- Research article
- Open Access
A clinical and EEG scoring system that predicts early cortical response (N20) to somatosensory evoked potentials and outcome after cardiac arrest
BMC Cardiovascular Disorders volume 8, Article number: 35 (2008)
Anoxic coma following cardiac arrest is a common problem with ethical, social, and legal consequences. Except for unfavorable somatosensory-evoked potentials (SSEP) results, predictors of unfavorable outcome with a 100% specificity and a high sensitivity are lacking. The aim of the current research was to construct a clinical and EEG scoring system that predicts early cortical response (N20) to somatosensory evoked potentials and 6-months outcome in comatose patients after cardiac arrest.
We retrospectively reviewed the records of all consecutive patients who suffered cardiac arrest outside our hospital and were subsequently admitted to our facility from November 2002 to July 2006. We scored each case based on early clinical and EEG factors associated with unfavorable SSEPs, and we assessed the ability of this score to predict SSEP results and outcome.
Sixty-six patients qualified for inclusion in the cohort. Among them, 34 (52%) had unfavorable SSEP results. At day three, factors independently associated with unfavorable SSEPs were: absence of corneal (14 points) and pupillary (21 points) reflexes, myoclonus (25 points), extensor or absent motor response to painful stimulation (28 points), and malignant EEG (11 points). A score >40 points had a sensitivity of 85%, a specificity of 84%, and a positive predictive value (PPV) of 85% to predict unfavorable SSEP results. A score >88 points had a PPV of 100%, but a sensitivity of 18%. Overall, this score had an area under ROC curves of 0.919. In addition, at day three, a score > 69 points had a PPV of 100% with a sensitivity of 32% to predict death or vegetative state.
A scoring system based on a combination of clinical and EEG findings can predict the absence of early cortical response to SSEPs. In settings without access to SSEPs, this score may help decision-making in a subset of comatose survivors after a cardiac arrest.
Despite improvements in cardiopulmonary resuscitation, 56% to 90% of patients who remain comatose after cardiac arrest have a poor outcome (death or permanent vegetative state) . For this reason, intensive care physicians are confronted with the ethical question of whether to continue treatment. In this context, early predictors of poor outcome would be valuable.
In the last few decades, several clinical and electrophysiological variables have been reported to be strongly associated with a poor outcome in comatose survivors of cardiac arrest; these include absence of pupillary and corneal reflexes, absent motor response to pain [2–5], myoclonus or epilepticus status [6, 7], an increase of neuron specific enolase (NSE) in serum , and a burst-suppression or isoelectric electro-encephalography (EEG) pattern [7, 9, 10]. However, in most cases, evidence predictive of poor outcome remains to be determined [1, 8, 11].
In contrast, bilateral absence of early cortical responses to somatosensory evoked potentials (SSEPs) demonstrated a 100% specificity for predicting poor outcome in this population [1, 5, 8, 12–17], but this electrophysiological procedure is not routinely performed in all ICUs. For example, in a systematic review of early prediction of poor outcome in anoxic-ischaemic coma, the prognostic value of SSEPs was studied in only 11 out of 33 studies (33%) . Therefore, alternatives are needed in settings without SSEPs.
We identified risk factors associated with unfavorable SSEP results; and based on these risk factors, we computed an early clinical and EEG score and assessed its predictive value, sensitivity, and specificity for predicting unfavorable SSEP results. Finally, we assessed the value of this score for predicting poor neurological outcomes in this patient population.
We conducted a retrospective cohort study of all consecutive patients who had suffered cardiac arrest outside the hospital and were subsequently admitted to the adult intensive care unit in the Caen University Hospital from November 2002 to July 2006. Patients who died or awoke within the first three days of admission were excluded from this analysis.
The institutional review board was consulted and considered that this protocol did not require Ethical approval given the observational and non-interventional nature of the study investigating routine care. Clinical variables collected at baseline were: age, sex, medical history (cardiovascular, respiratory, neurologic, metabolic diseases), cause of the arrest (cardiac, respiratory, other or unknown), time between arrest and cardiopulmonary resuscitation (<3 min, 3–5 min, >5 min), cardiac rhythm before cardiopulmonary resuscitation (ventricular fibrillation or tachycardia, asystole, pulseless rhythm), duration of cardiopulmonary resuscitation (<5 min, 5–15 min, >15 min), and scoring of disease severity within the first day in ICU as assessed by admission Simplified Acute Physiology Score type II (SAPS II)  and Acute Physiology and Chronic Health Evaluation (APACHE) II score .
