2520274-2014-00674
Report
- Report Number
- 2520274-2014-00674
- Event Type
- Injury
- Date Received
- February 19, 2014
- Report Date
- January 24, 2014
- Manufacturer
- SYNTHES USA
- Product Code
- HWC
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
DEVICE IS USED FOR TREATMENT, NOT DIAGNOSIS CLINICAL ORTHOPEDICS AND RELATED RESEARCH (2013) 471:2768¿2775. DEVICE IS AN UNKNOWN SCREW, QUANTITY 1. (B)(4). CANNOT BE DETERMINED WITHOUT A PART NUMBER. INVESTIGATION COULD NOT BE COMPLETED, NO CONCLUSION COULD BE DRAWN AS NO DEVICE WAS RETURNED AND NO LOT NUMBER WAS PROVIDED. MANUFACTURING RECORDS COULD NOT BE REVIEWED WITHOUT A LOT NUMBER. PLACEHOLDER.
JOURNAL ARTICLE RECEIVED: WHICH IMPLANT IS BETTER FOR TREATING REVERSE OBLIQUITY FRACTURES OF THE PROXIMAL FEMUR: A STANDARD OR LONG NAIL? GUVENIR OKCU MD, NADIR OZKAYIN MD,CEMIL OKTA MD, ISMET TOPCU MD, KEMAL AKTUGLU MD; CLINICAL ORTHOPEDICS AND RELATED RESEARCH (2013) 471:2768¿2775; REPORTED: A PILOT PROSPECTIVE RANDOMIZED CONTROLLED TRIAL THAT COMPARED THE EFFECTS OF STANDARD VERSUS LONG INTRAMEDULLARY HIP NAILS, SYNTHES DEVICES PROXIMAL FEMORAL NAIL - ANTIROTATION (PFN-A), FOR THE TREATMENT OF REVERSE OBLIQUITY FRACTURES OF THE PROXIMAL FEMUR. PATIENTS WERE RANDOMIZED INTO TWO GROUPS: 18 PATIENTS (GROUP 1) WERE TREATED WITH A 130 DEGREE STANDARD PFN-A WHICH WAS 24 CM IN LENGTH AND 22 PATIENTS (GROUP 2) WERE TREATED WITH A 130 DEGREE LONG PFN-A IN VARIABLE LENGTHS RANGING FROM 34 TO 42 CM. THE MEAN PATIENT AGE WAS 79 YEARS. IT WAS NOTED THAT THREE PATIENTS IN GROUP 1 AND FOUR IN GROUP 2 SUBSEQUENTLY DIED (DATE AND CAUSE UNSPECIFIED). AVERAGE FOLLOW-UP RANGE FOR GROUP 1 AND 2 WAS 14 MONTHS AND 14.5 MONTHS RESPECTIVELY. IN GROUP 2, ONE PATIENT WAS REVISED DUE TO A DEEP INFECTION (GRADE IIIB COMPLICATION) AND SIX PATIENTS EXPERIENCED MALUNION. THE AUTHORS CONCLUDED THAT LONG PFN-A NAILS OFFERED NO CLINICAL ADVANTAGE COMPARED TO STANDARD PFN-A NAILS FOR THE TREATMENT OF REVERSE OBLIQUITY FRACTURES OF THE PROXIMAL FEMUR. THIS REPORT IS FOR AN UNKNOWN SCREW. THIS IS REPORT 4 OF 4 FOR COMPLAINT (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 105098 | HWC | SYNTHES USA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |