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Palliative care in Neurological Disease

Surat Tanprawate, MD, FRCPT Division of Neurology, Department of Medicine Chiang Mai University

04-10-2011, Chaing Mai,Thailand


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Palliative care
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End of Life Care


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Patients with terminal cancer

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Patients with terminal cancer

It should be recognized as an important concept in the management of any patient with a progressive, incurable illness

So many neurologic illness are progressive and incurable


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Who do the neurologists see?

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Who do the neurologists see?

Worried well, headache/ migraine, numbness, dizziness, etc


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Who do the neurologists see?

Chronic neurological disorder: MS, spinal cord, dementia

Worried well, headache/ migraine, numbness, dizziness, etc


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Who do the neurologists see?


Acutely ill patients Chronic neurological disorder: MS, spinal cord, dementia

Worried well, headache/ migraine, numbness, dizziness, etc


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ART > SCIENCE


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What we have to learn?

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What we have to learn?


Learning process, not just knowledge

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What we have to learn?


Learning process, not just knowledge Different diseases have different problems
>> the same goal

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What we have to learn?


Learning process, not just knowledge Different diseases have different problems
>> the same goal

Humanity diversity

Thursday, October 6, 2011

What we have to learn?


Learning process, not just knowledge Different diseases have different problems
>> the same goal

Humanity diversity Knowing your function, and connect with


others
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The different view


Neurologist view

Palliative care team view

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The different view


Neurologist view

Holistic approach(physical, psychological, cultural, spiritual) Experience in symptoms control End of life decision Community center In-patient facilities for terminal care/respite Day hospice facilities Complementary therapies Bereavement counselling

Palliative care team view

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Neurologist

Palliative care

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Neurologist

Palliative care

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Neurologist

Palliative care

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Neurologist

Palliative care

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Improve QOL

Distress physical symptoms Feeling and psychological symptoms

Intervention
- Pharmacological -Nonpharmacological

Patient Family member


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Health care

Social

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Common neurological problems



Cognitive dysfunction, dementia> Alzheimers disease, other dementia Physical disability >stroke, motor neuron disease, Parkinsons disease, spinal cord disease, neuromuscular weakness

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Dementia and Alzheimers disease


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Dementia()

Decline of cognitive function () Cognitive function: memory, language,


motor ability, calculation

Its also involved psychological and

behavioral symptoms: depression, anxiety, hallucination, sleep problem, pain

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Alzheimers disease

Most common cause of dementia AD is a neurodegenerative disorder


40 35 30
Female Male

presented with progressive dementia

Percent of 20 Age Group


15 10 5 0

25

-64

-69

-74

-79

-84

-89

-94 90

30

65

70

75

80

85

Years
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95

-99

Alzheimers disease
Cognitive impairment
Physical disabilitylate stage

Psychiatric and behavioral symptoms


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Activity daily living

Stage of AD

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Management strategies
Prognostication, and dying from dementia Cognitive and communication ability
decline

Behavioral and psychological problems Challenging caregiver stress and


bereavement issues
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Prognostication questions in dementia

Patients question: How long do I have


before my mind is shot?

Health professionals question: Is s/he


eligible for palliative care? have to live ?

Familys question: How long does s/he Caregivers question: I am exhausted.


How much longer can I do this?
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Dementia hospice eligibility

Stage 7 or beyond according to the FAST scale

Unable to ambulate without assistance Unable to dress without assistance Unable to bathe without assistance Urinary or fecal incontinence, intermittent or constant No meaningful verbal communication, stereotypical phrases only, or ability to speak limited to six or fewer intelligible words Aspiration pneumonia Pyelonephritis or other upper UTI Septicemia Multiple stage 3 or 4 decubitus ulcers Fever that recurs after antibiotic therapy Inability to maintain sufcient uid and calorie intake, with 10 percent weight loss during the previous six months or serum albumin level less than 2.5 g per dL (25 g per L)

Plus one of the following within the past 12 months:

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Cognition and ability decline-1


Unrecognized symptoms-pain, physical illness to nd the hidden problem: patient
report, caregiver report, and direct observation

OA, peripheral neuropathy, other pain are


common
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change in behavior or mental status

Cognition and ability decline-II


Loss of functional ability unable to ambulate unable to bath, dress, or feed
independently

incontinent of bowel and bladder unable to communicate meaningfully (presence of medical complication)
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What does dying look like



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Decline in functional status Lack of desire to eat or drink Withdrawn Sleep- wake state Mottling of limbs Jaw movement Death rattle Co-morbid symptoms

Tube feed or not tube feed? Thats the question

The facts:

Effect on life span is an open question Increases suffering

Need for better pt/family education


Discussing benets and burdens of therapy Use neutral language Separate facts from your opinion Please offer your opinion Make allowances for special circumstances.

