FDA Adverse Event Death Summary report: N

UNKNOWN MECHANICAL HEART VALVE

MDR report key: 19940131 · Received August 8, 2024

Report

Report Number
2135147-2024-03867
Event Type
Death
Date Received
August 8, 2024
Date of Event
January 1, 2009
Report Date
August 8, 2024
Manufacturer
ABBOTT MEDICAL
Product Code
LWQ
PMA / PMN Number
P810002
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

B2 - DATE OF DEATH IS ESTIMATED. B3 - DATE OF EVENT IS ESTIMATED. D4 - THE UDI NUMBER IS NOT KNOWN AS THE PART AND LOT NUMBERS WERE NOT PROVIDED. LITERATURE: ARTICLE TITLE "AGE-SPECIFIC OUTCOMES OF BIOPROSTHETIC VS. MECHANICAL AORTIC VALVE REPLACEMENT: BALANCING REOPERATION RISK WITH ANTICOAGULATION BURDEN". SUMMARIZED PATIENT OUTCOMES/COMPLICATIONS OF A SINGLE CENTER STUDY THAT COMPARED THE OUTCOMES OF BIOPROSTHETIC VS. MECHANICAL AVR IN PATIENTS OLDER AND YOUNGER THAN 50 WERE REPORTED IN A RESEARCH ARTICLE "AGE-SPECIFIC OUTCOMES OF BIOPROSTHETIC VS. MECHANICAL AORTIC VALVE REPLACEMENT: BALANCING REOPERATION RISK WITH ANTICOAGULATION BURDEN" IN A SUBJECT POPULATION WITH MULTIPLE CO-MORBIDITIES INCLUDING SMOKING, RENAL IMPAIRMENT, HYPERTENSION, DIABETES, LIVER DISEASE, CHRONIC LUNG DISEASE, PRIOR MYOCARDIAL INFARCTION, PRIOR HEART FAILURE, STROKE, ATRIAL FIBRILLATION, PRIOR CARDIAC SURGERY, PRIOR PERCUTANEOUS CORONARY INTERVENTION, PRIOR TRANSCATHETER AORTIC VALVE INTERVENTION. SOME OF THE COMPLICATIONS REPORTED WERE DEATH, SURGICAL INTERVENTION (PACEMAKER), UNEXPECTED MEDICAL INTERVENTION (BLOOD TRANSFUSION), BLEEDING, ATRIAL FIBRILLATION, STROKE, RESPIRATORY FAILURE; THESE COMPLICATIONS ARE ANTICIPATED FOR THE PROCEDURE AND SUBJECT POPULATION. A MORE COMPREHENSIVE ASSESSMENT COULD NOT BE PERFORMED AS THE EVENT WAS NON-CONTEMPORANEOUSLY REPORTED THROUGH A LITERATURE REVIEW AND NO DEVICE OR INDIVIDUAL PATIENT INFORMATION WAS RECEIVED FOR ANALYSIS.

Description of Event or Problem · 0

THE ARTICLE, "AGE-SPECIFIC OUTCOMES OF BIOPROSTHETIC VS. MECHANICAL AORTIC VALVE REPLACEMENT: BALANCING REOPERATION RISK WITH ANTICOAGULATION BURDEN", WAS REVIEWED. THE ARTICLE PRESENTED A RETROSPECTIVE, SINGLE CENTER STUDY THAT COMPARED THE OUTCOMES OF BIOPROSTHETIC VS. MECHANICAL AVR IN PATIENTS OLDER AND YOUNGER THAN 50. DEVICES INCLUDED IN THE STUDY WERE ST. JUDE MECHANICAL VALVE, MEDTRONIC ATS, LIVANOVA PLC CARBOMEDICS SORIN, CRYOLIFE ON-X, EDWARDS LIFESCIENCES MAGNA, ABBOTT TRIFECTA, LIVANOVA PERCEVAL, AND MEDTRONIC HANCOCK. THE ARTICLE CONCLUDED THAT OUTCOMES OF MECHANICAL AND BIOPROSTHETIC VALVE REPLACEMENT WERE COMPARABLE IN PATIENTS OLDER THAN 50 YEARS. USING BIOPROSTHETIC VALVES IN PATIENTS YOUNGER THAN 50 YEARS WAS ASSOCIATED WITH A GREATER RATE OF VALVE REINTERVENTION, WITH NO BENEFICIAL EFFECT ON THE RISK OF BLEEDING OR STROKE. [THE PRIMARY AND CORRESPONDING AUTHOR WAS AMR ARAFAT, ADULT CARDIAC SURGERY DEPARTMENT, PRINCE SULTAN CARDIAC CENTER, RIYADH 12233, SAUDI ARABIA, WITH CORRESPONDING EMAIL: [email protected]]. THE TIME LINE OF THE STUDY WAS FROM 2009 TO 2020, WITH PHONE FOLLOW-UP IN JUNE 2021. A TOTAL OF 292 PATIENTS WERE INCLUDED IN THE STUDY, HOWEVER, THE NUMBER OF PATIENTS WHO RECEIVED AN ABBOTT DEVICE WAS NOT REPORTED. THE AVERAGE AGE FOR EACH GROUP WERE AS FOLLOWS: GROUP 1A = 64 YEARS; GROUP 2A = 58 YEARS; GROUP 1B = 38.5 YEARS; AND GROUP 2B = 31 YEARS. THE MAJORITY GENDER WAS MALE ACROSS ALL FOUR GROUPS. COMORBIDITIES INCLUDED SMOKING, RENAL IMPAIRMENT, HYPERTENSION, DIABETES, LIVER DISEASE, CHRONIC LUNG DISEASE, PRIOR MYOCARDIAL INFARCTION, PRIOR HEART FAILURE, STROKE, ATRIAL FIBRILLATION, PRIOR CARDIAC SURGERY, PRIOR PERCUTANEOUS CORONARY INTERVENTION, PRIOR TRANSCATHETER AORTIC VALVE INTERVENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2383387 UNKNOWN MECHANICAL HEART VALVE HEART-VALVE, MECHANICAL LWQ ABBOTT MEDICAL

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Death