Volume 56, Issue 4 pp. 577-582
Original Article

Cyclosporine for acute encephalopathy with biphasic seizures and late reduced diffusion

Yoshihiro Watanabe

Corresponding Author

Yoshihiro Watanabe

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

Correspondence: Yoshihiro Watanabe, MD, Department of Pediatrics, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama 232-0024, Japan. Email: [email protected]Search for more papers by this author
Hirotaka Motoi

Hirotaka Motoi

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Yoshitaka Oyama

Yoshitaka Oyama

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Kazushi Ichikawa

Kazushi Ichikawa

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Saoko Takeshita

Saoko Takeshita

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Masaaki Mori

Masaaki Mori

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Atsuo Nezu

Atsuo Nezu

Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan

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Shumpei Yokota

Shumpei Yokota

Department of Pediatrics, Yokohama City University School of Medicine, Yokohama, Japan

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First published: 13 January 2014
Citations: 9

Abstract

Background

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is the most common syndrome among the acute encephalopathies, and is associated with a high incidence of neurologic sequelae. This study examined the efficacy of cyclosporine (CsA) for the treatment of AESD.

Methods

Fourteen children with AESD were recruited and categorized as group A (not receiving CsA) and group B (receiving CsA). Clinical course, laboratory data, magnetic resonance imaging (MRI), and outcome were analyzed retrospectively. We divided the patients into three types according to the distribution of abnormalities on MRI: frontal lobe predominant type, unilateral cerebral hemisphere type, and diffuse type. We used the Pediatric Cerebral Performance Category scale (PCPC) and the Pediatric Overall Performance Category scale (POPC) as prognostic measures.

Results

Of the 14 children, five were boys (age range, 9–32 months). PCPC score was: 1 for seven patients, 2 for three patients, and 3 for four patients. There was no significant difference in PCPC between groups A and B (P = 0.293). POPC score was: 1 for six patients, 2 for five patients, and 3 for three patients. There was a significant difference in POPC between groups A and B when patients with the frontal lobe predominant type were excluded (P = 0.020).

Conclusions

CsA could improve the neurological prognosis of patients with AESD, except for those with frontal lobe predominant type.

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