Clinical procedures performed at days one and three were: pupillary light reflex (present/absent), motor response to painful stimulation (extensor or absent response/other response), corneal reflex (present/absent), tonic-clonic seizures (present/absent) and myoclonus (present/absent).
EEG and SSEPs were routinely performed in our center. For the purpose of this study, a neurophysiologist expert (O.E.) retrospectively reviewed all EEGs to allow similar definitions and increase homogeneity of the material. He was blinded to the clinical features at the time of recordings and to the outcome. EEG was recorded on at least a 10-channels system with needle electrodes using 10–20 international system (Fp1, Fp2, C3, C4, T5, T6, O1, and O2). The EEG patterns were classified at day one and day three according to the classification system of Synek et al [20, 21] [see Additional file 1]. EEG results were dichotomized as malignant and non-malignant, including benign and uncertain patterns. SSEPs were systematically performed the third day after cardiac resuscitation. However, if SSEPs recording was due on a weekend day, the recording was postponed to Monday. SSEps were recorded on Nicolet Viking IV using 6 channels: erb'point; C6sp; C'3 or C'4 controlateral to the stimulated hand and Fpz (ipsilateral ear was used as reference). The two remaining channels served as channels control: C'3 – C'4 (or C'3–C'4) on which N20 amplitude was measured and Fpz-C'3 (or Fpz-C'4) in order to check for long-latency component using larger time-window. Absence of early cortical responses to somatosensory evoked potentials were asserted only if the 3 following conditions were present: (i) correct peripheral (N10) and medullar (N13) component, (ii) no deflexion higher than 0.5 μV on C3–C'4 (or C'3–C'4) (iii) no late component on Fpz-C'3 (or Fpz-C'4). Two groups of patients were defined for statistical analysis according to SSEP results: Group 1, patients with bilateral absence of early cortical responses (unfavorable result of SSEPs) and Group 2, patients with uni- or bilateral presence of early cortical responses (favorable result of SSEPs).
Assessment of outcome
Neurological status at six months after cardiac arrest was recorded using the five grade Glasgow-Pittsburgh Cerebral Performance Category (GP-CPC) scale  [see Additional file 2]. Neurological outcome was classified as favorable (GP-CPC 1, 2, and 3) and unfavorable (GP-CPC 4 and 5).
Treatment and treatment restriction
All patients were treated without restriction for the first three days following cardiac arrest. They received standard intensive care management and monitoring, including induced hypothermia as recommended [23, 24]. Propofol, midazolam and sufentanyl were used as standard sedative and were stopped shortly before clinical assessment and EEG recording when this was possible. Hypothermia was induced using a endovascular cooling catheter (Icy™, Alsius, Irvine, CA, USA), inserted in the inferior vena cava via the femoral vein and connected to a cooling device (Coolgard 3000™, Alsius, Irvine, CA, USA), and was maintained during 24 hours. For patients which underwent cooling after resuscitation, clinical variables and neurophysiological tests were performed after rewarning. In our practice, bilateral lack of cortical response to SSEPs leads to active care withdrawal.
Quantitative variables were expressed as means ± standard deviation (SD) with their 95% confidence intervals (CI). Qualitative variables were expressed as percentages with their 95% CIs.
All analyses were replicated for day one and day three variables. Firstly, we investigated the univariate associations between clinical and EEG results (predictors) and outcomes (pejorative results of SSEPs and 6-month poor neurological outcome) using Fisher exact tests. Secondly, we constructed a multivariable model predicting the probability of outcome by performing a backward logistic regression that included variables associated at p < 0.25 in univariate analysis. Thirdly, we computed a score, based on the point system developed by Sullivan , using the beta coefficients of all risk factors that were significantly associated with outcomes in the multivariable analysis. The beta coefficients were multiplied by 10 to round them to the nearest integer and then were summed. Fourthly, we plotted Receiver Operating Characteristics (ROC) curves to estimate the capacity of the score to predict outcome using the Area Under Curve (c-index), sensitivity (Se) and specificity (Sp). We used SPSS 14.0 (Chicago, IL) for data analysis. All tests were two-sided and a p-value < 0.05 was considered statistically significant.
