The cognitive outcome of hemispherectomy in 71 children

被引:156
作者
Pulsifer, MB
Brandt, J
Salorio, CF
Vining, EPG
Carson, BS
Freeman, JM
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat, Boston, MA 02114 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Pediat Epilepsy Ctr, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
关键词
hemispherectomy; neuropsychology;
D O I
10.1111/j.0013-9580.2004.15303.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Long-term neuropsychological outcome was studied in 71 Patients Who Underwent hemispherectomy for severe and intractable seizures Lit The Johns Hopkins Hospital between 1968 and 1997 and who agreed to participate. Seizures were due to cortical dysplasias (n = 27), Rasmussen syndrome (n = 37). or vascular malformations or strokes (n = 7). Both presurgical and follow-up results are available and reported for 53 patients. Methods: Patients and caretakers were interviewed, and patients were administered standard measures of intelligence, receptive and expressive language visual-motor skills, adaptive/developmental functioning, and behavior. Results: Mean age at surgery was 7.2 years. At follow-up, Oil average 5.4 years after surgery. 65%, are seizure free, 49% are medication free, and, of those responding. none rated quality of life as worse than before surgery. Mean IQ was in the 70s for Rasmussen and vascular patients and in the 30s for cortical dysplasia patients. Language and visual-motor skills were consistent with IQ. For Rasmussen patients only, language was significantly more impaired for left than for right hemispherectomy, both before surgery and at follow-up. Adaptive skills were mildly impaired, with greatest impairment in the physical domain. Cognitive measures typically changed little between surgery and follow-up, With IQ change < 15 points for 34 of 53 patients of the remainder, 11 declined and eight improved. Behavior was free of major problems, but social interactions and activities were limited. Conclusions: The most significant predictor of cognitive skills at follow-up was etiology, with dysplasia patients scoring lowest in intelligence and language but not in visual motor skills. Regardless of etiology, most patients showed only moderate change in cognitive performance at follow-up.
引用
收藏
页码:243 / 254
页数:12
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