Safety Study of Post Intravenous tPA Monitoring in Ischemic Stroke (OPTIMIST)
Stroke, Ischemic Stroke
About this trial
This is an interventional health services research trial for Stroke focused on measuring IV tPA, Thrombolysis, Stroke, Ischemic, Monitoring
Eligibility Criteria
Inclusion Criteria:
- Ability to provide written informed consent (or a Legally Authorized Representative (LAR) available to provide informed consent) and comply with study assessments for the full duration of the study.
- Age 18-80 years
- Patients to be included will be diagnosed as having an acute ischemic stroke by history and physical exam and receive IV tPA within 4.5 hours of symptom onset according to current guidelines for acute stroke care.
- NIHSS at presentation <10
- Patients do not have ICU needs in the judgment of the treating ED physician or neurologist by the end of the tPA infusion
- NIHSS at the end of tPA infusion <10
Exclusion Criteria:
For patients receiving IV tPA according to the current standard of care, the following exclusion criteria apply:
- Age <17 or >80
- ICU need or indication by the end of the tPA infusion
- NIHSS >9 at presentation or at the end of the tPA infusion
- Indication/need for endovascular recanalization therapy
Sites / Locations
- The Johns Hopkins Hospital
Arms of the Study
Arm 1
Experimental
"Hopkins" post tPA monitoring protocol
Patients treated with IV tPA (intravenous tissue Plasminogen Activator) for acute stroke will be monitored in a non-ICU setting following the "Hopkins" post tPA monitoring protocol, a new schedule for vital signs and neurochecks. These patients will have vital signs and neurochecks every 15 minutes for two hours, then once upon admission to the stroke unit and after one hour, then every two hours for 8 hours and then every four hours until 24 hours post tPA.