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Successful Treatment of Intractable Hiccups with Benztropine / 대한소아신경학회지
Article in En | WPRIM | ID: wpr-40196
Responsible library: WPRO
ABSTRACT
In general, intractable hiccups are uncommon. Various drugs and interventions have been reported, but there is no consensus on the treatment of intractable hiccups. We report a patient with meningitis and rhombencephalitis who presented with intractable hiccups that were resolved following treatment with benztropine. A 17-year-old boy was admitted to another hospital with a two-week history of fever and headache. A cerebrospinal fluid (CSF) test showed an increased white blood cell (WBC) count (290/muL, monocytes 100%). He was diagnosed with meningitis and treated with ceftriaxone. Two days after admission, hiccups started and lasted for eight days, despite treatment with phenobarbital, diazepam, haloperidol, phenytoin, and chlorpromazine. He was transferred to our hospital for further evaluation and treatment. He was clinically diagnosed with rhombencephalitis based upon the findings of brain magnetic resonance imaging (MRI). The fever and headache disappeared one day later. However, the hiccups persisted, despite symptomatic treatment with chlorpromazine, gabapentin, and metoclopramide. The hiccups disappeared after one day of adding benztropine without relapse. Benztropine can be considered in the treatment of intractable hiccups.
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Full text: 1 Index: WPRIM Main subject: Phenobarbital / Phenytoin / Recurrence / Brain / Ceftriaxone / Magnetic Resonance Imaging / Monocytes / Benztropine / Cerebrospinal Fluid / Chlorpromazine Type of study: Guideline Limits: Adolescent / Humans / Male Language: En Journal: Journal of the Korean Child Neurology Society Year: 2014 Type: Article
Full text: 1 Index: WPRIM Main subject: Phenobarbital / Phenytoin / Recurrence / Brain / Ceftriaxone / Magnetic Resonance Imaging / Monocytes / Benztropine / Cerebrospinal Fluid / Chlorpromazine Type of study: Guideline Limits: Adolescent / Humans / Male Language: En Journal: Journal of the Korean Child Neurology Society Year: 2014 Type: Article