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Multiple Sclerosis: An Overview for Case Management Professionals

Multiple Sclerosis: An Overview for Case Management Professionals. Susan Raimondo Connecticut Chapter Offices in Hartford and Norwalk 860.913.2550 1.800.344.4867 www.ctfightsMS.org Susan.raimondo@nmss.org. Charlene Breen Care Management Associates/

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Multiple Sclerosis: An Overview for Case Management Professionals

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  1. Multiple Sclerosis: An Overview forCase Management Professionals Susan Raimondo Connecticut Chapter Offices in Hartford and Norwalk 860.913.2550 1.800.344.4867 www.ctfightsMS.org Susan.raimondo@nmss.org Charlene Breen Care Management Associates/ Connecticut Community Care, Inc. Toll-free: 800.654.2183 www.ctcommunitycare.org

  2. What does MS look like? • Julia—a 35yo white married mother who is exhausted all the time and can’t drive because of vision problems • Jackson—a 25yo African-American man who stopped working because he can’t control his bladder or remember what he read in the morning paper • Maria—a 10yo Hispanic girl who falls down a lot and whose parents just told her she has MS • Loretta—a 47yo white single woman who moved into a nursing home because she can no longer care for herself • Sam—a 45yo divorced white man who has looked and felt fine since he was diagnosed seven years ago • Karen—a 24yo single white woman who is severely depressed and worried about losing her job because of her diagnosis of MS • Richard—who was found on autopsy at age 76 to have MS but never knew it

  3. What is MS? • Neurological disease • Misguided immune cells • Multiple scars • Unpredictable • Variable • Often progressive

  4. What is MS? cont’d. • 2-3x women as men • Usually diagnosed between 20 and 50 • 200 people diagnosed every week in US • More common in Caucasians, especially those of northern European ancestry

  5. What Causes MS? Genetic Predisposition Environmental Trigger Autoimmunity Loss of myelin & nerve fiber

  6. The risk of getting MS is approximately: • 1/750 for the general population (0.1%) • 1/40 for person with a close relative with MS (3%) • 1/4 for an identical twin (25%) • 20% of people with MS have a blood relative with MS • The risk is higher in any family in which there are several family members with the disease (aka multiplex families).

  7. myelinated nerve fiber myelinated nerve fiber What happens in MS? “Activated” T cells... ...cross the blood-brain barrier… …launch attack on myelin & nerve fibers... …to obstruct nerve signals

  8. MS: A Timeline • 1396- Earliest recorded case of MS. • 1868- Charcot describes the disease and finds MS plaques (scars) on autopsy. • 1878- Louis Ranvier describes the myelin sheath (the primary target of MS in the central nervous system). • 1981- 1st MRI image of MS is published. • 1993- The first disease-modifying agent for MS—Betaseron—is approved in the U.S. • 1998- Bruce Trapp confirms that the nerve fibers are irreversibly damaged early in the disease course (probably accounting for the permanent disability that can occur). • 2014- There are several medications approved for the treatment of MS and more in the pipeline.

  9. How is MS diagnosed? • MS is a clinicaldiagnosis: • Signs and symptoms • Medical history • Laboratory tests • Magnetic resonance imaging (MRI) • Visual evoked potentials (VEP) • Lumbar puncture

  10. What tests may be used to help confirm the diagnosis? • Magnetic resonance imaging (MRI) • Visual evoked potentials (VEP) • Lumbar puncture

  11. How is MS diagnosed? • Requires dissemination in time and space: • Space: Evidence of scarring (plaques) in at least two separate areas of the CNS • Time: Evidence that the plaques occurred at different points in time • There must be no other explanation

  12. What is the prognosis? • One hallmark of MS is its unpredictability. • Approximately 1/3 will have a very mild course • Approximately 1/3 will have a moderate course • Approximately 1/3 will become more disabled • Characteristics that predict a better outcome: • Female, onset before age 35, sensory symptoms • Complete recovery following a relapse

  13. An Overview of Treatment Strategies

  14. What are the treatment strategies? • Management of MS falls into five general categories: • Treatment of relapses (aka exacerbations, flare-ups, attacks—that last at least 24 hours) • Symptom management • Disease modification • Rehabilitation (maintain/improve function) • Psychosocial support

  15. FDA-Approved Disease-Modifying Agents • Aubagio (teriflunomide) * • Avonex (interferon beta-1a) ** • Betaseron (interferon beta-1b) ** • Copaxone (glatiramer acetate) ** • Extavia (interferon beta-1b) ** • Gilenya (fingolimod)* • Novantrone (mitoxantrone)*** • Rebif (interferon beta-1a)** • Tecfidera (dimethyl fumarate)* • Tysabri (natalizumab)*** * oral ** by injection *** by infusion

  16. What do the disease-modifying drugs do? • All reduce attack frequency and severity, reduce scarring on MRI, and probably slow disease progression. • These medications are not designed to: • cure the disease • make people feel better • alleviate symptoms

  17. How important is early treatment? • The Society’s National Clinical Advisory Board recommends that treatment be considered as soon as a diagnosis of relapsing MS has been confirmed. • Irreversible damage to axons occurs even in the earliest stages of the illness. • Treatment is most effective during early, inflammatory phase • Treatment is least effective during later, neurodegenerative phase • No treatment has been approved for primary-progressive MS. • As of 2010, approximately 60% of people with MS are being treated with a disease-modifying therapy.

