Literature DB >> 29105055

The impact of hypsarrhythmia on infantile spasms treatment response: Observational cohort study from the National Infantile Spasms Consortium.

Scott T Demarest1, Renée A Shellhaas2, William D Gaillard3, Cynthia Keator4, Katherine C Nickels5, Shaun A Hussain6, Tobias Loddenkemper7, Anup D Patel8, Russell P Saneto9, Elaine Wirrell5, Iván Sánchez Fernández7, Catherine J Chu10, Zachary Grinspan11, Courtney J Wusthoff12, Sucheta Joshi2, Ismail S Mohamed13, Carl E Stafstrom14, Cynthia V Stack15, Elissa Yozawitz16, Judith S Bluvstein17, Rani K Singh18, Kelly G Knupp1.   

Abstract

OBJECTIVE: The multicenter National Infantile Spasms Consortium prospective cohort was used to compare outcomes and phenotypic features of patients with infantile spasms with and without hypsarrhythmia.
METHODS: Patients aged 2 months to 2 years were enrolled prospectively with new-onset infantile spasms. Treatment choice and categorization of hypsarrhythmia were determined clinically at each site. Response to therapy was defined as resolution of clinical spasms (and hypsarrhythmia if present) without relapse 3 months after initiation.
RESULTS: Eighty-two percent of patients had hypsarrhythmia, but this was not associated with gender, mean age, preexisting developmental delay or epilepsy, etiology, or response to first-line therapy. Infants with hypsarrhythmia were more likely to receive standard treatment (adrenocorticotropic hormone, prednisolone, or vigabatrin [odds ratio (OR) 2.6, 95% confidence interval (CI) 1.4-4.7] and preexisting epilepsy reduced the likelihood of standard treatment (OR 3.2, 95% CI 1.9-5.4). Hypsarrhythmia was not a determinant of response to treatment. A logistic regression model demonstrated that later age of onset (OR 1.09 per month, 95% CI 1.03-1.15) and absence of preexisting epilepsy (OR 1.7, 95% CI 1.06-2.81) had a small impact on the likelihood of responding to the first-line treatment. However, receiving standard first-line treatment increased the likelihood of responding dramatically: vigabatrin (OR 5.2 ,95% CI 2-13.7), prednisolone (OR 8, 95% CI 3.1-20.6), and adrenocorticotropic hormone (ACTH; OR 10.2, 95% CI 4.1-25.8) . SIGNIFICANCE: First-line treatment with standard therapy was by far the most important variable in determining likelihood of response to treatment of infantile spasms with or without hypsarrhythmia. Wiley Periodicals, Inc.
© 2017 International League Against Epilepsy.

Entities:  

Keywords:  Adrenocorticotropic hormone; Epilepsy; Prednisolone; Vigabatrin

Mesh:

Substances:

Year:  2017        PMID: 29105055      PMCID: PMC5863227          DOI: 10.1111/epi.13937

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  32 in total

1.  The underlying etiology of infantile spasms (West syndrome): information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification.

Authors:  John P Osborne; Andrew L Lux; Stuart W Edwards; Eleanor Hancock; Anthony L Johnson; Colin R Kennedy; Richard W Newton; Christopher M Verity; Finbar J K O'Callaghan
Journal:  Epilepsia       Date:  2010-08-17       Impact factor: 5.864

2.  The risk of lower mental outcome in infantile spasms increases after three weeks of hypsarrhythmia duration.

Authors:  Zvonka Rener Primec; Janez Stare; David Neubauer
Journal:  Epilepsia       Date:  2006-12       Impact factor: 5.864

Review 3.  The epidemiology and natural history of infantile spasms.

Authors:  L D Cowan; L S Hudson
Journal:  J Child Neurol       Date:  1991-10       Impact factor: 1.987

4.  Evidence-based guideline update: medical treatment of infantile spasms. Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Authors:  C Y Go; M T Mackay; S K Weiss; D Stephens; T Adams-Webber; S Ashwal; O C Snead
Journal:  Neurology       Date:  2012-06-12       Impact factor: 9.910

5.  Hypsarrhythmia assessment exhibits poor interrater reliability: a threat to clinical trial validity.

Authors:  Shaun A Hussain; Grace Kwong; John J Millichap; John R Mytinger; Nicole Ryan; Joyce H Matsumoto; Joyce Y Wu; Jason T Lerner; Raman Sankar
Journal:  Epilepsia       Date:  2014-11-10       Impact factor: 5.864

Review 6.  Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics.

