Multivariable prediction of seizure outcome one year after resective epilepsy surgery: development of a model with independent validation

PURPOSE To identify predictors of seizure-outcome after epilepsy surgery and validate the findings in an independent series of patients. To use the results to develop a predictive model. METHODS Sequential patients undergoing resective surgery for medically intractable epilepsy were identified at Yale New Haven Hospital (1987-1990, group 1) and Columbia Presbyterian Hospital (1991-1994, group 2). Information about seizure outcome and predictors of outcome was obtained from medical chart review. Good seizure-outcome was defined as having been seizure-free for one year beginning with discharge from the hospital. Multiple logistic regression was used to develop a model of predictors in group 1. It was then validated in group 2. RESULTS There were 133 patients in group 1 and 81 in group 2. In a multivariable analysis, independent predictors of outcome in group 1 were presence of mesial temporal sclerosis based on postsurgical pathological analysis (MTS) (relative risk (RR) = 1.47), having a known underlying etiology (RR = 1.32), and partial seizures only (RR = 1.17). In group 2, the findings for each factor were similar to those in group 1: MTS, RR = 1.49; etiology, RR = 1.32; and partial seizures, RR = 1.24. Used in combination, these three factors can identify patients with nearly a 100% chance of being seizure-free (all three factors present) versus less than a 50% chance (none of the three factors present). CONCLUSIONS With independent validation of the findings, we can be reasonably certain that the three factors identified in this analysis are meaningful and generalizable predictors of seizure outcome following epilepsy surgery. Use of predictive models should be considered in future studies to convert study results into clinically relevant statements about a particular patient's likelihood of surgical success.

[1]  Y. Løyning,et al.  Predictive Factors for Success in Surgical Treatment for Partial Epilepsy: A Multivariate Analysis , 1994, Epilepsia.

[2]  C. Binnie,et al.  Outcome following resective surgery for temporal lobe epilepsy: a prospective follow up study of 102 consecutive cases. , 1991, Journal of neurology, neurosurgery, and psychiatry.

[3]  P. Gloor,et al.  Results of surgical treatment in patients with bitemporal epileptiform abnormalities , 1989, Annals of neurology.

[4]  C E Elger,et al.  Prognostic Significance of Ictal and Interictal Epileptiform Activity in Temporal Lobe Epilepsy , 1994, Epilepsia.

[5]  A. Friedman,et al.  Predictors of Outcome of Epilepsy Surgery: Multivariate Analysis with Validation , 1996, Epilepsia.

[6]  J. Engel,et al.  Surgery for seizures. , 1996, The New England journal of medicine.

[7]  J. Engel,et al.  Outcome assessment for epilepsy surgery: The impact of measuring health‐related quality of life , 1995, Annals of neurology.

[8]  A. Saykin,et al.  Predictors of outcome after anterior temporal lobectomy , 1994, Neurology.

[9]  I. Fried,et al.  The anatomy of epileptic auras: focal pathology and surgical outcome. , 1995, Journal of neurosurgery.

[10]  G. Jackson,et al.  Preoperative MRI predicts outcome of temporal lobectomy , 1995, Neurology.

[11]  P. Riekkinen,et al.  Postoperative EEG and Electrocorticography: Relation to Clinical Outcome in Patients with Temporal Lobe Surgery , 1994, Epilepsia.

[12]  A. Alavi,et al.  Predictors of outcome after anterior temporal lobectomy , 1994, Neurology.

[13]  I. Jensen TEMPORAL LOBE EPILEPSY , 1976, Acta neurologica Scandinavica.

[14]  T. Rasmussen,et al.  Prognostic factors in the surgical treatment of temporal lobe epileptics , 1968, Neurology.

[15]  D. Commenges,et al.  A longitudinal assessment of seizure outcome and overall benefit from 100 cortectomies for epilepsy. , 1992, Journal of neurology, neurosurgery, and psychiatry.

[16]  T L Babb,et al.  Interhemispheric Propagation Time of Human Hippocampal Seizures , 1986, Epilepsia.

[17]  R. S. Sloviter,et al.  The functional organization of the hippocampal dentate gyrus and its relevance to the pathogenesis of temporal lobe epilepsy , 1994, Annals of neurology.

[18]  R. Worth,et al.  Clinical characteristics and predictive factors in 98 patients with complex partial seizures treated with temporal resection. , 1994, Archives of neurology.

[19]  J. Duncan,et al.  Seizure characteristics, pathology, and outcome after temporal lobectomy , 1987, Neurology.

[20]  F. Sharbrough,et al.  Depth Electrode Studies in Temporal Lobe Epilepsy: Relation to Quantitative Magnetic Resonance Imaging and Operative Outcome , 1995, Epilepsia.

[21]  G. Ojemann,et al.  Multidisciplinary prediction of seizure relief from cortical resection surgery , 1986, Annals of neurology.

[22]  S Shinnar,et al.  Do seizures beget seizures? An assessment of the clinical evidence in humans. , 1997, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

[23]  F. Andermann,et al.  Temporal Lobe Epilepsy After Prolonged Febrile Convulsions: Excellent Outcome After Surgical Treatment , 1993, Epilepsia.

[24]  T L Babb,et al.  Interhemispheric Propagation Time of Human Hippocampal Seizures: II. Relationship to Pathology and Cell Density , 1986, Epilepsia.

[25]  S. Berkovic,et al.  Febrile seizures and hippocampal sclerosis: frequent and related findings in intractable temporal lobe epilepsy of childhood. , 1995, Pediatric neurology.