Baseline characteristics and neurological outcome
Of the 109 consecutive patients resuscitated after a cardiac arrest outside the hospital and admitted to our intensive care unit during the study period, 66 fulfilled inclusion criteria for analysis: 34 (52%) in group 1 (unfavorable result of SSEPs) and 32 (48%) in group 2 (favorable result of SSEPs), as shown in Figure 1. Patient baseline characteristics are presented in Table 1. Fifteen patients (22%) underwent cooling after resuscitation (6 in group 1 and 9 in group 2). Only asystole as cardiac rhythm before CPR (odds ratio [OR] = 0.3; 95% CI = 0.1–1; p = 0.04), and duration of CPR > 15 min (OR = 0.3; 95% CI = 0.1–0.9; p = 0.03) were significantly associated with group 1. The neurological outcome at six months was favorable in 13 (20%) patients, all in group 2 (Figure 1).
Predictors of unfavorable result of SSEPs
In univariate analysis (Table 2), absence of corneal and pupillary reflexes, myoclonus, and extensor or absent motor response to painful stimulation was significantly associated with group 1 at day one and day three. A malignant EEG was also significantly associated with group 1 at day three. In multivariate logistic-regression analysis (Table 2), absence of corneal reflex, myoclonus, extensor or absent motor response to painful stimulation were independently associated with a unfavorable result of SSEPs, at both day one and day three. In addition, absence of pupillary reflex and a malignant EEG were also independently associated with group 1 at day three.
Score predictive of unfavorable result of SSEPs
At days one and three, the prediction models included three and five variables, respectively: myoclonus (30 points), extensor or absent motor responses to painful stimulation (17 points), and absence of corneal reflex (10 points) for day one, and extensor or absent motor responses to pain (28 points), myoclonus (25 points), absence of pupillary (21 points) and corneal (14 points) reflexes, and a malignant EEG (11 points) for day three.
As shown in Figures 2a and 2b respectively, the ROC curves for unfavorable result of SSEPs indicated a score ≥ 88.5 points with a positive predictive value of 100% and a sensitivity of 18% (95% CI = 8–27) at day three, but failed to determine a score with a positive predictive value of 100% at day one. The scores with the highest specificity and sensitivity were ≥ 28.5 points (day one; Sp = 75% [95% CI = 65–85], Se = 88% [95% CI = 80–96]) and ≥ 40.5 points (day three; Sp = 84% [95% CI = 76–93], Se = 85% [95% CI = 77–94]), with a positive predictive value of 79% and 85%, respectively. At days one and three, these scores predicted absence of early cortical responses to SSEPs with a false positive rate of 21% (day one) and 15% (day three).
Score predictive of unfavorable outcome (GP-CPC 4 or 5)
As shown Figures 3a and 3b, the ROC curves for unfavorable outcome determined a score ≥ 52 points at day one and a score ≥ 69 points at day three, with a positive predictive value of 100% and a sensitivity of 35.8% (95% CI = 24–47) and 32% (95%CI = 21–43), respectively. An unfavorable outcome was predicted in more than a quarter of the studied population with no false positives. The scores with the highest specificity and sensitivity were ≥ 22 points (day one; Sp = 92% [95% CI = 86–99], Se = 79% [95% CI = 70–89]) and ≥ 32 points (day three; Sp = 85% [95% CI = 76–93], Se = 85% [95% CI = 76–94]) with a positive predictive value of 98% and 96%, respectively. The presence of two or more predictors at day one or day three predicted an unfavorable outcome with a false positive rate of 2% and 4%, respectively.
Contribution of the score to predict the outcome among subjects with a favorable result of SSEPs
Among 32 patients with a favorable result of SSEPs, 19 patients had an unfavorable neurological outcome at six months (Figure 1). As shown in Figure 4, the scoring system with 100% specificity at day one (score ≥ 52 points) and at day three (score ≥ 69 points) predicted death or vegetative state in two and one patients, respectively. At day three, the score (≥ 32 points) with the highest sensitivity and specificity accurately predicted an unfavorable outcome in 9/19 (47%) patients, but failed in two.
Anoxic coma following cardiac arrest is a common problem with great ethical, social, and legal consequences. To our knowledge, except for unfavorable SSEP results, predictors of unfavorable outcome with a 100% specificity and a high sensitivity are lacking [1, 11]. We have identified an early clinical and electrophysiological score that has 100% predictive value of unfavorable result of SSEPs. In addition, we complemented this result with a score predictive of a poor neurological outcome (death or vegetative state) in more than two-thirds of patients, with a low false positive rate (4%) at day three. These results may have important implications in determining the level of care to be provided three days after cardiac arrest, if SSEPs cannot be performed.
