OHSU Parkinson Center
April 30, 2017 Linda Bryans, MACCC SLP-L Allison Lindauer, NP, PhD Lisa Mann, RN
Aimee Mooney, MSCCC-SLP-L Jennifer Wilhelm, PT, DPT, NCS Rosanne Yee, OTR-L
Key Challenges in Team Care Late Stage PD
OHSU PARKINSON CENTER
OHSU Parkinson Center
Overview • Compare and contrast rehab needs for
Advanced PD
• Identify discipline specific treatments • Coordinate inter-disciplinary team care
• Swallowing /Nutrition • Falls/Vision • Incontinence • Orthostatic hypotension
• Cognition/Mood • Communication • Pain
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Key Challenges in Advancing PD Nutrition, Feeding & Swallowing
Rosanne Yee, OTR Linda Bryans, MA, CCC-SLP
OHSU Parkinson Center
What? When? How? • What foods?
– Can be decided by ability to swallow, ability to manipulate food to mouth and foods that aid bowel movements (for constipation)
• When to eat? – Can be dependent on medications, energy level to maintain
proper posture during meal • How to make food?
– Can be decided on ability/endurance of balance and standing, energy and ability to use kitchen equipment, making the consistency allowed for swallow
• How much food? – Can be decided by caloric intake needed to maintain levels of
physical and cognitive activities, swallow abilities per bite
Interdisplinary Approach= Interplay with other team members
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Nutrition • Important to understand the role nutrition
plays in both neuroprotection and neurodegeneration.
• Recent studies have revealed the promise of some nutrients in reducing the risk of PD and other nutrients may be involved with increasing the risk or quicken disease progression
• Important to understand effects of food on medications
(The emerging role of nutrition in Parkinson's disease Seidl. Et al. Front. Aging Neurosci., 07 March 2014)
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Nutrients that may be Associated with an Increased Risk or Progression of PD • Dairy products
– the possible presence of neurotoxins, like pesticides in dairy products may increase the risk of PD
– mainly milk-strong positive association with the consumption of milk, but not cheese or yoghurt has been reported
(The emerging role of nutrition in Parkinson's disease Seidl. Et al. Front. Aging Neurosci., 07 March 2014)
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Nutrients that may be Associated with a Decreased Risk or Progression of PD
• Phytochemicals-Fruits and vegetables are rich sources of antioxidants
• Omega-3 polyunsaturated fatty acids-neuroprotective and has anti-inflammatory potential
• Soy-primary protein in soy appears to be neuroprotective • Caffeine- decrease triggers for neuroinflammation in
neuropathways may contribute to neuroprotection • Tea-Polyphenols in green and black tea provide potent
antioxidant-radicals • Alcohol-moderate consumption lowers the risk of PD. Red wine
especially neuroprotective (The emerging role of nutrition in Parkinson's disease Seidl. Et al. Front. Aging Neurosci., 07 March 2014)
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Nutrients: Questionable Role in PD
• Fat-saturated may increase risk of PD vs. high fat diet (8% protein) provided symptomatic and beneficial disease modifying activity
• Meat- red meat heme iron content may act as a toxin when not digested properly vs higher intake of iron is associated with neuroprotection in PD
• Carbohydrates-high glycemic index decrease the risk of PD vs High carbohydrate diets are associated with an increased risk of type 2 diabetes, which numerous studies indicate type 2 diabetes is associated with an increased risk of PD
(The emerging role of nutrition in Parkinson's disease Seidl. Et al. Front. Aging Neurosci., 07 March 2014)
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Nutrition and Medication Interactions
• All types of protein can interfere with Carbidopa-Levodopa absorption
• It is best to take the medication 30 to 60 minutes before eating protein and 1 to 2 hours after protein
• Take the medication along with foods that don’t contain proteins.
(National Parkinson Foundation (2017))
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Meal Preparation
• Barriers to participation and completion: – Fatigue (PT and SLP) – Posture (PT) – Pain (PT) – Vision (Neuro-opt/neuro-ophth) – Tremor (PT) – Rigidity (PT) – Cognition (SLP)
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Meal Preparation: OT Interventions • keep handles in and use the back burners if having balancing
problems • changing body positions: sit perching stool • good lighting • contrast colours: Equipment • gather ingredients all together before cooking • re-arrange kitchen for easier access to items used frequently • simple and less time depending recipes (limit multi task recipes) • use alarms/timers • use checklist to keep track of what has been done • Pacing: prep things throughout day, use crockpot
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Eating and Drinking • Barriers to participation and completion: • Dexterity • Wrist rigidity • Bradykinesia • Tremor • Decreased appetite (meds and olfactory issues) • Rigidity (increase caloric expenditure) • Posture • Vision • Fatigue (hand to mouth and chewing)
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Eating and Drinking: OT Interventions
• modify routines of meals: time of meals, texture, amount, environment
• only needed items on table • smaller portions • posture and proximity to table • Use of both hand • contrasting colours, proper lighting • adaptive equipment (plate guard, built up handles, off
set spoon and fork, liftware, Readi-steady glove, rocker knife, ergo knife, “nosey” cup, small opening bottles, non slip mats, box to raise eating surface)
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Feeding Habits that effect Swallowing
Observation during ADL’s: • Difficulty looking
down at the plate (make sure plate is in line of vision) • Mouth stuffing and rapid drinking • Tremor or stiffness interfere with self-feeding • Listening to patient/family about length of
mealtimes • Is my patient fatigued
from malnutrition or dehydration related to Dysphagia?
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Dysphagia in PD • Oral phase: PD can cause rigidity, tremor or dyskinesias in the muscles in the
tongue, jaw, lips and face which can impact the oral stage of the swallow. – Reduced or effortful chewing - Repetitive or excessive tongue movement (“tongue pumping") – Drooling - Reduced A-P transit – Decreased initiation - Oral residue
• Pharyngeal phase. PD can cause the swallow to be delayed, reduce pharyngeal contraction, reduced UES opening, reduce airway protection and reduce pharyngeal sensation.
– Choking or coughing while eating or drinking – Wet vocal quality after eating or drinking – Frequent throat clearing while eating or drinking – A sensation of food sticking in the throat
• Esophageal phase: PD can cause tightness in the cricopharyngeus muscle, reduced esophageal peristalsis and esophageal reflux.
