From the University of Virginia Health System.
Plast Reconstr Surg. 2022 Aug 1;150(2):290e-299e. doi: 10.1097/PRS.0000000000009338. Epub 2022 Jun 3.
When first described for breast reconstruction, the presence of acellular dermal matrices was associated with increased seroma formation and infection. However, clinical safety data have gradually improved with surgeon experience to an acceptable outcomes profile of acellular dermal matrix-assisted reconstruction when compared to submuscular implant coverage. In fact, acellular dermal matrix use potentially decreases capsular contracture rates and facilitates expansion for staged prepectoral breast reconstruction. Because of new regulatory requirements, the collection of unbiased, well-powered premarket approval data summarizing long-term clinical outcomes will be essential over the coming years to understand the clinical performance of acellular dermal matrix use in breast reconstruction. Currently, the authors can highlight the physiologic benefits of acellular dermal matrix use in breast reconstruction by evaluating the components of surgical wound healing that are favorably augmented by the implanted collagen substrate. Acellular dermal matrix takes advantage of the wound healing cascade to incorporate into the patient's tissues-a process that requires a coordinated inflammatory infiltrate and angiogenesis. The presence of acellular dermal matrix augments and modulates the wound healing process to its advantage by simultaneously increasing the invasion of appropriate cellular constituents to facilitate expeditious healing and accelerate angiogenesis. In this article, the authors summarize the wound healing literature to demonstrate the mechanisms acellular dermal matrices use to biointegrate and the literature in which cellular constituents and soluble growth factors are up-regulated in the presence of acellular dermal matrix. Lastly, the authors use their experimental observations of acellular dermal matrix incorporation to corroborate the literature.
当首次应用于乳房重建时,脱细胞真皮基质的存在与血清肿形成和感染增加有关。然而,随着外科医生经验的逐渐增加,与胸肌下植入物覆盖相比,脱细胞真皮基质辅助重建的临床安全性数据已逐渐改善,达到可接受的结果。事实上,与包膜挛缩率相比,脱细胞真皮基质的使用可能会降低包膜挛缩率,并为分期胸肌前置乳房重建提供扩张的便利。由于新的监管要求,在未来几年内,收集无偏见、有足够效力的上市前批准数据,总结长期临床结果对于了解脱细胞真皮基质在乳房重建中的临床性能至关重要。目前,作者可以通过评估植入胶原基质有利于增强的手术伤口愈合的组成部分,来强调脱细胞真皮基质在乳房重建中的生理益处。脱细胞真皮基质利用伤口愈合级联反应将自身整合到患者组织中——这一过程需要协调的炎症浸润和血管生成。脱细胞真皮基质的存在通过同时增加适当细胞成分的入侵,促进快速愈合和加速血管生成,从而有利于增强和调节伤口愈合过程。在本文中,作者总结了伤口愈合文献,以证明脱细胞真皮基质用于生物整合的机制,以及细胞成分和可溶性生长因子在脱细胞真皮基质存在时上调的文献。最后,作者使用他们对脱细胞真皮基质整合的实验观察来证实文献。