SSEPs are considered as the most accurate predictor of an unfavorable outcome in survivors after a cardiac arrest [1, 5, 8, 12–17]. SSEP assessment is superior to clinical or EEG tests in terms of low false positive rates and high prevalence of abnormal test results , and the results of SSEP assessment are less affected by metabolic changes and sedative drugs than are clinical features and EEG readings [26, 27]. In addition, SSEPs can be used in patients treated with hypothermia [16, 28, 29].
Our study confirmed the poor likelihood of awakening in patients who remained comatose after cardiac arrest, as 80% of our patients never regained consciousness. This result is consistent with results of previous studies that included only patients who remained unconscious 24 hours after cardiac arrest [2, 3, 5, 8, 17, 30].
We found that 51% of patients had no early cortical responses to SSEPs, in agreement with previous reports [5, 8, 17, 30]. Furthermore, the presence of early cortical responses to SSEPs was a poor predictor of a favorable outcome as previously reported [4, 5, 8]; indeed, only 40% (13/32) of our patients with a favorable result of SSEPs made a good recovery.
Because the results of SSEPs demonstrate 100% specificity as a predictor of poor outcome in half of patients in coma patients after a cardiac arrest [1, 5, 8, 12–17], we wanted to identify predictors of unfavorable SSEP result as potential substitutes for SSEPs, in settings without access to SSEPs. At day three, we identified a score (≥ 88.5 points) based on factors that were independently associated with an unfavorable SSEP results (Table 2) with 100% positive predictive value but low sensitivity (18%). In clinical practice, this score could allow early identification of a subgroup of irrecoverable patients for whom continued intensive care could be considered futile. In contrast, the scores with the highest specificity and sensitivity at days one and three could allow early identification of a large fraction of patients with unfavorable SSEPs results. However, the high false positive rate of these scores limits their use as potential substitutes for SSEPs, particularly when considering early withdrawal of intensive treatment.
Regarding poor neurological outcome, the score (Table 2) at day one and day three predicted death or vegetative state with 100% of specificity in one-quarter of our patients, suggesting that a definitive pejorative prognosis could be established early in a subset of patients for whom intensive treatment could be withdrawn. These scores combining simple clinical signs and EEG patterns, had a lower sensitivity than an unfavourable result of SSEPs alone. However, in patients with a favourable result of SSEPs, this scoring system could help in the identification of a subgroup of irrevocable patients.
However, the retrospective, single-center design of this study and the relatively small number of patients studied could limit the interpretation and the clinical relevance of our data. Another aspect that could limit the applicability of these data is that early withdrawal of treatment for patients with poor prognoses could result in a self-fulfilling prophesy of poor outcome. However, all of our patients were actively supported at least until SSEPs were assessed, and only a lack of bilateral cortical responses to SSEPs led to active care withdrawal.
We developed a scoring system based on a combination of early clinical and EEG factors that predicts with certainty an unfavorable result of SSEPs or a poor neurological outcome with a great accuracy in a subset of comatose survivors after a cardiac arrest. This scoring system had a lower sensitivity than an unfavourable result of SSEPs alone to predict death or vegetative state. However, this scoring system could assist clinicians, in settings without access SSEPs or when an early cortical response (N20) to SSEPs is present, in the early identification of a subgroup of irrecoverable patients for whom intensive treatment could be regarded futile and only palliative care could be given. This strategy needs to be confirmed by larger prospective trials.
Glasgow-Pittsburgh Cerebral Performance Category
Somatosensory Evoked Potentials
Receiver Operating Characteristics
Predictive Positive Value.
Zandbergen EG, de Haan RJ, Stoutenbeek CP, Koelman JH, Hijdra A: Systematic review of early prediction of poor outcome in anoxic-ischaemic coma. Lancet. 1998, 352: 1808-12. 10.1016/S0140-6736(98)04076-8.
Levy DE, Caronna JJ, Singer BH, Lapinski RH, Frydman H, Plum F: Predicting outcome from hypoxic-ischemic coma. JAMA. 1985, 253: 1420-6. 10.1001/jama.253.10.1420.
Edgren E, Hedstrand U, Kelsey S, Sutton-Tyrrell K, Safar P: Assessment of neurological prognosis in comatose survivors of cardiac arrest. BRCT I Study Group. Lancet. 1994, 343: 1055-9. 10.1016/S0140-6736(94)90179-1.
