Dr Zoltan Kaliszky - Epilepsy in Pregnancy

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Epilepsy service Consultants Epilepsy Nurse First fit Clinic Rapid review clinic Regular Clinic and Ward consults EEG Service led by Neurophysiologis t Consultant The future: Another Epilepsy Nurse ( or 2? ) Video Telemetry Unit? Another Consultant with interest in epilepsy

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'Epilepsy in Pregnancy' - Dr Zoltan Kaliszky (Consultant Neurologist for Cumbria Partnership NHS Foundation Trust) from the Cumbria Neuroscience Conference

Transcript of Dr Zoltan Kaliszky - Epilepsy in Pregnancy

Page 1: Dr Zoltan Kaliszky - Epilepsy in Pregnancy

Epilepsy service

Consultants Epilepsy Nurse First fit Clinic Rapid review clinic Regular Clinic and

Ward consults EEG Service led by

Neurophysiologist Consultant

The future: Another Epilepsy

Nurse ( or 2? ) Video Telemetry

Unit? Another Consultant

with interest in epilepsy

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EPILEPSY IN PREGNANCY

Zoltan Kaliszky MD.Consultant Neurologist

Cumbria Partnership NHS Trust

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Goals

Preconception planning and counselling

Teratogenic risk of specific antiepileptic drugs/

antiepileptic drug choices

Management of epilepsy during pregnancy

Management after delivery

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A. Preconception planning and counselling

The epilepsy itself is not a contraindication to pregnancy even if it requires AEDs.

Planned pregnancy- (changes 6-12 mo.) Over 90 % -remarkable event free/ good

outcome Assess seizure activity- controlled? Not? Any changes prior to pregnancy ( on VA? ?) Monotherapy ? / if not: lowest poss. dose There is 1.6-3.2 % risk of major congenital

malformation in the general population !

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A/2. Preconception planning and counselling

D/C medication prior to pregnancy? Consider if: seizure free for min. 2 years normal neuro exam + I/Q single type of seizure + neg.

EEG and: if the patient is willing to take the risk ! Determine a good baseline level with the lowest effective dose:- Obtain serum level 2 times wks. apart ( before the am. dose ) – this will be the range of effective level.

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A/3. Preconception planning

Review hx. of congenital malformations during prev. pregnancies

Discuss the increased risk Consider genetic consultation Change the drug used in previous

pregnancy AND: Start Folic acid 5 mg po./ day !

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AEDs - effect on hepatic enzymes

STRONG INDUCERS WEAK INDUCERS:

Phenobarbital Phenytoin Carbamazepine Primidone Oxcarbazepine Clobazam

Topiramate Lamotrigine Felbamate

NON INDUCERS: Valproate, Levetiracetam,Ethosuximide, Gabapentin,Clonazepam,Zonisamide

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Teratogenic risk of AEDs

The overall risk of major congenital malformation in the general population is

1.6-3.2 %. In general with the AED use it is 2-3x higher. 1. Valproate: first trimester exposure : 3 x

higher risk for malformation compare to the other AEDs; absolute risk: 6-9%.

Dose related risk: > 700 mg/d – 4%. ( = LTG <300 mg/d or CBZ 400 mg/d.)

VPA dose 1500mg – 20%.

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Other congenital malformations with VPA

Atrial septal defect Cleft palate Hypospadias Polydactyly Craniosynostosis autism

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Analysis of the NAAEDP Registry data

Not only the VPA but thee Phenobarbital has also highly increased risk – mainly cardiac malformations.

The VPA and PB has no overlap with the other AEDs.- the CBZ, LTG, PHT, LVT – cluster closely around 2-2.5%.

The risk ratio for malformation compared to Lamotrigine:

VPA: 5x, PB: 3x, TPM.: 2x.

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Other AEDs.

Topiramate: 1st. Trimester exposure – facial clefts. NAAEDP Registry: 1.4 % ( 10 fold increase

compare to the local control ) UK AED Pregnancy Register: 2.2% -facial

clefts Carbamazepine: EUROCAT ( European Surveillance of

Congenital Anomalies Antiepileptic Study ( -Spina bifida ( OR: 2.6% _ - but: it is 80 % less

than in case of VPA.