– Heartburn – Food coming back up into the throat or mouth after swallowing – Coughing after eating – Frequent coughing or throat clearing
-Tjaden. Speech and Swallowing in Parkinson's Disease (2008)
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PD Dysphagia Stats • 40-90% of persons with PD have dysphagia
– Rosenbeck & Jones (2007) – Leopold & Kagel (1997)
• Subjective dysphagia in 1/3 of community dwelling PD pts (higher numbers in advanced PD)
• Patients may remain clinically asymptomatic • Patients may have poor awareness of dysphagia • 15% of PD patients show silent aspiration • Dysphagia is more prevalent in advanced PD but often
does not correlate with disease severity • Moderate dysphagia: "The potential for aspiration that
is minimized by swallowing techniques and diet modifications"
– Yorkston, Miller, Strand (2004)
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Cough • Airway protective mechanisms such as swallowing and
cough may play a role in aspiration pneumonia • Cough is an important defense mechanism
– Important to remove mucus, foreign bodies from airways by generating a high expiratory flow
• Impairment of cough – Motor dysfunction – Sensory dysfunction
• In early stages of PD, the motor component of cough was impaired
• In late advanced stages of PD, both the motor and the sensory component of cough were impaired -Ebihara et al (2003) Impaired efficacy of cough in pts with PD
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Dysphagia Assessment • Clinical Assessment of Swallowing • Objective evaluation
– Modified Barium Swallow Study
(MBSS)
– Fiberoptic Endoscopic Evaluation of Swallowing (FEES)
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MBSS
• Diagnostic • Determine safest texture • Determine effectiveness of compensatory
strategies • Determine ability to safely maintain
nutrition/hydration • Education
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FEES
• Functional exam • Airway assessment • Vocal fold function • Secretion management • No exposure to radiation • Application of therapeutic techniques • Biofeedback
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Complications of Dysphagia
• Aspiration pneumonia • Malnutrition • Dehydration
• Aspiration pneumonia is a leading cause of
death in PD
– Fernandez & Lapane. (2002) Predictors of mortality among nursing home residents with a diagnosis of Parkinson's disease.
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Dysphagia Management
• Pt and caregiver education regarding s/s of dysphagia and aspiration
• Regular evaluations of pts with documented dysphagia • Compensatory Strategies
– Upright posture – Small bites/sips – Increase sensory input – Alternating liquids and solids – Chin tuck (maybe)
• Texture modification -Tjaden (2009)
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Therapeutic Exercises • Active ROM exercises for tongue, lips, larynx • Sustaining high pitch which engages pharyngeal
wall contraction • Effortful swallow to improve BOT retraction,
clearance of residue • Mendelsohn Maneuver to increase laryngeal
elevation • Shaker exercises to improve hyolaryngeal
excursion
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EMST and swallow safety • Promising treatment
– Expiratory Muscle Strength Training (EMST) – Randomized, blinded, sham-controlled study – EMST 5X/week for 4 weeks for 20 min per day – EMST group demonstrated improved swallow safety
as evidence by improved PA scores – EMST group demonstrated improvement of
hyolaryngeal function during swallow
– Troche et al (2010) Aspiration and swallowing in PD and rehabilitation with EMST
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Improving Cough in PD • Promising treatment
– EMST to improve cough – 10 mid stage PD pts with penetration or
aspiration on MBS – 4 weeks of EMST – Significant decrease in duration
of the Compression Phase Duration and Expiratory Phase Rise Time; decrease in EPRT resulted in significant increase in cough Volume Acceleration
– Significant decreases in PA scores after treatment
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Contributing factors to dysphagia in mid-late stage • Cognitive impairment • Impulsivity when self feeding • UE Tremor • Dyskinesias • Poor awareness of dysphagia • Posture • Fatigue • Vision
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A word about drooling • Reported in >56% of pts • Secretion management vs sialorrhea
– 55% of PWP c/o xerostomia • Changes in sensation • Things that were once automatic are no longer automatic • Oropharyngeal dysphagia • Treatments:
– Botox injections – Meds: anticholinergics (can cause confusion, hallucinations, constipation,
urinary retention, drowsiness) or adrenergic receptor antagonists • Strategies:
– Think swallow – Before talking – Before bending – When concentrating – Intermittently
-Srivanitchapoom, Pandey & Hallett (2014)
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When to talk about tube feeding…. • Important to understand pt's wishes • Usually in later stages of PD but some pts are more
proactive • s/s of dysphagia that are progressing • Conversation in conjunction with neurology/PCP • Offer support and understanding of implications of
TF • What does it mean to have TF?
– NPO? – Recreational PO? – Burden of PO – Extends life? – Prevents aspiration?
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I takes a village..... • Keep an eye out • Weight Loss • Food/liquid avoidance • Taking longer to finish a meal • Coughing with water • Wet/gurgly vocal quality • Congestion • Fever
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Key Challenges in Advancing PD Falls - Vision
Jennifer Wilhelm, PT, DPT, NCS Rosanne Yee, OTR-L
OHSU Parkinson Center
Falls
• Early PD: • 181 newly dx PWP vs 173 controls
– 64.1% of PWP fell over 7 years – 15% fell prior to dx; 13% within 1 year – Relative risk to controls: 3.1 – Higher rates of falls: higher age, UPDRS, PIGD
phenotype, dementia and lost to f/u
Hiorth Y et al; J Neurol 2017
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Falls
• Hospital in Australia retrospectively looked at 342,265 fall-related hospital admissions ≥65 years
• 2.5% of falls were in PWP – Higher rate of admission – Longer hospitalization stay
Paul SS et al; Eur J Neurol 2017
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Falls: where do they happen Fall location/circumstance PD admission
(n = 8628) Non PD
admission (n = 334,933)
Kitchen 2.2% 2.0% Bathroom 3.5% 4.1% Bedroom 3.2% 3.1% Elsewhere indoors at home 2.6% 2.6% Outdoors at home 3.6% 5.5% At home, unspecified 28.8% 29.0% Footpath 1.3% 2.7% Outdoors 1.5% 3.2% Residential living facility 28.6% 17.3% Healthcare facility 8.7% 7.0% Other buildings 1.7% 4.4% Unspecified/missing location 14.4% 19.3% Paul SS et al; Eur J Neurol 2017
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Falls and injuries Injury
PD admission (n =8487)
Non-PD admission
(n = 333,778) All fractures 34.9% 39.4% Hip fracture 17.0% 13.5% Other LE fracture 1.9% 5.1% UE fracture 6.3% 10.4% Other fracture 9.7% 10.5% TBI 3.1% 3.0% Other injury 29.4% 26.5% No injury 32.6% 31.0%
Paul SS et al; Eur J Neurol 2017
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Falls • PSP:
– Early postural instability: key in diagnosis
