  • Tolterodine: 2 mg PO BID
  • Imipramine: Usual dose 75 mg PO daily
  • Solifenacin: 5 mg PO daily
  • Darifenacin: Extended release 7.5 mg PO daily; may increase to 15 PO daily
  • Trospium: 20 mg PO BID
  • Intravesicular botox: 200 Units

 

Denervated bladder treated by:

  • Self-catheterization

Nocturia, night-time incontinence/urgency:

  • Desmopressin (DDAVP): 0.1-0.4 mg PO once at bed time

 

6) Bowel dysfunction:

Constipation: can be treated with combination of fiber and stool softeners.

  • High fiber diet and stool softeners
  • Docusate Sodium: 100 mg PO TID
  • Stimulants: Senna suppositories 2 tabs at bed time; digital stimulation sometimes used
  • Adopting a bowel regimen may help to regulate urges and incontinence

 

7) Sexual dysfunction

Erectile dysfunction:

Oral agents:

  • Sildenafil* 50-100 mg
  • Vardenafil* 5-20 mg
  • Tadalafil* 5-20 mg

*Give medication 30 minutes prior to intercourse; caution

advised in elderly and with cardiac disease.

Injectable agents (intracavernous):

  • Alprostadil:
    • Begin with 2.5 mcg and titrate by 2.5 mcg increments
    • Initial administered under supervision
    • Doses exceeding 40 mcg not recommended

Vaginismus:

  • Antispasmodics

Vaginal dryness:

  • Water based lubrication

 

8) Depression

It can be managed through counseling and/or medication.

Tricyclic antidepressant

  • Amitriptyline: 75-200 mg/day PO at night or in divided doses
  • Imipramine: 75-150 mg/day PO at night or in divided doses
  • Nortriptyline: 25-200 mg/day PO at night or in divided doses

Selective serotonin reuptake inhibitors (SSRIs)

  • Fluoxetine: 20-80 mg PO once daily
  • Paroxetine:
    • 20 mg PO once daily
    • May increase by 10 mg/day to maximum of 50 mg/day
  • Sertraline:
    • 50 mg PO once daily
  • Citalopram:
    • 20 mg PO once daily; may increase by 20 mg/week to maximum of 40 mg/day

Serotonin/norepinephrine reuptake inhibitors (SNRIs)

  • Duloxetine:
    • Start 30-60 mg PO once daily; target dose 60 mg/day
    • May titrate dose by 30 mg/day if needed; Max. 120 mg/day
  • Venlafaxine:
    • Start 37.5-75 mg daily; may increase by 75 mg/day as tolerated
    • Maximum 225 mg/day

 

Prognosis

  • Variable and unpredictable
  • If untreated, more than 50% of patients with multiple sclerosis will develop significant physical disability within 20-25 years from onset
  • 70% of patients lead active, productive lives with prolonged remission
  • 30% relapse in 1 year, 20% in 5-9 years, and 10% in 10-30 years
  • Untreated MS Patients are thought to have an average life expectancy 5-7 years shorter than that of the general population

 

D) Non-pharmacological treatments

  • Minimize exposure to exacerbating factors such as extreme temperature (hot tubs/saunas)
  • A cooling vest or cold beverages may help lower body temperature
  • Monitor for local sores and ulcers and take preventive measures before they become a source of infection
  • Aerobic exercise may help prevent deconditionin
  • Stretching exercises to help relieve stiffness
  • Assistance with energy conserving techniques e.g. timed rest periods
  • bBowel and bladder regimen to assist voiding; increase fiber and fluid intake
  • Recommend self-catheterization where required
  • Counseling: Psychologist, psychiatrist referral as required

 

MEDICATIONS:

ACUTE EXACERBATION-Medications

Corticosteroids

  • Methylprednisolone
  • Prednisone

Use: Acute exacerbations

Mechanism:

  • Decreases inflammation and the normal immune response through multiple mechanisms, also suppresses adrenal function in higher doses

Doses:

Methylprednisolone

  • 1-2 g/day IV usually for 3-5 days (but can be used up to 10 days). May be followed by tapering dose of oral prednisone (e.g. 100 mg x 1 dose then decrease by 10 mg daily until finished)

Prednisone

  • 500-1 g PO daily for 3-5 days followed by tapering doses

 

DISEASE MODIFYING-Medications

Interferon

Types:

  • Interferon Beta-1a (IFNb-1a)
  • Interferon Beta-1b (IFNb-1b)

