Division of Plastic and Reconstructive Surgery, University of Ottawa, Ottawa, Canada.
Division of General Surgery, University of Ottawa, Ottawa, Canada.
J Plast Reconstr Aesthet Surg. 2021 Jan;74(1):41-47. doi: 10.1016/j.bjps.2020.08.018. Epub 2020 Aug 15.
Alloderm and Dermacell are the two leading human acellular dermal matrices (ADM) in immediate breast reconstruction (IBR). Despite differences in sterility, consistency, thickness and cost, there are no comparative trials to date to compare patient-reported outcome measures (PROM) between the two products. The purpose of this study was to determine if there was a difference in patient-reported outcomes (as measured by the BREAST-Q) between patients reconstructed with Alloderm and Dermacell.
A single center, open-label, randomized control trial of patients undergoing IBR with an implant for breast cancer or breast cancer prophylaxis was performed. Patients were randomized to either Alloderm or Dermacell. Baseline demographic data were compared, and linear mixed models were used to identify associations with BREAST-Q over time.
Between June 2016 and October 2018, 62 patients were randomized into two groups, 31(50%) Alloderm and 31(50%) Dermacell. Of these, 23(74%) patients in the Alloderm group and 27(87%) patients of the Dermacell group filled out BREAST-Q questionnaires. Baseline BREAST-Q scores with respect to satisfaction with breasts, psychosocial well-being, sexual well-being, and physical well-being were similar between groups (p>0.05). At 3 months postoperatively, the Alloderm group had a statistically significant improvement with respect to satisfaction with breasts (67 vs 53, p = 0.03), satisfaction with overall results (85 vs 61, p = 0.003), satisfaction with the surgeon (89 vs 67, p = 0.01), and satisfaction with information provided (74 vs 59, p = 0.02). At 12 months postoperatively, there were no statistically significant differences in PROM between groups (p>0.05).
We report the first randomized controlled trial to date comparing patient-reported outcomes of the two most commonly used ADMs in IBR in Canada. Although a short-term analysis favors the use of Alloderm, there does not appear to be any difference in outcomes between the two products in the longer term.
Alloderm 和 Dermacell 是即刻乳房重建 (IBR) 中两种主要的人去细胞真皮基质 (ADM)。尽管在无菌性、一致性、厚度和成本方面存在差异,但迄今为止尚无比较试验来比较这两种产品的患者报告结局测量 (PROM)。本研究旨在确定接受植入物治疗乳腺癌或乳腺癌预防的 IBR 患者的患者报告结果 (以 BREAST-Q 衡量) 是否存在差异。
对接受 IBR 并植入乳房癌或乳腺癌预防用植入物的患者进行了一项单中心、开放性、随机对照试验。患者被随机分配到 Alloderm 或 Dermacell 组。比较基线人口统计学数据,并使用线性混合模型随时间识别与 BREAST-Q 的关联。
2016 年 6 月至 2018 年 10 月,62 名患者被随机分为两组,31 名(50%)患者使用 Alloderm,31 名(50%)患者使用 Dermacell。其中,Alloderm 组有 23 名(74%)患者和 Dermacell 组有 27 名(87%)患者填写了 BREAST-Q 问卷。两组间基线 BREAST-Q 评分在乳房满意度、心理社会幸福感、性健康和身体健康方面相似(p>0.05)。术后 3 个月,Alloderm 组在乳房满意度(67 对 53,p=0.03)、总体结果满意度(85 对 61,p=0.003)、对手术医生的满意度(89 对 67,p=0.01)和对提供信息的满意度(74 对 59,p=0.02)方面有统计学意义的改善。术后 12 个月,两组间 PROM 无统计学差异(p>0.05)。
我们报告了迄今为止加拿大比较两种最常用于 IBR 的 ADM 的患者报告结局的第一项随机对照试验。尽管短期分析有利于使用 Alloderm,但在较长时间内,这两种产品的结果似乎没有差异。