– Posterior falls – Dystonic rigidity of neck and upper trunk – Gait: “drunken sailor” (clumsy, slow and unsteady) – Gaze palsy:
• Difficulty scanning environment: curbs, obstacles, judging distances and going up/down stairs
– Impulsivity and poor insight into deficits – Can identify fallers with dual task conditions
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Falls
• PSP: Rapid progression of gait deficits – n = 50 pts with PSP followed
• To death (n = 21; mean duration 53.6 mo) • In ongoing fashion (n = 29; mean duration 46.2 mo)
– Loss of independent walking, inability to stand unassisted and requiring use of wheelchair
• Once you met 1 milestone: high probability of reaching others within 8 months
• All milestones occurred 59-62 mo from symptom onset; 36-39 mo from 1st visit
Goetz CG et al; Neurology. 2003
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Falls: PT
• PSP – Heel wedge in shoe: shift COG anterior – U-step walker – Increase step height to improve clearance – Posterior stepping strategies – Increase base of support for ADLs: “Strong
stance” – Work with OT regarding visual scanning
and SLP regarding impulsivity
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Falls
• MSA: – Can include cerebellar signs leading to ataxia – Often with bilateral involvement – Bradykinesia and rigidity – Initial symptoms in trunk and LEs – Can occur due to orthostatic hypotension – Often with urinary incontinence
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Falls
MSA-C • Coordination
exercises • Narrow BOS • Unstable
surfaces • Strengthen
trunk and hip/shoulder girdle muscles
MSA-P • Similar
treatments as PD
MSA-A • Address
orthostatic hypotension
• 4WW with seat
• Transport wheelchair
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Falls • Late Stage PD (study of n = 50; mean
duration of disease 17.94 yrs; H&Y 4/5) – Increased rate of falling with course of disease – Falls occurred in 50% of patients
• 28% had daily falls • 30% falls caused by freezing
– Caused an extreme impact on patients’ perceived health status
Coelho M et al; J Neurol. 2010 Sep;257(9):1524-32
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Falls: PT • Late Stage PD (study of n = 24; mean duration of
disease 11 yrs; H&Y 4) – Impaired postural control in quiet stance: both static
and dynamic – Decreased ability to balance when vision or
proprioception is disturbed • Delay in adapting balance strategy with sensory changes
– High reliance on vision: even if it is conflicted – Postural strategies usually are ineffective to keep
balance and avoid falls: especially if dynamic conditions or if sensory info is conflicting
Colnat-Coulbois S et al; Neuroscience. 2011
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Falls: PT
• Late Stage PD – Sensory integration training
• Try to decrease vision • Unstable surface: start with a towel
– Postural reactions: ankle, hip and stepping – Assistive equipment
• 4WW vs U-step walker: look at context • Wheelchair
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Freezing
• Causes: step initiation, turning, walking through doorways, crowds, stress, distraction
• 3 subtypes – Shuffling with small steps – Trembling in place – Total akinesia
• May be L-dopa responsive: ON/OFF
Snijders AH et al; Ann Neurology 2016
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Freezing • Correlated with
decline in miniBEST: – ↓ Anticipatory
reactions – ↓ Reactive postural
control – ↓ Dynamic postural
control
• Mechanisms: – Lack of APA: prevent
normal stepping pattern
• Treatment: weight shifting, lateral stepping
– Cognitive role: deficits in executive and visuospatial functions
• Treatment: external/sensory cues; SLP?
Vervoot G et al; Parkinsonism Relat Disord 2016 Jacobs JV et al; Exp Neurol. 2009 Kelly VE et al; Parkinsonism Relat Disord. 2015
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Treatment: Assistive Devices
• Single point cane: with or without laser, inverted walking stick
• Bilateral trekking poles • Walker
– FWW: increases falls with PD – 4WW – U-step walker
• Transport wheelchair • Manual wheelchair • Power wheelchair
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Falls/Vision: OT
Ocular and Visual disorders: • Impact on ADLs like walking, reading,
driving • typically have problems with internally
guided movements and postural control use vision to compensate
• (Ocular and Visual disorders in PD: Common but frequently overlooked. M.S. Ekker et al. Parkinsonism and Related Disorder (2017) 1-10)
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Falls/Vision: OT Ocular Disorders
• Dry eyes • Decrease blink rate • Blepharitis • Blepharospasm • Apraxia of eyelid opening
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Falls/Vision: OT Ocular Disorders Functional scan –Saccades tend to be slow and display delayed initiation –Pursuit movements become jerky and slow eye movements (cog-wheel) Depth Perception –Vergence becomes insufficient due to slowness of eye teaming and can result in eyestrain, headaches and double vision (diplopia) –Solution: eye exercises focused on concise movement and referral to neuro ophthalmology or neuro optometry
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Falls/Vision: OT Visual Disorders • Visual Processing
– Contrast sensitivity-problems seeing in low light during walking, ADLs and night driving. Solution: increase light. If too much glare yellow filtering glasses. Referral to Low vision optometry
– Colour discrimination-trouble with all colours except black and white. Solution: contrast colors
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Falls/Vision: OT Visual Disorders
• Visual Processing – Visuoperceptual issues:
• Detection of motion • Human movement • Facial recognition
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Falls/Vision: OT Visual Disorders • Visuospatial issues:
– Perception of space – Recognition of line orientation – Mental 3D rotation of object – ID figure embedded in complex figures – Visuospatial problem solving – Depth perception – Spatial working memory
Visuospatial dysfunction specifically associated to fatigue. (Is fatigue associated with cognitive dysfunction in early PD? B.M. Kluger at el. Parkinsonism and Related Disorders 37 (2017) 87-91)
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Falls/Vision: OT • PSP the predominant visual defects are:
– Vertical gaze palsy-vertical saccades slow and hypometric, both up and down direction
– impaired vergence – inability to modulate the linear vestibulo-
ocular reflex appropriately for viewing distance.
(The Disturbance of Gaze in Progressive Supranuclear Palsy: Implications for Pathogenesis A.L. Chen et al. Front Neurol. 2010; 1: 147.)
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Falls/Vision: OT • MSA Typical ocular features include:
– Blepharospasm-abnormal, involuntary blinking or spasm of the eyelids.
– excessive square-wave jerks-fixation instability – mild to mod saccade hypometria-undershooting
target – Impaired vestibular-ocular reflex (VOR)- eye
movement that is equal in magnitude but opposite in direction
– Nystagmus-involuntary movement of eye (Visual signs and symptoms of multiple system atrophy. Armstrong, Clin Exp Optom 2014 Nov;97(6):483-91.)
