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Page 1: Obat Neurologi dan Neuromuskular PSIK R - Drug Addicts · PDF fileOBAT NEUROLOGI dan NEUROMUSKULAR M. Bakhriansyah , H., ... samping obat: 1.Antikonvulasi 2.Hipnotik sedatif 3

OBAT NEUROLOGI OBAT NEUROLOGI dandan

NEUROMUSKULARNEUROMUSKULAR

M. M. BakhriansyahBakhriansyah, H., dr., , H., dr., M.KesM.Kes, , M.Med.EdM.Med.Ed

BagianBagian FarmakologiFarmakologi

BanjarbaruBanjarbaru

SasaranSasaran BelajarBelajar

DiDi akhirakhir pembelajaranpembelajaran, , mahasiswamahasiswa mampumampu

memahamimemahami mekanismemekanisme kerjakerja, , indikasiindikasi dandan efekefek

sampingsamping obatobat::

1.1.AntikonvulasiAntikonvulasi

2.2.HipnotikHipnotik sedatifsedatif

3.3.ParkinsonParkinson

4.4.PelemasPelemas OtotOtot

5.5.AnestesiAnestesi UmumUmum

6.6.AnestesiAnestesi LokalLokal

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Status Status EpilepticusEpilepticus

►► SE : SE : �� Continues seizures Continues seizures occuringoccuring 30 minutes 30 minutes ((epilepsiepilepsi foundation)foundation)

�� More than 30 minutes More than 30 minutes of continues seizures of continues seizures activity or 2 or more activity or 2 or more sequential seizures sequential seizures without full recovery of without full recovery of consciousness between consciousness between seizures (Dodson, seizures (Dodson, 1993)1993)..

►► Systemic and primary brain changes Systemic and primary brain changes �� related to related to

morbidity and mortality ratesmorbidity and mortality rates

�� Decreasing GABA inhibition. Decreasing GABA inhibition.

�� Increasing blood pressure (early stage) Increasing blood pressure (early stage) �� decreasingdecreasing

�� Acidosis (+)Acidosis (+)

�� Pulmonary edemaPulmonary edema

�� HyperthermiaHyperthermia

�� Mild Mild leukocytosisleukocytosis

�� GABAergicGABAergic mechanism failsmechanism fails

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►► Goal of therapy: to treat the epilepsy and to Goal of therapy: to treat the epilepsy and to minimaliseminimalise the side effectsthe side effects

Principal therapy:Principal therapy:

►►MonotherapyMonotherapy is better than is better than polypharmacypolypharmacy

►► Dosage is increased until the therapeutic effect or Dosage is increased until the therapeutic effect or toxicity effect are met. toxicity effect are met.

►► PolypharmacyPolypharmacy is introduced when is introduced when monotherapymonotherapydoes not workdoes not work

►► Avoiding the sudden withdrawal Avoiding the sudden withdrawal

Treatment flowchart for status Treatment flowchart for status

epilepticusepilepticus

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Medications Medications

BarbituratBenzodiazepinAsam valproatGabapentin

Lamotrigin

FenitoinKarbamazepinAsam valproatEtosuksimid

FenitoinKarbamazepin

GABA

Glutamate

Ca

Na

STATUS EPILEPTICUS

KarbamazepinKarbamazepin

►► Stabilize neural Stabilize neural

membrane by membrane by

decreasing Na, Ca and decreasing Na, Ca and

K flows through it.K flows through it.

►► avoid to be given with avoid to be given with

MAO inhibitor MAO inhibitor

consecutivelyconsecutively

FenitoinFenitoin

►► DifenilhidantoinDifenilhidantoin

derivatederivate

►►Mechanism of actions Mechanism of actions

are similar to are similar to

KarbamazepinKarbamazepin

►► Could be given orally, Could be given orally,

intra venous and intra intra venous and intra

muscularmuscular

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ValproicValproic AcidAcid

►► Increasing GABA Increasing GABA

transmission transmission

►► Sedation effect is Sedation effect is

minimalminimal

EtosuksimidEtosuksimid

►►Mechanism of action Mechanism of action is is

unknownunknown

►► Probably by inhibiting Probably by inhibiting

Ca channelCa channel

PhenobarbitalPhenobarbital

►► Stimulating GABA Stimulating GABA

receptorreceptor

►► SE: sedation, SE: sedation,

nistagmusnistagmus, ataxia and , ataxia and

allergyallergy

►► Inducing Inducing enzymenzym P450 P450

PrimidonPrimidon

►►Mechanism of actions Mechanism of actions

are unknownare unknown

►► Its active Its active metabolitmetabolit

has long half lifehas long half life

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GabapentinGabapentin

►► GABA agonist GABA agonist

►► Adjuvant therapyAdjuvant therapy

LamotriginLamotrigin

►► Stabilizing neuron and Stabilizing neuron and

affecting glutamate affecting glutamate

releaserelease

►► Adjuvant therapyAdjuvant therapy

►► SE: rash (prominent)SE: rash (prominent)

