Mendenhall Shaun D, Schmucker Ryan W, Daugherty Timothy H F, Kottwitz Katherine M, Reichensperger Joel D, Koirala Janak, Cederna Paul S, Neumeister Michael W
Springfield, Ill.; and Ann Arbor, Mich.
From the Institute for Plastic Surgery, the Laboratory for Regenerative Medicine and Applied Sciences, the Division of Infectious Diseases, Southern Illinois University School of Medicine; and the Section of Plastic Surgery, University of Michigan School of Medicine.
Plast Reconstr Surg. 2017 Jul;140(1):97-108. doi: 10.1097/PRS.0000000000003448.
Recent data suggest an increased risk for infection when acellular dermal matrix is used in breast reconstruction. This may be because some acellular dermal matrices are actually not terminally sterilized but are instead "aseptically processed." This study evaluates aseptic and sterile matrices for evidence of bacterial contamination and whether or not terminal sterilization affects matrix collagen architecture and stem cell ingrowth.
Five separate samples of 14 different matrices were analyzed by fluorescent in situ hybridization using a bacterial DNA probe to detect bacterial DNA on the matrices. Separate samples were incubated for bacteria, acid-fast bacilli, and fungi for 2 to 6 weeks to detect living organisms. The impact of terminal sterilization on the collagen network and stem cell ingrowth on the matrices was then assessed.
Traces of bacterial DNA were encountered on all matrices, with more bacteria in the aseptic group compared with the sterile group (3.4 versus 1.6; p = 0.003). The number of positive cultures was the same between groups (3.8 percent). Electron microscopy demonstrated decreased collagen organization in the sterile group. Stem cell seeding on the matrices displayed a wide variation of cellular ingrowth between matrices, with no difference between aseptic and sterile groups (p = 0.2).
Although there was more evidence of prior bacterial contamination on aseptically processed matrices compared with sterile matrices; clinical cultures did not differ between groups. Terminal sterilization does not appear to affect stem cell ingrowth but may come at the cost of damaging the collagen network.
CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, V.
近期数据表明,在乳房重建中使用脱细胞真皮基质时感染风险增加。这可能是因为一些脱细胞真皮基质实际上并未进行最终灭菌,而是“无菌处理”。本研究评估无菌和已灭菌基质是否存在细菌污染迹象,以及最终灭菌是否会影响基质胶原蛋白结构和干细胞向内生长。
使用细菌DNA探针通过荧光原位杂交分析14种不同基质的5个独立样本,以检测基质上的细菌DNA。将单独的样本培养2至6周以检测细菌、抗酸杆菌和真菌等活生物体。然后评估最终灭菌对基质胶原蛋白网络和干细胞向内生长的影响。
在所有基质上均检测到微量细菌DNA,无菌组中的细菌比已灭菌组更多(3.4对1.6;p = 0.003)。两组之间阳性培养物的数量相同(3.8%)。电子显微镜显示已灭菌组中胶原蛋白组织减少。基质上的干细胞接种显示不同基质之间细胞向内生长差异很大,无菌组和已灭菌组之间无差异(p = 0.2)。
尽管与已灭菌基质相比,无菌处理的基质上有更多先前细菌污染的证据,但两组之间的临床培养结果并无差异。最终灭菌似乎不会影响干细胞向内生长,但可能会以破坏胶原蛋白网络为代价。
临床问题/证据水平:治疗性,V级