Literature DB >> 32133641

Mortality in infantile spasms: A hospital-based study.

Chellamani Harini1, Elanagan Nagarajan1, Ann M Bergin1, Phillip Pearl1, Tobias Loddenkemper1, Masanori Takeoka1, Peter F Morrison2, David Coulter3, Gita Harappanahally4, Candice Marti1, Kanwaljit Singh5, Christopher Yuskaitis1, Annapurna Poduri1, Mark H Libenson1.   

Abstract

OBJECTIVE: To determine risk factors and causes for mortality during childhood in patients with infantile spasms (IS). We describe the overall goals of care for those who died.
METHODS: This is a retrospective chart review of IS patients born between 2000 and 2011. We examined potential risk factors for mortality, including etiology, neurologic impairment, medication use, persistence of epileptic spasms, and comorbid systemic involvement (requirement for G-tube feedings, respiratory interventions). For patients who died, we describe cause of death and resuscitation status or end-of-life care measures.
RESULTS: We identified 150 IS patients with median follow-up of 12 years. During the study period, 25 (17%) patients died, 13 before 5 years of age. Univariate analysis demonstrated that developmental delay, identifiable etiology, hormonal use for IS, persistence of epileptic spasms, polypharmacy with antiseizure medications, refractory epilepsy, respiratory system comorbidity, and the need for a G-tube were significant risk factors for mortality. In a multivariate analysis, mortality was predicted by persistence of epileptic spasms (odds ratio [OR] = 4.30, 95% confidence interval [CI] = 1.11-16.67, P = .035) and significant respiratory system comorbidity (OR = 12.75, 95% CI = 2.88-56.32, P = .001). Mortality was epilepsy-related in one-third of patients who died with sudden unexpected death in epilepsy (SUDEP), accounting for 88% of epilepsy-related deaths. Most deaths before age 5 years were related to respiratory failure, and SUDEP was less common (17%) whereas SUDEP was more common (45%) with deaths after 5 years. For the majority (67%) of patients with early mortality, an end-of-life care plan was in place (based on documentation of resuscitation status, comfort measures, or decision not to escalate medical care). SIGNIFICANCE: Mortality at our single-center IS cohort was 17%, and persistence of epileptic spasms and comorbid respiratory system disorders were the most important determinants of mortality. Early deaths were related to neurological impairments/comorbidities. SUDEP was more common in children who died after 5 years of age than in those who died younger than 5 years. Wiley Periodicals, Inc.
© 2020 International League Against Epilepsy.

Entities:  

Keywords:  SUDEP; infantile spasm; infantile spasm mortality; mortality

Year:  2020        PMID: 32133641     DOI: 10.1111/epi.16468

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


  7 in total

1.  A tale of two cohorts: Differing outcomes in infantile-onset focal epilepsy.

Authors:  Erin M Triplet; Katherine Nickels; Lily Wong-Kisiel; Anthony Fine; Elaine C Wirrell
Journal:  Epilepsia       Date:  2022-02-10       Impact factor: 5.864

Review 2.  Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic Encephalopathies.

Authors:  Elizabeth E Palmer; Katherine Howell; Ingrid E Scheffer
Journal:  Neurotherapeutics       Date:  2021-10-27       Impact factor: 6.088

3.  Safety and Effectiveness of Oral Methylprednisolone Therapy in Comparison With Intramuscular Adrenocorticotropic Hormone and Oral Prednisolone in Children With Infantile Spasms.

Authors:  Hong-Min Zhu; Chun-Hui Yuan; Meng-Qing Luo; Xiao-Long Deng; Sheng Huang; Ge-Fei Wu; Jia-Sheng Hu; Cong Yao; Zhi-Sheng Liu
Journal:  Front Neurol       Date:  2021-12-22       Impact factor: 4.003

4.  Classifying etiology of infantile spasms syndrome in resource-limited settings: A study from the South Asian region.

Authors:  Jithangi Wanigasinghe; Jitendra Kumar Sahu; Priyanka Madaan; Kanij Fatema; Kyaw Linn; Prem Chand; Prakash Poudel; Esmatullah Hamed; Mimi L Mynak; Samaahath Hassan
Journal:  Epilepsia Open       Date:  2021-10-25

Review 5.  EEG biomarkers for the diagnosis and treatment of infantile spasms.

Authors:  Blanca Romero Milà; Kavyakantha Remakanthakurup Sindhu; John R Mytinger; Daniel W Shrey; Beth A Lopour
Journal:  Front Neurol       Date:  2022-07-28       Impact factor: 4.086

6.  Automatic BASED scoring on scalp EEG in children with infantile spasms using convolutional neural network.

Authors:  Yuying Fan; Duo Chen; Hua Wang; Yijie Pan; Xueping Peng; Xueyan Liu; Yunhui Liu
Journal:  Front Mol Biosci       Date:  2022-08-10

7.  Brain Magnetic Resonance Imaging Findings in Infantile Spasms.

Authors:  Osama Y Muthaffar
Journal:  Neurol Int       Date:  2022-03-03
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.