Skip to main content
. 2021 Apr 12;14:17562864211007715. doi: 10.1177/17562864211007715

Table 2.

Outcome measures of patients undergoing thrombectomy with DA first-line versus SR first-line.

Outcome variable DA first-line SR first-line Unadjusted model
Adjusted model 1a
Adjusted model 2b
Effect size (95% CI) p-Value Effect size (95% CI) p-Value Effect size (95% CI) p-Value
Primary outcome
 Successful recanalization after first-device alonef 31/102 (30.4) 746/1123 (66.4) 0.22 (0.14–0.34)c <0.01 0.23 (0.15–0.37)c <0.01 0.24 (0.15–0.37)c <0.01
Secondary outcomes
 Complete recanalization after first-device aloneg 25/102 (24.5) 582/1123 (51.8) 0.30 (0.19–0.48)c <0.01 0.33 (0.20–0.53)c <0.01 0.31 (0.19–0.51)c <0.01
 Successful recanalization after first-passf 29/102 (28.4) 404/1123 (36.0) 0.71 (0.45–1.11)c 0.13 0.82 (0.52–1.29)c 0.39 0.83 (0.52–1.31)c 0.42
 Complete recanalization after first-passg 24/102 (23.5) 325/1123 (28.9) 0.76 (0.47–1.22)c 0.25 0.84 (0.51–1.37)c 0.48 0.83 (0.51–1.37)c 0.47
 Number of passes, median (IQR) 2 (1–4) 1 (1–2) 0.94 (0.68–1.20)d <0.01 0.79 (0.53–1.05)d <0.01 0.74 (0.48–1.01)d <0.01
 Use of rescue treatment 64/102 (62.8) 303/1123 (27.0) 4.56 (3.00–6.95)c <0.01 4.55 (2.92–7.08)c <0.01 4.51 (2.90–7.02)c <0.01
  Switching to other thrombectomy devices 58/102 (56.9) 45/1123 (4.0) 31.58 (19.30–51.67)c <0.01 27.67 (16.28–47.01)c <0.01 25.41 (15.18–42.53)c <0.01
  Intra-arterial thrombolysis 2/102 (2.0) 20/1123 (1.8) 1.10 (0.25–4.79)c 0.90 0.95 (0.21–4.37)c 0.95 1.15 (0.25–5.30)c 0.86
  Balloon angioplasty 12/102 (11.8) 167/1123 (14.9) 0.76 (0.41–1.43)c 0.40 0.81 (0.42–1.55)c 0.53 0.88 (0.46–1.68)c 0.70
  Stenting 11/102 (10.8) 158/1123 (14.1) 0.74 (0.39–1.41)c 0.36 0.79 (0.40–1.54)c 0.48 0.81 (0.41–1.58)c 0.54
 Successful recanalization after all proceduresf 86/102 (84.3) 1014/1123 (90.3) 0.58 (0.33–1.02)c 0.06 0.67 (0.37–1.21)c 0.18 0.74 (0.40–1.35)c 0.33
 Complete recanalization after all proceduresg 70/102 (68.6) 777/1123 (69.2) 0.97 (0.63–1.51)c 0.91 1.07 (0.68–1.68)c 0.77 1.02 (0.65–1.61)c 0.92
 Procedure duration, median (IQR), min 84 (50–150) 80 (50–123) 6.81 (−5.30 to 18.91)d 0.27 4.39 (−8.02 to 16.81)d 0.49 4.30 (−8.32 to 16.91)d 0.50
 mRS at 90 d, median (IQR) 3 (0–5) 3 (0–5) 0.94 (0.65–1.36)e 0.73 1.03 (0.70–1.50)e 0.90 0.99 (0.67–1.44)e 0.94
 mRS 0–1 at 90 d 37/95 (39.0) 423/1072 (39.5) 0.98 (0.64–1.51)c 0.92 1.11 (0.71–1.73)c 0.65 1.02 (0.66–1.59)c 0.93
 mRS 0–2 at 90 d 40/95 (42.1) 467/1072 (43.6) 0.94 (0.62–1.44)c 0.78 1.03 (0.67–1.60)c 0.88 0.96 (0.62–1.49)c 0.86
 mRS 0–3 at 90 d 46/95 (48.4) 583/1072 (54.4) 0.79 (0.52–1.20)c 0.26 0.85 (0.55–1.31)c 0.45 0.81 (0.53–1.25)c 0.34
Safety outcomes
 Intra-procedural embolization 6/102 (5.9) 61/1123 (5.4) 1.09 (0.46–2.58)c 0.85 0.79 (0.32–1.94)c 0.61 0.68 (0.27–1.73)c 0.42
 Any ICH within 24 h 34/96 (35.4) 237/1074 (22.1) 1.94 (1.24–3.01)c <0.01 1.78 (1.12–2.83)c 0.02 1.69 (1.06–2.69)c 0.03
 Symptomatic ICH within 24 hh 13/96 (13.54) 76/1068 (7.1) 2.05 (1.09–3.84)c 0.03 1.65 (0.84–3.26)c 0.15 1.51 (0.77–2.96)c 0.23
 Death within 90 d 15/95 (15.8) 181/1072 (16.9) 0.92 (0.52–1.64)c 0.78 0.82 (0.45–1.51)c 0.53 0.82 (0.45–1.48)c 0.51

Data are shown as the event number/total number (%), unless otherwise indicated.

a

Adjusted for the baseline variables with a significant difference of p < 0.05 between both groups, including occlusion site, tandem lesions, TOAST subtype, intravenous thrombolysis.

b

Adjusted for the propensity score.

c

The OR values were calculated using a binary logistic regression model.

d

The β-coefficients were calculated using a generalized linear model.

e

The common OR values were calculated using an ordinal logistic regression model and indicated the odds of improvement of 1 point on the mRS at 90 days.

f

Defined as mTICI of 2b-3.

g

Defined as mTICI of 3.

h

According to the Heidelberg Bleeding Classification.

CI, confidence interval; DA, direct aspiration; ICH, intracranial hemorrhage; IQR, interquartile range; mRS, modified Rankin Scale; mTICI, modified Thrombolysis in Cerebral Infarction; OR, odds ratio; SR, stent retriever; TOAST, Trial of ORG 10172 in Acute Stroke Treatment.