美国国立卫生研究院脑出血卒中量表的验证

IF 2.1 Q3 CLINICAL NEUROLOGY Stroke (Hoboken, N.J.) Pub Date : 2023-07-01 DOI:10.1161/svin.123.000834
Wendy Dusenbury, G. Tsivgoulis, Jason J. Chang, N. Goyal, Victoria Swatzell, A. Alexandrov, P. Lyden, A. Alexandrov
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引用次数: 1

摘要

我们试图确定美国国立卫生研究院卒中量表(NIHSS)是否比格拉斯哥昏迷量表(GCS)具有更大的判别力,以识别早期功能不良和血肿体积大的患者。我们前瞻性地收集了连续脑出血患者的临床评估、影像学和结果数据,并使用受试者操作特征分析、C‐统计量和DeLong检验确定了GCS和NIHSS预测不良功能结果(改良Rankin量表3-6)和血肿体积>30 cm 3的能力。我们研究了672名脑出血患者(平均年龄62±14岁;56%为男性;脑出血中位得分=1,四分位数间距(IQR)0-2;中位脑出血量7 cm 3,IQR 2–19),中位NIHSS为8(IQR 3–18),GCS为15(IQR 7–15)。NIHSS与GCS密切相关(r=−0.773;P<0.001)。入院NIHSS(C统计:0.91;95%CI,0.89–0.93)比GCS(0.78;95%CI,0.75–0.81)更好地预测出院不良功能结果(DeLong检验P<0.001在识别早期功能不良和血肿体积大的风险患者方面,GCS具有比GCS更大的辨别力。
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Validation of the National Institutes of Health Stroke Scale in Intracerebral Hemorrhage
We sought to determine if the National Institutes of Health Stroke Scale (NIHSS) has a greater discriminative power than Glasgow coma scale (GCS) to identify patients at risk of poor early functional outcomes and large hematoma volumes. We prospectively collected clinical assessments, imaging, and outcome data in consecutive patients with intracerebral hemorrhage, and determined the ability of GCS and NIHSS to predict poor functional outcome (modified Rankin scale 3–6) and hematoma volume >30 cm 3 using receiver operating characteristics analysis, C‐statistics, and the DeLong test. We studied 672 patients with intracerebral hemorrhage (mean age 62±14 years; 56% men; median intracerebral hemorrhage score=1, interquartile range (IQR) 0–2; median intracerebral hemorrhage volume 7 cm 3 , IQR 2–19) with median NIHSS of 8 (IQR 3–18) and GCS 15 (IQR 7–15). NIHSS correlated strongly to GCS (r=−0.773; P <0.001). Admission NIHSS (C‐statistic: 0.91; 95% CI, 0.89–0.93) predicted better than GCS (0.78; 95% CI, 0.75–0.81) discharge poor functional outcome (DeLong test P <0.001). NIHSS (0.82; 95% CI, 0.78–0.86) also discriminated better than GCS (0.78; 95% CI, 0.73–0.83) patients with large hematoma volume (DeLong test P =0.029). The NIHSS has a greater discriminative power than GCS to identify patients at risk of poor early functional outcomes and large hematoma volumes.
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