Validation of the 2HELPS2B Seizure Risk Score in Acute Brain Injury Patients
Background and Objective Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal hemorrhage (IPH)—collectively defined herein as acute brain injury (ABI). Most seizures in ABI are subclinical, mean...
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Published in | Neurocritical care Vol. 33; no. 3; pp. 701 - 707 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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New York
Springer US
01.12.2020
Springer Nature B.V |
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Abstract | Background and Objective
Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal hemorrhage (IPH)—collectively defined herein as acute brain injury (ABI). Most seizures in ABI are subclinical, meaning that they are only detectable with EEG. A method is required to identify patients at greatest risk of seizures and thereby in need of prolonged continuous EEG monitoring. 2HELPS2B is a simple point system developed to address this need. 2HELPS2B estimates seizure risk for hospitalized patients using five EEG findings and one clinical finding (pre-EEG seizure). The initial 2HELPS2B study did not specifically assess the ABI subpopulation. In this study, we aim to validate the 2HELPS2B score in ABI and determine its relative predictive accuracy compared to a broader set of clinical and electrographic factors.
Methods
We queried the Critical Care EEG Monitoring Research Consortium database for ABI patients age ≥ 18 with > 6 h of continuous EEG monitoring; data were collected between February 2013 and November 2018. The primary outcome was electrographic seizure. Clinical factors considered were age, coma, encephalopathy, ABI subtype, and acute suspected or confirmed pre-EEG clinical seizure. Electrographic factors included 18 EEG findings. Predictive accuracy was assessed using a machine-learning paradigm with area under the receiver operator characteristic (ROC) curve as the primary outcome metric. Three models (clinical factors alone, EEG factors alone, EEG and clinical factors combined) were generated using elastic-net logistic regression. Models were compared to each other and to the 2HELPS2B model. All models were evaluated by calculating the area under the curve (AUC) of a ROC analysis and then compared using permutation testing of AUC with bootstrapping to generate confidence intervals.
Results
A total of 1528 ABI patients were included. Total seizure incidence was 13.9%. Seizure incidence among ABI subtype varied: IPH 17.2%, SDH 19.1%, aSAH 7.6%, TBI 9.2%. Age ≥ 65 (
p
= 0.015) and pre-cEEG acute clinical seizure (
p
< 0.001) positively affected seizure incidence. Clinical factors AUC = 0.65 [95% CI 0.60–0.71], EEG factors AUC = 0.82 [95% CI 0.77–0.87], and EEG and clinical factors combined AUC = 0.84 [95% CI 0.80–0.88]. 2HELPS2B AUC = 0.81 [95% CI 0.76–0.85]. The 2HELPS2B AUC did not differ from EEG factors (
p
= 0.51), or EEG and clinical factors combined (
p
= 0.23), but was superior to clinical factors alone (
p
< 0.001).
Conclusions
Accurate seizure risk forecasting in ABI requires the assessment of EEG markers of pathologic electro-cerebral activity (e.g., sporadic epileptiform discharges and lateralized periodic discharges). The 2HELPS2B score is a reliable and simple method to quantify these EEG findings and their associated risk of seizure. |
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AbstractList | Background and Objective
Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal hemorrhage (IPH)—collectively defined herein as acute brain injury (ABI). Most seizures in ABI are subclinical, meaning that they are only detectable with EEG. A method is required to identify patients at greatest risk of seizures and thereby in need of prolonged continuous EEG monitoring. 2HELPS2B is a simple point system developed to address this need. 2HELPS2B estimates seizure risk for hospitalized patients using five EEG findings and one clinical finding (pre-EEG seizure). The initial 2HELPS2B study did not specifically assess the ABI subpopulation. In this study, we aim to validate the 2HELPS2B score in ABI and determine its relative predictive accuracy compared to a broader set of clinical and electrographic factors.
Methods
We queried the Critical Care EEG Monitoring Research Consortium database for ABI patients age ≥ 18 with > 6 h of continuous EEG monitoring; data were collected between February 2013 and November 2018. The primary outcome was electrographic seizure. Clinical factors considered were age, coma, encephalopathy, ABI subtype, and acute suspected or confirmed pre-EEG clinical seizure. Electrographic factors included 18 EEG findings. Predictive accuracy was assessed using a machine-learning paradigm with area under the receiver operator characteristic (ROC) curve as the primary outcome metric. Three models (clinical factors alone, EEG factors alone, EEG and clinical factors combined) were generated using elastic-net logistic regression. Models were compared to each other and to the 2HELPS2B model. All models were evaluated by calculating the area under the curve (AUC) of a ROC analysis and then compared using permutation testing of AUC with bootstrapping to generate confidence intervals.
