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Abstract Details

Management practices for West syndrome in South Asia
Child Neurology and Developmental Neurology
P16 - Poster Session 16 (5:30 PM-6:30 PM)
5-007

To study the management practices for West syndrome(WS) in the South Asian subcontinent. 

WS is the commonest infantile epileptic encephalopathy. There is paucity of literature on WS from south Asia.
Seven countries were surveyed using an online questionnaire. The questionnaire was sent to 223pediatric neurologists/pediatricians in India, Pakistan, Myanmar, Sri Lanka, Bhutan, Nepal, and Bangladesh. 

One-hundred-twenty-five responses were received[Response-rate:56%; India(76/165), Pakistan(22/22), Myanmar(9/11), Sri Lanka(6/8), Bhutan(5/10), Nepal(3/5), Bangladesh(2/2), and outliers(2/165; UK and UAE)]. Around 60% of responders observed male preponderance and an approximate lead-time-to-treatment of 4weeks-3months. The commonest etiology observed was static structural insult. 

Preferred first-choice drug (countrywise): India-ACTH(50%), oral steroids(38%), combination (hormonal+vigabatrin;8%), valproate(7%);  Pakistan-oral steroids(45.5%), vigabatrin(32%), ACTH(4.5%); Myanmar, Sri Lanka, and Nepal-oral steroids preferred; Bangladesh-ACTH(2/2); Bhutan- oral steroids(2/5), vigabatrin(3/5), ACTH(not used). ACTH and vigabatrin are not available in Myanmar and Nepal. The most commonly used preparation and regime for ACTH is long-acting synthetic corticotropin and maximal-dose-at-initiation-regime in India, Sri Lanka, and Bangladesh. In Pakistan, most responders follow a gradually-escalating-regime. Maximum dose of prednisolone ranges from 2-8mg/kg/day or 60mg/day- most common response from India:3-4mg/kg/day; Pakistan, Bhutan, and Bangladesh:2mg/kg/day; Sri Lanka, Nepal and Myanmar:5-8mg/kg/day or 60mg/day. The total duration of hormonal therapy (including tapering) ranges from 4-12weeks(59/81). Most responders consider cessation of spasms for 4weeks as complete response(55/125) and advise EEG(106/125) to check for hypsarrhythmia resolution. Difficult access to pediatric EEG in Bhutan and Nepal is concerning. Around 50% of responders follow a standard-operating-protocol for management. More than 95% of responders felt a need for more awareness.

 

This survey highlights the practices and challenges in the management of WS in South Asia. These include a longer lead-time-to-treatment, non-availability of natural ACTH, licensing issues with vigabatrin in most countries, preference for oral steroids/ vigabatrin over ACTH(except India and Bangladesh), difficult access to pediatric EEG, and non-availability of ACTH/vigabatrin in some countries. 

 

Authors/Disclosures
Priyanka Madaan
PRESENTER
Priyanka Madaan has nothing to disclose.
No disclosure on file
No disclosure on file
Jithangi Wanigasinghe (University of COlombo) No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
Jitendra Sahu, MD Jitendra Sahu has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Indian Journal of Pediatrics. The institution of Jitendra Sahu has received research support from Indian Council of Medical Research.