early onset parkinson’s disease: what nps need to know · 2018-04-03 · early onset...
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Early Onset Parkinson’s Disease: What NPs need to know
PATRICIA H. COX, DNP, MPH, FNP-BCASSISTANT PROFESSOR, UNIVERSITY OF PORTLAND
VISITING NURSE FACULTY, PARKINSON’S FOUNDATION
MELODY RASMOR, EdD, FNP, ARNP-BC, COHN-SASSISTANT CLINICAL PROFESSOR, WASHINGTON STATE UNIVERSITY
VISITING NURSE FACULTY, PARKINSON’S FOUNDATION
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Special thanks
The Parkinson’s Foundation is working toward a world without Parkinson’s disease. Formed by the merger of the National Parkinson Foundation (NPF) and the Parkinson’s Disease Foundation (PDF) in August 2016, the mission of the Parkinson’s Foundation is to invest in promising scientific research that will end Parkinson’s disease and improve the lives of people with Parkinson’s, and their families, through improved treatments, support and the best care.
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Disclosure statement:
We have nothing to disclose during our presentation.
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Objectives
Define Parkinson’s and describe prodromal symptoms Describe the pathophysiology of early Parkinson’s Discuss and analyze case studies of early prodromal
Parkinson’s Explore early interventions that NPs can use to assist
their patients Identify the elements of a Parkinson’s neuro
assessment
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Parkinson Disease Defined
A neurodegenerative movement disorder- It presents with motor deficits, cognitive, affect challenges, and autonomic nervous system dysfunction.
Dopamine depletion, is the hallmark of its motor presentation.
This presentation will hopefully provide a better understanding of the pathophysiology of Parkinson and early recognition of the disease.
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Facts 4,500 years ago – Ancient
Indian medicine –“kampavata”
1817 – James Parkinson - “the shaking palsy”
PD is the 2nd most common neurodegenerative disorder after Alzheimer’s Disease
1-2 million people in the U.S. 10 million people worldwide
The 14th leading cause of death
Occurrence expected to increase two-fold by 2005-2030 in individual aged > 50 years
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Costs
Exceeds 14.4 billion dollars in U.S. More than 6 billion dollars in direct medical costs Direct medical costs per patient estimated 10-14,000
dollars annually Direct + Indirect costs approximately 22,800 dollars
annually
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Disability
Reduced quality of life Impairment of activities of daily living
(walking, dressing, shopping) Impairment of instrumental activities
of daily living (meal preparation, money management, medication management)
Social isolation (embarrassed over physical symptoms of disease)
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Demographics
Gender differences- Men>women Younger age of onset- more symptoms Age not related to severity or progression 2-3% increase in older adults >65 years
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Risk Factors
Advancing Age
Men more likely than Women
Heredity- Having a close relative with Parkinson's increases the chances that you'll develop the disease. Risks still small unless you have many relatives in your family with Parkinson's.
Environmental Exposure- herbicides and pesticides may put you at a slightly increased risk of Parkinson's disease.
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Risk Factors
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Risk Factors
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Parkinson’s Definition
Neurological Motor Disease Affects Dopamine Neurons in Substantia
Nigra Pars Compacta Symptom onset correlates with
advanced neurodegeneration
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Parkinson’s Disease-4 Cardinal Symptoms
Tremor (resting) Muscle Rigidity Bradykinesia Postural Instability
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Parkinson Disease Motor Clinical Manifestations
Decreased arm swing when walking Micrographia (small hand writing) Hypophonia Masked face, decreased blinking Shuffling, slow gait Stooped posture
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CARDINAL SYMPTOMS OF PARKINSON’S DISEASE
https://www.youtube.com/watch?v=d0NYC1JICLA
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Pathophysiology
The substantia nigra pars compacta is located deep in the mid brain.