Use: Immunomodulating therapy

Mechanism:

  • Exact mechanism in the treatment of MS is unknown
  • Immunomodulatory effects include
    • Enhancement of suppressor T cell activity
    • Reduction of proinflammatory cytokines
    • Down-regulation of antigen presentation
    • Reduced trafficking of lymphocytes into the central nervous system

Dose:

Interferon Beta-1a (intramuscular)

  • 30 µg once weekly

Note:

  • Should be stored in a refrigerator at 2-8°C. Allow to reach room temperature (about 30 minutes) before giving the injection
  • Prefilled syringe can be stored at room temperature (between 15-30°C) for up to one week

Interferon Beta-1a (subcutaneous)

  • Titrate to 22-44 µg 3 times per week, at least 48 hours apart
  • 44 µg titration: 8.8 µg 3 times per week for 2 wks; then 22 µg 3 times per week for 2 wks; followed by 44 µg 3 times per week
  • 22 µg titration: Start 4.4 µg 3 times/week for 2 wks; then 11 µg 3 times/week for 2 wks; followed by 22 µg 3 times/week

Note: Interferon Beta-1a new HSA-free Fformulation liquid in a pre-filled syringe or pre-filled cartridge should be stored at 2-8°C. Allow warming to room temperature prior to use; do not use external heat sources such as hot water. It can also be stored for a limited time period at room temperature (up to 25°C), but not more than 1 month.

  • Stored at 2-8°C. Allow to warm to room temperature prior to use, Do not use external heat sources such as hot water
  • May be stored for a limited period at room temperature (up to 25°C), but not more than 1 month

General Care:

  • Protect injection from light and do not freeze
  • Rotate injection site with each injection, to minimize the likelihood of injection site reactions
  • NSAIDs, acetaminophen may be used for flu like symptoms

Interferon Beta-1b

Multiple sclerosis (relapsing)

  • Titration: Incerase by 0.0625 mg SC every 2 weeks as follows:
    • Week 1-2 = 0.0625 mg every other day
    • Week 3-4 = 0.125 mg every other day
    • Week 5-6 = 0.1875 mg every other day
    • Then 0.250 mg (target dose) every other day

Multiple sclerosis (secondary-progressive)

  • Titration: 0.125 mg SC every other day for 2 week as follows; then 0.250 mg every other day

Note: Store between 2-25°C. After reconstitution if not used immediately, refrigerate solution between 2 and 8°C and use within 3 hours of reconstitution.

 

IMMUNOMODULATOR

  • Glatimer acetate

Use: Immunomodulating therapy

Mechanism:

  • Complete mechanism in the treatment of MS is unknown
  • Supported hypothesis
    • Induces and activate T-lymphocyte suppressor cells specific for a myelin antigen
    • Interferes with the antigen-presenting function of certain immune cells opposing pathogenic T-cell function

Dose:

Glatiramer acetate:

  • 20 mg SC once daily

 

Sphingosine 1-phosphate receptor modulator

  • Fingolimod

Use: Immunomodulating therapy

Mechanism:

Complete mechanism in the treatment of MS is unknown

  • Binds to sphingosine 1-phosphate (S1P) receptors 1, 3, 4, and 5
  • Its binding to S1P receptors on lymphocytes induces S1P receptor down-regulation on lymphocytes, and blocks the capacity of lymphocytes to egress from lymph nodes, reducing the number of lymphocytes in peripheral blood
  • The amount of lymphocytes available to the central nervous system are decreased which reduces central inflammation

Dose:

Fingolimod:

  • 0.5 mg PO once daily

 

Pyrimidine synthesis inhibitor

  • Teriflunomide

Use: IRelapsing forms of multiple sclerosis (MS)

Mechanism:

Exact mechanism of action in MS is unknown

  • An immunomodulatory agent that inhibits pyrimidine synthesis by inhibiting dihydroorotate dehydrogenase enzyme
  • It also has anti-inflammatory effects

Dose:

Teriflunomide:

  • 7 mg PO or 14 mg PO once daily

Drug elimination procedure

 

Selective adhesion molecule inhibitor

  • Natalizumab

Use:Immunomodulation therapy

Mechanism(s):

Complete mechanism in the treatment of MS is unknown.

