Parkinson Disease Consensus

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    2012Consensus Guidelines

    for the Treatment of

    Parkinsons Disease

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    Authors note

    Prof. Dr. LIM Shen-Yang

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    From the Movement Disorders Council, Malaysian Society of Neurosciences

    Project Leader/Lead author:

    Prof. Dr. Lim Shen-Yang MBBS (Melbourne), MD (Melbourne), FRACP (Aust), Fellowships in Movement Disorders (Melbourne & Toronto)

    Co-authors:

    Prof. Datin Dr. Norlinah Mohd. IbrahimMBBCH, BAO, BMedSci, MRCP, Fellowship in Movement Disorders (London)

    Dr. Santhi Datuk Puvanarajah MBBS (Madras), MRCP (UK), AM (Malaysia)

    Dr. Lee Moon KeenMBBS (Malaya), Dip Clin Neurology (London), FRCP (Edinburgh), FAM (Malaysia)

    Dr. Chee Kok YoonMD (USM), MMed(Psych) (Malaysia), Fellowship in Neuropsychiatry (Melbourne)

    Dr. Shanthi ViswanathanMBBS (India), MRCP (Ireland), Fellowship in Neurology (Malaysia)

    Dr. Tan Ai HueyMD (UKM), MRCP (UK)

    Dr. Chris Chong Kang Tird

    MD (UKM), MRCP (UK), Fellowship in Movement Disorders (Monash)

    Assoc. Prof. Dr. Kamal Azrin Bin Abdullah @ Kalai Arasu A/L MuthusamyMBBS (Malaya), MSurg (Malaya), DPhil (Oxon)

    External Reviewers:

    Prof. Emeritus Dr. Niall Quinn MA, MD (Cantab), FRCP (UK), FAAN

    Assoc. Prof. Dr. Susan H. Fox BSc, MBChB, MRCP (UK), PhD

    Acknowledgments:

    Ms. Loh Hui Pin

    Mr. Yap Kian Yong Mr. Calvin Kuan

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    degenerativedisease

    older

    motor

    asymmetric

    Non-motor symptoms

    dopamine

    1

    1. Introduction - What is Parkinsons disease (PD)?

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    Contents

    Appendices

    1

    3

    15

    6

    20

    31

    13

    18

    29

    24

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    Diagnosing Parkinsons disease.

    9

    Table 1.

    2. Diagnosis of Parkinsons disease

    3

    Disorder Characteristic features

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    sporadic

    no test

    no cure worsens gradually well controlled

    restoring dopaminergic

    tailored

    2

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    BrainMRI

    Staging the severity of PD. Hoehn and Yahr (H&Y) stage

    medication status

    Table 2.

    5

    Hoehn & Yahr stage Description

    1

    2

    3

    4

    5

    ; ;

    ;

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    Disorder Characteristic features

    3

    5

    78

    9

    V

    3

    -

    As a general rule, patients presenting with movementdisorders below age 50 should undergo tests to rule out this condition. 9 ;

    >

    A

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    Figure 1.

    7

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    General approach.

    symptomatic troublesome

    as soon as, or very soon after, diagnosis patients preferences

    start low, go slow

    3. Initiation of antiparkinsonian medication -When and what to start

    6

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    should not be inappropriately delayed

    misconception saved for later

    non-dopaminergic

    Dopamine agonists.

    9

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    Levodopa (L-dopa). the most effective 33

    started at 50 mg daily every 3-7 days

    Individual doses 50-300 mg 8

    dyskinesias younger 35

    younger patients 9 lowest effective dose

    8

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    Anticholinergic agents. trihexyphenidyl benzhexol orphenadrine tremor

    dystonia7

    Experimental treatments. 7

    Non-pharmacologic management. physiotherapy

    occupational therapy speech therapy

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    Selegiline (e.g., Jumex and Selegos).

    mild antiparkinsonian putative neuroprotective rasagiline

    Table 3.

    Dopamine agonist Usual starting doseMaximum

    recommended dose

    5 3

    5

    5 5

    375 5

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    start low, go slow

    Dopaminergic side effects. dopaminergic3 nausea postural hypotension sleepiness confusionhallucinations impulse control disorders Domperidone

    MAO-B inhibitors.

    serotonin syndrome

    57

    Anticholinergic medications.

    Amantadine.

    4. Potential side effects of antiparkinsonianmedications

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    dietitian PD nurse specialists

    7

    alternative therapies acupuncture

    The importance of exercise. regular exercise 53

    Being informed & being involved. information 7 information booklets

    http://www.mpda.org.my

    support group 7 8

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    Wearing-off ON

    OFF motor fluctuations non-motor fluctuations unpredictable

    5. Motor response complications (motor fluctuations& dyskinesia) - What are they?

    Figure 2.

    (Wearing-off)

    Peak-dose dyskinesia A typical day

    TimeMedicationstarts to work

    PD

    medication

    PD

    medication

    PD

    medication

    Sympt

    oms a

    re

    allev

    iated

    Symptomsb

    egin

    toreturn

    (ON condition)

    (OFF condition)

    Symptoms

    adequately

    controlled

    Sym

    ptomsnot

    adequately

    co

    ntrolled

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    Patient diary.

