利用吲哚菁绿荧光成像技术实时识别危及生命的坏死性软组织感染。

IF 3 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Biomedical Optics Pub Date : 2024-06-01 Epub Date: 2024-05-14 DOI:10.1117/1.JBO.29.6.066003
Gabrielle S Ray, Samuel S Streeter, Logan M Bateman, Jonathan Thomas Elliott, Eric R Henderson
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引用次数: 0

摘要

意义重大:坏死性软组织感染(NSTI)是一种危及生命的感染,累计病死率高达 21%。NSTI 的最初表现并无特异性,经常导致误诊和治疗延误。目的:一项首创的观察性临床试验研究对以下假设进行了测试:静脉注射吲哚青绿(ICG)荧光并进行灌注成像后,受 NSTI 影响的组织中会出现可测量的荧光信号空洞。这一假设是基于 NSTI 与局部微血管血栓形成有关的既定知识:方法:在一家三级医疗中心急诊科就诊的 NSTI 高危成人患者被纳入前瞻性研究,并使用商用荧光成像仪进行成像。使用动态对比增强荧光成像技术量化了单帧荧光快照和一过灌注动力学参数--压迫斜率(IS)、峰值时间(TTP)强度和最大荧光强度(IMAX)。将临床变量(合并症、血液化验值)、荧光参数和荧光信噪比(SBR)与最终感染诊断进行比较:14 名患者入选并接受了成像检查(6 名 NSTI 患者、6 名蜂窝组织炎患者、1 名糖尿病相关性坏疽患者和 1 名骨髓炎患者)。临床变量显示,NSTI 和非 NSTI 患者组之间没有明显的统计学差异(P 值≥0.22)。所有 NSTI 病例的受影响组织都有明显的荧光信号空洞,包括肉眼无法看到的组织特征。所有蜂窝组织炎病例都表现出荧光增加的高充血反应,但没有明显的信号空洞。根据快照、IS、TTP 和 IMAX 参数图,NSTI 患者组的病变与背景组织 SBR 中值分别为 3.2 至 9.1、2.2 至 33.8、1.0 至 7.5 和 1.5 至 12.7。除 TTP 外,NSTI 患者组和蜂窝组织炎患者组之间的所有荧光参数差异均有统计学意义(P 值为 0.05):结论:通过基于灌注的 ICG 荧光成像技术,可以实时、准确地区分 NSTI 与非坏死性感染。
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Real-time identification of life-threatening necrotizing soft-tissue infections using indocyanine green fluorescence imaging.

Significance: Necrotizing soft-tissue infections (NSTIs) are life-threatening infections with a cumulative case fatality rate of 21%. The initial presentation of an NSTI is non-specific, frequently leading to misdiagnosis and delays in care. No current strategies yield an accurate, real-time diagnosis of an NSTI.

Aim: A first-in-kind, observational, clinical pilot study tested the hypothesis that measurable fluorescence signal voids occur in NSTI-affected tissues following intravenous administration and imaging of perfusion-based indocyanine green (ICG) fluorescence. This hypothesis is based on the established knowledge that NSTI is associated with local microvascular thrombosis.

Approach: Adult patients presenting to the Emergency Department of a tertiary care medical center at high risk for NSTI were prospectively enrolled and imaged with a commercial fluorescence imager. Single-frame fluorescence snapshot and first-pass perfusion kinetic parameters-ingress slope (IS), time-to-peak (TTP) intensity, and maximum fluorescence intensity (IMAX)-were quantified using a dynamic contrast-enhanced fluorescence imaging technique. Clinical variables (comorbidities, blood laboratory values), fluorescence parameters, and fluorescence signal-to-background ratios (SBRs) were compared to final infection diagnosis.

Results: Fourteen patients were enrolled and imaged (six NSTI, six cellulitis, one diabetes mellitus-associated gangrene, and one osteomyelitis). Clinical variables demonstrated no statistically significant differences between NSTI and non-NSTI patient groups (p-value0.22). All NSTI cases exhibited prominent fluorescence signal voids in affected tissues, including tissue features not visible to the naked eye. All cellulitis cases exhibited a hyperemic response with increased fluorescence and no distinct signal voids. Median lesion-to-background tissue SBRs based on snapshot, IS, TTP, and IMAX parameter maps ranged from 3.2 to 9.1, 2.2 to 33.8, 1.0 to 7.5, and 1.5 to 12.7, respectively, for the NSTI patient group. All fluorescence parameters except TTP demonstrated statistically significant differences between NSTI and cellulitis patient groups (p-value<0.05).

Conclusions: Real-time, accurate discrimination of NSTIs compared with non-necrotizing infections may be possible with perfusion-based ICG fluorescence imaging.

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来源期刊
CiteScore
6.40
自引率
5.70%
发文量
263
审稿时长
2 months
期刊介绍: The Journal of Biomedical Optics publishes peer-reviewed papers on the use of modern optical technology for improved health care and biomedical research.
期刊最新文献
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