From the Division of Neurocritical Care, Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD (A.M.G., P.A.N.).
Division of Brain Injury Outcomes (BIOS), Johns Hopkins University School of Medicine, Baltimore, MD (P.A.N., D.F.H.).
Stroke. 2020 Jan;51(1):129-136. doi: 10.1161/STROKEAHA.119.027085. Epub 2019 Nov 20.
Background and Purpose- Patients with active malignancy are at risk for intracerebral hemorrhage (ICH). We aimed to characterize perihematomal edema (PHE) and hematoma volumes after spontaneous nontraumatic ICH in patients with cancer without central nervous system involvement. Methods- Patients with active malignancy who developed ICH were retrospectively identified through automated searches of institutional databases. Control patients were identified with ICH and without active cancer. Demographic and cancer-specific data were obtained by chart review. Hematoma and PHE volumes were determined using semiautomated methodology. Univariate and multivariate linear regression models were created to assess which variables were associated with hematoma and PHE expansion. Results- Patients with cancer (N=80) and controls (N=136) had similar demographics (all >0.20), although hypertension was more prevalent among controls (=0.004). Most patients with cancer had received recent chemotherapy (n=45, 56%) and had recurrence of malignancy (n=43, 54%). Patients with cancer were thrombocytopenic (median platelet count 90 000 [interquartile range, 17 500-211 500]), and most had undergone blood product transfusion (n=41, 51%), predominantly platelets (n=38, 48%). Thirty-day mortality was 36% (n=29). Patients with cancer had significantly increased PHE volumes (23.67 versus 8.61 mL; =1.88×10) and PHE-to-ICH volume ratios (2.26 versus 0.99; =2.20×10). In multivariate analyses, variables associated with PHE growth among patients with cancer were ICH volume (β=1.29 [95% CI, 1.58-1.30] =1.30×10) and platelet transfusion (β=15.67 [95% CI, 3.61-27.74] =0.014). Variables associated with 30-day mortality were ICH volume (odds ratio, 1.06 [95% CI, 1.03-1.10] =6.76×10), PHE volume (odds ratio, 1.07 [95% CI, 1.04-1.09] =7.40×10), PHE growth (odds ratio, 1.05 [95% CI, 1.01-1.10] =0.01), and platelet transfusion (odds ratio, 1.48 [95% CI, 1.22-1.79] =0.0001). Conclusions- Patients with active cancer who develop ICH have increased PHE volumes. PHE growth was independent of thrombocytopenia but associated with blood product transfusion. Thirty-day mortality was associated with PHE and ICH volumes and blood product transfusion.
背景与目的- 患有活动性恶性肿瘤的患者有发生颅内出血(ICH)的风险。我们旨在描述无中枢神经系统受累的癌症患者自发性非外伤性 ICH 后血肿周围水肿(PHE)和血肿体积的特征。
方法- 通过对机构数据库的自动搜索,回顾性确定患有活动性恶性肿瘤且发生 ICH 的患者。对照患者通过 ICH 且无活动性癌症确定。通过病历回顾获得人口统计学和癌症特异性数据。使用半自动方法确定血肿和 PHE 体积。创建单变量和多变量线性回归模型,以评估哪些变量与血肿和 PHE 扩张相关。
结果- 癌症患者(N=80)和对照组(N=136)的人口统计学特征相似(均>0.20),尽管高血压在对照组中更为常见(=0.004)。大多数癌症患者最近接受过化疗(n=45,56%),且癌症复发(n=43,54%)。癌症患者血小板减少症(中位数血小板计数 90,000[四分位距,17,500-211,500]),大多数患者接受过血液制品输血(n=41,51%),主要是血小板(n=38,48%)。30 天死亡率为 36%(n=29)。癌症患者的 PHE 体积明显增加(23.67 与 8.61 mL;=1.88×10)和 PHE 与 ICH 体积比(2.26 与 0.99;=2.20×10)。在多变量分析中,与癌症患者 PHE 增长相关的变量是 ICH 体积(β=1.29[95%置信区间,1.58-1.30];=1.30×10)和血小板输血(β=15.67[95%置信区间,3.61-27.74];=0.014)。与 30 天死亡率相关的变量是 ICH 体积(比值比,1.06[95%置信区间,1.03-1.10];=6.76×10)、PHE 体积(比值比,1.07[95%置信区间,1.04-1.09];=7.40×10)、PHE 增长(比值比,1.05[95%置信区间,1.01-1.10];=0.01)和血小板输血(比值比,1.48[95%置信区间,1.22-1.79];=0.0001)。
结论- 发生 ICH 的活动性癌症患者的 PHE 体积增加。PHE 增长独立于血小板减少症,但与血液制品输血相关。30 天死亡率与 PHE 和 ICH 体积以及血液制品输血相关。