2022
DOI: 10.1016/j.bjps.2021.08.027
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Prepectoral implant-based breast reconstruction with TiLOOP® Bra Pocket – a single-centre retrospective study

Abstract: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, a… Show more

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Cited by 14 publications
(9 citation statements)
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References 28 publications
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“…Our preference is to use TiLOOP Bra Pocket™ due to its ease of use and its cost profile. [13][14][15][16][17] However, if the selected new implant, fits snuggly within the neo pocket, no mesh or ADM may be needed, or the use of internal bra sutures may be sufficient.…”
Section: Mesh or Adm Usagementioning
confidence: 99%
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“…Our preference is to use TiLOOP Bra Pocket™ due to its ease of use and its cost profile. [13][14][15][16][17] However, if the selected new implant, fits snuggly within the neo pocket, no mesh or ADM may be needed, or the use of internal bra sutures may be sufficient.…”
Section: Mesh or Adm Usagementioning
confidence: 99%
“…If there is discrepancy between the surface area of the implant selected and the overlying skin envelope and or the implant is >400 cc the implant will need the support of a mesh and or controlling with internal lateral bra sutures. Our preference is to use TiLOOP Bra Pocket™ due to its ease of use and its cost profile 13–17 . However, if the selected new implant, fits snuggly within the neo pocket, no mesh or ADM may be needed, or the use of internal bra sutures may be sufficient.…”
Section: Operative Techniquementioning
confidence: 99%
“…One retrospective multicenter study showed that major complications (need for additional surgery) occurred in 13.4% of patients using TiLOOP bra, minor complications (need for conservative treatment) in 15.6%, and implant loss in 8.7% 11 . Other previous studies reported that the risk of complications using TiLOOP bra in immediate or delayed‐immediate IBBR ranged from 2.4% to 30.2% 12–15 . It is also noted that other synthetic mesh alternatives, such as short‐term absorbable mesh (Seragyn ® ), reported a comparable rate of complications to ADM 16 …”
Section: Introductionmentioning
confidence: 96%
“…11 Other previous studies reported that the risk of complications using TiLOOP bra in immediate or delayedimmediate IBBR ranged from 2.4% to 30.2%. [12][13][14][15] It is also noted that other synthetic mesh alternatives, such as short-term absorbable mesh (Seragyn ® ), reported a comparable rate of complications to ADM. 16 However, most current studies comparing TiLOOP bra to other techniques for IBBR regarding postoperative complication profiling are small and retrospective. There are rarely randomized controlled trials (RCTs) or relevant meta-analyses.…”
Section: Introductionmentioning
confidence: 98%
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