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Falls/Vision: OT OTs evaluate functional vision to understand how it hinders and facilitate occupational performance • Modify and adapt the environment • Increase contrast • Reduce patterns • Improve lighting • Magnification • Organization • Simplify tasks • Improve search of environment • Refer as needed to neuro-ophthalmologist/neuro-
optometrist
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Falls: OT Examine home environment: • Rails for both sides stairs • Vertical grab bars when reaching overhead or opening doors • Remove clutter and throw rugs • Re-arrange environment to widen walking path and make
items more accessible • Good lighting and mark edges corners with contrasting colour
tape • Lower bars in clothes closet • Sit for shower, grooming and dressing • Education of family for future equipment needs for rapidly
progressing disease
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Falls: OT Retropulsion triggers • carrying things in both hands in front • pulling or dragging anything ex. tools for house
and garden work Retropulsion compensation strategies • carry objects with handles at the side • use push rolling kitchen, laundry, garden cart to
transport items • sit to do self care
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Key Challenges in Advancing PD Incontinence
Jennifer Wilhelm, PT, DPT, NCS Rosanne Yee, OTR-L
OHSU Parkinson Center
Incontinence • Seen primarily with MSA; can be early sign
due to autonomic dysfunction – 90.9% of MSA patients report symptoms
• PSP: 53.3% of patients report symptoms • Linked directly to quality of life
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Incontinence
• MSA and end stage PD – Storage problems: frequency, urgency, urge
incontinence, noctureia
• MSA - can also have and may need to catherized
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Toileting –behavioral modifications
Bladder • Record current habits/routine by using voiding diary • Monitor pm fluid intake
Bowel • Fiber and fluids • Height of toilet. • Exercise • Routine • Stress/rushing
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Weekly voiding diary
Monday Tuesday Wednesday Thursday Friday Saturday Sunday Comments Waking Breakfast mid-morning Lunch Early afternoon
Late afternoon
Supper Evening Bedtime Night
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Simple Voiding Diary
Document if you void or have an accident
Mon Tues Wed Thurs Fri Sat Sun
void
accident
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Incontinence: OT
Prevention: • Timing fluid intake • Timing regular trips to bathroom
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Incontinence: OT
Clothing Management: • Elastic waist pants • Velcro closure • Suspenders • Adult briefs/pads
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Incontinence OT • DME and adaptive equipment
– Elevated toilet seat • May need horseshoe/cutout for catherization • May need foot rests for bowel movements
– Condom catheter with Catheter clip – Incontinence pads/absorbent sheets. – Female/male urinal (non spill) – Catheter inserter – Bidet – Wet wipes – Commode
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Incontinence: PT • Bed Mobility
– Improve speed in getting up from bed – No Tempur-Pedic! – Technique – Satin
• “Sheet” in middle 1/3 of bed • Boxers
– Assistive equipment • Handrails • Safe T pole
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Incontinence: PT
• Mobility: able to get to bathroom on time? – Need for assistive equipment – Balance training
• Pelvic floor PT – Limited research in late stage PD or PD plus
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Incontinence: PT • Exercise-based behavioral therapy and urinary
incontinence in PD – n = 20 (17 completed study; 90% male; mean
duration of PD 6.9 ± 5.4 yrs) – Intervention: every 2 wks for total of 5 visits over
8 wks • 1st visit: dual channel EMG to pelvic floor for contraction
and relaxation; education; exercises: 45 pelvic floor contractions daily: 3 sets of 15 (1 set in lying, sitting and standing)
• 2nd visit: Education of urge-suppression strategy • 3rd + visits: offered additional biofeedback to promote
exercise compliance and reinforce bladder control strategies
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Incontinence: PT
• Outcomes: – 83.3% reduction in urinary incontinence – 94.4% reduction in urgency urinary
incontinence – 26.1% reduction in nocturia – Improvement in QOL scores from 71.1 ± 23.9
to 54.7 ± 15.4 (p = 0.002)
Vaughen CP et al; Neurology. 2011
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Incontinence: PT • TTNS: Transcutaneous-tibial nerve
stimulation – Inhibit detrusor overactivity through
afferent fibers to sacral cord – Potential use for both bladder and bowel
issues – As effective as extended release oxybutynin
in overactive bladder
Manríquez VS et al; Eur J Obstet Gynecol Reprod Biol. 2016
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Incontinence: PT • TTNS and PD (n=8 TTNS; n=5 sham)
– 30 min, 2x/wk x 5 wks: 200 µs, 10 Hz – ↓ urgency and nocturia – Improved urodynamic testing with increased volumes
• PTNS and PD (n=47) – 30 min, 1x/wk x 12 wks: 200 µs, 20 Hz – Significant ↓ daytime frequency, nocturia, urge incontinence
episodes and urgency episodes – Improved urodynamic testing with increased volumes
Perissinotto MC et al; J Wound Ostomy Continence Nurs. 2015 Kabay S et al; Urology. 2016
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Key Challenges in Advancing PD Orthostatic Hypotension
Jennifer Wilhelm, PT, DPT, NCS Lisa Mann, RN, BSN, MA
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Orthostatic Hypotension in PD • Causes
– Autonomic system dysregulation – Medications
• Symptoms – Lightheadedness, dizziness – Vision disturbance or syncope – Impaired thinking – Lethargy / fatigue / weakness – Pain (neck, shoulder, chest)
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Orthostatic Hypotension • Drop is SBP of at least 20 mm Hg or DBP of at least
10 mm Hg within 3 min of standing • Usually worse in the morning: nocturnal polyuria
results in reduced overall fluid volume • Other contributing factors
– Prolonged supine position – Quick position changes – Warm environment: lower BP in general – Ingestion of food
• Can lead to falls • Often multi-factorial for treatment
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Orthostatic Hypotension
• MSA: commonly seen due to autonomic dysfunction – Occurs in 53-68% of patients – Causes falls in 54.6% of patients – Only 12% of patients were symptomatic with 24 hr
testing • PSP: less common
– Present in 8-13.3% of patients, usually with no symptoms
Colosimo C et al; J Neurol. 2010 Schmidt C et al; Mov Disord. 2009
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Orthostatic Hypotension • Late stage PD (H&Y IV-5): often observed
– Present in 26% of patients; 8% of patients having syncope
– May not be as large of a problem: limited mobility prevents quick sit to stand
• 96% of patients had dysautonomic symptoms – Can occur due to medications (dopamine
agonists) – Incidence increases with higher age and longer
disease duration
Coelho M et al; J Neurol. 2010
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Orthostatic Hypotension
Complicating Factors • Medications
– PD meds – non-PD meds
• Environment • Activities
– Eating – Bathing – Exercise
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Orthostatic Hypotension • Medication evaluation/change • Environmental cautions • Medications to compensate
– fludrocortisone/Florinef ® – midodrine/Pro-Amatine®; – pyridostigmine/Mestinon® – droxidopa/Northera®
• Referral to Physical Therapy
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Orthostatic hypotension: Patient Education • No quick postural changes, especially after
awakening • Scheduling activities for later in the day • Avoiding
– Motionless standing activities – Warm environments – Valsalva maneuver
• Postprandial
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Orthostatic hypotension: Patient Education
• Non-pharmalogical interventions – ↑ use of caffeine, salt (8g/day), and fluids – ↓ alcohol intake – Eating smaller, more frequent meals (6/day) – Hydration: 1.5-2 L/day
• 2 8 oz glasses of water quickly: ↑ 20 mm Hg systolic BP in standing
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Orthostatic hypotension: Patient Education • Mechanical interventions
– Elevating head of bed up to 8” – Use of compression stockings (>15-20 mm Hg) or
abdominal binder • Coordinate with OT for difficulty with donning
– Abdominal binder – Reverse Trendelenberg – Wheelchair recommendations
• Elevating leg rests • Tilt feature
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Orthostatic hypotension: Patient Education • Exercise interventions:
– Maneuvers to increase BP: 20/10 mm Hg; 30 sec intervals • Squatting • Lower body muscle tensing • Crossing legs • Bending over
Krediet CT et al; Clin Auton Res. 2008 Krediet CT et al; Circulation. 2002
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Orthostatic Hypotension • Home evaluation/DME evaluation
– Commode next to bed – Barrier free way of getting to the
bathroom – Using bedside equipment – Condom catheter or bedside urinal – Good lighting
• Caregiver training
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Orthostatic Hypotension: PT • Monitor vitals during treatment • Exercise: swimming due to hydrostatic
pressure • LE exercises in bed or at EOB
– Hold knees to squeeze the legs before rising; do 10 times on each leg.
