๐Ÿ’ŠPharmacology for Nurses Unit 11 โ€“ Parkinson's and MS Drug Treatments

Parkinson's and multiple sclerosis are complex neurological disorders that significantly impact movement and quality of life. These conditions involve disruptions in neurotransmitter balance and immune system function, leading to progressive symptoms that require ongoing management. Treatment approaches for Parkinson's focus on restoring dopamine levels, while MS therapies aim to modulate the immune response and protect nerve fibers. Both conditions necessitate a multifaceted approach, combining medications with supportive care to optimize symptom control and slow disease progression.

What's the Deal with Parkinson's and MS?

  • Parkinson's disease (PD) is a progressive neurodegenerative disorder affecting movement, balance, and coordination
  • Caused by the loss of dopamine-producing neurons in the substantia nigra, a region of the brain involved in motor control
  • Symptoms include tremors, rigidity, bradykinesia (slowness of movement), and postural instability
  • Multiple sclerosis (MS) is an autoimmune disease that attacks the protective myelin sheath surrounding nerve fibers in the central nervous system (brain and spinal cord)
    • Leads to inflammation, scarring, and damage to the myelin, disrupting nerve impulse transmission
  • MS symptoms vary widely but can include muscle weakness, numbness, tingling, vision problems, fatigue, and difficulty with coordination and balance
  • Both PD and MS are chronic conditions that significantly impact a person's quality of life and require ongoing management with medications and supportive care

Key Players: Neurotransmitters and Pathways

  • Dopamine is a crucial neurotransmitter involved in the regulation of movement, reward, and motivation
    • In PD, the loss of dopamine-producing neurons leads to an imbalance in the basal ganglia, a group of brain structures that control movement
  • Acetylcholine is another neurotransmitter that plays a role in PD
    • An imbalance between dopamine and acetylcholine contributes to the motor symptoms of PD
  • Glutamate is an excitatory neurotransmitter that is thought to play a role in the damage to myelin in MS
    • Excessive glutamate release can lead to excitotoxicity, causing damage to neurons and oligodendrocytes (cells that produce myelin)
  • The nigrostriatal pathway is a dopaminergic pathway that connects the substantia nigra to the striatum (part of the basal ganglia)
    • This pathway is particularly affected in PD, leading to the characteristic motor symptoms
  • The immune system, particularly T cells and B cells, plays a central role in the pathogenesis of MS
    • Autoreactive T cells cross the blood-brain barrier and attack the myelin sheath, leading to inflammation and damage

Parkinson's Meds: The Usual Suspects

  • Levodopa (L-dopa) is a precursor to dopamine that can cross the blood-brain barrier and be converted to dopamine in the brain
    • Often combined with carbidopa (Sinemet) to prevent peripheral conversion of L-dopa to dopamine, reducing side effects like nausea and vomiting
  • Dopamine agonists (pramipexole, ropinirole) directly stimulate dopamine receptors, mimicking the action of dopamine
    • Can be used as monotherapy in early PD or as an adjunct to L-dopa in advanced stages
  • Monoamine oxidase B (MAO-B) inhibitors (selegiline, rasagiline) block the enzyme that breaks down dopamine, increasing its availability in the brain
  • Catechol-O-methyltransferase (COMT) inhibitors (entacapone, tolcapone) block the enzyme that metabolizes L-dopa, extending its duration of action
    • Often used in combination with L-dopa/carbidopa to manage wearing-off effects
  • Anticholinergics (trihexyphenidyl, benztropine) block the action of acetylcholine, helping to restore the balance between dopamine and acetylcholine in PD
    • Primarily used to manage tremor in younger patients

MS Treatments: Taming the Immune System

  • Disease-modifying therapies (DMTs) aim to reduce the frequency and severity of MS relapses and slow the progression of disability
  • Interferon beta (Avonex, Rebif, Betaseron) is a cytokine that modulates the immune response and has anti-inflammatory effects
    • Reduces the number of relapses and the development of new lesions on MRI
  • Glatiramer acetate (Copaxone) is a synthetic peptide that mimics myelin basic protein
    • Thought to shift the immune response from pro-inflammatory to anti-inflammatory, reducing damage to myelin
  • Natalizumab (Tysabri) is a monoclonal antibody that blocks the entry of immune cells into the central nervous system
    • Highly effective in reducing relapses and disability progression but carries a risk of progressive multifocal leukoencephalopathy (PML), a rare but serious brain infection
  • Fingolimod (Gilenya) is an oral medication that sequesters lymphocytes in lymph nodes, preventing their entry into the central nervous system
  • Dimethyl fumarate (Tecfidera) is an oral medication with immunomodulatory and neuroprotective properties
    • Reduces the number of relapses and the development of new lesions on MRI

