TY - JOUR
T1 - Neurological Prognostication After Hypoglycemic Coma
T2 - Role of Clinical and EEG Findings
AU - for the CCEMRC
AU - Bouyaknouden, Douaae
AU - Peddada, Teja N.
AU - Ravishankar, Nidhi
AU - Fatima, Safoora
AU - Fong-Isariyawongse, Joanna
AU - Gilmore, Emily J.
AU - Lee, Jong Woo
AU - Struck, Aaron F.
AU - Gaspard, Nicolas
AU - Struck, Aaron F.
AU - Husain, Aatif M.
AU - Fernandez, Andres
AU - Rodriguez-Ruiz, Andres
AU - Bagic, Anto
AU - Amin, Assad F.
AU - Foreman, Brandon
AU - Appavu, Brian L.
AU - Maciel, Carolina B.
AU - Hahn, Cecil D.
AU - Nwankwo, Chinasa
AU - Rubinos, Clio A.
AU - Wusthoff, Courtney J.
AU - Amorim, Edilberto
AU - Gerard, Elizabeth
AU - Ritzl, Eva K.
AU - Drislane, Frank W.
AU - Kapinos, Gregory
AU - Chen, Hai
AU - Britton, Jeffrey
AU - Szaflarski, Jerzy P.
AU - Yoo, Ji Yeoun
AU - Ding, Kan
AU - Chapman, Kevin
AU - Hirsch, Lawrence J.
AU - Huh, Linda L.
AU - Westover, M. Brandon
AU - Holmes, Manisha G.
AU - Ng, Marcus C.
AU - Mizrahi, Moshe A.
AU - Abend, Nicholas S.
AU - Gaspard, Nicolas
AU - Selioutski, Olga
AU - Taraschenko, Olga
AU - Mani, Ram
AU - Sainju, Rup K.
AU - Hantus, Stephen T.
AU - Herman, Susan T.
AU - LaRoche, Suzette M.
AU - Gofton, Teneille E.
AU - Loddenkemper, Tobias
N1 - Publisher Copyright:
© 2022, Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society.
PY - 2022/8
Y1 - 2022/8
N2 - Background: Hypoglycemic coma (HC) is an uncommon but severe clinical condition associated with poor neurological outcome. There is a dearth of robust neurological prognostic factors after HC. On the other hand, there is an increasing body of literature on reliable prognostic markers in the postanoxic coma, a similar—albeit not identical—situation. The objective of this study was thus to investigate the use and predictive value of these markers in HC. Methods: We conducted a retrospective, multicenter, cohort study within five centers of the Critical Care EEG Monitoring Research Consortium. We queried our electroencephalography (EEG) databases to identify all patients undergoing continuous EEG monitoring after admission to an intensive care unit with HC (defined as Glasgow Coma Scale < 8 on admission and a first blood glucose level < 50 mg/dL or not documented but in an obvious clinical context) between 01/01/2010 and 12/31/2020. We studied the association of findings at neurological examination (Glasgow Coma Scale motor subscale, pupillary light and corneal reflexes) and at continuous EEG monitoring(highly malignant patterns, reactivity, periodic discharges, seizures) with best neurological outcome within 3 months after hospital discharge, defined by the Cerebral Performance Category as favorable (1–3: recovery of consciousness) versus unfavorable (4–5: lack of recovery of consciousness). Results: We identified 60 patients (30 [50%] women; age 62 [51–72] years). Thirty-one and 29 patients had a favorable and unfavorable outcome, respectively. The presence of pupillary reflexes (24 [100%] vs. 17 [81%]; p value 0.04) and a motor subscore > 2 (22 [92%] vs. 12 [63%]; p value 0.03) at 48–72 h were associated with a favorable outcome. A highly malignant EEG pattern was observed in 7 of 29 (24%) patients with unfavorable outcome versus 0 of 31 (0%) with favorable outcome, whereas the presence of EEG reactivity was observed in 28 of 31 (90%) patients with favorable outcome versus 13 of 29 (45%) with unfavorable outcome (p < 0.001 for comparison of all background categories). Conclusions: This preliminary study suggests that highly malignant EEG patterns might be reliable prognostic markers of unfavorable outcome after HC. Other EEG findings, including lack of EEG reactivity and seizures and clinical findings appear less accurate. These findings should be replicated in a larger multicenter prospective study.
AB - Background: Hypoglycemic coma (HC) is an uncommon but severe clinical condition associated with poor neurological outcome. There is a dearth of robust neurological prognostic factors after HC. On the other hand, there is an increasing body of literature on reliable prognostic markers in the postanoxic coma, a similar—albeit not identical—situation. The objective of this study was thus to investigate the use and predictive value of these markers in HC. Methods: We conducted a retrospective, multicenter, cohort study within five centers of the Critical Care EEG Monitoring Research Consortium. We queried our electroencephalography (EEG) databases to identify all patients undergoing continuous EEG monitoring after admission to an intensive care unit with HC (defined as Glasgow Coma Scale < 8 on admission and a first blood glucose level < 50 mg/dL or not documented but in an obvious clinical context) between 01/01/2010 and 12/31/2020. We studied the association of findings at neurological examination (Glasgow Coma Scale motor subscale, pupillary light and corneal reflexes) and at continuous EEG monitoring(highly malignant patterns, reactivity, periodic discharges, seizures) with best neurological outcome within 3 months after hospital discharge, defined by the Cerebral Performance Category as favorable (1–3: recovery of consciousness) versus unfavorable (4–5: lack of recovery of consciousness). Results: We identified 60 patients (30 [50%] women; age 62 [51–72] years). Thirty-one and 29 patients had a favorable and unfavorable outcome, respectively. The presence of pupillary reflexes (24 [100%] vs. 17 [81%]; p value 0.04) and a motor subscore > 2 (22 [92%] vs. 12 [63%]; p value 0.03) at 48–72 h were associated with a favorable outcome. A highly malignant EEG pattern was observed in 7 of 29 (24%) patients with unfavorable outcome versus 0 of 31 (0%) with favorable outcome, whereas the presence of EEG reactivity was observed in 28 of 31 (90%) patients with favorable outcome versus 13 of 29 (45%) with unfavorable outcome (p < 0.001 for comparison of all background categories). Conclusions: This preliminary study suggests that highly malignant EEG patterns might be reliable prognostic markers of unfavorable outcome after HC. Other EEG findings, including lack of EEG reactivity and seizures and clinical findings appear less accurate. These findings should be replicated in a larger multicenter prospective study.
KW - Diabetic coma
KW - Electroencephalography
KW - Neurologic examination
KW - Patient outcome assessment
UR - https://www.scopus.com/pages/publications/85128361577
U2 - 10.1007/s12028-022-01495-2
DO - 10.1007/s12028-022-01495-2
M3 - Article
C2 - 35437670
AN - SCOPUS:85128361577
SN - 1541-6933
VL - 37
SP - 273
EP - 280
JO - Neurocritical Care
JF - Neurocritical Care
IS - 1
ER -