Authors:  Jo M Wilmshurst; William D Gaillard; Kollencheri Puthenveettil Vinayan; Tammy N Tsuchida; Perrine Plouin; Patrick Van Bogaert; Jaime Carrizosa; Maurizio Elia; Dana Craiu; Nebojsa J Jovic; Doug Nordli; Deborah Hirtz; Virginia Wong; Tracy Glauser; Eli M Mizrahi; J Helen Cross
Journal:  Epilepsia       Date:  2015-06-30       Impact factor: 5.864

Review 7.  Epidemiological data of West syndrome in Finland.

Authors:  R Riikonen
Journal:  Brain Dev       Date:  2001-11       Impact factor: 1.961

8.  Epidemiology of infantile spasms in Sweden.

Authors:  R Sidenvall; O Eeg-Olofsson
Journal:  Epilepsia       Date:  1995-06       Impact factor: 5.864

9.  Epidemiologic features of infantile spasms in Iceland.

Authors:  P Lúthvígsson; E Olafsson; S Sigurthardóttir; W A Hauser
Journal:  Epilepsia       Date:  1994 Jul-Aug       Impact factor: 5.864

10.  Infantile spasms in Down syndrome--effects of delayed anticonvulsive treatment.

Authors:  Monika Maria Eisermann; A DeLaRaillère; G Dellatolas; E Tozzi; R Nabbout; O Dulac; C Chiron
Journal:  Epilepsy Res       Date:  2003 Jun-Jul       Impact factor: 3.045

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  18 in total

Review 1.  West Syndrome: Questions Aplenty- Few Answers.

Authors:  Shivan Kesavan; Naveen Sankhyan
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Authors:  William Stacey; Mark Kramer; Kristin Gunnarsdottir; Jorge Gonzalez-Martinez; Kareem Zaghloul; Sara Inati; Sridevi Sarma; Jennifer Stiso; Ankit N Khambhati; Danielle S Bassett; Rachel J Smith; Virginia B Liu; Beth A Lopour; Richard Staba
Journal:  Epilepsy Res       Date:  2019-12-09       Impact factor: 3.045

Review 3.  Infantile Spasms-Have We Made Progress?

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Journal:  Curr Neurol Neurosci Rep       Date:  2018-04-19       Impact factor: 5.081

4.  Strength and stability of EEG functional connectivity predict treatment response in infants with epileptic spasms.

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5.  CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.

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Review 6.  CDKL5 Deficiency Disorder-Related Epilepsy: A Review of Current and Emerging Treatment.

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7.  Inequities in Therapy for Infantile Spasms: A Call to Action.

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Review 8.  Modeling epileptic spasms during infancy: Are we heading for the treatment yet?

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Journal:  Pharmacol Ther       Date:  2020-05-15       Impact factor: 12.310

9.  Rapid ictal transition of focal epilepsy to infantile spasms in neurofibromatosis type 1 captured with EEG.

Authors:  Shital H Patel; Robert P Carson; Lori C Jordan; Lindsay M Pagano
Journal:  Epilepsy Behav Rep       Date:  2020-06-08

10.  Comparative Effectiveness of Initial Treatment for Infantile Spasms in a Contemporary US Cohort.

Authors:  Zachary M Grinspan; Kelly G Knupp; Anup D Patel; Elissa G Yozawitz; Courtney J Wusthoff; Elaine Wirrell; Ignacio Valencia; Nilika S Singhal; Douglas R Nordli; John R Mytinger; Wendy Mitchell; Cynthia G Keator; Tobias Loddenkemper; Shaun A Hussain; Chellamani Harini; William D Gaillard; Ivan S Fernandez; Jason Coryell; Catherine J Chu; Anne T Berg; Renee A Shellhaas
Journal:  Neurology       Date:  2021-07-15       Impact factor: 11.800

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