Randomized Trial of Three Anticonvulsant Medications for Status Epilepticus.
Adolescent
Adult
Anticonvulsants
/ adverse effects
Benzodiazepines
/ therapeutic use
Child
Child, Preschool
Double-Blind Method
Drug Resistance
Female
Humans
Hypotension
/ chemically induced
Infusions, Intravenous
Injections, Intramuscular
Levetiracetam
/ adverse effects
Male
Middle Aged
Phenytoin
/ adverse effects
Status Epilepticus
/ drug therapy
Valproic Acid
/ adverse effects
Young Adult
Journal
The New England journal of medicine
ISSN: 1533-4406
Titre abrégé: N Engl J Med
Pays: United States
ID NLM: 0255562
Informations de publication
Date de publication:
28 11 2019
28 11 2019
Historique:
entrez:
28
11
2019
pubmed:
28
11
2019
medline:
18
12
2019
Statut:
ppublish
Résumé
The choice of drugs for patients with status epilepticus that is refractory to treatment with benzodiazepines has not been thoroughly studied. In a randomized, blinded, adaptive trial, we compared the efficacy and safety of three intravenous anticonvulsive agents - levetiracetam, fosphenytoin, and valproate - in children and adults with convulsive status epilepticus that was unresponsive to treatment with benzodiazepines. The primary outcome was absence of clinically evident seizures and improvement in the level of consciousness by 60 minutes after the start of drug infusion, without additional anticonvulsant medication. The posterior probabilities that each drug was the most or least effective were calculated. Safety outcomes included life-threatening hypotension or cardiac arrhythmia, endotracheal intubation, seizure recurrence, and death. A total of 384 patients were enrolled and randomly assigned to receive levetiracetam (145 patients), fosphenytoin (118), or valproate (121). Reenrollment of patients with a second episode of status epilepticus accounted for 16 additional instances of randomization. In accordance with a prespecified stopping rule for futility of finding one drug to be superior or inferior, a planned interim analysis led to the trial being stopped. Of the enrolled patients, 10% were determined to have had psychogenic seizures. The primary outcome of cessation of status epilepticus and improvement in the level of consciousness at 60 minutes occurred in 68 patients assigned to levetiracetam (47%; 95% credible interval, 39 to 55), 53 patients assigned to fosphenytoin (45%; 95% credible interval, 36 to 54), and 56 patients assigned to valproate (46%; 95% credible interval, 38 to 55). The posterior probability that each drug was the most effective was 0.41, 0.24, and 0.35, respectively. Numerically more episodes of hypotension and intubation occurred in the fosphenytoin group and more deaths occurred in the levetiracetam group than in the other groups, but these differences were not significant. In the context of benzodiazepine-refractory convulsive status epilepticus, the anticonvulsant drugs levetiracetam, fosphenytoin, and valproate each led to seizure cessation and improved alertness by 60 minutes in approximately half the patients, and the three drugs were associated with similar incidences of adverse events. (Funded by the National Institute of Neurological Disorders and Stroke; ESETT ClinicalTrials.gov number, NCT01960075.).
Sections du résumé
BACKGROUND
The choice of drugs for patients with status epilepticus that is refractory to treatment with benzodiazepines has not been thoroughly studied.
METHODS
In a randomized, blinded, adaptive trial, we compared the efficacy and safety of three intravenous anticonvulsive agents - levetiracetam, fosphenytoin, and valproate - in children and adults with convulsive status epilepticus that was unresponsive to treatment with benzodiazepines. The primary outcome was absence of clinically evident seizures and improvement in the level of consciousness by 60 minutes after the start of drug infusion, without additional anticonvulsant medication. The posterior probabilities that each drug was the most or least effective were calculated. Safety outcomes included life-threatening hypotension or cardiac arrhythmia, endotracheal intubation, seizure recurrence, and death.
RESULTS
A total of 384 patients were enrolled and randomly assigned to receive levetiracetam (145 patients), fosphenytoin (118), or valproate (121). Reenrollment of patients with a second episode of status epilepticus accounted for 16 additional instances of randomization. In accordance with a prespecified stopping rule for futility of finding one drug to be superior or inferior, a planned interim analysis led to the trial being stopped. Of the enrolled patients, 10% were determined to have had psychogenic seizures. The primary outcome of cessation of status epilepticus and improvement in the level of consciousness at 60 minutes occurred in 68 patients assigned to levetiracetam (47%; 95% credible interval, 39 to 55), 53 patients assigned to fosphenytoin (45%; 95% credible interval, 36 to 54), and 56 patients assigned to valproate (46%; 95% credible interval, 38 to 55). The posterior probability that each drug was the most effective was 0.41, 0.24, and 0.35, respectively. Numerically more episodes of hypotension and intubation occurred in the fosphenytoin group and more deaths occurred in the levetiracetam group than in the other groups, but these differences were not significant.
