Aesthet Surg J. 2023 Nov 16;43(12):1491-1498. doi: 10.1093/asj/sjad246.
Acellular dermal matrix (ADM) is frequently utilized in prepectoral breast reconstruction, but few studies have examined the role of ADM type in complication risk.
This study was performed to determine the impact of ADM type on early complication rates in 2-stage alloplastic prepectoral breast reconstruction.
We performed a cohort examination of all patients who underwent mastectomy with immediate 2-stage alloplastic prepectoral breast reconstruction with ADM support at Memorial Sloan Kettering Cancer Center from 2018 to 2021. ADM types utilized included AlloDerm (LifeCell Corporation, Branchburg, NJ), FlexHD (MTF Biologics, Edison, NJ), and SurgiMend (Integra LifeSciences Corporation, Princeton, NJ). Complication rates based on the number of tissue expanders (TEs) were determined for each ADM type. Performance of multivariate logistic regression determined the impact of ADM type on complication risk after accounting for confounders.
Overall, 726 patients (1054 TEs: 194 AlloDerm, 93 FlexHD, 767 SurgiMend) were included. The 3 cohorts differed in terms of mastectomy type (nipple-sparing: 23.5% of AlloDerm, 33.3% of FlexHD, 19.1% of SurgiMend, P = .038); ADM perforation (perforated: 94.8% of AlloDerm, 98.2% of FlexHD, 100% of SurgiMend, P < .001); and ADM size (AlloDerm: 153.2 cm2 [37.6], SurgiMend: 198.7 cm2 [10.4], FlexHD: 223.7 cm2 [37.9], P < .001). On univariate examination, no differences existed between ADM types for seroma, infection, exposure, malposition, or TE loss. Additionally, after adjustment for confounders with multivariate regression, no ADM type had higher odds of TE loss.
In this large cohort of prepectoral reconstruction patients, ADM type did not significantly affect the risk of complications. Additional prospective studies are warranted to better evaluate ADM choice for prepectoral breast reconstruction.
脱细胞真皮基质(ADM)常用于胸肌前置乳房重建,但很少有研究探讨 ADM 类型在并发症风险中的作用。
本研究旨在确定 ADM 类型对 2 期假体前置乳房重建中早期并发症发生率的影响。
我们对 2018 年至 2021 年期间在纪念斯隆凯特琳癌症中心接受即刻 2 期假体前置乳房重建并使用 ADM 支持的所有患者进行了队列研究。使用的 ADM 类型包括 AlloDerm(LifeCell Corporation,新泽西州布兰奇堡)、FlexHD(MTF Biologics,新泽西州爱迪生)和 SurgiMend(Integra LifeSciences Corporation,新泽西州普林斯顿)。基于组织扩张器(TE)的数量确定了每种 ADM 类型的并发症发生率。多变量逻辑回归分析确定了 ADM 类型在考虑混杂因素后对并发症风险的影响。
总体而言,共有 726 名患者(1054 个 TEs:194 个 AlloDerm、93 个 FlexHD、767 个 SurgiMend)入组。3 个队列在乳房切除术类型(保留乳头:23.5%的 AlloDerm、33.3%的 FlexHD、19.1%的 SurgiMend,P=0.038)、ADM 穿孔(穿孔:94.8%的 AlloDerm、98.2%的 FlexHD、100%的 SurgiMend,P<.001)和 ADM 大小(AlloDerm:153.2cm2[37.6],SurgiMend:198.7cm2[10.4],FlexHD:223.7cm2[37.9],P<.001)方面存在差异。单因素分析显示,在血清肿、感染、暴露、错位或 TE 丢失方面,ADM 类型之间无差异。此外,通过多变量回归调整混杂因素后,没有 ADM 类型 TE 丢失的可能性更高。
在本研究中,大量的胸肌前置重建患者中,ADM 类型并没有显著影响并发症的风险。需要进一步的前瞻性研究来更好地评估胸肌前置乳房重建中 ADM 的选择。