KlonazepamKlonazepam

►► Stimulating GABA Stimulating GABA

receptor receptor

FelbamatFelbamat

►► Stimulating GABA Stimulating GABA

receptor and inhibiting receptor and inhibiting

NMDA receptorNMDA receptor

►► Used unUsed un--frequentlyfrequently

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Parkinson diseaseParkinson disease

►► A progressive A progressive neurodegenerative neurodegenerative disorder associated disorder associated with loss of with loss of dopaminergicdopaminergicnigrostriatalnigrostriatal neurons.neurons.

►► Distinctive features:Distinctive features:�� Resting tremor, rigidity, Resting tremor, rigidity, bradikinetiabradikinetia, and , and postural instability postural instability

Principle therapyPrinciple therapy

►► Increasing the synthesis Increasing the synthesis and release of dopamine and release of dopamine (L(L--dopa+karbidopadopa+karbidopa, , amantadinamantadin))

►► Inhibiting Inhibiting dopamindopaminmetabolism metabolism ((selegilin/deprenilselegilin/deprenil))

►► Activating dopamine Activating dopamine receptor (receptor (bromocriptinebromocriptine, , pergolidepergolide))

►► Blocking Blocking muscarinicmuscarinic/ / cholinergic receptor cholinergic receptor ((trihexiphenidiletrihexiphenidile, , benzathropinebenzathropine, , diphenhidraminediphenhidramine))

To facilitate action of dopaminergic To suppress action of cholinergic

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Anti cholinergicAmantadine

L-dopa+karbidopa

Dopamine agonists drugsMAO B inhibitors

Protocol of therapyProtocol of therapy

LL--dovadova ((levodopalevodopa))

►► Dopamine precursor Dopamine precursor ��inactive forminactive form

►► Activated by Activated by decarboxilasedecarboxilase enzyme;enzyme;�� Brain Brain

�� Lever & kidneys Lever & kidneys �� can can not pass through BBB not pass through BBB �� bioavailability bioavailability countered by countered by karbidopa/benserazidekarbidopa/benserazide..

►► Interaction: Interaction: piridoxinepiridoxineincreases increases decarboxilateddecarboxilatedreaction. reaction.

►► On/off phenomenon On/off phenomenon (+) after 3(+) after 3--5 years 5 years application application ��mechanism ??? mechanism ??? Desensitization of Desensitization of dopamine receptordopamine receptor

►► Not a first line therapy Not a first line therapy

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SelegilineSelegiline ((deprenildeprenil))

►► Instead of inhibiting Instead of inhibiting

metabolism of dopamine:metabolism of dopamine:

�� Stimulating dopamine Stimulating dopamine

release.release.

�� NeuroNeuro--protective effect protective effect

►► + MOA inhibitors + MOA inhibitors �� crisis crisis

of hypertension. of hypertension.

BromociptineBromociptine & & PergolidePergolide

►► Dopamine receptor Dopamine receptor

agonists agonists

►► Action: Lesser than LAction: Lesser than L--dopadopa

►► As a single therapy at the As a single therapy at the

early stageearly stage

►► Combination with LCombination with L--dopa dopa

at the moderate and late at the moderate and late

stage. stage.

►► Tapering dose Tapering dose

TrihexiphenidileTrihexiphenidile & &

benzotropinebenzotropine

►► Action: less than LAction: less than L--

dopadopa

►► Adjuvant therapyAdjuvant therapy

►► Tapering doseTapering dose

DiphenhidramineDiphenhidramine

►► Anti cholinergic effect Anti cholinergic effect

at central level at central level

►► Anti histamineAnti histamine

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AmantadineAmantadine

►► Anti virusAnti virus

►► Mechanism: ??? May be by Mechanism: ??? May be by

facilitating dopamine facilitating dopamine

releaserelease

►► Action:Action:

�� Less than LLess than L--dopadopa

�� Better than anti cholinergicBetter than anti cholinergic

►► Early stage:Early stage:

�� Anti cholinergic orAnti cholinergic or

�� AmantadineAmantadine

►► When early stage therapy When early stage therapy

is not effective, Lis not effective, L--

dopa+karbidopadopa+karbidopa are are

started.started.