CONCLUSIONS
In the context of benzodiazepine-refractory convulsive status epilepticus, the anticonvulsant drugs levetiracetam, fosphenytoin, and valproate each led to seizure cessation and improved alertness by 60 minutes in approximately half the patients, and the three drugs were associated with similar incidences of adverse events. (Funded by the National Institute of Neurological Disorders and Stroke; ESETT ClinicalTrials.gov number, NCT01960075.).
Identifiants
pubmed: 31774955
doi: 10.1056/NEJMoa1905795
pmc: PMC7098487
mid: NIHMS1565235
doi:
Substances chimiques
Anticonvulsants
0
Benzodiazepines
12794-10-4
Levetiracetam
44YRR34555
Valproic Acid
614OI1Z5WI
Phenytoin
6158TKW0C5
fosphenytoin
B4SF212641
Banques de données
ClinicalTrials.gov
['NCT01960075']
Types de publication
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
2103-2113Subventions
Organisme : NINDS NIH HHS
ID : U01 NS073476
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS088023
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS059041
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS056975
Pays : United States
Organisme : NINDS NIH HHS
ID : U10 NS080369
Pays : United States
Organisme : NINDS NIH HHS
ID : U24 NS100651
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS059041
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS088023
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS073476
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS088034
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS056975
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS088034
Pays : United States
Investigateurs
Jaideep Kapur
(J)
Emily Gray
(E)
Sonya Gunter
(S)
Amy Fansler
(A)
Robert Silbergleit
(R)
William Barsan
(W)
Valerie Stevenson
(V)
Erin Bengelink
(E)
Deneil Harney
(D)
Mickie Speers
(M)
Joy Black
(J)
Natalie Fisher
(N)
Donna Harsh
(D)
Arthi Ramakrishnan
(A)
Lindsey Harris
(L)
Nia Bozeman
(N)
Aimee Spiteri
(A)
Yuko Palesch
(Y)
Jordan Elm
(J)
Caitlyn Meinzer
(C)
Holly Tillman
(H)
Wenle Zhao
(W)
Qi Pauls
(Q)
Chris Arnaud
(C)
Catherine R Dillon
(CR)
Jodie Riley
(J)
Teldon Alford
(T)
Cassidy Conner
(C)
Ellen Underwood
(E)
James Chamberlain
(J)
Kate Shreve
(K)
Peter Dayan
(P)
Nathan Kuppermann
(N)
Kurt Denninghoff
(K)
Rachel Stanley
(R)
Richard Ruddy
(R)
E Brooke Lerner
(EB)
J MIchael Dean
(JM)
Charles Casper
(C)
Lise Nigrovic
(L)
Walt Schalick
(W)
Doug Nelson
(D)
Bobbe Thomas
(B)
Shlomo Shinnar
(S)
Dan Lowenstein
(D)
Hannah Cock
(H)
Nathan Fountain
(N)
James Cloyd
(J)
Lisa Coles
(L)
Abhi Sathe
(A)
Scott Janis
(S)
Robin Conwit
(R)
Adam Hartman
(A)
Brandy Fureman
(B)
Eugen Trinka
(E)
David Treiman
(D)
Tom Bleck
(T)
David Wright
(D)
Jonathan Ratcliff
(J)
Alex Hall
(A)
Alaina Williams
(A)
Pamela Okada
(P)
Amanda Lee
(A)
Natasha Truesdale
(N)
Harold Simon
(H)
Nicholas Stanley
(N)
Lynn Babcock
(L)
Steven Chan
(S)
Mhadhumithaa Naresh
(M)
Venita Robinson
(V)
Maija Holsti
(M)
Jieun Hwang
(J)
Kristi Carlston
(K)
Michael Dela Cruz
(M)
Toni Harbour
(T)
Reena Karki
(R)
Roger Humphries
(R)
Theresa Mims
(T)
Joann Short
(J)
Daniel M Cohen
(DM)
Amy Nowakowski
