Table 3.
The impact of brain atrophy on clinical outcome.
Characteristics | Atrophy levels | No./No. (%) | P-value | OR (95%CI) | P | Adjusted OR (95%CI) | P |
---|---|---|---|---|---|---|---|
EFFICACY OUTCOME | |||||||
90-day outcome | |||||||
mRS, median (IQR) | Mild | 5 (1–6) | 0.137a | Reference | Reference | Reference | Reference |
Intermediate | 5 (2–6) | 1.23 (0.68, 2.34)c | 0.493 | 0.69 (0.34, 1.41)d | 0.311 | ||
Severe | 5 (3–6) | 1.96 (1.06, 3.65)c | 0.033 | 2.43 (1.17, 5.12)d | 0.018 | ||
mRS 0-3 | Mild | 32 (41.56) | 0.044b | Reference | Reference | Reference | Reference |
Intermediate | 29 (37.66) | 0.85 (0.44, 1.62) | 0.621 | 2.11 (0.82, 5.74) | 0.131 | ||
Severe | 18 (23.38) | 0.43 (0.21, 0.85) | 0.017 | 0.21 (0.07, 0.62) | 0.006 | ||
mRS 0-2 | Mild | 31 (40.25) | 0.045b | Reference | Reference | Reference | Reference |
Intermediate | 22 (28.57) | 0.59 (0.30, 1.16) | 0.128 | 1.13 (0.42, 3.08) | 0.814 | ||
Severe | 17 (22.08) | 0.42 (0.20, 0.84) | 0.016 | 0.18 (0.05, 0.58) | 0.006 | ||
mRS 0-1 | Mild | 26 (33.77) | 0.066b | Reference | Reference | Reference | Reference |
Intermediate | 17 (22.08) | 0.56 (0.27, 1.13) | 0.108 | 0.93 (0.32, 2.70) | 0.890 | ||
Severe | 14 (18.18) | 0.44 (0.20, 0.91) | 0.029 | 0.22 (0.06, 0.69) | 0.014 | ||
NIHSS SCORE | |||||||
Change from baseline at | Mild | 0.00 (−4.00–2.00) | 0.455a | Reference | Reference | Reference | Reference |
24 h, median (IQR) | Intermediate | 0.00 (−4.00, 2.00) | 1.78 (−1.44 to 5.00)e | 0.278 | 0.39 (−2.71 to 3.49)e | 0.805 | |
Severe | 0.00 (2.00, 2.00) | 2.48 (−0.74 to 5.70)e | 0.131 | 1.54 (−1.68 to 4.77)f | 0.346 | ||
Change from baseline at | Mild | −4.0 (−14.00, 2.00) | 0.285a | Reference | Reference | Reference | Reference |
5–7 d, median (IQR) | Intermediate | −2.00 (−15.00, 2.00) | 1.69 (−2.44 to 5.81)f | 0.421 | −0.87 (−4.56 to 2.82)f | 0.642 | |
Severe | 0.00 (−9.00, 4.00) | 3.78 (−0.35 to 7.90)f | 0.072 | 2.02 (−1.82 to 5.86)f | 0.300 | ||
ENIg | Mild | 14 (18.18) | 0.916b | Reference | Reference | Reference | Reference |
Intermediate | 13 (16.88) | 0.91 (0.39, 2.11) | 0.832 | 2.50 (0.77, 8.94) | 0.139 | ||
Severe | 15 (19.48) | 1.09 (0.48, 2.46) | 0.837 | 1.99 (0.65, 6.51) | 0.227 | ||
SAFETY OUTCOMES | |||||||
Mortality in hospital | Mild | 15 (19.48) | 0.770b | Reference | Reference | Reference | Reference |
Intermediate | 15 (19.48) | 1.00 (0.45, 2.23) | 1.000 | 0.90 (0.35, 2.34) | 0.832 | ||
Severe | 12 (15.58) | 0.76 (0.33,1.76) | 0.526 | 0.69 (0.22, 2.07) | 0.511 | ||
Mortality at 90 d | Mild | 29 (37.66) | 0.502b | Reference | Reference | Reference | Reference |
Intermediate | 34 (44.16) | 1.18 (0.62, 2.25) | 0.621 | 0.59 (0.22, 1.52) | 0.285 | ||
Severe | 36 (46.75) | 1.45 (0.77, 2.78) | 0.254 | 1.26 (0.47, 3.36) | 0.636 | ||
SICH | Mild | 4 (5.19) | 0.768b | Reference | Reference | Reference | Reference |
Intermediate | 3 (3.90) | 0.74 (0.14, 3.47) | 0.700 | 0.86 (0.13, 5.57) | 0.870 | ||
Severe | 5 (6.49) | 1.27 (0.32, 5.30) | 0.732 | 0.47 (0.08, 2.83) | 0.404 |
Wilcoxon test.
Chi-square test.
Common odds ratio.
Adjusted common odds ratio; adjusted estimates of outcome were calculated using multiple regression, taking the following variables into account: age, sex, dyslipidemia, atrial fibrillation, baseline NIHSS score, baseline PC-ASPECTS, mTICI, PC-CS, and onset to recanalization time.
β-values were estimated from a univariate linear regression model.
β-values were estimated from a multivariable linear regression model; adjusted estimates of outcome were calculated using multiple regression, taking the following variables into account: age, sex, dyslipidemia, atrial fibrillation, baseline NIHSS score, baseline PC-ASPECTS, mTICI, PC-CS, and onset to recanalization time.
ENI: early neurological improvement was estimated by a reduction of > 8 or return to 0 on NIHSS compared with baseline score at 24 h after EVT.
EVT, endovascular treatment; NIHSS, National Institutes of Health Stroke Scale; mRS, modified Rankin Scale score at 90 days.