  • Binds integrins on leukocyte cell walls, preventing migration into inflamed parenchymal tissue (monoclonal antibody)
  • Potentially blocks of T-lymphocyte migration into the CNS

Dose:

Natalizumab:

  • 300 mg IV infusion over 1 hour every 4 weeks

 

Immune modifiers/Antineoplastic

  • Mitoxantrone

Use: Immunosuppressant therapy

Mechanism:

  • Binds to nucleic acids and inhibits DNA and RNA synthesis
  • Replication is decreased by binding to DNA topoisomerase II
  • Inhibit the incorporation of uridine into RNA and thymidine into DNA
  • Active throughout entire cell cycle (cell-cycle nonspecific)

Dose:

Mitoxantrone:

  • 5-12 mg/m2 IV every 3 months for 2 years, with maximum lifetime cumulative dose of 140 mg/m2

 

Antineoplastic/Immunosuppressant

  • Cyclophosphamide

Use: Immunosuppressant therapy

Mechanism:

  • An alkylating agent that prevents cell division by cross-linking DNA strands and inhibiting DNA synthesis
  • Interferes with DNA replication and RNA transcription
  • It is a cell cycle phase nonspecific agent and potent immunosuppressive agent

Dose:

Cyclophosphamide

Various treatment protocols exists for cyclophosphamide and methylprednisolone one of them stated below:

  • 800 mg/m2 IV infusion given once every 4 weeks plus 1g of methyl prednisone. Dose adjustments based on preinfusion and 10day post-infusion WBC

 

SYMPTOMATIC TREATMENT-Medications

Antispasmodic

  • Baclofen
  • Tizanidine
  • Cannabinoids

Use: Spasticity

Mechanism:

Complete mechanism of action unknown.

Baclofen

  • It inhibits both monosynaptic and polysynaptic spinal reflexes, possibly by hyperpolarization of afferent terminals (resultant relief of muscle spasticity)

Tizanidine

  • It is chemically-related to clonidine and other α2-adrenergic agonists, which acts as a centrally acting muscle relaxant with anti-hypertensive properties
  • Presumably it reduces spasticity by increasing presynaptic inhibition of motor neurons

Dose:

Baclofen

  • 5-10 mg PO TID, may increase 5 mg/dose every 3days; Max. 80 mg/day

Tizanidine

  • 2-4 mg PO TID; may increase by 2-4 mg PO as needed to a maximum of 3 doses in 24 hrs, with at least 6-8 hrs interval between doses; Max. 36 mg/day

Dose in renal impairment:

  • CrCl <25: Decrease dose (e.g. 2-4 mg PO)

Cannabinoids

  • Buccal 1 spray every 4 hr, 4-5 sprays/day for MS, may start initially with 1 spray/day; increase every 1-2 d, Max ~12 sprays/day

 

Anticonvulsant:

  • Gabapentin
  • Carbamazepine

Gabapentin

Use: Neuropathic pain, Lhermitte's, Seizures

Mechanism:

Exact mechanism of action unknown.

  • It is structurally related to GABA (gamma-aminobutyric acid)
  • It does not affect the synthesis or uptake of GABA
  • High affinity gabapentin binding sites have been located throughout the brain

Dose:

Gabapentin

  • Begin at 100 to 300 mg TID; increase as tolerated every 3-7 days. Effective dose range: 900-1800 mg daily in 3 divided doses. Max dose: 2400 mg-3,600 mg/day

Dose in renal impairment:

  • CrCl 30-60: 200-700 mg twice daily
  • CrCl 16-29: 200-700 mg once daily
  • CrCl 15: 100-300 mg once daily
  • CrCl <15: Decrease dose proportionately to creatinine clearance
  • Hemodialysis: Single dose of 125-350 mg as supplement every 4 hrs of dialysis

 

Carbamazepine

Use: Neuropathic pain, Lhermitte's, Seizures

Mechanism:

  • Decreases synaptic transmission
  • Within CNS by affecting sodium channels in neurons
  • It had anticonvulsant, anticholinergic, antineuralgic, antidiuretic, muscle relaxant, antimanic, antidepressive, and antiarrhythmic properties

Dose:

Carbamazepine

  • 100-200 mg/day PO; may increase upto maximum of 600-1,600 mg
  • Monitor: CBC and risk of bone marrow suppression within first 2 months of initiating therapy

 

Analgesic; Neuropathic pain

  • Pregabalin
  • Cannabinoids

Pregabalin

Primary use: Neuropathic pain may assist with Lhermitte's; used for partial onset seizures in some countries

Mechanism:

Exact mechanism of action is unknown.