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The Levetiracetam ( Keppra )

UK Pregnancy Registry: 671 first trimester exposure/ 304

monotherapy Only 2 major congenital malformation

case: 1. inguinal hernia ( dose: 4000mg/d ) 2. reflux - requiring op. – ( dose;

2000mg/d ) NAAEDP Registry: risk: 2.4 % - with 450

exposures.

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AED polytherapy

Lamotrigine and Carbamazepine – modest major congenital malformation risk change in any polytherapy combination which does not contain VPA.

Major CM rate increase in case of Lamotrigine and any other AED: 2.9 % but with VPA: 9.1 %

Also: In case of Carbamazepine and other AED

this increase is 2.5 % but with VA: 15.4 %

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Repeated major congenital malformation risk

The risk is 35.7% if the first pregnancy ended up with major cong. malformation.

It is 57% if it happens with VPA.

The maternal genetic influence predisposes to teratogenicity and compounds the AED risk.

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AED - teratogenic dose effect

EURAP Study ( International Registry of AEDs and Pregnancy )

4 drugs studied: CBZ, LTG, Pb, VPA The lowest major cong. malformation

rate: Lamotrigine less than 300 mg/d ( 1.7%) Carbamazepine less than 400 mg/d

( 2.0%) CBZ > 1000 mg/d- 7.7% LTG > 300 mg/d – 3.6% VPA and Pb – much higher with ALL

doses.

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Stratification of risk for occurrence of major congenital malformation

Probably the safest AEDs: LTG,CBZ,LVT, PTHProbably have lower risk than Valproate:OXC, ZNS, GBPHave significant risk greater than other AED:Topiramate ( oral clefts)Phenobarbital ( cardiac defects)Valproate ( spina bifida, hypospadias )

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Seizures during pregnancy Increased frequency: 20-33% During labour: 3.5 % ( EURAP study ) Causes : sex hormone concentration changes AED metabolism Sleep deprivation New stresses Non-compliance Note: Seizure during the month before

conception – 3.7x increase in the risk of seizure in the peripartum period.

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Risk of seizure to the fetus:GTC – maternal and fetal hypoxia and acidosis - Fetal heart rate deceleration - Miscarriages - stillbirth Non-convulsive seizures: - trauma and its consequences ( ruptured fetal membranes, etc.)Obstetric risk in case of AED use:Mildly increased risk for :pre-eclampsia ( OR: 1.8 )Gestational HTN ( OR 1.5)Vaginal bleeding late in pregnancy ( OR: 1.9)Delivery before 34 wks of gestation (OR: 1.5)

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Management of AED levels during pregnancy

The clearance of most AED increases during pregnancy leading to decreased serum concentration.

Causes: 1. hepatic enzymatic induction 2.increased volume distribution 3.increased renal blood flow 4. alterations in drug absorption 5. altered concentration of albumin and

alfa-1 glycoproteins

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Lamotrigine level

May decrease remarkably because of the primary elimination happens via hepatic glucoronidation.

Needs close monitoring and correction Recommendation: Check the level 2 times prior to pregnancy Check the level every month during pregnancy Check the level at delivery and weekly later

until it is 25% higher only than the pre-pregnancy level – TOXICITY !!!

Needs fast dose decrease after delivery !

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Other postconception follow up

Level in case of other AEDs: - before conception ( x 2 ) At the beginning of each trimester In the last month Post delivery ( Phenytoin + Valproate – needs free level ! ) High level U/S at 14-18 wks. Alfa – fetoprotein at 14-16 wks ( on VPA/ or

CBZ ) If abn.: amniocentesis ( AFP+ Ach-esterase –

97% sensitivity)

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Supplementation

1. Vit-K.: in case of enzyme inducing AED. - increased risk of haemorrhagic dz. of the newborn

b/o.deficiency of vit.-K dependent clotting factors.- Suppl.: 20 mg. po./d from 36 wks of gestation +

1 mg. im to the baby at birth.

2. Folate: 5 mg from the time of the planning - decreases the risk for cong. malformations incl.

neural tube defects Decreases the risk of spontaneous abortion Improves the chance for better IQ.

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Breast feeding

Ratios between the breast milk and the serum level:

VPA.: 0.1 PTH.: 0.19 Pb.: 0.36 CBZ.: 0.41 Be careful with Pb., Primidone, benzo –

sedation Safe breast feeding practice – sitting on

the floor, etc.

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Thank you. Any question?