人工智能联合脑梗死体积预测醒后卒中患者预后不良的价值

Value of artificial intelligence combined with cerebral infarct volume in predicting poor prognosis in wake-up stroke patients

  • 摘要:
    目的 探讨人工智能Alberta卒中项目早期CT评分(ASPECTS)联合弥散加权成像(DWI)脑梗死体积预测醒后卒中(WUS)患者预后不良的价值。
    方法 选取2022年9月—2023年6月开封市中心医院收治的100例未知时间窗醒后急性缺血性卒中患者为研究对象,均行急诊头颅非对比增强CT与磁共振成像(MRI)扫描,后续接受再灌注治疗。治疗后随访3个月,依据改良Rankin量表(mRS)评分将患者分为预后良好组(mRS≤2分)和预后不良组(mRS>2分),比较2组基线资料、ASPECTS及DWI脑梗死体积。采用多因素Logistic回归分析筛选影响预后的因素,通过受试者工作特征(ROC)曲线评估人工智能ASPECTS联合DWI脑梗死体积的诊断效能。
    结果 随访3个月后,患者预后不良率为32.00%(32/100)。预后不良组入院时人工智能ASPECTS低于预后良好组, DWI脑梗死体积大于预后良好组,差异有统计学意义(P < 0.05)。多因素Logistic分析结果显示,年龄(OR=2.190, 95%CI: 1.412~3.398)、血压变异(OR=1.726, 95%CI: 1.192~2.500)、入院时同型半胱氨酸水平(OR=1.902, 95%CI: 1.268~2.854)、入院时D-二聚体水平(OR=2.275, 95%CI: 1.274~4.064)、入院时白细胞计数(OR=2.614, 95%CI: 1.484~4.606)、入院时中性粒细胞与淋巴细胞比值(OR=2.921, 95%CI: 1.350~6.323)、入院时美国国立卫生研究院卒中量表评分(OR=3.171, 95%CI: 1.754~5.731)及入院时DWI脑梗死体积(OR=3.586, 95%CI: 1.634~7.869)为预后不良的影响因素,人工智能ASPECTS高为保护因素(OR=0.534, 95%CI: 0.352~0.810, P < 0.05)。联合预测模型的灵敏度、特异度、曲线下面积分别为96.88%、85.29%、0.947, 其中灵敏度与AUC均高于单独预测(P < 0.05), 特异度与单独预测相当。
    结论 人工智能ASPECTS与DWI脑梗死体积联合应用可显著提升WUS患者预后不良的预测效能,为临床决策提供更精准的预后评估工具,具有指导个性化治疗的价值。

     

    Abstract:
    Objective To investigate the predictive value of artificial intelligence-based Alberta Stroke Program Early CT Score (ASPECTS) combined with diffusion-weighted imaging (DWI) cerebral infarct volume for poor prognosis in wake-up stroke (WUS) patients.
    Methods A total of 100 patients with acute ischemic stroke after waking up with unknown time window admitted to Kaifeng Central Hospital from September 2022 to June 2023 were selected as the research objects. All patients underwent emergency non-contrast-enhanced cranial CT and magnetic resonance imaging (MRI) scan, followed by reperfusion therapy. The patients were followed up for 3 months after treatment, and were divided into good prognosismodified Rankin Scale(mRS) ≤ 2 and poor prognosis groups mRS >2 according to the mRS score. The baseline data, artificial intelligence ASPECTS, and DWI cerebral infarct volumes were compared between the two groups. Multivariate logistic regression analysis was used to identify prognostic factors, and receiver operating characteristic (ROC) curves were employed to evaluate the diagnostic efficacy of artificial intelligence ASPECTS combined with DWI cerebral infarct volume.
    Results After 3 months of follow-up, the poor prognosis rate of patients was 32.00% (32/100). The artificial intelligence ASPECTS at admission in the poor prognosis group was lower than that in the good prognosis group, and the DWI cerebral infarction volume at admission was larger than that in the good prognosis group, with statistically significant differences (P < 0.05). The results of multivariate logistics analysis showed that age (OR=2.190; 95%CI, 1.412 to 3.398), blood pressure variability (OR=1.726; 95%CI, 1.192 to 2.500), homocysteine (OR=1.902; 95%CI, 1.268 to 2.854), D-dimer (OR=2.275; 95%CI, 1.274 to 4.064), white blood cell count (OR=2.614; 95%CI, 1.484 to 4.606), neutrophil-to-lymphocyte ratio (OR=2.921; 95%CI, 1.350 to 6.323), National Institutes of Health Stroke Scale score (OR=3.171; 95%CI, 1.754 to 5.731), and DWI infarct volume (OR=3.586; 95%CI, 1.634 to 7.869) were identified as factors affecting poor prognosis (P < 0.05), while high artificial intelligence ASPECTS was identified as a protective factor (OR=0.534; 95%CI, 0.352 to 0.810; P < 0.05). The sensitivity, specificity and area under the curve of the combined prediction model were 96.88%, 85.29% and 0.947, respectively. The sensitivity and AUC of the combined prediction model were higher than that of the single prediction (P < 0.05), and the specificity was similar to that of the single prediction.
    Conclusion The combined application of artificial intelligence ASPECTS and DWI infarct volume significantly enhances predictive efficacy for poor prognosis in WUS patients, providing a more accurate prognostic evaluation tool for clinical decision-making, and it has the value of guiding personalized treatment.

     

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