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Palliative care in stroke patient


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Stroke

Stroke is one of the three biggest killers in Thailand. Two types:

Infarction Hemorrhage

Death range from 8-20% in rst 30 days (higher for hemorrhage)

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Stroke care: palliative care aspect


Palliative cares role in stroke care

Acute stroke: end of life care Long term care in stoke with severe disability

Death is mainly from cardiac (AMI, arrhythmias) or respiratory (aspiration, pneumonia embolism) Brain swelling

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End of life care in acute stroke

Ethical aspects of care - end of life issues including withdrawal of treatment

Early decisions about withholding cardiopulmonary resuscitation are avoided. There is full discussion with the patient (if possible) and family/carer about reasons for withdrawal/ futility of treatment to allow all concerned to understand treatment goals. There is accurate documentation of plans of care and discussions between the multidisciplinary team, the patient and family/carer.

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Various case of stroke with disability

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Various case of stroke with disability

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Various case of stroke with disability

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Various case of stroke with disability

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Palliative care in motor neuron disease

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--Motor Neuron Disease-Amyotrophic Lateral Sclerosis (ALS)

Progressive, degenerative neurologic disease


of unknown etiology

Involve: upper and lower motor neurons


==: LMN: weakness, atrophy, fasciculation ==: UMN: hyperreexia, spasticity due to lateral corticospinal tract degeneration

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--Motor Neuron Disease-:Symptoms: Amyotrophic Lateral Sclerosis (ALS)

Weakness of body muscles causing :: limb weakness Progressive, degenerative neurologic disease :: dysphagia of unknown etiology :: respiratory failure Involve: upper and lower motor neurons :: speech difculty

==: LMN: weakness, atrophy, fasciculation ==: UMN: hyperreexia, Memory and Cognitive spasticity due to lateral corticospinal tract function are spared... degeneration

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Signs and symptoms

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Signs and symptoms

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Signs and symptoms

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Signs and symptoms

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Secretion management
: decrease saliva production Medication use>>Benztropine, amitriptyline, artane : remove saliva>>increase uid intake, humidied air

Thursday, October 6, 2011

Secretion management
: decrease saliva production Medication use>>Benztropine, amitriptyline, artane : remove saliva>>increase uid intake, humidied air

Dysarthria Dysphagia

: speech therapy

: Decreased caloric and uid intake may lead to worsening of symptoms, such as weakness, muscle atrophy, fatigue : Initially management includes the modication of food and liquid consistency : Discussion for PEG
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Secretion management
: decrease saliva production Medication use>>Benztropine, amitriptyline, artane : remove saliva>>increase uid intake, humidied air

Muscle spasm & weakness


: Early PT/OT

Cramps

: Quinine sulfate 200 mg twice daily, Tizanidine 2-4 mg twice daily

Dysarthria Dysphagia

: speech therapy

: Decreased caloric and uid intake may lead to worsening of symptoms, such as weakness, muscle atrophy, fatigue : Initially management includes the modication of food and liquid consistency : Discussion for PEG
Thursday, October 6, 2011

Secretion management
: decrease saliva production Medication use>>Benztropine, amitriptyline, artane : remove saliva>>increase uid intake, humidied air

Muscle spasm & weakness


: Early PT/OT

Cramps

: Quinine sulfate 200 mg twice daily, Tizanidine 2-4 mg twice daily

Dysarthria Dysphagia

: speech therapy

Respiratory care
: initiate discussion regarding the patientss goals and how the goal can be best achieved : respect the right of patients to refuse or withdraw treatment

: Decreased caloric and uid intake may lead to worsening of symptoms, such as weakness, muscle atrophy, fatigue : Initially management includes the modication of food and liquid consistency : Discussion for PEG
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To cure sometimes

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To cure sometimes To relieve often

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To cure sometimes To relieve often To comfort always

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Dr.Surat Tanprawate, MD, MSc(Lond.), FRCP(T)


Division of Neurology, Department of Medicine, CMU

My Deep Gratitude to

Ass. Prof. Siwaporn Chankrachang

Thank You for Your Kind Attention

WWW.OPENNEURONS.COM
Thursday, October 6, 2011

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