  18. MS Symptoms vs Relapses…How Are They Different? • MS symptoms are chronic or ongoing indicators of MS lesion damage to certain areas of the brain and/or spinal cord • MS relapses are sudden flare-ups or symptom attacks that typically last several days to several weeks Joy and Johnston, eds. Multiple Sclerosis: Current Status and Strategies for the Future. Washington, DC: National Academies Press; 2001

  19. How are relapses treated? • Not all relapses require treatment • Mild, sensory sx are allowed to resolve on their own. • Sx that interfere with function (e.g., visual or walking problems) are usually treated • 3-5 day course of IV methylprednisolone—with/without an oral taper of prednisone • High-dose oral steroids used by some neurologists • H.P. Acthar® gel • Plasmapheresis • Rehabilitation to restore lost function • Psychosocial support

  20. What are possible symptoms? • Fatigue (most common) • Visual problems • Bladder and/or bowel dysfunction • Sexual dysfunction • Emotional disturbances (depression, mood swings) • Cognitive difficulties (memory, attention, processing) (Heat can worsen many symptoms)

  21. What are possible symptoms? cont’d. • Sensory changes (tingling, numbness) • Pain (neurogenic, musculoskeletal) • Spasticity • Gait, balance and coordination problems • Weakness, paralysis • Speech/swallowing problems • Tremor These are symptoms of a number of illnesses, making diagnosis difficult. (Heat can worsen many symptoms)

  22. A Word about Temperature Sensitivity • 70-80% experience heat sensitivity • 20% experience cold sensitivity • Slight elevations in core body temperature (related to ambient temperature, exercise, fever, hot baths/showers) can cause temporary worsening of MS symptoms—a pseudoexacerbation • Cooling strategies (A/C, scarves/vests, cold liquids, cool showers) can help maintain core body temperature If a person with MS has a fever, symptoms can worsen rapidly. Important to find the source of the infection.

  23. How are MS symptoms managed? • Symptom management continues throughout the disease course • Effective symptom management involves a combination of medication, rehabilitation strategies, emotional support—and good coordination of care • Virtually every medication used to treat MS symptoms is used off-label Many symptoms are invisible and misunderstood.

  24. Cycle of MS Symptoms:Related and Interdependent  FatigueDepression Sexuality issues Cognitive function  Spasticity Constipation  Sleep  Bladder& Bowel problems

  25. Managing MS Fatigue • > 80% of people with MS experience fatigue; many identify it as their most disabling symptom • Along with cognitive dysfunction, fatigue is the most common cause of early departure from the workforce • MS fatigue is easily misunderstood by family members and employers as laziness/disinterest

  26. Managing MS Fatigue, cont’d. Strategies: • Identify/address contributory factors • Disrupted sleep; muscle fatigue; disability-related fatigue; depression; medications • Develop comprehensive treatment plan • Energy conservation: planning/prioritizing; mobility aids; environmental modifications • Exercise regimen • Medications: amantadine, modafinil, armodafinil

  27. Managing Bladder Dysfunction • 80% of people with MS experience bladder problems. • Major cause of embarrassment and social isolation. Types • Storage dysfunction • Small, spastic bladder in which small quantity of urine triggers the urge to void • Sx include: urgency, frequency, incontinence, nocturia • Tx includes: anticiholinergic/antimuscarinicmedication

  28. Managing Bladder Dysfunction, cont’d. Types, cont. • Emptying dysfunction • Bladder fails to empty  risk of UTI • Sx include: urgency, frequency, nocturia, incontinence • Tx includes: ISC and anticholinergic/antimuscarinic medications

  29. Managing Bowel Problems • Experienced by 50% of people with MS • Constipation—most common -Loose stool (related to impaction) • Bowel incontinence—least common • Managed best with regular bowel routine • Adequate fluid/fiber intake • Exercise • OTC products as needed • Anticholinergic medications added to manage incontinence

  30. Improving Mobility • 80-90% of people experience mobility impairment due to weakness, imbalance, sensory problems, or spasticity • Management strategies: • Dalfampridine (Ampyra) to improve walking (speed; weakness) • Spasticity management • Exercise/gait training • Mobility aids for weakness, balance, and fatigue issues

  31. Improving Mobility, cont’d. • Ataxia/Tremor • Less common MS symptom, but very disabling • No effective treatments at this time • Medications that may be tried: propranolol; primidone; acetazolamide; buspirone; clonazepam • Occupational therapy, weighting; assistive devices • Thalamic surgery for tremor (generally poor results)

