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Long-term outcome of phenobarbital treatment for epilepsy in rural China: A prospective cohort study

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机构: [1]Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3050, Australia; [2]Univ Melbourne, Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic 3050, Australia; [3]Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China; [4]Capital Med Univ, Beijing Neurosurg Inst, Beijing, Peoples R China; [5]China Assoc Epilepsy, Beijing, Peoples R China; [6]Fudan Univ, Inst Neurol, Shanghai 200433, Peoples R China; [7]Jiaozuo Peoples Hosp, Jiaozuo, Henan Province, Peoples R China; [8]Yangzhou Univ, Clin Med Coll, Dept Neurol, Yangzhou, Jiangsu, Peoples R China; [9]Universal Love Hosp, Mudanjiang, Heilongjiang Pr, Peoples R China; [10]Netherlands Fdn, SEIN Epilepsy Inst, Heemstede, Netherlands; [11]WHO Collaborating Ctr Res Training & Treatment Ep, Heemstede, Netherlands; [12]UCL Inst Neurol, Dept Clin & Expt Epilepsy, London WC1N 3BG, England; [13]Epilepsy Soc, Gerrards Cross, England; [14]UCL Inst Neurol, Dept Clin & Expt Epilepsy, Queen Sq, London WC1N 3BG, England
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关键词: Epilepsy Phenobarbital Outcome China

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Purpose: To evaluate the long-term outcome of phenobarbital treatment for convulsive epilepsy in rural China, and to explore factors associated with overall seizure outcomes. Methods: We carried out follow-up assessments of people who took part in an epilepsy community management program conducted in rural counties of six provinces in China. People with convulsive epilepsy who were previously untreated (or on irregular treatment) were commenced on regular treatment with phenobarbital. Information was collected using a standardized questionnaire by face-to-face interviews of the individuals (and their families where necessary). Information collected included treatment status, medication change, seizure frequency, and mortality. Key Findings: Among the 2,455 people who participated in the original program, outcomes were successfully ascertained during the follow-up assessment in 1986. Among them, 206 had died. Information on treatment response was obtained in 1,780 (56% male; mean age 33.9years, range 384; mean duration of follow-up 6.4years). Among them, 939 (53%) were still taking phenobarbital. The most common reasons for stopping phenobarbital were seizure freedom or substantial seizure reduction, socioeconomic reasons, and personal preference. Four hundred fifty-three individuals (25%) became seizure-free for at least 1year while taking phenobarbital, 88% of whom did so at daily doses of 120mg or below. Four hundred six (23%) reported adverse events, which led to withdrawal of phenobarbital in <1%. The most common adverse effects were malaise/somnolence (7.4%), dizziness (3%), and lethargy (2.6%). At the follow-up assessment, 688 (39%) individuals had been seizure free for at least the previous year. People with persistent seizures had significantly longer duration of epilepsy and higher number of seizures in the 12months before treatment. People who were taking AED treatment irregularly at recruitment were less likely to become seizure-free. Significance: We observed long-term benefits of regular treatment with phenobarbital for convulsive epilepsy in rural China. One hundred years after the discovery of its antiepileptic effect, phenobarbital is still playing an important role in the management of epilepsy.

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出版当年[2012]版:
大类 | 2 区 医学
小类 | 2 区 临床神经病学
最新[2023]版:
大类 | 1 区 医学
小类 | 2 区 临床神经病学
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出版当年[2011]版:
Q1 CLINICAL NEUROLOGY
最新[2023]版:
Q1 CLINICAL NEUROLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2011版] 出版当年五年平均 出版前一年[2010版] 出版后一年[2012版]

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第一作者机构: [1]Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3050, Australia; [2]Univ Melbourne, Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic 3050, Australia; [3]Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China;
通讯作者:
通讯机构: [10]Netherlands Fdn, SEIN Epilepsy Inst, Heemstede, Netherlands; [11]WHO Collaborating Ctr Res Training & Treatment Ep, Heemstede, Netherlands; [12]UCL Inst Neurol, Dept Clin & Expt Epilepsy, London WC1N 3BG, England; [13]Epilepsy Soc, Gerrards Cross, England; [14]UCL Inst Neurol, Dept Clin & Expt Epilepsy, Queen Sq, London WC1N 3BG, England
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