Parkinson's Disease Handout

Incidence Approximately 1 in 100 people over the age of 60
Prevalence Approximately 1 in 100 people over the age of 60
Age of Onset Typically between 55 and 65 years old, though early-onset Parkinson's can occur before the age of 50
AT Required 80-90%
Medical Coding Information
ICD-11:
ICD-10-CM: See content
OMIM:
UMLS:
MeSH:
GARD:

Introduction

Parkinson's Disease Handout

Name of Disorder: Parkinson's Disease

Formal Name: Parkinson's Disease (PD)

Demographic Information:

  • Incidence: Approximately 1 in 100 people over the age of 60
  • Prevalence: About 1% of the population over 60 years old
  • Gender: More common in men than women
  • Onset Age: Typically between 55 and 65 years old, though early-onset Parkinson's can occur before the age of 50

Coding:

  • ICD-11: 8A00
  • OMIM: 168600
  • UMLS: C0030567
  • MeSH: D010300
  • GARD: 7251

Medical Features and Pathophysiology:

  • Etiology:
Parkinson's Disease (PD) is a neurodegenerative disorder characterized by the progressive loss of dopamine-producing neurons in the substantia nigra, a region of the brain that controls movement. The exact cause of PD is unknown, but it is believed to involve a combination of genetic and environmental factors. Mutations in specific genes, such as LRRK2, PARK7, PINK1, PRKN, and SNCA, have been associated with familial forms of the disease. Environmental factors, such as exposure to pesticides and heavy metals, are also thought to contribute to the risk of developing PD.
  • Pathology:
The hallmark pathological feature of PD is the presence of Lewy bodies, which are abnormal aggregates of the protein alpha-synuclein, within neurons. These Lewy bodies disrupt normal cellular function and lead to the death of dopamine-producing neurons. The loss of dopamine in the basal ganglia, a brain region involved in controlling movement, results in the characteristic motor symptoms of PD. Additionally, non-motor symptoms, such as cognitive impairment and psychiatric disturbances, may occur due to the involvement of other neurotransmitter systems.
  • Symptoms:
- Motor Symptoms:

- Tremor at rest (often described as "pill-rolling" tremor) - Bradykinesia (slowness of movement) - Rigidity (muscle stiffness) - Postural instability (impaired balance and coordination) - Non-Motor Symptoms: - Cognitive impairment and dementia - Psychiatric symptoms (depression, anxiety, hallucinations, and psychosis) - Autonomic dysfunction (constipation, orthostatic hypotension, urinary incontinence) - Sleep disturbances (REM sleep behavior disorder, insomnia)

  • Diagnosis:
Diagnosis of PD is primarily clinical, based on the presence of characteristic motor symptoms and response to dopaminergic therapy. Imaging studies, such as dopamine transporter (DAT) scans, can support the diagnosis by demonstrating reduced dopamine activity in the basal ganglia. Genetic testing may be considered in cases with a family history of PD or early-onset disease.

Assistive Suggestions and Requirements:

  • Requirement Percentage for Assistive Technology:
A significant percentage of individuals with PD will benefit from assistive technology, particularly as the disease progresses and motor symptoms become more disabling.
  • Assistive Technology Suggestions:
- Mobility Aids:

- Canes or Walkers: To assist with balance and prevent falls. - Wheelchairs: For individuals with severe mobility impairments. - Communication Aids: - Voice Amplifiers: To assist with hypophonia (soft speech). - Speech Generating Devices (SGDs): For individuals with severe speech difficulties. - Home Modifications: - Grab Bars and Handrails: To enhance safety and prevent falls. - Adjustable Beds: To improve comfort and ease of movement. - Feeding Aids: - Adaptive Utensils: For individuals with tremor or reduced hand dexterity.

  • Access Modalities:
- Switch Access: For individuals with severe motor impairments to control communication devices and computers.

- Voice-Controlled Systems: Beneficial for those who retain good vocal strength. - Touchscreen Devices: Useful for those with adequate hand dexterity.

Care Management and Therapeutic Techniques:

  • Aims:
- To manage symptoms and maintain the highest possible level of independence and quality of life.

- To provide supportive care and address complications through a multidisciplinary approach. - To offer education and support to patients and caregivers.

  • SLP Suggestions:
- Assessment and Intervention:

- Regular speech and swallowing assessments to monitor changes and adjust therapy plans accordingly. - Techniques to improve speech clarity and address hypophonia (soft speech). - Swallowing techniques to ensure safe swallowing and reduce the risk of aspiration. - Augmentative and Alternative Communication (AAC): - Introduction of AAC devices early in the disease progression to ensure familiarity and ease of use as the disease progresses.

