It was reported that the patient experienced hypertension.An ekosonic endovascular device, 106x12cm was selected for use in a bilateral pulmonary embolism case.There was an e322 alarm on channel b of the control unit.Channel a was working, and all medications were infusing without issue.Channel b was restarted, and the issue was resolved.However, the patient was reported to be hypertensive, and it was undetermined whether the hypertension was a result of the ekos device or procedure.The remainder of ekos therapy was completed without further issue.
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