Byun Jung-Ick, Lee Soon-Tae, Jung Keun-Hwa, Sunwoo Jun-Sang, Moon Jangsup, Lim Jung-Ah, Lee Doo Young, Shin Yong-Won, Kim Tae-Joon, Lee Keon-Joo, Lee Woo-Jin, Lee Han-Sang, Jun Jinsun, Kim Dong-Yub, Kim Man-Young, Kim Hyunjin, Kim Hyeon Jin, Suh Hong Il, Lee Yoojin, Kim Dong Wook, Jeong Jin Ho, Choi Woo Chan, Bae Dae Woong, Shin Jung-Won, Jeon Daejong, Park Kyung-Il, Jung Ki-Young, Chu Kon, Lee Sang Kun
Departments of Neurology, Seoul National University Hospital, Seoul, South Korea.
Program in Neuroscience, Seoul National University College of Medicine, Seoul, South Korea.
PLoS One. 2016 Jan 15;11(1):e0146455. doi: 10.1371/journal.pone.0146455. eCollection 2016.
To evaluate the seizure characteristics and outcome after immunotherapy in adult patients with autoimmune encephalitis (AE) and new-onset seizure.
Adult (age ≥18 years) patients with AE and new-onset seizure who underwent immunotherapy and were followed-up for at least 6 months were included. Seizure frequency was evaluated at 2-4 weeks and 6 months after the onset of the initial immunotherapy and was categorized as "seizure remission", "> 50% seizure reduction", or "no change" based on the degree of its decrease.
Forty-one AE patients who presented with new-onset seizure were analysed. At 2-4 weeks after the initial immunotherapy, 51.2% of the patients were seizure free, and 24.4% had significant seizure reduction. At 6 months, seizure remission was observed in 73.2% of the patients, although four patients died during hospitalization. Rituximab was used as a second-line immunotherapy in 12 patients who continued to have seizures despite the initial immunotherapy, and additional seizure remission was achieved in 66.6% of them. In particular, those who exhibited partial response to the initial immunotherapy had a better seizure outcome after rituximab, with low adverse events.
AE frequently presented as seizure, but only 18.9% of the living patients suffered from seizure at 6 months after immunotherapy. Aggressive immunotherapy can improve seizure outcome in patients with AE.
评估自身免疫性脑炎(AE)伴新发癫痫的成年患者免疫治疗后的癫痫特征及预后。
纳入年龄≥18岁、接受免疫治疗且随访至少6个月的AE伴新发癫痫患者。在初始免疫治疗开始后2 - 4周及6个月时评估癫痫发作频率,并根据发作减少程度分为“癫痫缓解”“发作减少>50%”或“无变化”。
分析了41例新发癫痫的AE患者。初始免疫治疗后2 - 4周时,51.2%的患者无癫痫发作,24.4%的患者癫痫发作显著减少。6个月时,73.2%的患者癫痫缓解,尽管有4例患者在住院期间死亡。12例尽管接受了初始免疫治疗仍持续发作的患者使用利妥昔单抗作为二线免疫治疗,其中66.6%的患者实现了额外的癫痫缓解。特别是那些对初始免疫治疗表现出部分反应的患者,在使用利妥昔单抗后癫痫预后更好,不良事件发生率低。
AE常表现为癫痫发作,但免疫治疗6个月后仅18.9%的存活患者仍有癫痫发作。积极的免疫治疗可改善AE患者的癫痫预后。