Related manufacturer reference number: 2017865-2020-04331.Related manufacturer reference number: 2017865-2020-04332.Related manufacturer reference number: 2017865-2020-04337.It was reported that the patient presented in the hospital with pericarditis.The physician noted that the implantable cardioverter defibrillator, right atrial lead, right ventricular lead, or left ventricular lead could have contributed to the infection.An echocardiogram was performed on (b)(6) 2020 and revealed that the patient had developed cardiac tamponade.An emergent pericardiocentesis was performed on (b)(6) 2020, as well as a right ventricular lead revision.The patient continued to decline after procedure, experienced cardiogenic shock, and deceased on (b)(6) 2020.
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