Changing the paradigm of 1-stage total callosotomy for the treatment of pediatric generalized epilepsy.
Changing the paradigm of 1-stage total callosotomy for the treatment of pediatric generalized epilepsy.
复制标题
改变一期全胼胝体切开术治疗小儿全身性癫痫的范例。
DOI:
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发表时间:
2008
期刊:
影响因子:
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通讯作者:
Dong
中科院分区:
文献类型:
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作者:
K. Shim;Young;H. Kim;Jun;Joong;Dong
OBJECT
The authors propose that anterior callosotomy -- thought to have some advantages over total callosotomy -- is not superior to total callosotomy for prevention of seizure propagation or other complications.
METHODS
The study comprised 34 patients in whom generalized epilepsy syndrome or frontal lobe seizures with a secondary generalization were diagnosed. Preoperatively, all patients suffered from disabling drop attacks or intense head-drop seizures, and some patients also experienced other types of seizures. The male/female ratio was 22:12, and patients ranged in age between 1 to 19 years (mean 8.7 years). The follow-up period ranged from 1.08 to 5.0 years (mean 2.58 years). Seizure outcome, parental assessment of daily function, and parental satisfaction with the outcome was assessed postoperatively.
RESULTS
After undergoing 1-stage total callosotomy, drop attacks disappeared completely in 25 patients during the follow-up period, and in 6 patients the frequency of drop attacks decreased to < 10% of baseline. With regard to other types of seizures, seizures resolved completely in 12 patients, and in another 18 seizure frequency decreased. Two patients experienced a transient disconnection syndrome for 2 and 4 weeks. One patient experienced ataxic hemiparesis for 3 weeks before it completely abated. The overall daily function of the patients improved, and all parents were satisfied with the surgical outcome.
CONCLUSIONS
For pediatric generalized epilepsy syndrome, 1-stage total callosotomy will be the first choice in treatment for controlling generalized seizures.