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. 2023 Oct 31;16:17562864231207508. doi: 10.1177/17562864231207508

Table 3.

Outcome.

Outcome AM C OR (95% CI)
Primary safety endpoint
 Major bleeding event* 4 (5.0) 46 (4.9) 1.03 (0.36–2.94)
Secondary safety endpoint
 SICH_ECASS* 4 (5.1) 40 (4.3) 1.67 (0.69–4.04)
 SICH_HBC* 4 (5.1) 46 (4.9) 1.20 (0.46–3.10)
 Systemic bleeding* 0 (0) 6 (0.6) n.a.
 Mortality 25 (31.6) 153 (16.3) 2.37 (1.43–3.93)
 Prolonged length of hospital stay 8 (10.1) 33 (3.5) 3.09 (1.37–6.93)
Primary efficacy endpoint
 NI 20% or more 42 (53.2) 582 (62.1) 0.69 (0.44–1.10)
 NI 30% or more 40 (50.6) 539 (57.5) 0.76 (0.48–1.20)
Secondary efficacy endpoint
 NIHSS decrease 4 or more 30 (38.0) 375 (40.0) 0.92 (0.57–1.47)
 NIHSS decrease 8 or more 17 (21.5) 192 (20.5) 1.06 (0.61–1.86)

Data are n (%). AM: n = 79; C: n = 937. Logistic regression was performed to compare the occurrence of each endpoint in the active malignancy group with the control group. Results are presented as OR and 95% CI.

*

Stroke treatment related.

AM, active malignancy group; C, control group; CI, confidence interval; n.a., not applicable; NI, neurological improvement during hospital stay; NIHSS, National Institute of Health Stroke Scale; OR, odds ratio; SICH_ECASS, symptomatic intracranial hemorrhage according to ECASS III Classification; SICH_HBC, symptomatic intracranial hemorrhage according to Heidelberg Bleeding Classification.