FDA Adverse Event Death Summary report: N

REBAR

MDR report key: 12436030 · Received September 7, 2021

Report

Report Number
2029214-2021-01117
Event Type
Death
Date Received
September 7, 2021
Date of Event
September 1, 2017
Report Date
September 7, 2021
Manufacturer
MICRO THERAPEUTICS, INC. DBA EV3
Product Code
KRA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TU
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

BILGIN, C., DURMUS, Y., HAKI, C. ET AL. DIRECT ASPIRATION THROMBECTOMY EXPERIENCE WITH THE SOFIA 6F CATHETER IN ACUTE ISCHEMIC STROKE. JPN J RADIOL 39, 605¿610 (2021). DOI.ORG/10.1007/S11604-021-01090-Z. AGE OR DATE OF BIRTH: THIS VALUE IS THE AVERAGE AGE OF THE PATIENTS REPORTED IN THE ARTICLE AS SPECIFIC PATIENTS COULD NOT BE IDENTIFIED. SEX: THIS VALUE REFLECTS THE GENDER OF THE MAJORITY OF THE PATIENTS REPORTED IN THE ARTICLE AS SPECIFIC PATIENTS COULD NOT BE IDENTIFIED. DATE OF EVENT: PLEASE NOTE THAT THIS DATE IS BASED OFF OF THE DATE OF PUBLICATION OF THE ARTICLE [OR THE DATE THAT THE ARTICLE WAS ACCEPTED FOR PUBLICATION] AS THE EVENT DATES WERE NOT PROVIDED IN THE PUBLISHED LITERATURE. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

BILGIN, C., DURMUS, Y., HAKI, C. ET AL. DIRECT ASPIRATION THROMBECTOMY EXPERIENCE WITH THE SOFIA 6F CATHETER IN ACUTE ISCHEMIC STROKE. JPN J RADIOL 39, 605¿610 (2021). DOI.ORG/10.1007/S11604-021-01090-Z. MEDTRONIC LITERATURE REVIEW FOUND REPORTED OF PATIENT COMPLICATIONS IN ASSOCIATION WITH SOLITAIRE THROMBECTOMY. THE PURPOSE OF THIS ARTICLE WAS TO EVALUATE THE USEFULNESS OF THE SOFIA 6F CATHETER IN MECHANICAL THROMBECTOMY WITH THE DIRECT ASPIRATION FIRST PASS TECHNIQUE. THE AUTHORS REVIEWED 148 CASES OF PATIENTS TREATED FOR ACUTE ISCHEMIC STROKE BETWEEN SEPTEMBER 2017 TO JANUARY 2019 USING DIRECT ASPIRATION THROMBECTOMY. OF THE 148 PATIENTS, THE AVERAGE AGE WAS 64 YEARS, 67 WERE FEMALE AND 81 WERE MALE. THE ARTICLE DOES NOT STATE ANY TECHNICAL ISSUES DURING USE OF THE REBAR MICROCATHETER OR SOLITAIRE STENT RETRIEVER. THERE WAS NO COMPLICATION DIRECTLY RELATED TO THE SOFIA CATHETER. IT WAS NOTED INITIAL ASPIRATION THROMBECTOMY COULD NOT BE PERFORMED IN 18 PATIENTS DUE TO EXTREME TORTUOSITY, INSUFFICIENT CATHETER LENGTH, OR SEVERE STENOSIS. SUCCESSFUL RECANALIZATION WAS ACHIEVED IN 90 PATIENTS. THE FOLLOWING INTRA- OR POST-PROCEDURAL OUTCOMES WERE NOTED: THE RATE OF MORTALITY WAS 14.1% (21 PATIENTS) AFTER THE PROCEDURE. REFER TO MANUFACTURER REPORT 2029214-2021-01116 FOR DETAILS PERTAINING TO THE RELATED REPORTABLE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1329472 REBAR CATHETER, CONTINUOUS FLUSH KRA MICRO THERAPEUTICS, INC. DBA EV3

Patients

Seq Age Sex Outcome Treatment
1 64 YR Death