Pharmacological monitoring of antiepileptic drugs in epilepsy patients on haemodialysis.


Journal

Epileptic disorders : international epilepsy journal with videotape
ISSN: 1950-6945
Titre abrégé: Epileptic Disord
Pays: United States
ID NLM: 100891853

Informations de publication

Date de publication:
01 Feb 2020
Historique:
pubmed: 8 2 2020
medline: 3 11 2020
entrez: 8 2 2020
Statut: ppublish

Résumé

To retrospectively evaluate the pharmacological profiles of antiepileptic drugs (AEDs) in epilepsy patients during haemodialysis using therapeutic drug monitoring data. The serum concentration of AEDs was collected before and after haemodialysis, and the clearance rate and concentration-to-dose ratio were calculated as pharmacological parameters. Thirty-six patients were enrolled in the study (25 males, 11 females; age: 65.3 ± 14.8 years). In 24 of the 36 patients, epilepsy was associated with cerebrovascular disorders, and diabetes was the most common reason for haemodialysis in 16 patients. With regards to seizure type, focal aware seizures were less frequent than focal impaired awareness seizures and focal-to-bilateral tonic-clonic seizures. Interictal EEG showed intermittent rhythmic slow waves and intermittent slow waves more often than spikes or sharp waves. Levetiracetam was the most commonly used AED and led to the highest percentage of responders (80%; 16/20 patients). However, the clearance rate of levetiracetam during dialysis was highest among the antiepileptic drugs used, requiring supplementary doses after haemodialysis in all 20 patients. Valproic acid was not effective for focal epilepsy for patients on haemodialysis, and non-responders to phenytoin had low serum concentration of phenytoin both before and after haemodialysis. The pre-haemodialysis concentration of levetiracetam tended to be higher than the reference range, suggesting a potential risk of overdosing before haemodialysis. The pre- and post-haemodialysis concentrations of valproic acid tended to be lower than the reference range, suggesting a potential risk of underdosing. The concentration-to-dose ratios for levetiracetam, valproic acid, phenytoin, and carbamazepine were significantly lower after than before haemodialysis. The majority of patients with epilepsy on haemodialysis had cerebrovascular diseases, and therapeutic drug monitoring for levetiracetam, valproic acid, and phenytoin, before and after haemodialysis, is needed to ensure proper dosing.

Identifiants

pubmed: 32031531
pii: epd.2020.1139
doi: 10.1684/epd.2020.1139
doi:

Substances chimiques

Anticonvulsants 0
Levetiracetam 44YRR34555

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-102

Auteurs

Kunihiko Araki (K)

Department of Neurology, Nagoya University Graduate School of Medicine, Aichi.

Tomohiko Nakamura (T)

Department of Neurology, Nagoya University Graduate School of Medicine, Aichi,, Department of Laboratory Medicine, Nagoya University Hospital, Aichi.

Yuko Takeuchi (Y)

Department of Neurology, Masuko Memorial Hospital, Aichi.

Saori Morozumi (S)

Department of Neurology, Nagoya Daini Red Cross Hospital, Aichi.

Katsunori Horie (K)

Department of Nephrology, Aoi Central Hospital, Aichi.

Yasushi Kobayashi (Y)

Department of Neurology, Okazaki City Hospital, Aichi.

Osamu Kawakami (O)

Department of Neurology, Anjo Kosei Hospital, Aichi.

Fumio Sobue (F)

Department of Neurology, Miai Clinic, Aichi.

Takuya Ueda (T)

Department of Nephrology, Aoi Clinic, Aichi.

Kensuke Hamada (K)

Department of Neurology, Kamiiida Daiichi General Hospital, Aichi.

Tetsuo Ando (T)

Department of Neurology, Anjo Kosei Hospital, Aichi.

Yushi Inoue (Y)

National Epilepsy Center, NHO Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka.

Keizo Yasui (K)

Department of Neurology, Nagoya Daini Red Cross Hospital, Aichi.

Kunio Morozumi (K)

Department of Nephrology, Masuko Memorial Hospital, Aichi.

Shoichi Maruyama (S)

Department of Nephrology, Nagoya University Graduate School of Medicine, Aichi, Japan.

Masahisa Katsuno (M)

Department of Neurology, Nagoya University Graduate School of Medicine, Aichi.

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Classifications MeSH