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. 2016 Apr 14;5:1–6. doi: 10.1016/j.ensci.2016.04.002

Table 5.

Summary comparing data of five clinical trials and a cohort in Joinville/Brazil (JOINVASC IA).

Study
N
IAT/IVT
NIHSS range
IV rt-PA TICI
2B/3
LSN to
groin
(mdn)
mRS 0–2 at 90 days
sICH
Device complications Mortality
IVT IAT IVT IAT IVT IAT IVT IAT
MR CLEAN
500
233/267
18
(14–21)
17
(14–22)
90% 59% 200 29% 53% 2.7% 3.6% Embol. 13 22% 21%
EXTENDED IA
70
35/35
17
(12–20)
16
(13–20)
76% 72% 200 29% 53% 2.7% 3.6% Perf.1 19% 10%
ESCAPE
315
165/150
13
(9–19)
17
(13–20)
100% 86% 210 40% 71% 6% 0% Perf.1
Embol.2
20% 9%
SWIFT PRIME
196
98/98
17
(13–19)
17
(13–20)
98% 88% 224 36% 60% 3% 0% SAH 4 12% 9%
REVASCAT
206
103/103
17
(12–19)
17
(14–20)
73% 66% 269 28% 44% 1.9% 1.9% Perf.5
Embol.5
16% 18%
JOINVASC IA
113
31/82
16
(14–21)
19
(17–24)
81% 71% 217 37% 55% 12% 10% Perf.1 39% 26%

NIHSS indicates baseline National Institute of Neurological Disorders and Stroke Scale; rt-PA: recombinant tissue-type plasminogen activator; TICI 2b/3: patients in IAT group achieving thrombolysis in cerebral infarction grade 2b or 3 reperfusion according to Thrombolysis in Cerebral Infarction Score. LSN: last time seen normal to groin puncture; mRS: functional independence at modified Rankin scale; sICH: symptomatic intracerebral hemorrhage after IVT or IAT; Embol. Catheter embolization; Perf. Vessel perforation.