  • Binds to alpha2-delta subunit of voltage-gated calcium channels within the CNS, inhibiting excitatory neurotransmitter release
  • Produces antinociceptive and antiseizure effects

Dose:

Pregabalin

  • 75-150 mg PO BID; Max. dose 600 mg daily in 2-3 divided doses

Dose in renal impairment:

Cannabinoids

  • Buccal 1 spray every 4 hr, 4-5 sprays/day for MS, may start initially with 1 spray/day; increase every 1-2 d, Max. ~12 sprays/day

 

Benzodiazepine

  • Diazepam

Use: Spasticity, anxiety, sedation

Mechanism:

  • Binds to benzodiazepine receptors and enhances GABA effects
  • Depresses the CNS, produces skeletal muscle relaxation, has anticonvulsant properties due to enhanced presynaptic inhibition

Dose:

Diazepam

  • 5-10 mg PO TID PRN; can be given as monotherapy or in combination

 

Dopamine agonist

  • Amantadine

Use: Fatigue

Mechanism: Unclear

Dose:

Amantadine

  • 100 mg PO BID; Max. 300 mg PO daily in divided doses

 

Central nervous system stimulant

  • Modafinil

Use: Fatigue in MS

Mechanism:

Exact mechanism of action is unknown.

  • It may exert its stimulant effects by decreasing GABA-mediated neurotransmission

Dose:

Modafinil:

  • 100 mg PO BID

 

Selective serotonin reuptake inhibitors (SSRIs)

  • Fluoxetine

Use: MS induced fatigue, depression

Mechanism:

  • Inhibits the presynaptic reuptake of neurotransmitters and increases synaptic serotonin concentration and potentiates its effect
  • Little effect on the reuptake of norepinephrine or dopamine
  • Does not significantly bind to alpha-adrenergic, histamine, or cholinergic receptors

Dose:

Fluoxetine

  • Start 20 mg/PO daily every morning; may increase dose gradually after several weeks if inadequate response; Max. 80 mg/day

 

Potassium channel blocker

  • Fampridine - Approved by Health Canada
  • Dalfampridine - Approved by FDA

Use: Help to improve walking in patients with MS

Mechanism:

Exact mechanism of action is unknown.

  • Inhibits potassium channels
  • Delay repolarization and prolongs the duration of action potentials, improves conduction of action potentials in demyelinated axons

Dose:

Fampridine/Dalfampridine

  • 10 mg PO every 12 hr

 

Opioid analgesic

  • Tramadol

Use: Pain management

Mechanism:

The precise mechanism is unclear but may be related to:

  • The binding of its active metabolites to mu opioid receptors in the CNS which inhibits reuptake of serotonin and norepinephrine
  • The binding causes inhibition of ascending pain pathway which in turns alter the perception of and response to pain

Dose:

Tramadol

  • 50-400 mg PO daily as tolerated

 

Anticholinergic

  • Oxybutynin
  • Tolterodine
  • Solifenacin
  • Darifenacin
  • Trospium

Use: Urinary incontinence

Mechanism:

  • Antagonizes the action of acetylcholine at postganglionic receptors
  • Relaxes bladder smooth muscle, inhibits involuntary detrusor muscle contractions

Dose:

Oxybutynin

  • 5 mg PO BID or TID; Max. of 5 mg PO 4 times a day

Tolterodine

  • 2 mg PO BID

Solifenacin

  • 5 mg PO daily, if tolerated may increase to 10 mg once daily
  • Note: Maximum 5 mg/day if on potent CYP3A4 inhibitor

Darifenacin

  • 7.5 mg PO daily; may increase if required at least after 2 weeks to 15 mg PO daily

Trospium

  • Immediate release: 20 mg PO BID
  • Extended release: 60 mg PO daily

 

Neuromuscular blocking agent, (Botulinum toxin)

  • Botox

Use: Muscle spasticity, Urinary incontinence

Mechanism:

  • Blocks neuromuscular conduction by binding to receptor sites on motor nerve terminals, inhibits release of acetylcholine and produces a state of denervation that could last for weeks-months

Dose:

Botox (intramuscular)

  • Exact dosage and number of injection sites are based on patient size, extent and location of muscles involved, severity of spasticity, presence of local muscle weakness, and response to prior treatment

Botox (intravesical)

  • Recommended dose is 200 Units
  • Treatment benefits usually last a minimum of three months.

