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. Author manuscript; available in PMC: 2014 Oct 1.
Published in final edited form as: Mayo Clin Proc. 2013 Oct;88(10):10.1016/j.mayocp.2013.07.015. doi: 10.1016/j.mayocp.2013.07.015

TABLE 3.

Subgroup Analysisa

Subgroup analysis No. of
cohorts
RR 95% CI P value for difference
between the subgroupsb
Mortality
  Duration of therapy from stroke onset
    ≤6 h 4 1.07 0.75–1.50 .39
    ≥6 h 2 0.76 0.38–1.51
  Study location
    US 4 0.86 0.65–1.15 .08
    Non-US 2 1.43 0.87–2.36
  Study setting
    Multicenter 5 0.98 0.76–1.25 NA
    Monocenterc 1 NA NA

mRS score ≤1
  Duration of therapy from stroke onset
    ≤6 h 3 1.05 0.80–1.38 .56
    >6 h 2 0.73 0.23–2.36
  Study location
    US 3 1.06 0.82–1.38 .85
    Non-US 2 1.14 0.59–2.19
  Study setting
    Multicenter 5 1.02 0.84–1.23 NA
    Monocenterc 1 NA NA

mRS score ≤2
  Duration of therapy from stroke onset
    ≤6 h 3 1.06 0.83–1.35 .38
    >6 h 2 0.71 0.30–1.69
  Study location
    US 3 1.04 0.86–1.26 70
    Non-US 2 1.19 0.61–2.32
  Study setting
    Multicenter 5 1.02 0.84–1.24 NA
    Monocenterc 1 NA NA

mRS score ≤3
  Duration of therapy from stroke onset
    ≤6 h 3 1.05 0.94–1.16 26
    >6 h 2 0.78 0.48–1.28
  Study location
    US 3 1.03 0.90–1.18 .88
    Non-US 2 1.03 0.89–1.20
  Study setting
    Multicenter 5 1.03 0.93–1.14 NA
    Monocenterc 1 NA NA

sICH
  Duration of therapy from stroke onset
    ≤6 h 4 0.96 0.62–1.58 .63
    >6 h 2 1.50 0.27–8.42
  Study location
    US 3 1.06 0.59–1.92 77
    Non-US 3 0.89 0.42–1.89
  Study setting
    Multicenter 5 1.02 0.64–1.63 .55
    Monocenterc 1 0.42 0.02–7.71
a

mRS = modified Rankin scale; NA = not applicable/available; RCT = randomized controlled trial; RR = risk ratio; sICH = symptomatic intracranial hemorrhage.

b

P<.10 implies that difference between the 2 subgroups is significant, and it may explain the heterogeneity observed in the overall analysis.

c

Sen et al22; in this RCT, no patient died and authors did not report the mRS score as an outcome.