TY - JOUR
T1 - Predicting hematoma expansion after primary intracerebral hemorrhage
AU - Brouwers, H. Bart
AU - Chang, Yuchiao
AU - Falcone, Guido J.
AU - Cai, Xuemei
AU - Ayres, Alison M.
AU - Battey, Thomas W.K.
AU - Vashkevich, Anastasia
AU - McNamara, Kristen A.
AU - Valant, Valerie
AU - Schwab, Kristin
AU - Orzell, Susannah C.
AU - Bresette, Linda M.
AU - Feske, Steven K.
AU - Rost, Natalia S.
AU - Romero, Javier M.
AU - Viswanathan, Anand
AU - Chou, Sherry H.Y.
AU - Greenberg, Steven M.
AU - Rosand, Jonathan
AU - Goldstein, Joshua N.
PY - 2014/2
Y1 - 2014/2
N2 - IMPORTANCE: Many clinical trials focus on restricting hematoma expansion following acute intracerebral hemorrhage (ICH), but selecting those patients at highest risk of hematoma expansion is challenging. OBJECTIVE: To develop a prediction score for hematoma expansion in patients with primary ICH. DESIGN, SETTING, AND PARTICIPANTS: Prospective cohort study at 2 urban academic medical centers among patients having primary ICH with available baseline and follow-up computed tomography for volumetric analysis (817 patients in the development cohort and 195 patients in the independent validation cohort). MAIN OUTCOMES AND MEASURES: Hematoma expansion was assessed using semiautomated software and was defined as more than 6 mL or 33% growth. Covariates were tested for association with hematoma expansion using univariate and multivariable logistic regression. A 9-point prediction score was derived based on the regression estimates and was subsequently tested in the independent validation cohort. RESULTS: Hematoma expansion occurred in 156 patients (19.1%). In multivariable analysis, predictors of expansion were as follows: warfarin sodium use, the computed tomography angiography spot sign, and shorter time to computed tomography (<6 vs >6 hours) (P <.001 for all), as well as baseline ICH volume (<30 [reference], 30-60 [P =.03], and >60 [P =.005] mL). The incidence of hematoma expansion steadily increased with higher scores. In the independent validation cohort (n = 195), our prediction score performed well and showed strong association with hematoma expansion (odds ratio, 4.59; P <.001 for a high vs low score). The C statistics for the score were 0.72 for the development cohort and 0.77 for the independent validation cohort. CONCLUSIONS AND RELEVANCE: A 9-point prediction score for hematoma expansion was developed and independently validated. The results open a path for individualized treatment and trial design in ICH aimed at patients at highest risk of hematoma expansion with maximum potential for therapeutic benefit.
AB - IMPORTANCE: Many clinical trials focus on restricting hematoma expansion following acute intracerebral hemorrhage (ICH), but selecting those patients at highest risk of hematoma expansion is challenging. OBJECTIVE: To develop a prediction score for hematoma expansion in patients with primary ICH. DESIGN, SETTING, AND PARTICIPANTS: Prospective cohort study at 2 urban academic medical centers among patients having primary ICH with available baseline and follow-up computed tomography for volumetric analysis (817 patients in the development cohort and 195 patients in the independent validation cohort). MAIN OUTCOMES AND MEASURES: Hematoma expansion was assessed using semiautomated software and was defined as more than 6 mL or 33% growth. Covariates were tested for association with hematoma expansion using univariate and multivariable logistic regression. A 9-point prediction score was derived based on the regression estimates and was subsequently tested in the independent validation cohort. RESULTS: Hematoma expansion occurred in 156 patients (19.1%). In multivariable analysis, predictors of expansion were as follows: warfarin sodium use, the computed tomography angiography spot sign, and shorter time to computed tomography (<6 vs >6 hours) (P <.001 for all), as well as baseline ICH volume (<30 [reference], 30-60 [P =.03], and >60 [P =.005] mL). The incidence of hematoma expansion steadily increased with higher scores. In the independent validation cohort (n = 195), our prediction score performed well and showed strong association with hematoma expansion (odds ratio, 4.59; P <.001 for a high vs low score). The C statistics for the score were 0.72 for the development cohort and 0.77 for the independent validation cohort. CONCLUSIONS AND RELEVANCE: A 9-point prediction score for hematoma expansion was developed and independently validated. The results open a path for individualized treatment and trial design in ICH aimed at patients at highest risk of hematoma expansion with maximum potential for therapeutic benefit.
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U2 - 10.1001/jamaneurol.2013.5433
DO - 10.1001/jamaneurol.2013.5433
M3 - Article
C2 - 24366060
AN - SCOPUS:84893873177
SN - 2168-6149
VL - 71
SP - 158
EP - 164
JO - JAMA Neurology
JF - JAMA Neurology
IS - 2
ER -