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The Combined Lysis of Thrombus in Brain Ischemia Using Transcranial Ultrasound and Systemic rt-PA (CLOTBUST) study was a phase II randomized trial which compared continuous transcranial Doppler ultrasound insonation, in subjects with ultrasound evidence of MCA occlusion being given IV rt-PA, to sham insona-tion. ° There was an increased rate of arterial recanalization with the continuous insonation (49% vs. 30%, p = 0.03) and no increased risk of sICH. [Pg.54]

A reversed bridging approach has been proposed by Keris et al. In this study, 12 patients (three ICA occlusions and nine MCA occlusions) out of the 45 enrolled (all with an NIHSS score >20) were randomized to receive an initial lA infusion of 25 mg of rt-PA over 5-10 minutes, followed by IV infusion of another 25 mg over 60 minutes, within 6 hours of stroke onset (total combined dose 50 mg with a maximum dose of 0.7 mg/kg). The remaining 33 patients were assigned to a control group and did not undergo any thrombolysis. TIMI 2 and 3 recanalization occurred in 1 of 12 and 5 of 12 of the patients, respectively. There were no symptomatic ICHs. At 12 months, 83% of the patients in the thrombolysis group were functionally independent, whereas only 33% of the control subjects had a good outcome. [Pg.69]

Corbett D, Hamilton M, Colboume F. Persistent neuroprotection with prolonged postischemic h3fpothermia in adult rats subjected to transient middle cerebral artery occlusion. Exp Neurol 2000 163 200-206. [Pg.120]

Other interferences which may occur in flame AAS are ionization of the analyte, formation of a thermally stable compound e.g., a refractory oxide or spectral overlap (very rare). Non-flame atomizers are subject to formation of refractory oxides or stable carbides, and to physical phenomena such as occlusion of the analyte in the matrix crystals. Depending on the atomizer size and shape, other phenomena such as gas phase reactions and dimerization have been reported. [Pg.105]

On the skin, g-cymene may cause erythema, dryness, and defatting. However, 4% p-cymene in petroleum did not produce irritation in 25 humans after a 48-hour closed patch test or after 10 daily applications to the same spot on the backs of subjects. Undiluted g-cymene applied to rabbit skin for 24 hours under occlusion was moderately irritating. The LDso by skin absorption is greater than 5 g/% in rabbits. [Pg.201]

Many pathological conditions, including ischemia/reperfusion, inflammation, and sepsis may induce tissues to simultaneously produce both superoxide and nitric oxide. For example, ischemia allows intracellular calcium to accumulate in endothelium (Fig. 20). If the tissue is reperfused, the readmission of oxygen will allow nitric oxide as well as superoxide to be produced (Beckman, 1990). For each 10-fold increase in the concentration of nitric oxide and superoxide, the rate of peroxynitrite formation will increase by 100-fold. Sepsis causes the induction of a second nitric oxide synthase in many tissues, which can produce a thousand times more nitric oxide than the normal levels of the constitutive enzyme (Moncada et al., 1991). Nitric oxide and indirectly peroxynitrite have been implicated in several important disease states. Blockade of nitric oxide synthesis with N-methyl or N-nitroarginine reduces glutamate-induced neuronal degeneration in primary cortical cultures (Dawson et al., 1991). Nitroarginine also decreases cortical infarct volume by 70% in mice subjected to middle cerebral artery occlusion (Nowicki et al., 1991). Myocardial injury from a combined hy-... [Pg.40]

The survey covered a period of 3 years of potential exposure, but exposure levels were not reported. No adverse dermal effects were observed on the arms or legs of subjects after a 6-day application of polymer fibers containing commercial octabromobiphenyl mixture under an occlusive covering no additional information was reported (Waritz et al. 1977). [Pg.187]

Brachial artery response to 5-minute wrist cuff occlusion and release % dilation from baseline to 60 seconds after cuff release (P=.05) significant increase in flow-mediated vasodilation of normal control subjects compared with ED over entire curve (P=.014). [Pg.506]

Following a pre-treatment phase of female subjects with soap washing on the legs, baseline visual scaling scores were determined according to the following grades in Table 17.1. In the occlusion studies Hilltop chambers with 0.3 ml of test solutions or control were attached to the skin surface... [Pg.178]

Of greater therapeutic relevance is the zone lying peripheral to the region of dense ischemia and perfused at somewhat higher CBF levels the ischemic penumbra. In baboons subjected to MCA occlusion, CBF was measured along with the extracellular potassium concentration and sensory evoked poten-... [Pg.44]

It was noted in spontaneously hypertensive rats, subjected either to permanent or transient (2-h) MCAO that vasogenic edema and gliosis, as visualized immunohistochemically, were more widespread after transient occlusion although infarctions were larger after permanent occlusion (Nordborg et al. 1994). [Pg.136]

Zhang R. L., ChoppM., Chen H., Garcia J.H., and Zhang Z. G. (1993) Postischemic (1 hour) hypothermia significantly reduces ischemic cell damage in rats subjected to 2 hours of middle cerebral artery occlusion. Stroke 24,1235-1240. [Pg.90]

Similarly, Schmid-Elsaesser et al. (7) reported a synergistic effect of hypothermia when added to therapy with either tirilizad or magnesium (Mg). In this study, rats were subjected to transient ischemia of 90 min duration using a suture occlusion model. Hypothermia was administered intraischemically and animals were rewarmed simultaneous with reperfusion. Subjects were treated with various combinations of the three agents, in a systematic fashion. A stepwise increase in the reduction in infarct volume was observed between Tirilizad + Mg, hypothermia alone, and hypothermia + tirilizad + Mg in combination. [Pg.97]

Williams et al. (1997) described renal ischemia-reperfusion injury in rats. The animals were anesthetized and subjected to 45min of bilateral renal occlusion using atraumatic vascular clamps before renal perfusion was reestablished. After various time interval (up to lweek) blood urea nitrogen, creatinine and myeloperoxidase activity in the kidney were determined. The protective effects of an intracellular adhesion molecule monoclonal antibody were tested. [Pg.124]

The Shelanski/Shelanski test employs occlusive patches in contact with the skin of the upper arm for 24 h in a similar fashion to the Draize RIPT described above. However, the patches are placed on the same test site each time with a total of 15 sets applied during induction. The test site is evaluated before application of a new patch to the site. If inflammation has developed, the patch is placed on an adjacent uninflamed site. Two to 3 weeks after the induction period, subjects are challenged by application of a patch to be remained in place for 48 h. Test sites are evaluated for erythema and edema at patch removal and the incidence of positive responses is reported. [Pg.375]

A 1-in square of Webril is saturated with liquid, or up to 0.5 g of viscous substances, and applied to the surface of the pad to be applied to the skin. The patch is applied to the upper back and sealed in place with occlusive tape. The patch is removed after 24 h, the area is evaluated and a fresh patch applied. The procedure is repeated daily for up to 21 days. Lanman et al. (1968) increased the sensitivity of the assay by increasing the number of test subjects from 10 to 24. [Pg.381]

In the hospital, ECG and laboratory tests are performed promptly to determine the subsequent treatment strategy. When car-diomyocytes die, contractile proteins (troponin) or myocardial enzymes (creatine kinase, CK-MB) are liberated and can be detected in blood for diagnostic purposes. Marked elevation of the ST segment in the ECG raises the strong suspicion of a complete occlusion of a coronary artery (ST elevation MI, STEMI). In these MI patients, reperfusion of the affected area as early and as completely as Luellmann, Color Atlas of Pharmacology All rights reserved. Usage subject to terms... [Pg.320]


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