Factors associated with outcomes of severe acute necrotizing encephalopathy: A multicentre experience in Malaysia

Author:

Lee Vanessa Wan Mun1ORCID,Khoo Teik Beng1,Teh Chee Ming2,Heng Hock Sin3,Li Limin4,Yusof Yusma Lyana Md5,Yahaya Nor Azni6,Dharshini Sangita7,Wong Sau Wei8,Nickson Tai9,

Affiliation:

1. Paediatric Neurology Unit Hospital Tunku Azizah Kuala Lumpur Malaysia

2. Pediatric Neurology Unit Hospital Pulau Pinang Pulau Pinang Malaysia

3. Pediatric Neurology Unit Sabah Women and Children Hospital Kota Kinabalu Malaysia

4. Division of Pediatric Neurology, Department of Paediatrics, Faculty of Medicine University Malaya Kuala Lumpur Malaysia

5. Pediatric Unit, Faculty of Medicine Universiti Teknologi Mara Selangor Darul Ehsan Malaysia

6. Paediatric Neurology Unit Hospital Raja Perempuan Zainab II Kota Bharu Malaysia

7. Pediatric Neurology Unit Subang Jaya Medical Centre Selangor Darul Ehsan Malaysia

8. Paediatric Neurology Unit Hospital Pakar Kanak‐Kanak Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia

9. Paediatric Unit Hospital Umum Sarawak Sarawak Malaysia

Abstract

AbstractThis case series compared clinical variables and various combinations of immunotherapy received with outcomes of patients with severe acute necrotizing encephalopathy (ANE). We performed a retrospective review of clinical variables, immunotherapy received, and outcomes (based on the modified Rankin Scale) in Malaysia between February 2019 and January 2020. Twenty‐seven children (12 male), aged 7 months to 14 years (mean 4 years) at diagnosis were included. Of these, 23 had an ANE severity score of 5 to 9 out of 9 (high risk). Eleven patients received tocilizumab (four in combination with methylprednisolone [MTP], seven with MTP + intravenous immunoglobulin [IVIG]) and 16 did not (two received MTP alone, 14 received MTP + IVIG). Nine died. Among the survivors, six had good outcomes (modified Rankin Score 0–2) at 6 months follow‐up. All patients who received tocilizumab in combination with MTP + IVIG survived. Twenty children received first immunotherapy within 48 hours of admission. No significant association was found between the timing of first immunotherapy with outcomes. Those with brainstem dysfunction (p = 0.016) were observed to have poorer outcomes. This study showed a trend towards better survival when those with severe ANE were treated with tocilizumab in combination with MTP + IVIG. However, larger studies will be needed to determine the effect of this regime on the long‐term outcomes.

Funder

Ministry of Health

King's College London

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

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