 

Antidiuretic

  • Desmopressin

Use: Nocturia

Mechanism:

  • Increases cyclic adenosine monophosphate (cAMP) in renal tubular cells with increase in water permeability in distal tubules and collecting ducts leading to decreased urine volume and increased urine osmolality
  • Increases plasma levels of von Willebrand factor, factor VIII, and t-PA

Dose:

Desmopressin

  • 0.1-0.4 mg PO daily at bedtime

 

Antidepressants

  • Tricyclic antidepressant (TCAs)
  • Selective serotonin reuptake inhibitors (SSRIs)
  • Serotonin/norepinephrine reuptake inhibitor (SNRIs)

Tricyclic antidepressants (TCAs)

  • Amitriptyline
  • Imipramine
  • Nortriptyline

Use: Depression

Mechanism:

  • Inhibits the presynaptic reuptake of neurotransmitters, increases synaptic serotonin and/or norepinephrine
  • Also has significant anticholinergic properties

Dose:

Amitriptyline

  • Start 25-50 mg/day; may increase dose gradually; usual effective dose 75 to 200 mg PO daily or in divided doses; Max. 300 mg/day

Imipramine

  • Start 75 mg/day and increase dose gradually to 150 mg PO daily or in divided doses; Max. 200 mg/day

Nortriptyline

  • 25-50 mg/day PO; may increase gradually to 200 mg/day, if needed

 

Selective serotonin reuptake inhibitors (SSRIs)

  • Fluoxetine
  • Paroxetine
  • Sertraline
  • Citalopram

Use: Depression

Mechanism:

  • Inhibits the presynaptic reuptake of neurotransmitters, increases synaptic serotonin concentration
  • Little effect on the reuptake of norepinephrine or dopamine
  • Does not significantly bind to alpha-adrenergic, histamine, or cholinergic receptors

Dose:

Fluoxetine

  • Start 20 mg PO daily in the morning; may increase dose gradually after several weeks if inadequate response; Max. 80 mg/day

Paroxetine

  • Immediate-release: Start 20 mg PO daily in the morning; may increase dose gradually by 10 mg/day after at least 1 week of interval; Max. 50 mg/day
  • Controlled-release (CR): Start 25 mg PO daily in the morning; may increase dose gradually by 12.5 mg/day after at least 1 week of interval; Max. 62.5 mg/day

Sertraline

  • Start 50 mg PO in the morning or at bedtime once daily; may increase dose gradually after at least 1 week of interval; usual dose 50-100 mg/day; Max. 200 mg/day

Citalopram

  • Start 20 mg PO in the morning or at bedtime once daily; may increase dose gradually after at least 1 week of interval; usual dose 20-40 mg/day; Max. 60 mg/day

 

Serotonin/norepinephrine reuptake inhibitors (SNRIs)

  • Duloxetine
  • Venlafaxine

Use: Depression, pain

Mechanism:

Exact mechanism of action is unknown.

  • A potent serotonin and norepinephrine reuptake inhibitor
  • Weakly inhibits dopamine reuptake

Dose:

Duloxetine

  • 30-60 mg PO once daily; target dose 60 mg/day; may titrate dose by 30 mg/day if needed; Max. 120 mg/day

Venlafaxine

  • 37.5-75 mg PO daily; may increase in ≤75 mg/day increments at intervals of ≥4 days as tolerated (maximum daily dose: 225-375 mg)

 

Stool softener

  • Docusate sodium

Use: Stool softener

Mechanism:

  • Facilitates mixture of stool fat and water
  • May also promote electrolyte and water secretion into the colon

Dose:

Docusate sodium

  • 100 mg PO TID

 

Phosphodiesterase type 5 inhibitors (PDE5 inhibitors)

  • Sildenafil
  • Tadalafil
  • Vardenafil

Use: Erectile dysfunction

Mechanism:

  • Does not directly cause penile erections
  • Inhibits the enzyme phosphodiesterase type 5 (PDE5), which inactivates cGMP
  • Enhances effects of nitric oxide released during sexual stimulation
  • Nitric oxide activates guanylatecyclase enzyme and increasecGMP level which leads to smooth muscle relaxation of corpus cavernosumhence promotes increased blood flow and subsequent erection

Dose:

Sildenafil

  • 50-100 mg PO, prior to intercourse (~1 hour before)

Tadalafil

  • 5-20 mg PO, prior to intercourse (at least 30 minutes)

Vardenafil

  • 5-20 mg PO, prior to intercourse (~1 hour before)

 

Prostaglandin

  • Alprostadil

Use: Erectile dysfunction

Mechanism:

  • Vasodilator - relaxes arterial smooth muscle and dilates cavernosal arteries

Dose:

Alprostadil

  • 2.5-40 mg intracavernosal injection

 

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Clinical Trials:
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Pipeline Agents:
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Pharmacist Resources:

Pharmacists are becoming more involved in assisting with the management of self-injected MS medications, with increasing need for closer monitoring of efficacy and side effects.