(A)
Cindy Lin
(C)
Erin Fisher Kenny
(E)
Elizabeth Jones
(E)
Misty Ottman
(M)
Dale Steele
(D)
Lisa H Merck
(LH)
Erin Ryan
(E)
Kristin Basso
(K)
Lesley D'Urso
(L)
Nina Gentile
(N)
Derek Isenberg
(D)
Hannah Reimer
(H)
Vernon Sayoc Kalugdan
(V)
Claude Hemphill
(C)
Debbie Yi Madhok
(D)
Jeany Duncan
(J)
Dominica Randazzo
(D)
Kathleen Brown
(K)
Bobbe Thomas
(B)
Gina Nauman
(G)
Matthew Ledda
(M)
Sean Gillen
(S)
Vanessa Grant
(V)
James Quinn
(J)
Anita Visweswaran
(A)
Rosen Mann
(R)
Cheryl Vance
(C)
Daniel K Nishijima
(DK)
Kyle Pimenta
(K)
Alexander J Rogers
(AJ)
Noelle Herzog
(N)
Jonathan Bennett
(J)
Christine Eisenhart
(C)
Opeolu Adeoye
(O)
Jason McMullan
(J)
Brandon Foreman
(B)
Sara Keegan
(S)
Danny Thomas
(D)
Duke Wagner
(D)
Michelle Biros
(M)
Brian Driver
(B)
Audrey Hendrickson
(A)
Jamie Stang
(J)
Christopher Lewandowski
(C)
Joseph Miller
(J)
Kaleem Chaudhry
(K)
Shannen Berry
(S)
Craig Warden
(C)
Rachel Blake
(R)
Jennifer N B Cook
(JNB)
Erin Sabolick
(E)
Antoine Selman
(A)
Katrina Kissman
(K)
Monica Moore
(M)
J Stephen Huff
(JS)
Lea Becker
(L)
Jan Claassen
(J)
Angela Velazquez
(A)
Cristina Falo
(C)
Zlatan Coralic
(Z)
Jackie Grupp-Phelan
(J)
Jill Baren
(J)
Angela Ellison
(A)
Ashley Woodford
(A)
Ima Samba
(I)
Marlena Kittick
(M)
Robert W Hickey
(RW)
Rose Azrak
(R)
Ralph Riviello
(R)
John Massey
(J)
Lisa Bonacquisti
(L)
Steven Levine
(S)
Sergey Motov
(S)
Christian Fromm
(C)
Rukhsana Hossain
(R)
Antonios Likourezos
(A)
Illya Pushkar
(I)
Thomas Terndrup
(T)
Salman Khaliqdina
(S)
Michael Hill
(M)
Bjorn Peterson
(B)
Alexia Terwilliger
(A)
Joseph Holm
(J)
Kyra Wicklund
(K)
Sandi Wewerka
(S)
Robert Welch
(R)
Claire Pearson
(C)
Vijaya Arun Kumar
(VA)
Farhan Ayaz
(F)
Saikat Bhuiyan
(S)
Valerie H Mika
(VH)
Daniel Rubalcava
(D)
Juan Mondragon
(J)
Victor Gonzalez
(V)
Maha Khalil
(M)
Lola Morgan
(L)
Floyd Jones
(F)
Lorraine Dishman
(L)
Thomas Henry Neuro
(TH)
Ford Erickson
(F)
Abbey Staugaitis
(A)
Chloe Lawyer
(C)
Kathleen Miller
(K)
Clif Callaway
(C)
Alexandra Urban
(A)
Sara DiFiore
(S)
Peter Adams
(P)
Brian Baum
(B)
Kristina Hart
(K)
Sarah Parker
(S)
Jason Nomura
(J)
Barbara Davis
(B)
Tom Aufderheide
(T)
Amanda Emmrich
(A)
Melissa Mena
(M)
Jacob Labinski
(J)
Chinwe Ogedegbe
(C)
Diana McCarthy
(D)
Arelis Villot-Santiago
(A)
Joshua Goldstein
(J)
Eric S Rosenthal
(ES)
Abigail Cohen
(A)
Chun Mei Su
(C)
Greg Tirrell
(G)
Melissa Howell
(M)
Angela Lumba
(A)
Kim Quayle
(K)
Sri Chinta
(S)
Debra Robinson
(D)
Thomas Henry
(T)
Marissa Hendrickson
(M)
Dan Nerheim
(D)
Eric Jaton
(E)
Lisa Merck
(L)
Barbara Biney
(B)
Christopher Gibson
(C)
Erica Dahlmeier
(E)
Katherine Blackburn
(K)
Oluwarotimi Vqughan-Ogunlus
(O)
Shahriar Zehtabchi
(S)
Richard Sinert
(R)
Bryce Petty
(B)
Maria Kwok
(M)
Brooke Peery
(B)
Julie Ochs
(J)
Leonor Suarez
(L)
Scott Youngquist
(S)
Margaret Carlson
(M)
Nadege Gilles
(N)
Sarah Weingast
(S)
Barney Stern
(B)
Jennifer Hopp
(J)
Virginia Ganley
(V)
Joseph Ornato
(J)
Christopher Hogan
(C)
Alan Payne
(A)
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2019 Massachusetts Medical Society.
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