Neoplastic and Non-Neoplastic Causes of Acute Intracerebral Hemorrhage on CT: The Diagnostic Value of Perihematomal Edema
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Neoplastic and Non-Neoplastic Causes of Acute Intracerebral Hemorrhage on CT: The Diagnostic Value of Perihematomal Edema. / Nawabi, Jawed; Hanning, Uta; Broocks, Gabriel; Schön, Gerhard; Schneider, Tanja; Fiehler, Jens; Thaler, Christian; Gellissen, Susanne.
in: CLIN NEURORADIOL, Jahrgang 30, Nr. 2, 06.2020, S. 271-278.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Neoplastic and Non-Neoplastic Causes of Acute Intracerebral Hemorrhage on CT: The Diagnostic Value of Perihematomal Edema
AU - Nawabi, Jawed
AU - Hanning, Uta
AU - Broocks, Gabriel
AU - Schön, Gerhard
AU - Schneider, Tanja
AU - Fiehler, Jens
AU - Thaler, Christian
AU - Gellissen, Susanne
PY - 2020/6
Y1 - 2020/6
N2 - OBJECTIVE: The aim of this study was to investigate the diagnostic value of perihematomal edema (PHE) volume in non-enhanced computed tomography (NECT) to discriminate neoplastic and non-neoplastic causes of acute intracerebral hemorrhage (ICH).METHODS: In this retrospective study, from 560 patients with acute ICH 91 patients fulfilled the inclusion criteria and were classified into neoplastic and non-neoplastic ICH. For each patient, ICH and total hemorrhage volume (ICH + PHE) were segmented semiautomatically. The PHE volume and relative PHE were further calculated and all parameters were compared between the different groups. Additionally, hematoma density was measured and compared between the groups.RESULTS: The PHE volume and relative PHE on NECT were significantly higher in neoplastic vs. the non-neoplastic ICH (p = 0.003 and p < 0.001, respectively). Absolute ICH volume, symptom time onset to CT and ICH localization showed no significant difference between the two groups (p > 0.1). Univariate receiver operating characteristics (ROC) analysis revealed a high diagnostic performance for relative PHE in the discrimination of neoplastic and non-neoplastic ICH with an optimal cut-off of 0.50 (area under the curve, AUC 0.81, 60.0% sensitivity, 91.8% specificity), followed by PHE (AUC 0.69) and hematoma density (AUC 0.68).CONCLUSION: Relative PHE with a cut-off of >0.50 is a specific and simple indicator for neoplastic causes of acute ICH and a potential tool for clinical implementation. This observation needs to be validated in an independent patient cohort.
AB - OBJECTIVE: The aim of this study was to investigate the diagnostic value of perihematomal edema (PHE) volume in non-enhanced computed tomography (NECT) to discriminate neoplastic and non-neoplastic causes of acute intracerebral hemorrhage (ICH).METHODS: In this retrospective study, from 560 patients with acute ICH 91 patients fulfilled the inclusion criteria and were classified into neoplastic and non-neoplastic ICH. For each patient, ICH and total hemorrhage volume (ICH + PHE) were segmented semiautomatically. The PHE volume and relative PHE were further calculated and all parameters were compared between the different groups. Additionally, hematoma density was measured and compared between the groups.RESULTS: The PHE volume and relative PHE on NECT were significantly higher in neoplastic vs. the non-neoplastic ICH (p = 0.003 and p < 0.001, respectively). Absolute ICH volume, symptom time onset to CT and ICH localization showed no significant difference between the two groups (p > 0.1). Univariate receiver operating characteristics (ROC) analysis revealed a high diagnostic performance for relative PHE in the discrimination of neoplastic and non-neoplastic ICH with an optimal cut-off of 0.50 (area under the curve, AUC 0.81, 60.0% sensitivity, 91.8% specificity), followed by PHE (AUC 0.69) and hematoma density (AUC 0.68).CONCLUSION: Relative PHE with a cut-off of >0.50 is a specific and simple indicator for neoplastic causes of acute ICH and a potential tool for clinical implementation. This observation needs to be validated in an independent patient cohort.
KW - Journal Article
U2 - 10.1007/s00062-019-00774-4
DO - 10.1007/s00062-019-00774-4
M3 - SCORING: Journal article
C2 - 30899965
VL - 30
SP - 271
EP - 278
JO - CLIN NEURORADIOL
JF - CLIN NEURORADIOL
SN - 1869-1439
IS - 2
ER -