  • Special Educator Suggestions:
- Cognitive Rehabilitation:

- Activities designed to enhance executive function, memory, and attention. - Use of memory aids, such as notebooks or electronic organizers. - Behavioral Strategies: - Structured routines to manage apathy and maintain engagement in activities. - Positive reinforcement to encourage participation and effort in tasks.

  • Occupational Therapist Suggestions:
- Daily Living Skills:

- Training in the use of adaptive equipment for self-care activities (e.g., dressing, grooming). - Techniques to conserve energy and manage fatigue. - Home and Environmental Modifications: - Assessing and modifying the home environment to ensure safety and accessibility. - Recommendations for ergonomic furniture and tools to support independence.

Recommendations on AAC and Other Details:

  • Text-Based AAC:
- Use of text-to-speech apps and devices for individuals who retain good literacy skills.

- Predictive text features to speed up communication.

  • Symbol-Based AAC:
- For individuals with cognitive impairments affecting literacy, symbol-based systems like Picture Communication Symbols (PCS) can be useful.

- Dynamic display devices that can grow with the userโ€™s needs.

References:

  • Jankovic, J. (2008). Parkinsonโ€™s disease: clinical features and diagnosis. Journal of Neurology, Neurosurgery & Psychiatry, 79(4), 368-376.
  • Kalia, L. V., & Lang, A. E. (2015). Parkinson's disease. The Lancet, 386(9996), 896-912.
  • Schapira, A. H. V. (2009). Neurobiology and treatment of Parkinson's disease. Neurology, 72(21 Supplement 4), S1-S136.

Additional Information:

Parkinson's Disease (PD) is a chronic and progressive movement disorder that affects millions of people worldwide. The exact cause of PD is unknown, but it is believed to involve a combination of genetic and environmental factors. The disease is characterized by the gradual loss of dopamine-producing neurons in the substantia nigra, a region of the brain that controls movement. The loss of dopamine leads to the hallmark motor symptoms of PD, including tremor, bradykinesia, rigidity, and postural instability.

In addition to motor symptoms, individuals with PD may experience a range of non-motor symptoms, such as cognitive impairment, psychiatric disturbances, autonomic dysfunction, and sleep disturbances. These non-motor symptoms can significantly impact quality of life and may even precede the onset of motor symptoms.

Diagnosis of PD is primarily clinical, based on the presence of characteristic motor symptoms and response to dopaminergic therapy. Imaging studies, such as dopamine transporter (DAT) scans, can support the diagnosis by demonstrating reduced dopamine activity in the basal ganglia. Genetic testing may be considered in cases with a family history of PD or early-onset disease.

Management of PD requires a multidisciplinary approach to address the diverse needs of affected individuals. Pharmacological treatments, such as levodopa and dopamine agonists, are commonly used to manage motor symptoms. Deep brain stimulation (DBS) may be considered for individuals with advanced PD who do not respond adequately to medication. Non-pharmacological interventions, including physical therapy, occupational therapy, and speech-language therapy, are essential for maintaining function and improving quality of life.

Support groups and advocacy organizations provide valuable resources and support for individuals with PD and their families. Engaging in advocacy efforts can help improve access to services, funding for research, and public awareness. Ongoing research into the underlying mechanisms of PD and the development of new treatments offers hope for future advancements in PD care.

In conclusion, Parkinson's Disease is a complex and multifaceted disorder that requires comprehensive management and support. Early diagnosis and intervention, along with ongoing care from a multidisciplinary team, can significantly improve the quality of life for individuals with PD.

Epidemiology and Demographics

Etiology and Pathophysiology

What causes Parkinson's Disease Handout?

What does Parkinson's Disease Handout do to the body?

Clinical Features and Stages

Diagnosis

Diagnostic Criteria

Genetic Testing

Differential Diagnosis

Assistive Technology and AAC Interventions

Communication Devices

Mobility Aids

Access Modalities

Environmental Control Units

Clinical Recommendations

๐Ÿ—ฃ๏ธ For Speech-Language Pathologists

โœ‹ For Occupational Therapists

๐Ÿšถ For Physical Therapists

๐Ÿ“Š For Applied Behavior Analysts

๐ŸŽ“ For Special Educators

๐Ÿ‘ฅ For All Staff and Caregivers

Care Management

Medical Management

Positioning and Handling

Feeding and Swallowing

Psychosocial Support

Educational Support

IEP Goal Examples

Accommodations and Modifications

Transition Planning

Support and Resources

๐Ÿ›๏ธ Foundations and Research

๐ŸŒ Online Communities

๐Ÿ“š Educational Resources

๐Ÿ’ฐ Financial Assistance

References

Version: 1.0
Created: 2025-10-24
Last Reviewed: 2025-10-24
Next Review:

Disclaimer: This comprehensive clinical guide is designed for healthcare professionals, educators, and families. For specific medical advice, please consult with qualified healthcare providers.