Madl C, Grimm G, Kramer L, Yeganehfar W, Sterz F, Schneider B, Kranz A, Schneeweiss B, Lenz K: Early prediction of individual outcome after cardiopulmonary resuscitation. Lancet. 1993, 341: 855-8. 10.1016/0140-6736(93)93061-5.
Chen R, Bolton CF, Young B: Prediction of outcome in patients with anoxic coma: a clinical and electrophysiologic study. Crit Care Med. 1996, 24: 672-8. 10.1097/00003246-199604000-00020.
Wijdicks EF, Parisi JE, Sharbrough FW: Prognostic value of myoclonus status in comatose survivors of cardiac arrest. Ann Neurol. 1994, 35 (2): 239-243. 10.1002/ana.410350219.
Thomke F, Marx JJ, Sauer O, Hundsberger T, Hâgele S, Wiechelt J, Weilemann SL: Observations on comatose survivors of cardiopulmonary resuscitation with generalized myoclonus. BMC Neurology. 2005, 5: 14-10.1186/1471-2377-5-14.
Zandbergen EG, Hijdra A, Koelman JH, Hart AA, Vos PE, Verbeek MM, de Haan RJ, PROPAC Study Group: Prediction of poor outcome within the first 3 days of postanoxic coma. Neurology. 2006, 66: 62-8. 10.1212/01.wnl.0000191308.22233.88.
Edgren E, Hedstrand U, Nordin M, Rydin E, Ronquist G: Prediction of outcome after cardiac arrest. Crit Care Med. 1987, 15: 820-5. 10.1097/00003246-198709000-00004.
Bassetti C, Bomio F, Mathis J, Hess CW: Early prognosis in coma after cardiac arrest: a prospective clinical, electrophysiological, and biochemical study of 60 patients. J Neurol Neurosurg Psychiatr. 1996, 61: 610-5. 10.1136/jnnp.61.6.610.
Wijdicks EF, Hijdra A, Young GB, Bassetti CL, Wiebe S, Quality Standards Subcommittee of the American Academy of Neurology: Practice parameter: prediction of outcome in comatose survivors after cardiopulmonary resuscitation (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2006, 67: 203-10. 10.1212/01.wnl.0000227183.21314.cd.
Madl C, Kramer L, Domanovits H, Woolard RH, Gervais H, Gendo A, Eisenhuber E, Grimm G, Sterz F: Improved outcome prediction in unconscious cardiac arrest survivors with sensory evoked potentials compared with clinical assessment. Crit Care Med. 2000, 28: 721-6. 10.1097/00003246-200003000-00020.
Nakabayashi M, Kurokawa A, Yamamoto Y: Immediate prediction of recovery of consciousness after cardiac arrest. Intensive Care Med. 2001, 27: 1210-4. 10.1007/s001340100984.
Zingler VC, Krumm B, Bertsch T, Fassbender K, Pohlmann-Eden B: Early prediction of neurological outcome after cardiopulmonary resuscitation: a multimodal approach combining neurobiochemical and electrophysiological investigations may provide high prognostic certainty in patients after cardiac arrest. Eur Neurol. 2003, 49: 79-84. 10.1159/000068503.
Robinson LR, Micklesen PJ, Tirschwell DL, Lew HL: Predictive value of somatosensory evoked potentials for awakening from coma. Crit Care Med. 2003, 31: 960-7. 10.1097/01.CCM.0000053643.21751.3B.
Tiainen M, Kovala TT, Takkunen OS, Roine RO: Somatosensory and brainstem auditory evoked potentials in cardiac arrest patients treated with hypothermia. Crit Care Med. 2005, 33: 1736-40. 10.1097/01.CCM.0000171536.63641.D9.
Fischer C, Luauté J, Némoz C, Morlet D, Kirkorian G, Mauguière F: Improved prediction of awakening or nonawakening from severe anoxic coma using tree-based classification analysis. Crit Care Med. 2006, 34: 1520-4. 10.1097/01.CCM.0000215823.36344.99.
Le Gall JR, Lemeshow S, Saulnier F: A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA. 1993, 270: 2957-63. 10.1001/jama.270.24.2957.
Knaus WA, Draper EA, Wagner DP, Zimmerman JE: APACHE II: a severity of disease classification system. Crit Care Med. 1985, 13: 818-29. 10.1097/00003246-198510000-00009.
