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Advanced Neurology                                                                  Seizures and CKD






                        Dialysis‑related dose   adjustments  US: 50% daily dose as   post-HD supplementation  UK: No additional   dosing adjustments   recommended   Dialysis‑related dose   adjustments  US: Consider post-HD   supplementation dose.   Evidence remains not fully   clear  UK: Evidence not   fully clear. Does not   recommend additional   post-HD supplementation   dosing at present








                        eGFR (mL/min/1.73 m 2 )   related dose adjustments  US: No dosing adjustments   needed for eGFR GF30.   Maximum 300 mg daily   with slow titration for   eGFR < 30 UK: No dosing adjustments   needed for eGFR ≥ 30.   Upper limit of dosing to be   250 mg daily for patients   with eGFR < 30  eGFR   (mL/min/1.73 m 2 )   related dose   adjustments  US: Dosing   reduction for   eGFR < 60 may   be needed. Advice   to prescribe with   caution  UK: Advise to












                        Potential   nephrotoxicities  Only a single   reported case of   nephritis  Potential   nephrotoxicities  Interstitial nephritis   with antiepileptic   hypersensitivity   syndrome




                        Interactions with   other AEDs  Reduces   10-hydroxycarbozepine   levels  Interactions with   other AEDs  Reduces clonazepam,   levetiracetam and   valproic acid levels  Lamotrigine levels   could be increased by   valproic acid







                        % of urinary   excretion  Approximately   95%   AED: Antiepileptic drug; CYP450: Cytochrome P450; eGFR: estimated glomerular filtration rate; HD: Hemodialysis; UK: United Kingdom; US: United States  % of urinary   excretion  Approximately   10%  AED: Antiepileptic drug; eGFR: estimated glomerular filtration rate; GABA: Gamma-aminobutyric acid; HD: Hemodialysis; UK: United Kingdom; US: United States





                        Metabolism  Hepatic   metabolism   through   CYP450   system  Metabolism  Hepatic   metabolism




                        Protein   binding  <15%                       Protein   binding  Between 50%   and 55%
                    Table 10. Properties and metabolism of lacosamide






                        Primary   mechanism of   action  Inactivation of slow   voltage-gated sodium   channels, whilst not   interfering with fast   inactivation  Table 11. Properties and metabolism of lamotrigine  Primary   mechanism of   action  Blockade of   voltage-gated sodium   channels, reduction   of glutamate,   enhancement of   GABA release




                        AED (reference range   in mg/L)  Lacosamide [9,130,131,135,160-162]  (10 – 20)  AED (reference range   in mg/L)  Lamotrigine [9,130,131,135,139,163-165]  (2.5 – 15)










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                                                                                       https://doi.org/10.36922/an.314
            Volume 2 Issue 2 (2023) olume 2 Issue 2 (2023)
            V                                               17                         https://doi.org/10.36922/an.314
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