It was reported that the patient had hypotension, myocardial stunning, and arrythmia which led to death.A 1.50mm rotapro was selected for use.During the procedure, it was noted that the patient experienced hypotension, myocardial stunning, and arrythmia which led to death.Neither the device nor the procedure caused or contributed to the patient's complication based on the physician's opinion.The procedure was not completed due to the patient death and the device was buried together with the patient.
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