The rate of stent thrombosis at 48 hours was significantly lower in the cangrelor group than in the placebo group , and the difference was still significant in 30 days . The death rate at 48 hours was significantly reduced the cangrelor group than in the placebo group , though at 30 days, this difference was no longer significant . Somewhat counterintuitively, in the subgroup of 1659 patients who didn’t have an elevation in the troponin level at baseline, the primary end point was reduced in the cangrelor group , as compared with the placebo group . As a result, exploratory analyses had been performed in the overall study population to judge the following two composite clinical end points: death, Q-wave myocardial infarction, or stent thrombosis; and loss of life, Q-wave myocardial infarction, or ischemia-powered revascularization.Usage of an autoinjector maximized the velocity and ease of intramuscular delivery and reduced delays in initiating intravenous access. The relationships among benzodiazepine dose, respiratory depression, and subsequent dependence on endotracheal intubation are poorly characterized, but higher doses of benzodiazepines may actually reduce the amount of airway interventions. Our data are consistent with the finding that endotracheal intubation is certainly additionally a sequela of continuing seizures than it is an adverse aftereffect of sedation from benzodiazepines.11 In regards to to the mechanism of drug action, our temporal data are consistent with what will be expected: the intramuscular route delivers the medication more rapidly following the paramedics’ arrival at the scene than the intravenous route, but its onset of action is faster after intravenous administration than after intramuscular administration.