DysphagiaoBowel incontinenceoConstipation•MusculoskeletaloFatigueoWeaknessoAtaxic Movements oSpasticityoFoot Drop•NeurooEmotional labilityoScanning SpeechoImpaired judgment•SensoryoBlurred visionoNumbness/ParesthesiaoDiminished sense of temperature•ReproductiveoLoss of sensationMales – impotenceDiagnosis of MS•Symptomso2 or more episodes lasting 24 hours separated by one monthoExacerbations & remissions with worsening of symptoms over 6 months ORoGradual worsening of symptoms without recovery over 6 months•LP – CSF shows increase in protein•MRI – lesions visibleoShows lesions that aren’t normally seen on CT scanoActually measures the size of lesionsTreatment of MSDisease Modifying Drugs*S/E: flu-like symptoms 24-48 hrs, but subside within 2-3 months•Drugs that modify course of the Disease:oAvonex (Interferon beta 1-a)IM Q weekoBetaseron (Interferon beta 1-b)SC Q other DayoCopaxone (Glatiramer acetate)SC QDoRebif (Interferon beta 1-a)SC 3 times a weekoTysabriEvery four weeks by IVInfusion in a registered infusion centerTreatment for Exacerbations•Solu-Medrol (methylprednisolone) oMost commonly used corticosteroids in MSoShortens duration of relapse by its anti-inflammatory effects•Plasmapheresis (Plasma Exchange) oOnly considered for the 10% or so who do not respond to the standard steroidsPlasmapheresis•Blood is cycled through a machine•Plasma portion of the blood is separated and removed•This removes harmful antibodies – Immunoglobulins•Plasma is replaced with plasmanate, NSS or albumin. Symptom Treating Drugs•Baclofen (Lioresal) – spasticity or diazepam•Amitriptyline (Elavil) – pain/paresthesia•Bupropion (Wellbutrin) – depression/fatigue•Oxybutynin (Ditropan) – bladder dysfunctionAtaxia treated with: •Neurontin – antiseizure med.•Inderal – beta adrenergic blockers•Klonopin – benzodiazepines Goals of Treatment•Promotion of physical mobility•Avoidance of injury•Achievement of bowel and bladder continence•Improvement in cognitive function•Promotion of speech and swallowing mechanisms•Development of coping strengths•Improved home maintenance•Adaptation to sexual functionCollaborative Management•Promote mobility / water exercise•Promote nutrition •Promote rest and comfort measures•EducationoBladder/Bowel trainingoAvoidance of infection2
Degenerative Neurologic DisordersoAvoidance of heat/humidityMyasthenia GravisOverview•Autoimmune disease•Antibody mediated destruction of acetylcholine receptors at the neuromuscular junction•Can occur at any ageRisk Factors:•Peak incidence in the 20 to 30 age range•Three times more common in womenClinical Manifestations•Initial Symptoms in 50% of pts.:oPtosis – drooping of upper eyelidoDiplopia – double vision•As disease progresses additional symptoms appear:oDifficulty chewing or swallowingoProximal extremity weaknessoRespiratory muscle weakness (May require mechanical ventilation)o