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Hospital Emergency Treatment of Convulsive Status Epilepticus: Comparison of Pathways From Ten Pediatric Research Centers.
Vasquez, Alejandra; Gaínza-Lein, Marina; Sánchez Fernández, Iván; Abend, Nicholas S; Anderson, Anne; Brenton, J Nicholas; Carpenter, Jessica L; Chapman, Kevin; Clark, Justice; Gaillard, William D; Glauser, Tracy; Goldstein, Joshua; Goodkin, Howard P; Lai, Yi-Chen; Loddenkemper, Tobias; McDonough, Tiffani L; Mikati, Mohamad A; Nayak, Anuranjita; Payne, Eric; Riviello, James; Tchapyjnikov, Dmitry; Topjian, Alexis A; Wainwright, Mark S; Tasker, Robert C.
Afiliação
  • Vasquez A; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Maryland.
  • Gaínza-Lein M; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Maryland; Facultad de Medicina, Universidad Austral de Chile, Valdivia, Chile.
  • Sánchez Fernández I; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Maryland; Department of Child Neurology, Hospital Sant Joan de Déu, Universidad de Barcelona, Barcelona, Spain.
  • Abend NS; Division of Neurology, The Children's Hospital of Philadelphia, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Anderson A; Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Brenton JN; Department of Neurology and Pediatrics, University of Virginia Health System, Charlottesville, Virginia.
  • Carpenter JL; Center for Neuroscience, Children's National Medical Center, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia.
  • Chapman K; Departments of Pediatrics and Neurology, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado.
  • Clark J; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Maryland.
  • Gaillard WD; Center for Neuroscience, Children's National Medical Center, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia.
  • Glauser T; Division of Neurology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio.
  • Goldstein J; Ruth D. & Ken M. Davee Pediatric Neurocritical Care Program, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Goodkin HP; Department of Neurology and Pediatrics, University of Virginia Health System, Charlottesville, Virginia.
  • Lai YC; Section of Pediatric Critical Medicine, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Loddenkemper T; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Maryland.
  • McDonough TL; Division of Child Neurology, Department of Neurology, Columbia University Medical Center, Columbia University, New York, New York.
  • Mikati MA; Division of Pediatric Neurology, Duke University Medical Center, Duke University, Durham, North Carolina.
  • Nayak A; Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Payne E; Division of Child and Adolescent Neurology, Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Riviello J; Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Tchapyjnikov D; Division of Child and Adolescent Neurology, Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Topjian AA; Division of Critical Care Medicine, The Children's Hospital of Philadelphia, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Wainwright MS; Ruth D. & Ken M. Davee Pediatric Neurocritical Care Program, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Division of Child Neurology, Department of Neurology, Seattle Children's Hospital, Seattle, Washington.
  • Tasker RC; Departments of Neurology and Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts. Electronic address: Robert.Tasker@childrens.harvard.edu.
Pediatr Neurol ; 86: 33-41, 2018 09.
Article em En | MEDLINE | ID: mdl-30075875
OBJECTIVE: We aimed to evaluate and compare the status epilepticus treatment pathways used by pediatric status epilepticus research group (pSERG) hospitals in the United States and the American Epilepsy Society (AES) status epilepticus guideline. METHODS: We undertook a descriptive analysis of recommended timing, dosing, and medication choices in 10 pSERG hospitals' status epilepticus treatment pathways. RESULTS: One pathway matched the timeline in the AES guideline; nine pathways described more rapid timings. All pathways matched the guideline's stabilization phase in timing and five suggested that first-line benzodiazepine (BZD) be administered within this period. For second-line therapy timing (initiation of a non-BZD antiepileptic drug within 20 to 40 minutes), one pathway matched the guideline; nine initiated the antiepileptic drug earlier (median 10 [range five to 15] minutes). Third-line therapy timings matched the AES guideline (40 minutes) in two pathways; eight suggested earlier timing (median 20 [range 15 to 30] minutes). The first-line BZD recommended in all hospitals was intravenous lorazepam; alternatives included intramuscular midazolam or rectal diazepam. In second-line therapy, nine pathways recommended fosphenytoin. For third-line therapy, eight pathways recommended additional boluses of second-line medications; most commonly phenobarbital. Two pathways suggested escalation to third-line medication; most commonly midazolam. We found variance in dosing for the following medications: midazolam as first-line therapy, fosphenytoin, and levetiracetam as second-line therapy, and phenobarbital as third-line therapy medications. CONCLUSIONS: The pSERG hospitals status epilepticus pathways are consistent with the AES status epilepticus guideline in regard to the choice of medications, but generally recommend more rapid escalation in therapy than the guideline.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Tratamento de Emergência / Hospitalização / Anticonvulsivantes Tipo de estudo: Guideline Limite: Adolescent / Child / Child, preschool / Humans / Infant País/Região como assunto: America do norte Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Tratamento de Emergência / Hospitalização / Anticonvulsivantes Tipo de estudo: Guideline Limite: Adolescent / Child / Child, preschool / Humans / Infant País/Região como assunto: America do norte Idioma: En Ano de publicação: 2018 Tipo de documento: Article