Fujimoto K; J Neurol. 2009
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Orthostatic Hypotension: PT
• Implications for exercise – Study of MSA pts (n=15)
• Exercise: Supine position, pedaling cycle ergometer at workloads of 25, 50 and 75 W, each for 3 min
• BP ↓ and stayed low for 10 min post exercise
• Vasodilation of skeletal muscle without compensatory vasoconstriction in other large vascular beds
Smith GD et al; J Physiol 1995
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Cognition in PD Incidence: >40% experience cognitive impairment after 10 years, 75% of people have Dementia Type: heterogenic; yet: Working Memory Processing Speed Executive Functioning Learning Efficiency (slower, more reps)
Impact: Independence (driving), Safety, Quality of Life, Carepartner Burnout, Emotional and Psychological Health
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Continuum of Cognitive Changes in PD Mild cognitive impairment is common in nondemented Parkinson's disease (PD) patients and may be a harbinger of dementia. The Movement Disorder Society commissioned a task force to delineate diagnostic criteria for mild cognitive impairment in PD. The proposed diagnostic criteria are based on a literature review and expert consensus.
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PD-MCI Criteria
I. Inclusion criteria • Diagnosis of Parkinson's disease as based on the UK PD Brain Bank Criteria20
• Gradual decline, in the context of established PD, in cognitive ability reported by either the patient or informant, or observed by the clinician • Cognitive deficits on either formal neuropsychological testing or a scale of global cognitive abilities (detailed in section III) • Cognitive deficits are not sufficient to interfere significantly with functional independence, although subtle difficulties on complex functional tasks may be present II. Exclusion criteria • Diagnosis of PD dementia 18
• Other primary explanations for cognitive impairment (e.g., delirium, stroke, major depression, metabolic abnormalities, adverse effects of medication, or head trauma) • Other PD-associated comorbid conditions (e.g., motor impairment or severe anxiety, depression, excessive daytime sleepiness, or psychosis) that, in the opinion of the clinician, significantly influence cognitive testing
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Dementia 1. APHASIA: Difficulty with language 2. APRAXIA: Difficulty with performing tasks 3. AGNOSIA: Struggles with recognizing
known/familiar objects 4. EXECUTIVE FUNCTION: Creating difficulty
with planning, sequencing, organizing 5. Behaviorally/Personality Changes “ The loss of mental functions involving
thinking, memory, reasoning and language to such an extent that it interferes with a person’s daily living.”
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“Must Knows” • See patients as EARLY in their Diagnosis as
possible • Education for patients and caregivers is KEY • Encourage patients to DO DO DO for
themselves! • Exercise (both physical and mental is
IMPERATIVE) • Give your patients Home Programs that are
specific & intense • Encourage check-ins every 6 months • ANTICIPATE needs as PD progresses
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Questions SLP’s can answer: • Can they continue to live alone Independently?
• What level of residential care would be best?
• Are they safe while eating (i.e.: risk of aspiration?)
• Can they remember to take their medications on time?
• How can I get them to stop wandering?
• How can I reduce Care-giver Strain?
• Do they need Occupational Therapy? Do they need Physical Therapy?
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ASHA: Roles of SLP’s Working with Individuals with Dementia-based Communication Disorders Identification: Screening (i.d. sensory
impairment, hearing, vision); consider mood, medications
Assessment: selecting and
administering clinically, culturally and linguistically appropriate approaches to diagnosis and assessment of cognitive-communication disorders of dementia across the course of the underlying disease complex
Intervention: identifying appropriate
evidence-based practice techniques for direct intervention with persons with dementia and indirect intervention through their caregivers and environmental modifications.
Counseling: to individuals with
Dementia and their significant others about nature of their dementia and its course
Collaboration: To develop intervention plans for maintaining cognitive-communication and functional abilities at highest level throughout the disease course
Case Management: serve as
coordinator or team leader to ensure appropriate and timely delivery of comprehensive management plan
Education
Advocacy
Research
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Treatment Considerations • Direct: facilitate cognitive-communication
function • Indirect: environmental modifications,
development of therapeutic routines & activities and caregiver training.
Caregiver training is essential to optimal
outcomes for individuals with dementia.
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(ASHA) Technical Report SLP Tx for deficits in Cognition
DIRECT: facilitate cognitive-communication function • Spaced Retrieval Training • Reminiscence • Montessori Based
activities • Graphic and written cues
in Memory Wallets and books
• Exploration of participation in cognitively stimulating activities; assistance in establishing community activities which enhance life
INDIRECT: environmental modifications; caregiver training
• Caregiver training in use of strategies and aides for successful cuing of patient in home and community environments
• Caregiver training in communication strategies
• Environmental modifications
• Development of therapeutic routines and activities
101
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Factors which make cognitive function worse:
• Medication • Pain • Poor sleep • Fatigue • Low mood/depression • Stress • Over stimulation/distraction
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Patient Education: Key for all SLP Interventions for deficits in Cognition
• Patient and Caregiver education about cognition strengths and weaknesses, their impact on ADL’s, and type of supervision required
• Patient and Caregiver education about factors which contribute to difficulties with cognition (fatigue, stress, pain, depression, anxiety, sleep, meds)
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Area of Cognition Speech Therapy Speed of Information Processing
•Training in Speaker Control Strategies
Attention
•Guidance in energy conservation strategies/fatigue management (coord with OT) •Instruction in environmental modifications to maximize attention
Memory
•Development of external aides and environmental modifications in the home to support reduced skills (resources: epill.com) •Training in Internal Memory Strategies(repetition, visualization, association, location, attention) •Teaching of External Memory Compensations (daily journals, calendars, white boards, checklists, routines)
Executive Function •Education in Initiation Strategies (daily plan, scheduled routine activities, use of a timer to get started, dry erase board for caregivers)
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SLP Treatment for Energy & Speed of Processing and Attention Training in energy conservation
strategies/fatigue management (coord with OT) Training in Speaker Control Strategies
Environmental Modification to
maximize attention (ie, reduce distractions, do one task at a time)
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SLP Treatment for Memory Patient Education: Memory is an ACTIVE
process; you must consciously manipulate the information to get in into your brain.
