FDA Adverse Event Death Summary report: N

CONFORMABLE GORE® TAG® THORACIC ENDOPROSTHESIS

MDR report key: 6983596 · Received October 27, 2017

Report

Report Number
2017233-2017-00558
Event Type
Death
Date Received
October 27, 2017
Date of Event
April 19, 2017
Report Date
December 7, 2017
Manufacturer
W.L. GORE & ASSOCIATES
Product Code
MIH
PMA / PMN Number
P040043
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

IN LITERATURE THE FOLLOWING INFORMATION WAS OBTAINED: (B)(6) JOURNAL VOL. 26. PAGE 51(APR 19, 2017). FROZEN ELEPHANT TRUNK TECHNIQUE REPORT OF CONFORMABLE GORE TAG THORACIC ENDOPROSTHESIS ON ASCENDING ARCH REPLACEMENT KAJIYAMA T, SATO N, MATSUE H, ISHIDA M, KO Y, MATSUDA A. FIFTEEN (15) PATIENTS WHO HAD BEEN IMPLANTED WITH CONFORMABLE GORE TAG THORACIC ENDOPROSTHESIS WITH FROZEN ELEPHANT TRUNK TECHNIQUE (TAR-FET) AND 13 PATIENTS WHO HAD BEEN IMPLANTED WITH ARTIFICIAL BLOOD VESSEL BY OPEN CHEST SURGERY (TAR-ET). THE PATIENT BACKGROUND AS FOLLOWS. MEAN AGE: TAR-FET 70.3+-13.3 TAR-ET 66.2+-17.7, THE RESULT IS AS FOLLOWS. OPERATION TIME: TAR-FET 533.5+-1.2 TAR-ET 502.8+-75.0 CPB TIME: TAR-FET 209.4+-57.1 MIN TAR-ET 284.2+-64.9 P<0.0016, BLOOD TRANSFUSION VOLUME: TAR-FET 1266.7+-474.4ML TAR-ET 2929.2+-1013.5 P<0.0001, INTUBATION TIME: TAR-FET 69.9+-62.6 HR TAR-ET 79.1+-47.6, ICU TIME: TAR-FET 8.3+-9.7 DAY TAR-ET 8.7+-9.7. REGARDING THE HEALTH HAZARD, 2 PATIENTS OF TAR-FET DIED DURING PROCEDURE AND 1 PATIENTS OF TAR-FET SUFFERED PARAPARESIS THOUGH, THE AUTHOR REPORTED THAT TAR-FET WAS CONSIDERED MORE BENEFICIAL THAN TAR-ET SINCE TAR-FET WAS LESS INVASIVE THERAPIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
763744 CONFORMABLE GORE® TAG® THORACIC ENDOPROSTHESIS SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH W.L. GORE & ASSOCIATES

Patients

Seq Age Sex Outcome Treatment
1 Death