首页> 外文期刊>Epilepsia: Journal of the International League against Epilepsy >Clinical predictors of the long-term social outcome and quality of life in juvenile myoclonic epilepsy: 20-65 years of follow-up
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Clinical predictors of the long-term social outcome and quality of life in juvenile myoclonic epilepsy: 20-65 years of follow-up

机译:青少年肌阵挛性癫痫的长期社会预后和生活质量的临床预测指标:随访20-65年

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Objective The long-term social outcome in patients with juvenile myoclonic epilepsy (JME) is still controversial. The aim of this study was both to investigate the long-term social outcome in relation to clinical variables and to identify epilepsy-related factors that affect the quality of life (QoL) in JME patients with a follow-up of at least 20 years. Methods A retrospective selection of 33 of 90 patients (21 female) from a tertiary epilepsy center diagnosed with JME and followed for ≥20 years (mean 37.8 years) was studied. All patients were evaluated with a thorough review of their medical records, and a subsequent face-to-face or telephone interview. QOLIE-31-P questionnaire (QoL In Epilepsy) and Beck Depression Inventory-II were used to assess the QoL and the presence and severity of depressive symptoms, respectively. Results Of 33 patients, 18 (54.5%) became seizure-free; in 4 of the patients (22.2%), antiepileptic drug (AED) treatment was discontinued. Early and long-term seizure freedom improves both social adjustment (p = 0.02) and occupational integration (p = 0.02) and associates with a better QoL (odds ratio [OR] 2.25). A high seizure burden highly affects both aspects of personal life - family and work; notably the occurrence of frequent and/or late onset generalized tonic-clonic seizures increases the risk of concomitant diseases (p = 0.05) and lifelong AED treatment (p = 0.03), decreases the patient's employability (p = 0.02), increases the rate of employment disability pension (p = 0.05), and considerably increases public/social spending. Seizure freedom significantly increases the QoL (p = 0.001), whereas more severe courses of epilepsy (OR 3.2), AED side effects (p = 0.04), depression (p = 0.02), and sleep disturbances (OR 2.7) considerably decrease the patient's QoL. Significance Although patients with JME are a heterogeneous group, several predictors for the long-term social, family, educational, and occupational outcome have been identified in our study and should be considered in the effort to both improve the patient′s QoL as well as preserve economic resources.
机译:目的青年肌阵挛性癫痫(JME)患者的长期社会结局仍存在争议。这项研究的目的是调查与临床变量有关的长期社会结局,并确定影响JME患者并至少随访20年的生活质量(QoL)的癫痫相关因素。方法对90例JME确诊为JME的癫痫病中心患者中的33例(21名女性)进行回顾性选择,随访时间≥20年(平均37.8年)。对所有患者进行了彻底的病历审查,随后进行了面对面或电话采访。使用QOLIE-31-P问卷(癫痫中的QoL)和贝克抑郁量表II分别评估QoL,抑郁症状的存在和严重程度。结果33例患者中无18例(54.5%)无癫痫发作。在4例患者中(22.2%),停止了抗癫痫药(AED)的治疗。早期和长期的癫痫发作自由度可改善社会适应能力(p = 0.02)和职业融合(p = 0.02),并具有更好的QoL(比值比[OR] 2.25)。癫痫发作高负担严重影响个人生活的两个方面-家庭和工作;值得注意的是,频繁和/或迟发的全身性强直阵挛发作增加了并发疾病的风险(p = 0.05)和终生AED治疗(p = 0.03),降低了患者的就业能力(p = 0.02),增加了患病率就业残疾养恤金(p = 0.05),并大大增加了公共/社会支出。癫痫发作的自由度显着提高了QoL(p = 0.001),而更严重的癫痫病程(OR 3.2),AED副作用(p = 0.04),抑郁症(p = 0.02)和睡眠障碍(OR 2.7)大大降低了患者的生活质量重要性尽管JME患者属于异类人群,但在我们的研究中已确定了长期社会,家庭,教育和职业结局的几种预测因素,在改善患者的QoL以及保存经济资源。

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