Memory has 3 Stages: Input: when information is coming into
your brain; effected by: Storage: maintaining information;
consolidation with info you already know Retrieval: ability to access information
when it is needed.
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Memory Strategies: the “why” • Remember to take medications as prescribed • Remember to use good posture strategies • Remember and keep medical appointments • Remember how to use adaptive equipment
and assistive devices • Remember to use safety swallow precautions • Remember golf score or bridge score • Remember stories that your granddaughter
tells you
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Internal Strategies Repetition Association Visualization Location Mnemonics First Letter
External Strategies Write it down!!! Calendar/dry erase board Diary/memory book Paper & Pencil by each
telephone Timers (epill.com) Memory Shrine Established routines Checklists Signs & Labels
Training Memory Strategies
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SLP Treatment for Executive Function: Training Initiation Strategies Consistent & predictable routines Checklists for tasks: “Things to do before
leaving the house”: 1. Turn off the lights, TV and Stove 2. Check to make sure I have my meds 3. Lock the Doors 4. Set the Alarm
Make a daily plan and schedule activities Use timer to help get started Dry erase board: Caregiver writes down the
plan for TODAY
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Effective Instructional Strategies
• Encourage appropriate independence • Simplify complex tasks • Avoid multiple sensory cues • Avoid over stimulation
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Academy of Neurologic Communication Disorders and Sciences
Evidence Based Practice Guidelines for the Management of Communication Disorders in
Neurologically Impaired Individuals : DEMENTIA
• Spaced Retrieval Training • Montessori-Based Interventions • Validation Therapy • Graphic and Written Cues • FOCUSED Caregiver Training Program
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Montessori-based interventions
• Based on work done with children by Maria Montessori in the early 1900s and continuing today.
• Basic technique is to create structured,
stimulating activities that are appropriate to an individual's cognitive abilities, allowing engagement in tasks and the opportunity for social interaction.
• Activities can be conducted individually with clients or in groups.
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Validation therapy
• A method of communication initially described by Naomi Feil, a gerontological social worker
• Basic technique is to validate (through
words, gestures) what the person with dementia says, regardless of accuracy or basis in fact, rather than correcting or re-orienting the person
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Graphic and written cues • Basic technique involves providing written
factual information and/or familiar photos to facilitate communication
• Capitalizes on recognition memory and the
ability to read aloud, both of which may be relatively preserved in many individuals with Alzheimer's dementia
• Photographs and words can be incorporated
into memory books/wallets, memo boards, and activity calendars
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FOCUSED caregiver training program FOCUSED is an acronym for the key features of the communication enhancement program: F = functional and face-to-face; O = orient to topic; C = continuity of topic-concrete topics; U = unstick any communication blocks; S = structure with yes/no and choice questions; E = exchange conversation--encourage interaction; D = direct, short, simple sentences Designed to be used with both family and professional caregivers
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Cognitive Intervention: 5 evidence-based principles for enhancing learning in Dementia
1. Strengthen memory traces with repetition 2. Engage the non-declarative memory system:
active involvement promotes better learning 3. Reduce errors during learning. Minimizing
errors during learning is essential b/c every time an error is repeated, this erroneous response is strengthened. (Spaced Retrieval)
4. Structure intervention so clients focus attention on a single task
5. Use salient cues to aid successful retrieval (free recall harder than cued recall or forced choice)
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Other considerations re: Cognition
• Cognitive Stimulation • Maintain participation in as many activities
as possible- and train caregivers about this!!
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Utilizing the knowledge and power of Neuroplasticity
• Neuroplasticity: The ability of the brain to change and adapt to circumstances of injuries by forming new pathways, making new cells and getting bigger.
• Patient Message: “You can make a difference in the course of your disease by what you choose to do.” – Exercise – Cognitive Fitness – Emotional Resilience
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Recommendation • Exercise in Stimulating environment
with a range of cognitive and sensory stimulating activates
• Exercise with others • Cognitive Stimulating activities • Creativity • Connectedness • Cognitive Behavioral Therapy
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Updated Evidence for Cog Rehab in PD
• Watermeyer, T. J., Hindle, J. V., Roberts, J., Lawrence, C. L., Martyr, A., Lloyd-Williams, H., ... & Clare, L. (2016). Goal Setting for Cognitive Rehabilitation in Mild to Moderate Parkinson’s Disease Dementia and Dementia with Lewy Bodies. Parkinson’s Disease, 2016.
• Vlagsma, T. T., Koerts, J., Fasotti, L., Tucha, O., Van
Laar, T., Dijkstra, H., & Spikman, J. M. (2016). Parkinson's patients’ executive profile and goals they set for improvement: Why is cognitive rehabilitation not common practice?. Neuropsychological rehabilitation, 26(2), 216-235.
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Key Challenges to Late Stage PD
Communication Linda Bryans, MA, CCC-SLP-L
Aimee Mooney, MS, CCC-SLP-L
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Patient’s Communication
Care Path
Stage 1 Normal Speech
Processes
Stage 2 Detectable Speech
Disturbance
Stage 3 Reduction in speech
intelligibility
Stage 4 Natural speech
supplemented by Augmentative and
Alternative Communication
Stage 5 No Functional
Speech
What’s going on with your speech and writing?
Is your voice soft? Are you or others noticing changes in your voice?
Do others ask you to repeat? Is your voice soft? Are you noticing stuttering or mumbling?
Is your voice soft? Are you mumbling? Are you talking less or avoiding some communication situations?
Are you giving up on conversations? Is your voice inaudible? Are you communicating less, to a smaller group of people? Have you limited your topics and messages?
Do you rely on nonverbal ways of communicating with your carepartner, family and friends? Have you stopped or limited your participation in conversations?
Assessment
Your PCO health care provider or Speech-Language Pathologist (SLP) will listen for any changes in your voice, loudness or speech.
Your SLP will listen to your speech and voice and evaluate for changes in loudness, voice quality, articulation and overall speech intelligibility. An ENT or SLP may look at your voice box.
Your SLP will listen to your speech and voice and evaluate for changes in loudness, voice quality, articulation and overall speech intelligibility . Your SLP will help you identify best strategies for your needs.
Your SLP will: -Listen to your speech and voice and evaluate for changes in overall speech intelligibility. -Evaluate of your communication needs. -Conduct a formal augmentative and alternative communication (AAC) assessment.
