Epilepsy Outcome at Four Years in a Randomized Clinical Trial Comparing Oral Prednisolone and Intramuscular ACTH in West Syndrome.

Author: ArambepolaCarukshi, JayasundaraKasun, RanganathanShalini Sri, WanigasingheJithangi, WeerasingheAshangi, WickramarachchiPiyumi

Paper Details 
Original Abstract of the Article :
BACKGROUND: This article explores the role of initial treatment on control of spasms and other epilepsies at four years in children previously treated for West syndrome. METHODS: The Sri Lanka Infantile Spasm Study is a prospective clinical trial evaluating response to intra-muscular adrenocorticot...See full text at original site
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引用元:
https://doi.org/10.1016/j.pediatrneurol.2021.01.008

データ提供:米国国立医学図書館(NLM)

West Syndrome: Long-Term Epilepsy Outcomes after ACTH or Prednisolone Treatment

This study examines the long-term epilepsy outcomes in children with West syndrome, a severe form of epilepsy that typically begins in infancy. The authors compare the outcomes of children who were initially treated with intramuscular adrenocorticotropic hormone (ACTH) to those who received oral prednisolone. The findings indicate that at four years of age, a majority of children with West syndrome continued to experience seizures, regardless of the initial treatment received. The study also highlights the importance of early intervention in West syndrome, as spasm control at day 14 did not appear to influence the long-term epilepsy outcome.

West Syndrome: A Persistent Challenge

The research reveals the challenges associated with treating West syndrome, a severe form of epilepsy that often persists into childhood. It highlights the importance of early intervention and underscores the need for long-term seizure management strategies. It's like navigating a complex desert landscape where each step requires careful planning and attention to ensure the best possible outcome. This research provides valuable insights into the long-term effects of different treatments for West syndrome, offering a crucial roadmap for clinicians caring for these children.

Navigating the Desert of Epilepsy

This research highlights the ongoing quest for effective treatments for epilepsy, a complex neurological disorder that affects millions worldwide. It underscores the importance of early intervention and emphasizes the need for personalized treatment plans to manage seizures effectively. It's a journey through the desert of epilepsy, where each step forward brings us closer to a future where individuals with epilepsy live fulfilling lives free from debilitating seizures.

Dr.Camel's Conclusion

Imagine West syndrome as a relentless sandstorm, disrupting the brain's electrical activity. This research explores different approaches to combat this storm, offering insights into the long-term effects of treatment. While the journey to managing epilepsy is challenging, this research provides valuable knowledge for clinicians and families navigating this complex neurological disorder.

Date :
  1. Date Completed 2022-01-25
  2. Date Revised 2022-01-25
Further Info :

Pubmed ID

33836476

DOI: Digital Object Identifier

10.1016/j.pediatrneurol.2021.01.008

Related Literature

SNS
PICO Info
in preparation
Languages

English

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