Applications of Adipose Tissue Micrografts (ATM) and Dermis Micrografts (DMG) in Wound Healing: A Scoping Review of Clinical Studies.

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Konstantinos Zapsalis, Orestis Ioannidis, Elissavet Anestiadou, Maria Pantelidou, Konstantinos Siozos, Christos Xylas, Georgios Gemousakakis, Angeliki Cheva, Chryssa Bekiari, Antonia Loukousia, Savvas Symeonidis, Stefanos Bitsianis, Manousos-Georgios Pramateftakis, Efstathios Kotidis, Ioannis Mantzoros, Stamatios Angelopoulos
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引用次数: 0

Abstract

Adipose tissue micrografts (ATM) and dermis micrografts (DMG) have emerged as promising autologous therapies in regenerative wound care, leveraging mechanically disaggregated cell-matrix constructs to modulate the wound microenvironment and promote tissue repair. This scoping review systematically analyzed clinical studies investigating ATMs and DMGs in acute and chronic wounds. Eight studies, comprising randomized controlled trials, observational studies, and case series, were identified, involving diverse wound types such as burns, ulcers, surgical dehiscence, and posttraumatic defects. All interventions utilized mechanical disaggregation (Rigenera® system) to produce micrografts, which were applied via perilesional injection, scaffold-assisted delivery, or topical administration. Outcomes consistently demonstrated accelerated re-epithelialization, enhanced angiogenesis, improved scar remodeling, and low complication rates. In select studies, micrografts were combined with platelet-rich fibrin or stromal vascular fraction, suggesting potential synergistic effects. While one randomized trial showed superior healing outcomes with DMGs over collagen scaffolds, others yielded mixed results, likely reflecting heterogeneity in methodology and outcome measures. Overall, the available clinical evidence supports the safety, feasibility, and biological activity of micrograft-based therapies. However, larger, standardized, and mechanistically driven studies are required to validate their efficacy and define optimal protocols across wound etiologies.

脂肪组织微移植(ATM)和真皮微移植(DMG)在伤口愈合中的应用:临床研究综述
脂肪组织微移植物(ATM)和真皮微移植物(DMG)已经成为再生伤口护理中有前途的自体治疗方法,利用机械分解的细胞基质结构来调节伤口微环境并促进组织修复。本综述系统分析了急性和慢性创伤中atm和dmg的临床研究。八项研究,包括随机对照试验、观察性研究和病例系列,涉及不同的伤口类型,如烧伤、溃疡、手术开裂和创伤后缺陷。所有干预措施均采用机械分解(Rigenera®系统)产生微移植物,通过病灶周围注射、支架辅助输送或局部给药。结果一致显示加速再上皮化,增强血管生成,改善疤痕重塑和低并发症发生率。在一些选定的研究中,微移植物与富血小板纤维蛋白或间质血管组分联合使用,提示潜在的协同作用。虽然一项随机试验显示dmg比胶原蛋白支架的愈合效果更好,但其他试验的结果好坏参半,可能反映了方法和结果测量的异质性。总的来说,现有的临床证据支持微移植物治疗的安全性、可行性和生物活性。然而,需要更大规模、标准化和机械驱动的研究来验证其有效性,并确定跨伤口病因的最佳方案。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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