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1 ients, 71 received alteplase and 75 received tenecteplase.
2 re assigned to the alteplase group and 52 to tenecteplase.
3 s selective to t-PA and its close derivative tenecteplase.
4 7.1%, p = 0.05) when compared with full-dose tenecteplase.
5 aphic flow patterns, compared with full-dose tenecteplase.
6  therapy with eptifibatide administered with tenecteplase.
7 nogen activator, reteplase, lanoteplase, and tenecteplase.
8 ents were randomly assigned (1:1) to receive tenecteplase 0.25 mg/kg (maximum 25 mg) or alteplase 0.9
9 lase (0.9 mg per kilogram of body weight) or tenecteplase (0.1 mg per kilogram or 0.25 mg per kilogra
10                           The higher dose of tenecteplase (0.25 mg per kilogram) was superior to the
11 -combination regimen of 50% of standard-dose tenecteplase (0.27 microg/kg) plus high-dose eptifibatid
12 kg/min infusion) was compared with full-dose tenecteplase (0.53 microg/kg).
13 owever, in patients with target mismatch (33 tenecteplase, 35 alteplase), treatment with tenecteplase
14 B trial (tissue plasminogen activator versus tenecteplase), 49 centers carried out 2-year follow-up.
15 of recombinant tissue plasminogen activator (tenecteplase, 5 mg/kg) worsened APAP-induced liver injur
16 titutes of Health Stroke Scale score change: tenecteplase, 6; alteplase, 1; P<0.001) and better late
17 titutes of Health Stroke Scale score change: tenecteplase, 7; alteplase, 2; P=0.018) and less parench
18                                              Tenecteplase, a genetically engineered mutant tissue pla
19 tion (TIMI) 10, TIMI 14, and Integrillin and Tenecteplase acute MI trials.
20 reperfusion therapy in STEMI (streptokinase, tenecteplase, alteplase, and reteplase) were included.
21 imary PCI or fibrinolytic therapy with bolus tenecteplase (amended to half dose in patients >/=75 yea
22                  Of 71 patients (35 assigned tenecteplase and 36 assigned alteplase) contributing to
23 ological outcomes did not differ between the tenecteplase and alteplase groups.
24        Combination therapy with reduced-dose tenecteplase and eptifibatide leads to faster, more stab
25 t detect any significant differences between tenecteplase and placebo in the primary end point of 30-
26                                              Tenecteplase and reteplase are comparable with accelerat
27 c stroke, 1 that demonstrated superiority of tenecteplase and the other that showed no difference bet
28  STEMI and alteplase (accelerated infusion), tenecteplase, and reteplase should be considered over st
29 d between accelerated infusion of alteplase, tenecteplase, and reteplase with parenteral anticoagulan
30                        For major bleeding, a tenecteplase-based regimen tended to be associated with
31               We pooled 2 clinical trials of tenecteplase compared with alteplase for the treatment o
32 day 30, a total of 12 patients (2.4%) in the tenecteplase group and 16 patients (3.2%) in the placebo
33 eeding occurred in 32 patients (6.3%) in the tenecteplase group and 6 patients (1.2%) in the placebo
34 d day 7, a total of 6 patients (1.2%) in the tenecteplase group and 9 (1.8%) in the placebo group die
35 Stroke occurred in 12 patients (2.4%) in the tenecteplase group and was hemorrhagic in 10 patients; 1
36 occurred in 13 of 506 patients (2.6%) in the tenecteplase group as compared with 28 of 499 (5.6%) in
37 e of penumbral salvaged (68% [SD 28] for the tenecteplase group vs 68% [23] for the alteplase group;
38 nts did not differ between groups (32 in the tenecteplase group, three considered probably or definit
39 re were more intracranial hemorrhages in the tenecteplase group.
40                            Together, the two tenecteplase groups had greater reperfusion (P=0.004) an
41                  The newer thrombolytic drug tenecteplase has been investigated in one randomised tri
42         This sub-study of the Integrilin and Tenecteplase in Acute Myocardial Infarction (INTEGRITI)
43                                Evaluation of tenecteplase in larger trials of patients with acute str
44 enemia also increased thrombus resistance to tenecteplase-induced thrombolysis in vivo.
45                                              Tenecteplase may offer an improved efficacy and safety p
46  improved patient outcomes when treated with tenecteplase (modified Rankin scale score 0-1: odds rati
47 ed out-of-hospital cardiac arrest to receive tenecteplase or placebo during cardiopulmonary resuscita
48        Patients were drawn from the low-dose tenecteplase plus eptifibatide arm of the INTEGRITI stud
49 nation reperfusion therapy with reduced-dose tenecteplase plus eptifibatide on continuous ST-segment
50  randomized, double-blind trial, we compared tenecteplase plus heparin with placebo plus heparin in n
51 he dose-confirmation regimen of reduced-dose tenecteplase plus high-dose eptifibatide was associated
52 ticoagulants (RR 1.47 [95% CI 1.10-1.98] for tenecteplase plus parenteral anticoagulants plus glycopr
53 failed in clinical trials and currently only tenecteplase remains to be tested as a potential alterna
54 thin 6 h of STEMI enrolled in the Enoxaparin Tenecteplase-Tissue-Type Plasminogen Activator With or W
55 e of either alteplase (tPA) (2 to 5 mg/h) or tenecteplase (TNK) (0.5 mg/h) for a total of 8 h.
56 -TIMI 23 evaluated enoxaparin with full-dose tenecteplase (TNK) and half-dose TNK plus abciximab.
57 mbinations of eptifibatide with reduced-dose tenecteplase (TNK) in ST-elevation myocardial infarction
58 ed by the administration of the thrombolytic Tenecteplase (TNK, 1.5 mg/kg, IV bolus) in the presence
59                      We investigated whether tenecteplase-treated patients had a different 24-hour re
60                                              Tenecteplase-treated patients had greater early clinical
61                             In the Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis (A
62 e aimed to assess the efficacy and safety of tenecteplase versus alteplase within 4.5 h of stroke ons
63 omized (1:1) comparison of thrombolysis with tenecteplase versus placebo in normotensive patients wit
64 morrhage (by SITS-MOST definition, 1/52 [2%] tenecteplase vs 2/51 [4%] alteplase, p=0.55; by ECASS II
65                                              Tenecteplase was administered to 525 patients and placeb
66  tenecteplase, 35 alteplase), treatment with tenecteplase was associated with greater early clinical
67                                              Tenecteplase was associated with significantly better re
68                                         When tenecteplase was used without adjunctive antithrombotic
69 the hypotheses that reperfusion therapy with tenecteplase would be superior to alteplase in improving

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