Montreal, Quebec, Canada.
From the Plastic and Reconstructive Surgery Department, Notre-Dame Hospital, University of Montreal Hospital Center.
Plast Reconstr Surg. 2018 Apr;141(4):919-928. doi: 10.1097/PRS.0000000000004216.
BACKGROUND: Despite benefits in reducing capsular contractures, textured implants have been associated with significant pitfalls, such a propensity for biofilm formation. Few studies have investigated whether the use of acellular dermal matrix on textured implants produces similar findings. This study aims to characterize biofilm formation at the capsular-acellular dermal matrix interface with scanning electron microscopy. METHODS: The authors performed a prospective observational pilot study in patients undergoing two-stage expander-to-permanent implant exchange. Patients were inflated with Biocell or Siltex expanders, and specimens from the capsular-pectoralis interface and capsular-acellular dermal matrix interface were obtained and examined under scanning electron microscopy for capsular ingrowth and biofilm formation using the Van Herdeen Biofilm Grading System and the Biofilm Thickness Grading Scale. RESULTS: Nine patients including 14 breasts (28 capsular samples in total) were examined. Thick biofilm formation was observed in all specimens from the capsular-acellular dermal matrix interface with Biocell and 25 percent of capsule-pectoralis interface, whereas no biofilm formation was found in Siltex implants. For Biocell implants, a significant difference in biofilm coverage between the upper and lower poles was observed using the Van Herdeen Biofilm Grading System (p = 0.0028) and the Biofilm Thickness Grading Scale (p = 0.0161). CONCLUSIONS: Biocell implants produce a significant rate of biofilm formation over acellular dermal matrix-covered capsules, which is not present in the muscular region or in Siltex implants. Further randomized controlled trials will further elucidate the clinical impact of using acellular dermal matrices with macrotextured implants. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.
背景:尽管纹理植入物在减少包膜挛缩方面有好处,但它也存在着一些重大缺陷,例如容易形成生物膜。很少有研究调查在使用脱细胞真皮基质的情况下,纹理植入物是否会产生类似的结果。本研究旨在通过扫描电子显微镜来描述包膜-脱细胞真皮基质界面的生物膜形成。
方法:作者对接受两阶段扩张器-永久性植入物更换的患者进行了前瞻性观察性试点研究。患者使用 Biocell 或 Siltex 扩张器充气,然后从包膜-胸肌界面和包膜-脱细胞真皮基质界面获得标本,并通过扫描电子显微镜使用 Van Herdeen 生物膜分级系统和生物膜厚度分级量表检查包膜内生长和生物膜形成情况。
结果:共检查了 9 名患者的 14 个乳房(共 28 个包膜样本)。所有使用 Biocell 的包膜-脱细胞真皮基质界面的标本都观察到厚的生物膜形成,而在 25%的包膜-胸肌界面的标本中则没有发现生物膜形成。对于 Biocell 植入物,使用 Van Herdeen 生物膜分级系统(p = 0.0028)和生物膜厚度分级量表(p = 0.0161)观察到生物膜覆盖范围在上极和下极之间存在显著差异。
结论:Biocell 植入物在覆盖有脱细胞真皮基质的包膜上产生了很高的生物膜形成率,而在肌肉区域或 Siltex 植入物中则没有。进一步的随机对照试验将进一步阐明使用带有宏观纹理植入物的脱细胞真皮基质的临床影响。
临床问题/证据水平:治疗,IV。
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