Your SLP will help you identify the best speech generating device and low technology options to meet your communication needs.
Intervention
If your voice is noticeably soft or hoarse, you may benefit from Lee Silverman Voice Treatment (LSVT) to improve loudness and quality of your voice.
If your voice is noticeably soft or hoarse and speech slurred, you may benefit from Lee Silverman Voice Treatment (LSVT) to improve loudness and quality of your voice.
-You may benefit from LSVT to improve loudness and speech. -Have an attention getting strategy -Consider voice amplification as needed -Suggest changes in your environment for more effective communication
No matter how difficult it is to “talk”, you CAN still communicate. Consider a speech generating device to use when oral speech is inadequate. Consider voice amplification if voice is weak and volume is low.
Consider a speech generating device for functional communication and daily needs. You will learn how to use the speech device for conversation and telephone.
Patient Education Your SLP will give you information about possible changes in your speech and communication due to PD. Other services are available through the PCO.
Your SLP will provide you with information about: -LSVT -Ways to make your speech more understandable -Ways to enhance your written and verbal communication -Planning and preparation for further changes in communication.
Your SLP will discuss enhancement techniques: -LSVT -Loudness and rate exercises if needed -Learning to use low technology strategies -Preparing for other “tools” for speech and written communication.
Your SLP will provide you and your communication partners will information about resources for a communication system. The system will most likely include: -Your natural speech, gestures, and facial expressions; -Low and/or high tech
i t
Your SLP can help provide information and ways to change your communication system as needed. The ways you use your communication system are based on the time of day, medication regimen, your communication partners, and the disease progression.
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Late Stage PD • Stages 4 and 5 • Most patients have had LSVT….maybe • More barriers to successful LSVT outcomes • Complexity of communication disorder in context
of progression of disease and other health issues • May need to used combined interventions • Care Partner support and education
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How can I help my pt with advanced PD? • Prioritizing needs and interventions
– What is important to my pt? • Refresher LSVT with multimodality communication support as
needed….and if pt is able/interested • Team approach to managing complex problems in PD
– SLP spear heads communication – OT can facilitate access of supports – PT can support with positioning – All disciplines can support communication
• Refer to SLP if pt is struggling with cognition or communication • Encourage use of loud voice, communication supports, communication
strategies
• Care Partner support and education
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Treatment considerations
Four purposes of communication
(Light, 1988) – Express wants and needs
– Information exchange
– Social closeness
– Social etiquette
“Communication is not only the essence of being human, but
also a vital property of life.” John Piece
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Communication Disorders in Older Adults -Palmer et al (2016)
Predictor of: Smaller social networks
Fewer positive social
exchanges
Less frequent participation in social
activities
Higher levels of loneliness
Potentially leading to:
Social isolation
Reduced social
participation
Increased loneliness
Placing older adults at risk for:
Increased risk for mental and physical
health problems
Holt-Lunstad, J., Smith, T. B., & Layton, J. B. (2010). Social relationships and mortality risk: a meta-analytic review. Kawachi,I.,&Berkman,L.F.(2001).Social ties and mental health.
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PD are at risk for decreased participation and social isolation
• PD patients socialize less • PD patients avoid participation in
communication
• Wertheimer, Gottuso, Nuno, Walton, Duboille, Tuchman, & Ramig (2014) • Miller, et al (2006)
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Keeping pts engaged and staying socially connected…including 4 purposes of communication
• Modified goals ? cued LOUD • Tailoring therapy to pts needs, motivation, abilities,
endurance • Social participation • Consider complexity of communication challenges
– Hypokinetic dysarthria – Cognitive communication challenges – Apathy?
• Amplification – Personal amplifier – Amplified telephone
• Augmentative Alternative Communication – Supported communication
• Care partner education
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Communication Supports
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A shift toward aided approaches Fried-Oken, Beukelman & Hux, (2012)
• Expressive language less efficient
• Verbal participation decreases • Telephone use declines or is
avoided • Conversations become
imbalanced
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Communication demands Settings
• Employment • Home • Groups • Community events
Partners
• Familiar/Unfamiliar Topics
• Familiar vs. unfamiliar
Modes of communication • Telephone • Face to face, spontaneous • Written • Electronic (email, text)
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Partners and Modes:
Partners • Primary partner? • Most skilled? • Spends most time with ? • Willing to learn new
communication skills? • Willing to teach others
how to communicate with individual?
Modes • Influence by the situation,
intent, content and individuals involved
• Performance is multi-modal
• Modes uniquely constrain types of information conveyed
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Communication Supports
UNAIDED: Natural • Speech • Vocalization • Gestures • Eye gaze • Body language • Sign language • Partner co-
construction
AIDED: Low & High tech • Paper and pencil • Communication
books boards and cards
• Speech generating devices
• Mobile technologies and apps
flex
ible
mu l t i -modal
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Low tech options – Paper/pencil
– Communication books
– Photo albums
– Pictures
– Newspapers
– Communication boards
– White board
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Low tech options – Cards – Remnants – Written choice and
continuum lines – Paper and pencil – Lanyards
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Low tech options: pre-planned scripts
• Can be prepared with conversation partner
• Used over telephone • Order food, set up
appt, ask directions • Explain PD, ask for
support • Personal information • MUST be practiced
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AAC tools people report using: • Address
book/Resident/staff directory
• Calendar • Comm. Board • Comm. photo booklet • Church bulletin • Computer • Cookbook • Electronic photo frame • E-mail • Gestures/ sign
language/ pantomime • Letters/Mail
• Magazine/Ads/Newspaper • Maps • Museum brochures • Newsletters (school,
neighborhood) • Numbers • Paper & pen/writing • Photos & photo albums • Post it notes • Scrap book • Show Me • Skype
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High tech options
• Dedicated speech generating devices
• Mobile technology devices
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Mobile Technology • Social acceptance • Consumer empowerment in accessing assist • Connections to social network • Native applications • Multiple Communication applications: ProLoquo2Go Lingraphica SmallTalk Pictello Scene and Heard Verbally Sounding Board Doceri White Board
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Shift to environmental modifications “Engineering the environment” means ... • Using ALL previous compensations and
determining what CURRENTLY fits.
• training use of natural supports • training partners
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Natural environmental supports • Pointing to weather pictures in newspaper to
indicate time of day • Using mail received from the bank to indicate
questions about finances • Flipping through pictures in photo book during
family visit • Remnant boxes • Sharing news about religious services by looking at
bulletin together • Native apps on mobile devices (weather, photos,
calendar, maps, etc)
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As person with PD loses speech/voice/language, partner assumes more responsibility for interaction and message co-construction.
Evidence shows training is effective in improving communication activities and participation.