How These Drugs Work Their Magic

  • Parkinson's medications primarily work by restoring the balance of dopamine in the brain
    • L-dopa is converted to dopamine, dopamine agonists stimulate dopamine receptors, and MAO-B and COMT inhibitors prevent the breakdown of dopamine
  • Anticholinergics in PD help to restore the balance between dopamine and acetylcholine, which is disrupted due to the loss of dopamine-producing neurons
  • MS treatments focus on modulating the immune response to reduce inflammation and damage to the myelin sheath
    • Interferons and glatiramer acetate shift the immune response towards an anti-inflammatory state
    • Natalizumab and fingolimod prevent immune cells from entering the central nervous system, reducing inflammation and damage
  • Some MS treatments, like dimethyl fumarate, also have neuroprotective properties that may help to preserve neuronal function and slow the progression of disability

Side Effects: The Not-So-Fun Part

  • Parkinson's medications can cause a range of side effects, depending on the specific drug and individual patient
    • L-dopa can cause nausea, vomiting, and dyskinesias (involuntary movements) at higher doses
    • Dopamine agonists can cause drowsiness, hallucinations, and impulse control disorders (gambling, hypersexuality)
    • MAO-B inhibitors can cause insomnia, headache, and gastrointestinal upset
    • Anticholinergics can cause dry mouth, constipation, urinary retention, and cognitive impairment, especially in older patients
  • MS treatments also have potential side effects that need to be monitored and managed
    • Interferons can cause flu-like symptoms (fever, chills, fatigue) after injection, as well as depression and liver enzyme elevations
    • Glatiramer acetate can cause injection site reactions (redness, pain, swelling) and post-injection flushing
    • Natalizumab carries a risk of PML, a serious brain infection that requires close monitoring with MRI and JC virus antibody testing
    • Fingolimod can cause bradycardia (slow heart rate), macular edema (swelling in the retina), and rarely, PML
    • Dimethyl fumarate can cause flushing, gastrointestinal upset, and rarely, PML

Nursing Know-How: Administration Tips

  • Parkinson's medications should be administered on a regular schedule to maintain consistent dopamine levels and optimize symptom control
    • L-dopa/carbidopa should be given 30-60 minutes before meals or 2 hours after meals to maximize absorption
    • Dopamine agonists and MAO-B inhibitors can be given with or without food
    • Anticholinergics should be started at low doses and titrated slowly to minimize side effects
  • MS treatments require careful patient education and monitoring for side effects and treatment response
    • Interferons and glatiramer acetate are administered by subcutaneous or intramuscular injection, and patients should be taught proper injection technique and rotation of injection sites
    • Natalizumab is given by intravenous infusion every 4 weeks, and patients should be monitored for signs of PML (changes in cognition, vision, or motor function)
    • Oral medications like fingolimod and dimethyl fumarate require regular monitoring of blood work (liver enzymes, lymphocyte counts) and patient education on potential side effects

Real Talk: Patient Education and Support

  • Patients with Parkinson's and MS face significant physical, emotional, and social challenges that require ongoing support and education
  • Nurses play a key role in helping patients and their families understand the disease process, treatment options, and coping strategies
    • Encourage patients to stay active and engage in regular exercise, as this can help to maintain mobility, balance, and overall well-being
    • Provide resources for support groups, counseling, and occupational/physical therapy to help patients adapt to living with a chronic condition
  • Medication adherence is crucial for optimal symptom management and disease control
    • Educate patients on the importance of taking medications as prescribed and reporting any side effects or concerns to their healthcare provider
    • Assist patients in developing strategies for remembering to take medications, such as using pill boxes, setting alarms, or enlisting the help of family members
  • Emphasize the importance of regular follow-up with healthcare providers to monitor disease progression, adjust treatment plans, and address any new symptoms or concerns
    • Encourage patients to keep a symptom diary or log to track changes in their condition and share this information with their healthcare team
  • Provide emotional support and validation for patients and their families, acknowledging the challenges they face and offering hope for effective management and improved quality of life


ยฉ 2024 Fiveable Inc. All rights reserved.
APยฎ and SATยฎ are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.

ยฉ 2024 Fiveable Inc. All rights reserved.
APยฎ and SATยฎ are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.