Results
A total of 1528 ABI patients were included. Total seizure incidence was 13.9%. Seizure incidence among ABI subtype varied: IPH 17.2%, SDH 19.1%, aSAH 7.6%, TBI 9.2%. Age ≥ 65 (
p
= 0.015) and pre-cEEG acute clinical seizure (
p
< 0.001) positively affected seizure incidence. Clinical factors AUC = 0.65 [95% CI 0.60–0.71], EEG factors AUC = 0.82 [95% CI 0.77–0.87], and EEG and clinical factors combined AUC = 0.84 [95% CI 0.80–0.88]. 2HELPS2B AUC = 0.81 [95% CI 0.76–0.85]. The 2HELPS2B AUC did not differ from EEG factors (
p
= 0.51), or EEG and clinical factors combined (
p
= 0.23), but was superior to clinical factors alone (
p
< 0.001).
Conclusions
Accurate seizure risk forecasting in ABI requires the assessment of EEG markers of pathologic electro-cerebral activity (e.g., sporadic epileptiform discharges and lateralized periodic discharges). The 2HELPS2B score is a reliable and simple method to quantify these EEG findings and their associated risk of seizure. BACKGROUND AND OBJECTIVESeizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal hemorrhage (IPH)-collectively defined herein as acute brain injury (ABI). Most seizures in ABI are subclinical, meaning that they are only detectable with EEG. A method is required to identify patients at greatest risk of seizures and thereby in need of prolonged continuous EEG monitoring. 2HELPS2B is a simple point system developed to address this need. 2HELPS2B estimates seizure risk for hospitalized patients using five EEG findings and one clinical finding (pre-EEG seizure). The initial 2HELPS2B study did not specifically assess the ABI subpopulation. In this study, we aim to validate the 2HELPS2B score in ABI and determine its relative predictive accuracy compared to a broader set of clinical and electrographic factors. METHODSWe queried the Critical Care EEG Monitoring Research Consortium database for ABI patients age ≥ 18 with > 6 h of continuous EEG monitoring; data were collected between February 2013 and November 2018. The primary outcome was electrographic seizure. Clinical factors considered were age, coma, encephalopathy, ABI subtype, and acute suspected or confirmed pre-EEG clinical seizure. Electrographic factors included 18 EEG findings. Predictive accuracy was assessed using a machine-learning paradigm with area under the receiver operator characteristic (ROC) curve as the primary outcome metric. Three models (clinical factors alone, EEG factors alone, EEG and clinical factors combined) were generated using elastic-net logistic regression. Models were compared to each other and to the 2HELPS2B model. All models were evaluated by calculating the area under the curve (AUC) of a ROC analysis and then compared using permutation testing of AUC with bootstrapping to generate confidence intervals. RESULTSA total of 1528 ABI patients were included. Total seizure incidence was 13.9%. Seizure incidence among ABI subtype varied: IPH 17.2%, SDH 19.1%, aSAH 7.6%, TBI 9.2%. Age ≥ 65 (p = 0.015) and pre-cEEG acute clinical seizure (p < 0.001) positively affected seizure incidence. Clinical factors AUC = 0.65 [95% CI 0.60-0.71], EEG factors AUC = 0.82 [95% CI 0.77-0.87], and EEG and clinical factors combined AUC = 0.84 [95% CI 0.80-0.88]. 2HELPS2B AUC = 0.81 [95% CI 0.76-0.85]. The 2HELPS2B AUC did not differ from EEG factors (p = 0.51), or EEG and clinical factors combined (p = 0.23), but was superior to clinical factors alone (p < 0.001). CONCLUSIONSAccurate seizure risk forecasting in ABI requires the assessment of EEG markers of pathologic electro-cerebral activity (e.g., sporadic epileptiform discharges and lateralized periodic discharges). The 2HELPS2B score is a reliable and simple method to quantify these EEG findings and their associated risk of seizure. Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal hemorrhage (IPH)-collectively defined herein as acute brain injury (ABI). Most seizures in ABI are subclinical, meaning that they are only detectable with EEG. A method is required to identify patients at greatest risk of seizures and thereby in need of prolonged continuous EEG monitoring. 2HELPS2B is a simple point system developed to address this need. 2HELPS2B estimates seizure risk for hospitalized patients using five EEG findings and one clinical finding (pre-EEG seizure). The initial 2HELPS2B study did not specifically assess the ABI subpopulation. In this study, we aim to validate the 2HELPS2B score in ABI and determine its relative predictive accuracy compared to a broader set of clinical and electrographic factors. We queried the Critical Care EEG Monitoring Research Consortium database for ABI patients age ≥ 18 with > 6 h of continuous EEG monitoring; data were collected between February 2013 and November 2018. The primary outcome was electrographic seizure. Clinical factors considered were age, coma, encephalopathy, ABI subtype, and acute suspected or confirmed pre-EEG clinical seizure. Electrographic factors included 18 EEG findings. Predictive accuracy was assessed using a machine-learning paradigm with area under the receiver operator