Postoperative Time and Anatomic Location Influence Skin Graft Reperfusion Assessed With Laser Speckle Contrast Imaging

医学 灌注 头皮 微循环 坏死 斑点图案 外科 缺血 病理 放射科 内科学 计算机科学 人工智能
作者
André Pinho,Ana Brinca,Joana Xará,Mariana Batista,Ricardo Vieira
出处
期刊:Lasers in Surgery and Medicine [Wiley]
卷期号:56 (6): 564-573 被引量:4
标识
DOI:10.1002/lsm.23815
摘要

OBJECTIVES: Under optimal conditions, afferent and efferent human skin graft microcirculation can be restored 8-12 days postgrafting. Still, the evidence about the reperfusion dynamics beyond this period in a dermato-oncologic setting is scant. We aimed to characterise the reperfusion of human skin grafts over 4 weeks according to the necrosis extension (less than 20%, or 20%-50%) and anatomic location using laser speckle contrast imaging (LSCI). METHODS: Over 16 months, all eligible adults undergoing skin grafts following skin cancer removal on the scalp, face and lower limb were enroled. Perfusion was assessed with LSCI on the wound margin (control skin) on day 0 and on the graft surface on days 7, 14, 21 and 28. Graft necrosis extension was determined on day 28. RESULTS: Forty-seven grafts of 47 participants were analysed. Regardless of necrosis extension, graft perfusion equalled the control skin by day 7, surpassed it by day 21, and stabilised onwards. Grafts with less than 20% necrosis on the scalp and lower limb shared this reperfusion pattern and had a consistently better-perfused centre than the periphery for the first 21 days. On the face, the graft perfusion did not differ from the control skin from day 7 onwards, and there were no differences in reperfusion within the graft during the study. CONCLUSION: Skin graft reperfusion is a protracted process that evolves differently in the graft centre and periphery, influenced by postoperative time and anatomic location. A better knowledge of this process can potentially enhance the development of strategies to induce vessel ingrowth into tissue-engineered skin substitutes.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
刚刚
刚刚
君故发布了新的文献求助10
1秒前
1秒前
1秒前
有轨电车前的红绿灯完成签到,获得积分10
2秒前
2秒前
科研通AI6.4应助a海w采纳,获得10
3秒前
科研通AI6.4应助a海w采纳,获得10
3秒前
科研通AI6.4应助a海w采纳,获得10
3秒前
科研通AI6.4应助a海w采纳,获得10
3秒前
科研通AI6.2应助a海w采纳,获得10
3秒前
科研通AI6.2应助a海w采纳,获得10
3秒前
科研通AI6.2应助a海w采纳,获得10
4秒前
科研通AI6.2应助a海w采纳,获得10
4秒前
科研通AI6.4应助a海w采纳,获得10
4秒前
科研通AI6.4应助a海w采纳,获得10
4秒前
林天完成签到,获得积分10
4秒前
4秒前
落后悟空完成签到,获得积分10
4秒前
怡然铃铛发布了新的文献求助10
5秒前
zmy发布了新的文献求助10
6秒前
bkagyin应助zyj采纳,获得10
6秒前
吱吱发布了新的文献求助10
6秒前
不知名热心网友完成签到,获得积分10
6秒前
木子完成签到,获得积分10
7秒前
7yin秦发布了新的文献求助30
7秒前
8秒前
wwww完成签到,获得积分10
8秒前
阿木应助111采纳,获得10
8秒前
8秒前
小蘑菇应助雷欧采纳,获得10
9秒前
李玲玲完成签到,获得积分10
10秒前
科研通AI6.2应助耿怀肖采纳,获得10
10秒前
天天快乐应助滕青寒采纳,获得10
11秒前
12秒前
12秒前
CipherSage应助a海w采纳,获得10
12秒前
科研通AI6.4应助a海w采纳,获得10
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7622244
求助须知:如何正确求助?哪些是违规求助? 9197534
关于积分的说明 19715344
捐赠科研通 7193777
什么是DOI,文献DOI怎么找? 3272947
关于科研通互助平台的介绍 2435355
邀请新用户注册赠送积分活动 2268327