• identify vocabulary for external lexicon • support use of tools in different settings • initiate conversation during late stages of PD • train other partners
Communication Partner training (see updated Systematic review by Simmons-Mackie et al, 2016)
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Communication Partner training:
Communication ramp!
Communication access
Minimizes communication disability
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Train partners to facilitate Comprehension
• Face to Face; get attention 1st
• Manage the environment • Speak slowly, allow to
respond • Augmented inpwith pictures
• One direction at a time • Written choice • Yes/no choice
Expression • “Should I finish his
sentences? • Support all forms of
communication • Count to 10 before
expecting a response • Set up a way to “come
back to that later.”
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Training Communication Partners 1. ID partner behaviors that elicit desired client
outcomes 2. Start small and expand after mastery 3. Use Systematic Instruction CHOOSE to take strategic approach: imPAACT Program (Kent-Walsh &
McNaughton, 2005) Communication Partner Instruction Model
(CPI) (Kent-Walsh & McNaughton, 2005 ). Self anchored Rating Scale (SARS) (Fox,
2012)
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Amplification
• Crutch or support • When amplification should be considered • Amplified telephone application
– Public Utility Commission (PUC) – http://www.puc.state.or.us/rspf/tdapapp.pdf
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PUC Speech-to-Speech
• http://www.oregonrelay.com/ • 711 or 877-735-7525 • Speech-to-Speech (STS) allows a
speech-disabled person to voice his/her conversation.
• A specially trained STS operator repeats the words of the person with a speech disability or synthesizer output to the other person.
• No special equipment is needed to use this service
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Team supported communication How can we work together as a team to support communication?
– Can they provide input regarding their care/goals/needs? (express needs)
– Can they tell you about their weekend? (exchange
info) – Can you get to know them? (social closeness)
– Can your pt greet you? (social etiquette)
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Supporting participation For example…. • Intervention several years ago with group tx,
LSVT, medialization thyroplasty • Withdrawing from conversations • “It’s not just being heard” • Fast moving conversations • Initiation
– He just doesn’t talk at home • Refresher LSVT in context of conversational
strategies • Involving wife, family and friends • Invite PWP to participate • Practice strategies to stay in conversation
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Pain
• Pain and PD: Recent cross-sectional survey (n =181; Germany; H&Y 1-5) – 95% of PWP reported pain
• 91% > 6 months • 79% > 1 yr • 40% > 5 yrs
– Type: back, nerve, joint, head, abdomen, traumatic, after surgery, infection
Buhmann C et al; J Neurol 2017
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Pain
% of patients given a certain therapy
% of patients reporting at least some efficacy
% of patients reporting at only temporary effect
Buhmann C et al; J Neurol 2017
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Pain
• PD and Pain Study – n = 450 with PD; n = 98 without PD – PD patients: average duration: ~6 yrs
• 61.8% had chronic pain; 5.6% had non-chronic pain (control: 58.2% had chronic pain)
• Chronic pain: 60.1% “PD pain” – Direct pain: 61.7%
» “off” dystonia, “neuropathic” pain, akathisia, deep aching, myalgia, cramps, stiffness, articular or abdominal discomfort
– Indirect pain: 38.3%
Nègre-Pagès L et al; Mov Disord. 2008
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Pain
• PD and Pain study con’t – Pain topography
Non PD pain
(n=111)
PD pain indirect (n = 64)
PD pain direct
(n = 103) Head 12.6% 10.9% 8.7%
Back 44.1% 60.9% 12.6%
UE 23.4% 14.1% 21.4%
LE 31.5% 29.7% 67%
Nègre-Pagès L et al; Mov Disord. 2008
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Kings Parkinson’s Pain Scale
• 7 domains: – Musculoskeletal pain – Chronic pain – Fluctuation-related
pain – Nocturnal pain
(includes RLS) – Orofacial pain – Discoloration:
Swelling/edema – Radicular pain
• Each item is scored by severity (0-3)
• Multiplied by frequency (0-4)
• Results in a subscore of 0 to12
• Sum gives the total score (0 to 168)
Chaudhuri KR Mov Disorders 2015
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Pain
• Late stage PD – Varies greatly between studies
• 24% of patients reported severe, disabling pain • 67.3% of PD patients (avg 6 yr duration) with pain
(Negre-Pages (2008): see next slide) – Paresthesias: 20% – Dystonia: 48%
Coelho M et al; J Neurol. 2010
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Pain
• MSA: – 70.6% of pts had complaints of pain
associated with disease progression – Often affect extremities > neck/spine – Most common: sensory symptoms
• Cold or burning sensations • Paresthesia • Numbness
– Dystonia: can be related to levodopa
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Pain
• MSA/(PSP): Antecollis (head drop) – Stretching – Positioning (work with OT) – Tilt-in-space wheelchair – *Botox NOT used due to concerns with
swallowing
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Pain • PSP:
– 40%-56% of patients reported symptoms – Often non-specific – Dystonia: axial (antecollis or extension of neck)
or flexion of hands – Case study for chronic neck pain
• IV administration of lidocaine x 30 min every 2 wks: dramatic improvement in pain for 10 days and improvement in QOL
Colosimo et al; J Neurol. 2010 Shrag A et al; Mov Disord. 2010 Schlesinger I et al; Clin Neuropharmacol. 2009
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Pain
• Musculoskeletal – Related to rigidity, postural changes and co-
morbidities • Dystonia
– Occurs during “off” or peak dose • Neuropathic
– Radicular pain from compressive root lesions, focal or peripheral neuropathy
• Central – Unusual burning, unrelated to motor phenomena – Neurontin
• Akathisia: inner restlessness – Restless leg syndrome
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Pain • Musculoskeletal
– Most common type of pain – Found in #1 low back, knee, shoulder – Re-balance muscles: stretch the flexors – Education: joint protection – Rotational exercises to decrease rigidity – Bracing – Consider ortho or pain consult: injections or
other intervention
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Pain • Stretching: passive and caregiver
training • Kinesiotape • Palm shields • Splinting • Paraffin bath • Collar (headmaster collar) • TENS • Manua therapy
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Pain
• Dystonia – Common in foot, neck or trunk
(Camptocormia/Pisa syndrome) – Relationship to medication timing? – Botox – Bracing for neutral joint position
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Pain • Dystonia
– Stretching to maintain ROM – Non-weight bearing treatment:
• Yoga toes or foam (pedicure) when sleeping – Weight-bearing treatment:
• Taping 2 pennies to head of 2nd MTP: tone inhibition orthotic
• Taping to ankle for subtalar neutral: Supramalleolar Orthosis (SMO) + tone inhibition plate
– Rigid taping for Upper Trap – Botox: coordinate for home program
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Pain
• Neuropathy – Mineral ice – Compression stockings – ROM exercises – TENS/IFC/micro-current