Encourage

Advise patient to

  • Establish prescribed routine for medication use
  • Maintain regular activity but avoid overwork and fatigue
  • Educate on importance of self-catheterizations techniques for inadequate bladder emptying ( where indicated )

Drugs

  • Consider concurrent risk factors and interaction of disease state with the prescribed therapy
  • Dispense and track medications and encourage maintenance of diaries
  • Monitor drug therapy by following the patient through his/her treatment course and progress
  • Assess response, side effects, and toxicities, and communicate to the physician promptly
  • Evaluate cost and affordability and insurance coverage for patients

Unlabeled/Alternate uses:

Includes but are not limited to:

  • Methylprednisolone
    • Acute spinal cord injury
    • Various inflammatory processes
  • Mitoxantrone
    • Hodgkin's lymphoma, non-Hodgkin's lymphomas
    • Leukemias
    • Breast cancer
  • Methotrexate
    • Ectopic pregnancy
    • Crohn's disease
    • Systemic lupus erythematosus
  • Cyclophosphamide
    • Myasthenia gravis
    • Idiopathic thrombocytopenic purpura (ITP), chronic
    • Rheumatoid disorders,( in severe cases)
  • Azathioprine
    • Crohn's disease (CD) and ulcerative colitis (UC)
    • Atopic dermatitis
    • Autoimmune hepatitis

Counseling

  • Ensure patient is well informed about disease and its treatment
  • Suggest high fluid intake and a high-fiber diet to prevent or treat constipation
  • Include family or social support in lifestyle modification
  • Offer advice and make calls to support groups, agencies or physician offices to assist and enhance patient care
  • May serve as an interface between the patient and physician and/or patient and health insurance plan

Alerts

  • Remissions can occur spontaneously, which make objective treatment evaluations difficult
  • Advise rest during periods during acute phase of a relapses
  • Infections, including minor upper respiratory infections, increase the risk of MS exacerbations

Tips

  • Adherence to the medication should be assessed at each visit
  • MS patients should receive regular follow-up with a neurologist/clinic

Expected outcome

  • Highly variable and unpredictable
  • Approximately 60-70% of patients lead active, productive lives with prolonged remissions
  • MS Patients are thought to have mildly reduced average life expectancy (~5-7 years shorter) than that of the general population

 

2. Scales and Tables

 

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References:

Core Resources:

  • Brust J, ed. Current Diagnosis and Treatment (Neurology). 2nd edition. New York: McGraw-Hill; 2011
  • Compendium of Pharmaceuticals and Specialties (CPS). Canadian Pharmacist association. Toronto: Webcom Inc. 2012
  • Day RA, Paul P, Williams B, et al (eds). Brunner & Suddarth's Textbook of Canadian Medical-Surgical Nursing. 2nd ed. Philadelphia: Lippincott Williams and Wilkins; 2010
  • Foster C, Mistry NF, Peddi PF, Sharma S, eds. The Washington Manual of Medical Therapeutics. 33rd ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2010
  • Freedman MS, Selchen D, Arnold DL, et al. Treatment Optimization in MS: Canadian MS Working Group Updated Recommendations. Can J Neurol Sci. 2013; 40(3):307-23
  • Gray J, ed. Therapeutic Choices. Canadian Pharmacists Association. 6th ed. Toronto: Webcom Inc. 2011
  • Katzung BG, Masters SB, Trevor AJ, eds. Basic and Clinical Pharmacology. 11th ed. New York: McGraw-Hill; 2009
  • Longo D, Fauci A, Kasper D, et al (eds). Harrison's Principles of Internal Medicine. 18th ed. New York: McGraw-Hill; 2011
  • McPhee SJ, Papadakis MA, eds. Current Medical Diagnosis & Treatment. 49th ed. New York: McGraw-Hill; 2010
  • Pagana KD, Pagana TJ eds. Mosby's Diagnostic and Laboratory Test Reference. 9th ed. St. Louis: Elsevier-Mosby; 2009
  • Rowland LP and Pedley TA, eds. Merritt's Neurology. 12th ed. Philadelphia: Lippincott Williams and Wilkins; 2010
  • Skidmore-Roth L. ed. Mosby's drug guide for nurses. 9th ed. St. Louis: Elsevier-Mosby; 2011
  • Skidmore-Roth L, ed. Mosby's nursing drug reference. 24th ed. St. Louis: Elsevier-Mosby; 2011