These neurons are large dopamine neurons that degenerate in PD
Literally all patients receive a late diagnosis since motor symptoms, required for diagnosis, are manifested when approximately 60% of the neurons of the substantia nigra pars compacta (SNpc) are lost
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SUBSTANTIA NIGRA PARS COMPACTA
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How Is Prodromal (Early) Parkinson’s Disease Different?
Non-Motor Neurological Disease Preceded PD Diagnosis Affects Dopamine Neurons in the SNpc Characterized by premotor PD features Onset prior to advanced neurodegeneration
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Life course of disease and need for early diagnosis
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Why isn’t it identified earlier? Mean delay 3-6 years from first symptoms, some
for 10+ years Underreporting & Under-recognition of NMS
• Lack of PCP systematic questioning & knowledge
• Lack of inter-professional collaboration• “I’m just getting old.”• The great copycat• Knowledge inadequacies
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Prodromal Symptoms
Olfactory impairment(hyposmia)-90% REM Sleep Behavior Disorder Autonomic Dysfunction Anxiety/Depression/Apathy Mild Cognitive Impairment (MCI) Fatigue Hallucinations Restless leg (Akathisia) Diffuse Pain Seborrhea/melanoma Decreased blink response
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Movement Disorder Society (MDS) Prodromal PD Criteria
Diagnosis of prodromal PD relies on clinical non-motor markers
Speed of progression from prodromal PD to PD is unpredictable
Criteria is based on estimated risks and symptoms Criteria development relied on prospective studies Estimates criteria predicts prodromal PD with >80%
likelihood
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Prodromal PD in Primary Care
Increased Awareness of Prodromal PD
Evidence is only informative
Diagnosis still relies on MDS Clinical Criteria for PD
Proposed Algorithm
Put Algorithm here
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Why NPs need to know more
Early Parkinson’s-vague symptoms Patients frustrated with multiple diagnosis Complex disease with no diagnostic test Lack of diagnosis, delayed referrals, delayed
treatment
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Why should we evaluate patients with Non-motor symptoms?
Time to plan Physiotherapies to prolong quality of life NPs incorporate patient’s feelings and thoughts Early referral allows for neurology evaluation and
possible treatments/studies
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How can NPs evaluate patients early to make a difference?
Know your patient’s normal to detect subtle changes Broaden your differential for olfactory/gustatory
changes Mimics other disease processes: Sleep disturbances,
IBS, essential tremor, stress incontinence, depression, dementia, metabolic diseases, cerebrovascular disease, Lewy body disease, Huntington disease, multisystem atrophy-so think Parkinson’s
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Time for a Case Study
So…you have a 50 something year old white female coming to see you and she discloses she is in the process of getting a divorce and she is depressed. She reports that her boss has noticed some postural changes and shuffling. She has no tremor, no constipation and she does Jazzercise 2-3 x week.
She has HTN, Thyroid Disease, Metabolic syndrome, is Vitamin D deficient and she is post-menopausa1. She works full time, is a non-smoker and drinks a glass of wine per night.
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The Michael J Fox Foundation
https://www.michaeljfox.org/foundation/news-detail.php?watch-our-latest-video-what-is-parkinson-disease
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Here is the Neuro Exam
Conduct a dexterity test-Ask patient to finger tap. Maintained speed over 10-15 seconds and maintained amplitude. Slowing speed, decreasing amplitude, pauses/arrests in finger and foot taps are consistent with bradykinesia
Observe walking-gait, ataxia, freezing, limitations in turning
Observe for reduced arm swing Observe rising out of a chair. Perform the Pull Test.
www.toolkit.parkinson.org/sites/toolkit.parkinson.org/files
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Questions?
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Acknowledgements
Gwyn M. Vernon, M.S.N., R.N., C.R.N.P.Co-Founder and National Director, Parkinson's Disease Foundation
The Edmond J. Safra Visiting Nurse Faculty Program
Nikkiel Lefebre, RN, BSN, MN, FNP
Elizabeth Teeling, BSc, RN-BSN, MN, FNP
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References
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References
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Melody with “Parky” and Nikkiel Lefebre