Changes in Real-world Practice Patterns of Antiepileptic Drugs for Status Epilepticus: A Nationwide Observational Study in Japan.
epilepsy
fosphenytoin
levetiracetam
phenytoin
seizure
Journal
Neurologia medico-chirurgica
ISSN: 1349-8029
Titre abrégé: Neurol Med Chir (Tokyo)
Pays: Japan
ID NLM: 0400775
Informations de publication
Date de publication:
15 Mar 2020
15 Mar 2020
Historique:
pubmed:
6
2
2020
medline:
3
2
2021
entrez:
4
2
2020
Statut:
ppublish
Résumé
Intravenous (i.v.) phenytoin/fosphenytoin is recommended as the second-line therapy of antiepileptic drugs in patients with status epilepticus (SE). i.v. Levetiracetam is regarded as an effective and safe equivalent with i.v. phenytoin/fosphenytoin. However, i.v. levetiracetam is not covered by public health insurance for SE in most countries. For this study, we performed the real-world practice pattern survey of antiepileptic drugs for status epilepticus using the nationwide inpatient database. We used the Japanese Diagnosis Procedure Combination inpatient database in Japan and identified all cases of emergency admission attributable to status epilepticus from March 2011 through March 2018. We described the patient characteristics and practice pattern of antiepileptic drugs. The analysis conducted for this study examined 31,472 cases. As the second-line therapy, the use of i.v. levetiracetam increased rapidly from 2016; 35% of cases received i.v. levetiracetam in 2017. By contrast, the use of i.v. phenytoin/fosphenytoin decreased from 2016. In-hospital mortality decreased year-by-year. No year-by-year change was observed for deaths within 24 h, length of hospital stay, drug-induced hepatitis, or drug-induced eruption. Although the use of levetiracetam for treatment of SE is not compensated by public health insurance in Japan, i.v. levetiracetam use is increasing dramatically as the second-line SE therapy. We propose that health insurance coverage be extended to include i.v. levetiracetam treatment for SE.
Identifiants
pubmed: 32009125
doi: 10.2176/nmc.oa.2019-0225
pmc: PMC7073701
doi:
Substances chimiques
Anticonvulsants
0
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
156-163Références
Jpn Hosp. 2016 Aug;(35):35-44
pubmed: 30226960
Eur J Neurol. 2010 Mar;17(3):348-55
pubmed: 20050893
Epilepsy Res. 2015 Aug;114:52-8
pubmed: 26088885
Neurol Clin. 1995 Aug;13(3):529-48
pubmed: 7476818
J Epidemiol. 2017 Oct;27(10):476-482
pubmed: 28142051
J Neurosci. 1997 Oct 1;17(19):7532-40
pubmed: 9295398
Neurocrit Care. 2012 Aug;17(1):3-23
pubmed: 22528274
Medicine (Baltimore). 2017 Jun;96(25):e7206
pubmed: 28640109
Neurol Res. 2002 Dec;24(8):842-8
pubmed: 12500711
J Clin Neurosci. 2015 Jun;22(6):959-63
pubmed: 25899652
J Neurophysiol. 2011 Sep;106(3):1227-39
pubmed: 21653714
Epilepsia. 2006 Jul;47(7):1128-35
pubmed: 16886975
Epilepsia. 2015 Oct;56(10):1515-23
pubmed: 26336950
Seizure. 2017 Jul;49:8-12
pubmed: 28528211
Epilepsy Curr. 2016 Jan-Feb;16(1):48-61
pubmed: 26900382
Epilepsy Behav. 2018 Aug;85:37-44
pubmed: 29906700
Epilepsia. 2015 Mar;56(3):348-55
pubmed: 25684068
Acad Emerg Med. 2004 Mar;11(3):244-52
pubmed: 15001403
Anaesthesia. 2001 Jul;56(7):648-59
pubmed: 11437765
N Engl J Med. 1998 Sep 17;339(12):792-8
pubmed: 9738086
Epilepsy Behav. 2017 Apr;69:186-222
pubmed: 28237319
BMJ Open. 2013 Apr 29;3(4):
pubmed: 23633419