Online Pharmacological Resources:

  • e-Therapeutics
  • Lexicomp
  • RxList
  • Epocrates

Journals/Clinical Trials:

  • Beck RW, Chandler DL, Cole SR et al. Interferon β-1a for early multiple sclerosis: CHAMPS trial subgroup analyses. Annals of Neurology 2002;51:481-490
  • Cohen JA, Barkhof F, Comi G, et al. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med 2010;362:402-415
  • Cohen JA, Coles AJ, Arnold DL, et al. Alemtuzumab versus interferon beta 1a as first-line treatment. Lancet. 2012;380(9856):1819-28
  • DOI: 10.1016/S0140-6736(12)61769-3
  • Comi G, Martinelli V, Rodegher M, et al. Affect of Glatiramer acetate on conversion to clinically definite multiple sclerosis (CDMS) in patients with clinically isolated syndrome (PreCISe study): a randomised, double-blind, placebo-controlled trial. Lancet. 2009;374:1503-11
  • Ebers GC; PRISMS (Prevention of Relapses and Disability by Interferon beta-1a Subcutaneously in Multiple Sclerosis) Study Group. Randomized double-blind placebo-controlled study of interferon beta-1a in relapsing/remitting multiple sclerosis. Lancet.1998;352:1498-1504
  • Gold R, Kappos L, Arnold DL et al. Placebo-Controlled Phase 3 Study of Oral BG-12 for Relapsing Multiple Sclerosis. N Engl J Med 2012;367:1098-1107
  • Jacobs LD, Cookfair DL, Rudick RA, et al; The Multiple Sclerosis Collaborative Research Group (MSCRG). Intramuscular interferon beta-1a for disease progression in relapsing multiple sclerosis. Ann Neurol. 1996;393:285-94
  • Kappos L, Radue EM, O'Connor P, et al. A Randomized, Placebo-Controlled Trial of Natalizumab for Relapsing Multiple Sclerosis. N Engl J Med 2006;354:899-910
  • Kappos L, Radue EM, O'Connor P, et al for the FREEDOMS Study Group. A placebo-controlled trial of oral fingolimod in relapsing multiple sclerosis. N Engl J Med 2010;362:387-401
  • Krapf H, Morrissey SP, Zenker O, et al. Effect of Mitoxantrone on MRI in progressive MS: results of the MIMS trial. Neurology. 2005;65:690-695
  • Kurtzke JF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology 1983;33:1444-52
  • McDonald WI, Compston A, Edan G et al. Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple Sclerosis. Ann Neurol 2001;50:121-7
  • Miller DH, Weinshenker BG, Filippi M, et al. Differential diagnosis of suspected multiple sclerosis: a consensus approach. Mult Scler. 2008;14(9):1157-74
  • Rooney WD, Goodkin DE, Schuff N, et al. 1H MRSI of normal appearing white matter in multiple sclerosis. Mult Scler. 1997;3(4):231-7
  • Rosati G. The prevalence of multiple sclerosis in the world: an update. Neurological Sciences 2001;22:117-139
  • Rudick RA, Stuart WH, Calabresi PA, et al for the SENTINEL Investigators. Natalizumab plus interferon beta-1a for relapsing multiple sclerosis. N Engl J Med. 2006;354 (9):911-23

 

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Reviewers

EXPERT REVIEWER:
Mark Freedman, MSc, MD, FAAN FRCPC, Professor of Medicine (Neurology), University of Ottawa, Director, Multiple Sclerosis Research Unit, The Ottawa Hospital-General Campus, Ottawa, ON Canada
.......................................... PHARMACY REVIEWER:
Tejal Patel, B.Sc.(Pharm), Pharm.D., Clinical Assistant Professor, School of Pharmacy, University of Waterloo, ON Canada

 
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