Abstract
Purpose
To explore the efficacy and safety of intravenous immunoglobulin (IVIG) in the treatment of severe Japanese encephalitis (JE).
Methods
A retrospective study of 124 children diagnosed with the severe or very severe form of JE was undertaken. There were 62 cases in the IVIG group and control group. The efficacy, safety, and tolerability of IVIG were evaluated 3 days, as well as 1, 2, and 3 weeks after IVIG, respectively, and the prognosis was assessed at 6 months.
Results
Cox regression survival analysis suggested that the IVIG group reached the criteria for efficacious treatment faster than that in the control group. The duration of unconsciousness and the number of days of seizures, a dull response to light, the pyramidal sign, and meningeal-irritation sign in the IVIG group were shorter than those in the control group (p < 0.05). The number of complications occurring in the IVIG group (including gastrointestinal bleeding and pneumonia) was less than that in the control group (p < 0.05). Cox regression survival analysis suggested that age (p = 0.003) and imaging abnormalities (p = 0.042) had an effect on the efficacy of IVIG treatment. The Liverpool Outcome Score at 6 months showed that the prognosis of the IVIG group was better than that of the control group (p < 0.05). IVIG treatment was safe and tolerable.
Conclusion
IVIG showed good efficacy, safety, and tolerance for treatment of the severe form of JE. The age and imaging abnormalities of patients affect the efficacy of IVIG treatment.
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Data availability
The dataset generated during and/or analyzed during the study is available from the corresponding author upon reasonable request.
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Acknowledgements
We sincerely thank all the children and their parents for their cooperation during this study.
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D.C. contributed to the acquisition and interpretation of data, and was involved in drafting the manuscript. Y.H. conceived of the study, participated in its design, and helped to draft the manuscript. X.L.P., Y.Z., and P.W. participated in the design of the study and undertook statistical analyses. L.J. revised the manuscript critically for important intellectual content. All authors approved the final version of the manuscript.
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The study protocol was approved by the Scientific and Ethical Committee of the Children’s Hospital of Chongqing Medical University (Chongqing, China).
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Written informed consent was obtained from the accompanying relative/guardian of the child.
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Chen, D., Peng, X., Zhan, Y. et al. Efficacy and safety of intravenous high-dose immunoglobulin in treatment of the severe form of Japanese encephalitis. Neurol Sci 43, 3911–3918 (2022). https://doi.org/10.1007/s10072-022-05891-6
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DOI: https://doi.org/10.1007/s10072-022-05891-6