DR.RAHUL ANAND YADAV MD DM(NEONATOLOGY) HOD KKCTH When to us use? - - PowerPoint PPT Presentation

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DR.RAHUL ANAND YADAV MD DM(NEONATOLOGY) HOD KKCTH When to us use? - - PowerPoint PPT Presentation

DR.RAHUL ANAND YADAV MD DM(NEONATOLOGY) HOD KKCTH When to us use? Whic ich type of se seiz izur ures? es? How much(d (dose ose of d drug) g) to us use? Ho How lo long g to us use? MANDAN MISHRA SANKARACHA CHARY


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DR.RAHUL ANAND YADAV MD DM(NEONATOLOGY) HOD KKCTH

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 When to us

use?

 Whic

ich type of se seiz izur ures? es?

 How much(d

(dose

  • se of d

drug) g) to us use?

 Ho

How lo long g to us use?

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MANDAN MISHRA SANKARACHA CHARY RYA

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1)Eye witness 2)Logic 3)Guidelines by authority in subject

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 Normal Neonatal Brain  Neonatal convulsions  Drug Action  Conclusions

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 Disturbed balance

between excitatory and inhibitory neurotransmitters

 Excitatory:Glutamat

e

 Inhibitory:Gaba

Glutamate tamate Gaba

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 Subtle seizures  Multi focal clonic  Generalized tonic  Myoclonic

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  • Depends upon levels of

cytosolic calcium levels.

  • When cytosolic calcium levels

are high, signal to noise ratio is altered resulting in seizures.

  • Levetiracetam inhibits the

release and influx of calcium into cytosol thereby reducing the signal to noise ratio

  • Synaptotagmin is a calcium

sensor for exocytosis in pre synaptic vesicle leading to excitatory NT release into synaptic junction.

  • SV2A regulates the activity of

synaptotagmin leading to inhibition of calcium mediated exocytosis.

  • Levetiracetam acts as an

agonist of synaptic vesicle protein 2A

 Signal

al to noise ratio

 SV2A

2A agonist ist

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 Can be used in neonates  Do not use in subtle and generalized tonic

seizures

 “Use in Myocloni

  • nic seizur

ures, es, especi cial ally ly stimulus ulus sen ensi siti tive ve thalamocort mocortical ical myoclonus

  • nus”
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“DOES NOT EXIST”

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 When to use?  Which type of seizure to use?  How much to use?  How long to use?

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DIAZEPAM

Status Epilepticu s LEVETIRACET AM

4 hours NOT REDUCED

EPILEPSY RISK

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LEVETIRACETAM PHENOBARBITONE

 Respiratory depressant

action absent

 Myocardial depressant

action absent

 Metabolic demand:?  Multifocal clonic

seizure:use unknown

 Myocloni

clonic: c:more more useful ul

 Drug

g interac acti tions

  • ns

ab absent ent

 Respiratory depressant

action present

 Myocardial depressant

action present

 Metabolic

demand:Decreased

 Multifocal clonic

seizure:useful

 Myocl

clonic

  • nic: less useful

 Drug interact

ractions ions present ent

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LEV EVETIR ETIRAC ACETA ETAM VALPR LPROAT OATE

 Liver dysfunction

absent

 In instances where

there is increased levels of ammonia,it is safe

 Pharmacoresistance

not seen(MDR protein)

 Liver dysfunction

present

 In instances where

there is increased levels of ammonia,it is unsafe

 Pharmacoresistance

seen

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  • Loading dose :40mg/kg(some units start

with 20mg/kg)

  • 1cc=100mg…
  • “Accidental overdose reported but non fatal!”
  • Maintainance dose

< 7 days-10mg/kg q8h > 7 days-20mg/kg q12h

  • Can use higher doses in exceptional

circumstances

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 Dentate gyrus is a part of Hippocampus  Involved in episodic memory formation and

exploration of new environment

 LEV ,on prolonged use has potential side

effects due to effect on dentate gyrus

 Manifestations include

Hyperactivity,psychosis ,tremors

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 Routinely don’t use  Can be used in stimulus sensitive myoclonic

convulsions

 Higher doses tolerated better  Stop as soon as primary etiology is better