FDA Adverse Event Injury Summary report: N

LIGACLIP EXTRA TITANIUM CLIPS

MDR report key: 9491045 · Received December 18, 2019

Report

Report Number
3005075853-2019-24547
Event Type
Injury
Date Received
December 18, 2019
Report Date
December 5, 2019
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
FZP
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). BATCH # UNK. PUBLICATION YEAR OF 2019. THIS REPORT IS RELATED TO A JOURNAL ARTICLE; THEREFORE, NO PRODUCT WILL BE RETURNED FOR ANALYSIS. THE LOT/BATCH WAS NOT PROVIDED; THEREFORE, A MANUFACTURING RECORD EVALUATION COULD NOT BE PERFORMED. ATTEMPTS ARE BEING MADE TO OBTAIN THE FOLLOWING INFORMATION:   DOES THE AUTHOR/SURGEON BELIEVE THAT THE ETHICON DEVICE CAUSED OR CONTRIBUTED TO THE PATIENT COMPLICATIONS MENTIONED IN THE ARTICLE? IF YES, PLEASE EXPLAIN. TO DATE NO RESPONSE HAS BEEN PROVIDED. IF FURTHER DETAILS ARE RECEIVED AT A LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING REVIEW OF A JOURNAL ARTICLE, TITLE: THE USE OF PLASMAKINETIC CAUTERY COMPARED TO CONVENTIONAL ELECTROCAUTERY FOR DISSECTION OF ABDOMINAL FREE FLAP FOR BREAST RECONSTRUCTION: SINGLE-CENTRE, RANDOMIZED CONTROLLED STUDY. AUTHOR : WHITNEY T. H. CHOW, GEORGETTE ONI, VENKAT V. RAMAKRISHNAN, MAT GRIFFITHS. CITATION: GLAND SURG 2019;8(3):242-248; DOI: 10.21037/GS.2018.12.04. THIS PROSPECTIVE RANDOMIZED BLINDED STUDY AIMED TO INVESTIGATE WHETHER THE USE OF THE PLASMAKINETIC CAUTERY CONFERS CLINICAL BENEFITS OVER CONVENTIONAL ELECTROCAUTERY DIATHERMY IN ABDOMINAL FLAP DISSECTION DURING BREAST RECONSTRUCTION. FROM JANUARY 2014 TO NOVEMBER 2014, A TOTAL OF 40 PATIENTS WERE BLINDLY RANDOMIZED TO EITHER ¿GROUP 1- CONVENTIONAL ELECTROCAUTERY¿ (N=20, MEAN AGE: 55 YEARS, MEAN BMI: 29 KG/M2) OR ¿GROUP 2-PLASMAKINETIC CAUTERY¿ (N=20, MEAN AGE: 54 YEARS, MEAN BMI 27.9 KG/M2) WITH THE RATIO OF 1:1, FOR THE DISSECTION OF THE ABDOMINAL FREE FLAP. DURING SURGERY, BLEEDING VESSELS WERE CAUTERIZED EXCEPT FOR LARGE PERFORATING BRANCHES, WHICH WERE CLIPPED WITH LIGACLIPS (ETHICON). VICRYL MESH (ETHICON) WAS ROUTINELY PLACED UNDER THE RECTUS SHEATH ON CLOSURE. THE CLOSURE OF THE ABDOMINAL WOUND IN LAYERS WITH 3/0 VIRCYL (ETHICON) TO THE FASCIA, STRATAFIX BARBED SUTURES (ETHICON) TO DERMIS AND DERMBOND TOPICAL SKIN ADHESIVE (ETHICON) FOR WOUND FINAL APPROXIMATION. COMPLAINTS INCLUDED SEROMA FORMATION (N=27) WHERE 4, 14 AND 9 SEROMAS WERE DETECTED AT DAYS 7, 14 AND 42 POST-OPERATION RESPECTIVELY AND ONLY ONE SEROMA REQUIRED DRAINAGE DURING THEIR OUTPATIENT VISIT AT 14 DAYS POST-OPERATION. OTHER COMPLAINTS ARE HEMATOMA (N=3) WHICH REQUIRED FURTHER SURGERY TO EVACUATE THE HEMATOMA, AND SUSPECTED WOUND INFECTION (N=1) WHO NEED ANTIBIOTICS POST-DISCHARGE. IN CONCLUSION, THIS STUDY DEMONSTRATES THAT THERE ARE NO SIGNIFICANT DIFFERENCES BETWEEN THE USE OF PLASMAKINETIC CAUTERY AND CONVENTIONAL ELECTROCAUTERY FOR ABDOMINAL FREE FLAP DISSECTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1286485 LIGACLIP EXTRA TITANIUM CLIPS CLIP, IMPLANTABLE FZP ETHICON ENDO-SURGERY, LLC.

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention