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First‐year complications after immediate breast reconstruction with a biological and a synthetic mesh in the same patient: A randomized controlled study

by editor | Oct 6, 2020 | Breast, Evidence, Published

Hansson, E.Edvinsson, A‐C.Elander, A.Kölby, L.Hallberg, H. Journal of Surgical Oncology, 13 October 2020 DOI: https://doi.org/10.1002/jso.26227 Abstract Background Even though meshes and matrices are widely used in breast reconstruction, there is little high‐quality...

TIGR Matrix surgical mesh – a two-year follow-up study and complication analysis in 65 immediate breast reconstructions

by editor | Feb 1, 2018 | Evidence, Published Breast reconstruction

Hallberg, H.Lewin, R.Elander, A.Hansson, E. Published online: 07 June 2018. J Plast Surg Hand Surg. 52(4):253. DOI: 10.1080/2000656X.2018.1478841 Abstract In recent years, it has become increasingly popular to use matrices, such as acellular dermal matrices,...

Recent posts

  • Comparing Complications of Biologic and Synthetic Mesh in Breast Reconstruction: A Systematic Review and Network Meta-Analysis 6 February, 2023
  • Are patients most satisfied with a synthetic or a biological mesh in dual-plane immediate breast reconstruction after 5 years? A randomized controlled trial comparing the two meshes in the same patient 18 November, 2022
  • Mastectomy and Immediate Breast Reconstruction with Pre-Pectoral or Sub-Pectoral Implant: Assessing Clinical Practice, Post-Surgical Outcomes, Patient’s Satisfaction and Cost 2 October, 2022
  • Prophylactic onlay mesh at emergency laparotomy: promising early outcomes with long-acting synthetic resorbable mesh 1 August, 2022
  • A Retrospective Study Assessing the Outcomes of Immediate Prepectoral and Subpectoral Implant and Mesh-Based Breast Reconstruction 29 June, 2022
  • Press Release CE MDR TIGR Matrix 12 January, 2022
Copyright 2023 © Novus Scientific • Virdings Allé 2, 754 50 Uppsala, SWEDEN • TIGR® Matrix Surgical Mesh received 510(k) clearance by the FDA in 2010 and carries the CE-mark since 2011.