    Peak-dose dyskinesia Biphasic dyskinesia

    ;

    Table 4.

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    Dyskinesia. wriggling peak-dose

    biphasic

    Figure 3. involuntary movements

    Figure A. Tremor (shakes).

    Figure B. Dyskinesia (wriggling).

    ON

    Figure C. Dystonia (twisting). OFF

    A.

    B.

    C.

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    Treatment of dyskinesia.

    misconception overdosed

    the exactsame dose

    Amantadine (Pk-Merz).

    Motor response complications that are refractory to adjustment of oralmedications.

    19

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    Treatment of motor fluctuations. dose and/or frequency

    addition dopamine

    agonist entacapone

    beneficial effects on night-time sleep

    Controlled-release L-dopa erratically absorbed 7

    gradually, especiallyin a patient who is at higher risk of side effects

    18

    6. Treatment of motor fluctuations & dyskinesia

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    Other DBS targets. 78

    Lesional (ablative) surgery. 7

    Apomorphine (APO-go) (subcutaneous infusion or injections).

    Jejunal L-dopa (Duodopa).

    21

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    Percutaneous endoscopicgastrostomy (PEG)

    Infusion pump

    CassettecontainingDuodopa

    Intestinal tubing

    Figure 6.

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    Wire tunneledunder the skin

    Tiny electrodes stimulate a deeppart of the brain (subthalamicnucleus / STN or globuspallidus internus / GPi)

    Battery

    Cloth pouch containingapomorphine reservoir& small infusion pump

    Apomorphine delivered via veryfine plastic tubing, & butteryneedle sited under the skin

    Figure 4.

    Figure 5.

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    Figure 7.

    25

    Intrinsic toPD

    Medicationeffect

    Modifying factors(gender, genetic,

    etc.)

    V

    Disease progression & Age

    A A

    Evolution of NMS

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    largenegative impact specifically asked about;

    24

    8. The non-motor symptoms of Parkinsons disease

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    Non-motor symptoms Treatment Options Comments

    Depression

    3

    53

    5 Z 5

    V 55 55 5 3 55 375875 X75375

    5

    ;

    ;

    A

    8 ;

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    Appendix 1: Parkinsons Disease DrugIdentication Chart

    Comtan 200mg tabEntacapone

    Madopar 100/25mg cap

    Madopar 200/50mg tab

    Madopar HBS 100/25mg cap

    Levodopa/Benserazide

    Bromocriptine

    Stalevo 50(50/12.5/200mg)tab

    Stalevo 100(100/25/200mg)tab

    Stalevo 150(150/37.5/200mg)tab

    Stalevo 200(200/50/200mg)tab

    Levodopa/Carbidopa/Entacapone

    Parlodel 2.5mg tab

    Sinemet 25/100mg tab

    Sinemet 25/250mg tab

    Sinemet CR 50/200mg tab

    Levodopa/Carbidopa

    Levodopa-Based Medications

    Direct Dopamine Agonists (Ergot)

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    Non-motor symptoms Treatment Options Comments

    Orthostatic hypotension (OH)

    3

    3

    5 AA 5

    3

    A

    X

    8

    3

    3

    5

    A ; ;

    3 A V5 3 A

    V 5

    Constipation

    Urinary frequency andurgency, nocturia(overactive bladder)

    Erectile dysfunction

    Drooling

    PD-related pain

    A A 5 A 3

    3 X

    X

    3 A

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    Appendix 2 - Patient diary (for motor uctuationsand dyskinesia)

    DAY ONE DATE:

    Time

    ONwithoutdyskinesia

    ON withminordyskinesia

    ON withtroublesomedyskinesia

    OFF Asleep L-dopa intake(please stateexact time)

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    Trihexyphenidylhydrochloride

    Norex 100mg tab

    Benzhexol 2mg tab

    Direct Dopamine Agonists (Non-Ergot)

    Others

    Piribedil

    Sifrol 1mg tab

    Pramipexole

    Pramipexole extendedrelease

    Trivastal Retard 50mg SR tab

    Sifrol 0.125mg tab

    Ropinirole

    Ropinirole prolongedrelease

    Rotigotine transdermalpatch

    Requip 0.25mg tab

    Requip 1mg tab

    Requip 2mg tab

    Requip PD 2mg tab

    Requip PD 4mg tab

    Neupro

    Sifrol ER 0.375mg tab

    Sifrol ER 1.5 mg tab

    Selegiline

    Jumex 5mg tab

    Selegos 5mg tab

    Orphenadrine

    Amantadine PK-Merz 100mg tab

    2mg 4mg 6mg 8mg

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    References 1. 2.

    3.

    4. 5. 6.

    7.

    8. 9.

    10. 11. 12. 13. 14. 15. 16. 17. 18.

    19. 20.

    21. 22. 23.

    24. 25. 26.

    27. 28.

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    54. 55. 56. 57.

    58. 59. 60. 61.

    62. 63.

    64.

    65.

    66. 67.

    68.

    69. 70.

    71. 72.

    73.

    74. 75. 76.