Synek VM: EEG abnormality grades and subdivisions of prognostic importance in traumatic and anoxic coma in adults. Clin Electroencephalogr. 1988, 19: 160-6.
Synek VM: Prognostically important EEG coma patterns in diffuse anoxic and traumatic encephalopathies in adults. J Clin Neurophysiol. 1988, 5: 161-74.
Cummins RO, Chamberlain DA, Abramson NS, Allen M, Baskett P, Becker L, Bossaert L, Delooz H, Dick W, Eisenberg M: Recommended guidelines for uniform reporting of data from out-of-hospital cardiac arrest: the Utstein Style. Task Force of the American Heart Association, the European Resuscitation Council, the Heart and Stroke Foundation of Canada, and the Australian Resuscitation Council. Ann Emerg Med. 1991, 20: 861-74. 10.1016/S0196-0644(05)81441-6.
Bernard SA, Gray TW, Buist MD, Jones BM, Silvester W, Gutteridge G, Smith K: Treatment of comatose survivors of out-of-hospital cardiac arrest with induced hypothermia. N Engl J Med. 2002, 346: 557-63. 10.1056/NEJMoa003289.
Hypothermia after Cardiac Arrest Study Group: Mild therapeutic hypothermia to improve the neurologic outcome after cardiac arrest. N Engl J Med. 2002, 346: 549-56. 10.1056/NEJMoa012689.
Sullivan LM, et al: Presentation of multivariate data for clinical use: The Framingham Study risk score functions. Stat Med. 2004, 23: 1631-1660. 10.1002/sim.1742.
Koht A, Schatz W, Schmidt G, Schramm J, Watanabe E: Effects of etomidate, midazolam, and thiopental on median nerve somatosensory evoked potentials and the additive effects of fentanyl and nitrous oxide. Anesth Analg. 1988, 67: 435-41. 10.1213/00000539-198805000-00003.
Sloan TB, Fugina ML, Toleikis JR: Effects of midazolam on median nerve somatosensory evoked potentials. Br J Anaesth. 1990, 64: 590-3. 10.1093/bja/64.5.590.
Stecker MM, Cheung AT, Pochettino A, Kent GP, Patterson T, Weiss SJ, Bavaria JE: Deep hypothermic circulatory arrest: I. Effects of cooling on electroencephalogram and evoked potentials. Ann Thorac Surg. 2001, 71: 14-21. 10.1016/S0003-4975(00)01592-7.
Kottenberg-Assenmacher E, Armbruster W, Bornfeld N, Peters J: Hypothermia does not alter somatosensory evoked potential amplitude and global cerebral oxygen extraction during marked sodium nitroprusside-induced arterial hypotension. Anesthesiology. 2003, 98: 1112-8. 10.1097/00000542-200305000-00013.
Jorgensen EO, Holm S: The natural course of neurological recovery following cardiopulmonary. Resuscitation. 1998, 36: 111-22. 10.1016/S0300-9572(97)00094-4.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/8/35/prepub
The authors want to thank Elisabeth Munoz Leconte, Patrick Chevrel, Max Courbier and Roger Viquelin for their valuable assistance.
Previous Presentation: The work has been presented in part at the annual congress of the Société de Réanimation de Langue Française (SRLF) held in January 2007, Paris, France.
The authors declare that they have no competing interests.
CD and DG initiated the study, and the design. OE reviewed all EEGs and SSEPs. JJP, CG and CD performed the statistical analysis and were involved in the interpretation of the results. CD wrote the manuscript, and JJP and PC helped to draft the manuscript. OE, DDC, MR, BB and PC contributed to the conception and design of the study and revision of the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: EEG pattern according to the classification system of Synek [20, 21]. The data provided represent the EEG pattern according to the classification system of Synek. (DOC 19 KB)
Additional file 2: Neurological outcome according to the Glasgow-Pittsburgh Cerebral Performance Category (GP-CPC) . The data provided represent the five grades Glasgow-Pittsburgh Cerebral performance category (GP-CPC) scale (DOC 19 KB)
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Daubin, C., Guillotin, D., Etard, O. et al. A clinical and EEG scoring system that predicts early cortical response (N20) to somatosensory evoked potentials and outcome after cardiac arrest. BMC Cardiovasc Disord 8, 35 (2008). https://doi.org/10.1186/1471-2261-8-35
- Cardiac Arrest
- Positive Predictive Value
- Receiver Operating Characteristic Curve
- Vegetative State
- Cerebral Performance Category