Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 5 of 5 for “"alteplase"”.
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Mean Arterial Pressure in Acute Ischemic Stroke Study
… Today, 25 years after the FDA’s approval of alteplase, practitioners continue to use BP parameters of 185/110 and 180/105 to guide the initiation of alteplase bolus and infusion, although the shift to the use of NIBP devices challenges the validity of these dated parameters. Theoretically, by …
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Perfil sociodemográfico e avaliação de escores preditores de risco de sangramento intracraniano em pacientes com acidente vascular cerebral isquêmico submetidos à trombólise endovenosa em hospital do nordeste brasileiro
… realizada através da trombólise endovenosa com alteplase, o que demonstrou aumentar as chances de bom desfecho neurológico. Apesar da eficácia, os eventos adversos mais temidos desta modalidade terapêutica são as hemorragias intracranianas sintomáticas, cujo risco pode variar entre 2% e 7%. …
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Saving the Brain Matter(s): Improving Stroke Outcomes Utilizing a Direct to CT Workflow
… ischemic stroke patients eligible for potential alteplase treatment was increase from one nurse to two nurses until the decision to use or not use alteplase was made. After the interdisciplinary team developed the workflow over 140 healthcare professionals from multiple departments were educated …
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Improving Stroke Documentation on a Stroke Unit
… which were patients who either received alteplase (TPA= 19); did not receive alteplase (NTPA= 34); had Intracerebral Hemorrhagic Stroke (ICH= 30); or were suspected of stroke/ Transient Ischemic Attack (TIA= 15). Next, stroke chart audits were done to determine whether or not the nursing …
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The role and essence of pilot trials and subgroup analysis in cardiovascular research: the IMPI trial experience
… 1 results showed that at 50mg, intrapericardial alteplase was safe in facilitating complete pericardiocentesis, while phase two showed that it was feasible to recruit, randomised and follow up patients in line with the study protocol. However, we identified participant retention as a considerable …