  32. Managing Spasticity • Experienced by 40-60% of people with MS (more common in the lower extremities) • Management strategies: • Stretching • Oral medication (baclofen, tizanidine, clonazapam, gabapentin, cyproheptidine, dantrolene, dopaminergic agonists) • Baclofen pump • Botox injections; nerve blocks; surgery • Some spasticity is useful to counteract weakness

  33. Managing Sexual Dysfunction • 40-80% of people with MS • Reduced libido (behavioral/environmental strategies) • Sensory disturbances (anticonvulsant medications) • Women • Reduced lubrication (gels) • Men • Erectile dysfunction (pharmacotherapy; implants) • Other contributory factors • Managing symptoms that interfere with sexual activity/pleasure (fatigue, spasticity, bladder dysfunction) • Managing medications to promote comfort and responsiveness (anticholinergic; antidepressants; fatigue & spasticity meds) • Feelings and attitudes – education and counseling

  34. Managing Pain • 75% of people with MS experience pain • Neuropathic (central) pain • Paroxysmal pain (trigeminal neuralgia; headache) • Anticonvulsants • Continuous pain (dysesthesias) • Tricyclics; anticonvulsants • Secondary pain • Musculoskeletal pain • Physical therapy; NSAIDs • Spasticity—As described previously

  35. Speech Issues • 40-50% experience speech/voice disorders • Dysarthria – impaired volume control, articulation, emphasis • Dysphonia – altered voice, pitch control, breathiness, hoarseness • Speech/language assessment: • Oral peripheral examination, voice eval, communication profile • Treatment: includes exercises, strategies and compensatory techniques to improve speech clarity, augmentative device or ACC, if needed

  36. Swallowing Issues • Dysphagia – less common symptom • Swallowing assessment, clinical history, examination, videofluoroscopy (modified barium swallow) • Treatment • Exercises • Dietary modifications/positioning while eating/chewing strategies • Non-oral feeding options, if needed

  37. Visual Impairments • Optic Neuritis – • inflammation of the optic • nerve can cause: • Blurred vision • Dimming of colors • Pain when eye is moved • Blind spots • Loss of contrast sensitivity • Nystagmus: • Jerky eye movement • World is “wiggling”

  38. Cognitive Symptoms • Correlates with number of lesions, lesion area, and brain atrophy • Can occur at any time in the course of the disease • Can occur with any disease course • Being in an exacerbation is a risk factor for • cognitive dysfunction

  39. Cognitive Symptoms, cont’d. • Most common problems: memory, attention/concentration, information processing • Treatments: • Disease-modifying therapy, donepezil • Cognitive rehabilitation (primarily compensatory) Cognitive symptoms are often misunderstood.

  40. Managing Depression • >50% of people with MS will experience a major depressive episode • Suicide in MS is 7x higher than in the general population • Greatest risk factor for suicide in MS is depression • Depression is under-recognized, under-diagnosed and under-treated in MS • Recommended treatment: psychotherapy + medication + exercise

  41. Other Affective Disorders • Bipolar disorder • 10 times the rate of general population • Mood swings • Rapid changes in feelings - anger, irritability, sadness - are very common • Anxiety disorder • As common as depression, particularly in the early phases of the disease • Pseudobulbar affect • Pathological laughing and weeping • Euphoria • In progressive MS, person may be excessively happy given their situation.

  42. Serious Complications • Urosepsis • Aspiration pneumonia • Pulmonary dysfunction • Skin breakdown • Untreated depression • Osteoporosis

  43. Uncertain diagnosis Unpredictable course and outcomes Invisible symptoms Potential physical and/or cognitive disability Diminished self-esteem Impact on relationships and family systems Uncertain financial future What are the psychosocial challenges?

  44. What are essential psychosocial interventions? • Disease-related education to enhance people’s understanding of the disease, adaptive coping strategies, and available resources • Support for the ongoing grieving process as activities and roles are altered by the disease

  45. What are essential psychosocial interventions? cont’d. • Help with important life transitions—diagnosis, disease progression, disability • Assessment and treatment of emotional and/or cognitive problems • Support for family members

  46. What role does rehabilitation play? • Rehabilitation offers structured, problem-focused, interdisciplinary interventions to: • Enhance/maintain function, comfort, safety, and independence over the course of the disease • Educate for self-management and behavior change

  47. What role does rehabilitation play? cont’d. • Rehabilitation offers structured, problem-focused, interdisciplinary interventions to: • Identify appropriate assistive devices and environmental modifications • Prevent injuries and unnecessary complications • Empower individual and family

  48. Rehabilitation and MS: Medicare coverage for maintenance programs • Jimmo Settlement - Maintenance Therapy • Skilled therapy services are covered when an assessment of the patient’s condition demonstrates that skilled care is necessary for the performance of a safe and effective maintenance program to maintain the patient’s current condition or prevent or slow further deterioration.

  49. Long-term Services and Supports • 60% of people with MS have activity limitation • 20-25% need long-term care services • 14,000 in nursing homes • 60% of nursing home residents with MS are under 60 years of age

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