►► Final stage: dopamine Final stage: dopamine

agonists medications and agonists medications and

MAO inhibitors. MAO inhibitors.

Headache/Headache/CephalgiaCephalgia

►►MigraineMigraine

►► Tension headacheTension headache

►► Cluster headacheCluster headache

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MigraineMigraine

►► Mechanism: Mechanism: �� GeneticGenetic

�� VascularVascular

�� Neural Neural

�� Neurotransmitter serotoninNeurotransmitter serotonin

�� Neurotransmitter dopamineNeurotransmitter dopamine

�� Activation of Activation of symphaticsymphaticnervous systemnervous system

►► NSAIDsNSAIDs + caffeine + caffeine ((asetaminophenasetaminophen, acetic , acetic salicilicsalicilic acid, etc)acid, etc)

►► Serotonin receptor Serotonin receptor agonists (ergotamine, agonists (ergotamine, dihidroergotaminedihidroergotamine, , sumatriptanesumatriptane, , naratriptanenaratriptane, , rizatriptanerizatriptane, , zolmatriptanezolmatriptane))

►► Dopamine antagonist Dopamine antagonist ((metochlopramidemetochlopramide, CPZ, , CPZ, proCPZproCPZ) )

Protocol of therapyProtocol of therapy

Serotonin receptor agonists (SC/IM/IV), orDopamine receptor antagonist (IM/IV)

Serotonin receptor agonists (oral/nasal/SC), orDopamine receptor antagonist (oral)

NSAIDs, orSerotonin receptor agonist (oral)

Heavy migraine

Moderate migraine

Mild migraine

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NSAIDsNSAIDs

►► SE: SE: dispepsiadispepsia

Stimulator of serotonin (5Stimulator of serotonin (5--HTHT11) receptors: ) receptors:

1.1. ergotamine, ergotamine, dihidroergotaminedihidroergotamine

►► Non selective 5Non selective 5--HTHT1 1 receptor agonistreceptor agonist

►► Contra indication: CHD, pregnancy, peripheral Contra indication: CHD, pregnancy, peripheral

blood vessel constriction, level and kidney blood vessel constriction, level and kidney

disorders.disorders.

2. 2. triptantriptan

►► Selective 5Selective 5--HTHT11 receptor agonistreceptor agonist

►► RizatriptanRizatriptan: quickest onset, highest : quickest onset, highest

efficacyefficacy

►► NaratriptanNaratriptan: in contrast: in contrast

►► MonotherapyMonotherapy is unadvisableis unadvisable

►► Contra indication: cardiovascular diseasesContra indication: cardiovascular diseases

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Dopamine antagonistsDopamine antagonists

►► Adjuvant therapyAdjuvant therapy

►► Increasing gut motilityIncreasing gut motility

►► Also could treat: Nausea & Also could treat: Nausea & vomit vomit

PreventionPrevention

►► 3 times per month3 times per month

►► Beta blockers (Beta blockers (propanololpropanolol, , timololtimolol))

►► Anti convulsive agents Anti convulsive agents ((valproicvalproic acid)acid)

►► MAO inhibitors MAO inhibitors ((phenelzinephenelzine, , isokarbosazideisokarbosazide))

►► SerotonergicSerotonergic agents agents ((metisergidemetisergide, , siproheptadinesiproheptadine))

►► Ca antagonist (Ca antagonist (verapamilverapamil))

TensionTension headacheheadache

►►Usually bilateralUsually bilateral

►►Usually following anxiety or depressionUsually following anxiety or depression

►►Therapy:Therapy:

�� NSAIDsNSAIDs + + coffeinecoffeine

�� Muscle relaxant agentsMuscle relaxant agents

►►Prevention: Prevention: amitriptilineamitriptiline a.na.n

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Cluster headacheCluster headache

►► PeriorbitalPeriorbital pain pain

(temporal bone pain)(temporal bone pain)

►► Some signs and Some signs and

symptoms related to symptoms related to

eyeseyes

►►Mechanism: ??? May Mechanism: ??? May

be be serotonergicserotonergic

transmission disordertransmission disorder

►► Therapy:Therapy:

�� PrednisonPrednison

�� LithiumLithium

�� MetisergidMetisergid

�� ErgotamineErgotamine

�� Na Na valproicvalproic

�� VerapamilVerapamil