接受治疗的儿童期发病癫痫的自然病史:前瞻性、长期的人群研究

来源 :世界核心医学期刊文摘(神经病学分册) | 被引量 : 0次 | 上传用户:sgrsrg
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It is not well known how often drug resistance, a major clinical problem, occurs early or late in the course of epilepsy and how often epilepsy follows a continuous, remitting or relapsingremitting pattern. To provide evidence if, in fact, different patterns of evolution of drug resistance and remission exist, a prospective, long- term population- based study of 144 patients followed on the average for 37.0 years (SD 7.1, median 40.0, range 11- 42) since their first seizure before the age of 16 years was performed. At the end of follow- up, 67% of 144 patients were in terminal remission, on or off antiepileptic drugs. Early remission, starting within the first year of treatment, was seen in 45 patients (31% ). In 23 (16% ) of them, first remission continued, uninterrupted by relapse, to terminal remission. Late remission with a mean delay of 9 years was achieved by a further 72 patients (50% ), including 46 (32% ) patients who achieved terminal remission without any relapse and suggested, together with 23 patients, a remitting course. Following a relapse after early or late remission, 28 (19% ) patients achieved terminal remission, suggesting a remitting- relapsing pattern. Altogether 20 patients (14% ) did not re- enter remission, indicating a worsening course of epilepsy. Twenty- seven (19% ) patients were drug- resistant from the start to the end of follow- up. In conclusion, half the patients with childhood- onset epilepsy will eventually enter terminal remission without relapse and a fifth after relapse. One- third will have a poor long- term outcome in terms of persistent seizures after remission or without any remission ever. It is not well known how often drug resistance, a major clinical problem, occurs early or late in the course of epilepsy and how often epilepsy follows a continuous, remitting or relapsingremitting pattern. To provide evidence if, in fact, different patterns of evolution of drug resistance and remission exist, a prospective, long-term population-based study of 144 patients followed on the average for 37.0 years (SD 7.1, median 40.0, range 11-42) since their first firstizure before the age of 16 years was performed . At the end of follow-up, 67% of 144 patients were in terminal remission, on or off antiepileptic drugs. Early remission, starting within the first year of treatment, was seen in 45 patients (31%). %) of them, first remission continued, uninterrupted by relapse, to terminal remission. Late remission with a mean delay of 9 years was achieved by a further 72 patients (50%), including 46 (32%) patients who achieved terminal remission without any relapse and suggest ed together with 23 patients, a remitting course. Following a relapse after early or late remission, 28 (19%) patients achieved terminal remission, suggesting a remitting- relapsing pattern. Altogether 20 patients (14%) did not re- enter remission , indicating a worsening course of epilepsy. Twenty-seven (19%) patients were drug- resistant from the start to the end of follow-up. In conclusion, half the patients with childhood- onset epilepsy will eventually arrive at terminal remission without relapse and a fifth after relapse. One-third will have a poor long-term outcome in terms of persistent seizures after remission or without any remission ever.
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