characteristic (ROC) curve as the primary outcome metric. Three models (clinical factors alone, EEG factors alone, EEG and clinical factors combined) were generated using elastic-net logistic regression. Models were compared to each other and to the 2HELPS2B model. All models were evaluated by calculating the area under the curve (AUC) of a ROC analysis and then compared using permutation testing of AUC with bootstrapping to generate confidence intervals. A total of 1528 ABI patients were included. Total seizure incidence was 13.9%. Seizure incidence among ABI subtype varied: IPH 17.2%, SDH 19.1%, aSAH 7.6%, TBI 9.2%. Age ≥ 65 (p = 0.015) and pre-cEEG acute clinical seizure (p < 0.001) positively affected seizure incidence. Clinical factors AUC = 0.65 [95% CI 0.60-0.71], EEG factors AUC = 0.82 [95% CI 0.77-0.87], and EEG and clinical factors combined AUC = 0.84 [95% CI 0.80-0.88]. 2HELPS2B AUC = 0.81 [95% CI 0.76-0.85]. The 2HELPS2B AUC did not differ from EEG factors (p = 0.51), or EEG and clinical factors combined (p = 0.23), but was superior to clinical factors alone (p < 0.001). Accurate seizure risk forecasting in ABI requires the assessment of EEG markers of pathologic electro-cerebral activity (e.g., sporadic epileptiform discharges and lateralized periodic discharges). The 2HELPS2B score is a reliable and simple method to quantify these EEG findings and their associated risk of seizure. |
Author | Moffet, Eric W. Haider, Hiba A. Jadeja, Neville Gaspard, Nicolas Subramaniam, Thanujaa Struck, Aaron F. Rodriguez-Ruiz, Andres A. Dhakar, Monica B. Lee, Jong Woo Hirsch, Lawrence J. Gilmore, Emily J. Osman, Gamaledin |
Author_xml | – sequence: 1 givenname: Eric W. orcidid: 0000-0002-4168-7596 surname: Moffet fullname: Moffet, Eric W. organization: Department of Neurology, University of Wisconsin School of Medicine and Public Health, Department of Neurology, Northwestern University Feinberg School of Medicine – sequence: 2 givenname: Thanujaa surname: Subramaniam fullname: Subramaniam, Thanujaa organization: Department of Neurology, University of Wisconsin School of Medicine and Public Health – sequence: 3 givenname: Lawrence J. surname: Hirsch fullname: Hirsch, Lawrence J. organization: Department of Neurology, Yale University School of Medicine – sequence: 4 givenname: Emily J. surname: Gilmore fullname: Gilmore, Emily J. organization: Department of Neurology, Yale University School of Medicine – sequence: 5 givenname: Jong Woo surname: Lee fullname: Lee, Jong Woo organization: Department of Neurology, Brigham and Women’s Hospital, Harvard Medical School – sequence: 6 givenname: Andres A. surname: Rodriguez-Ruiz fullname: Rodriguez-Ruiz, Andres A. organization: Department of Neurology, Emory University School of Medicine – sequence: 7 givenname: Hiba A. surname: Haider fullname: Haider, Hiba A. organization: Department of Neurology, Emory University School of Medicine – sequence: 8 givenname: Monica B. surname: Dhakar fullname: Dhakar, Monica B. organization: Department of Neurology, Emory University School of Medicine – sequence: 9 givenname: Neville surname: Jadeja fullname: Jadeja, Neville organization: Department of Neurology, UMass Memorial Medical Center – sequence: 10 givenname: Gamaledin surname: Osman fullname: Osman, Gamaledin organization: Department of Neurology, Henry Ford Hospital – sequence: 11 givenname: Nicolas surname: Gaspard fullname: Gaspard, Nicolas organization: Department of Neurology, Yale University School of Medicine, Département de Neurologie, Université Libre de Bruxelles, Hôspital Erasme – sequence: 12 givenname: Aaron F. surname: Struck fullname: Struck, Aaron F. email: afstruck@wisc.edu organization: Department of Neurology, University of Wisconsin School of Medicine and Public Health |
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Keywords | Critical care EEG Seizure Acute brain injury 2HELPS2B Continuous EEG |
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Snippet | Background and Objective
Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and... Seizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and non-traumatic intraparenchymal... Background and ObjectiveSeizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and... BACKGROUND AND OBJECTIVESeizures are common after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhage (aSAH), subdural hematoma (SDH), and... |
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SubjectTerms | Brain Injuries - complications Brain Injuries - diagnosis Brain research Coma Consortia Convulsions & seizures Critical care Critical Care Medicine Datasets Electroencephalography Epilepsy Hemorrhage Hospitalization Humans Intensive Internal Medicine Medicine Medicine & Public Health Monitoring, Physiologic Neurology Original Work Patients Regression analysis Risk Factors Seizures - diagnosis Seizures - etiology Traumatic brain injury |
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Title | Validation of the 2HELPS2B Seizure Risk Score in Acute Brain Injury Patients |
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