RESOLUTE INTEGRITY RX
Report
- Report Number
- 9612164-2015-01207
- Event Type
- Death
- Date Received
- July 6, 2015
- Date of Event
- December 7, 2013
- Report Date
- October 6, 2015
- Manufacturer
- MEDTRONIC IRELAND
- Product Code
- NIQ
- PMA / PMN Number
- P110013
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
CEC HAS ADJUDICATED THE PREVIOUSLY REPORTED DEATH WAS NOT RELATED TO THE STUDY DEVICE.
THE PATIENT HAD A HISTORY OF HYPERTENSION, HYPERLIPIDEMIA, DIABETES AND PREVIOUS PCI. INDEX PROCEDURE WAS PROMPTED BY STABLE ANGINA. DURING THE INDEX PROCEDURE THE 3 RSINT STENTS WERE IMPLANTED IN THE FOLLOWING VESSELS, 2 IN THE CX AND THE 3RD IN THE 2ND OM. DURING A STAGED PROCEDURE APPROX. 1 MONTH LATER ANOTHER 4 RESOLUTE INTEGRITY DRUG-ELUTING STENTS WERE IMPLANTED IN THE RCA. IT WAS ASSESSED THAT THE STROKE AND CARDIAC DEATH WERE NOT RELATED TO THE STUDY STENTS.
EVALUATION CODES, RESULTS:INHERENT RISK OF PROCEDURE ¿ (CVA/STROKE,DEATH) EVALUATION CODES, CONCLUSIONS: INHERENT RISK OF PROCEDURE ¿ (CVA/STROKE,DEATH) (B)(4).
THREE RESOLUTE INTEGRITY DRUG-ELUTING STENTS WERE IMPLANTED; ONE IN THE 2ND DIAGONAL, LCX AND 2ND OM DURING THE INDEX PROCEDURE. APPROXIMATELY 4 DAYS POST INDEX PROCEDURE PATIENT SUFFERED CEREBROVASCULAR DISORDER PATIENT WAS HOSPITALISED FOR TREATMENT. APPROXIMATELY 3 MONTHS POST INDEX PROCEDURE PATIENT EXPIRED. CAUSE OF DEATH WAS CARDIAC DEATH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 436644 | RESOLUTE INTEGRITY RX | STENT, CORONARY, DRUG-ELUTING | NIQ | MEDTRONIC IRELAND |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00076 YR | Death| H |