Abstract

BackgroundUtilising fluorescence optical imaging (FOI), the distribution of an intravenously applied colouring agent indocyanine green (ICG) can be analysed with the potential to identify malperfusion by little to no tissue enhancement. Systemic sclerosis (SSc) is characterised by the presence of digital ulcers reflecting progressive vasculopathy.The objective was to investigate the potential of FOI in the detection of disturbed microcirculation in the hands and fingers of patients with SSc and to link FOI findings to clinical signs of ischemia such as digital ulcers and pitting scars.MethodsIn this cross-sectional study, 63 patients with SSc and 26 healthy subjects were examined. FOI was performed in all 89 individuals and compared to clinical data and capillaroscopic findings assembled for the SSc cohort.ResultsHealthy subjects showed initial ICG signals in their fingertips in 93.6%, SSc patients in 78.5% (limited SSc) and 43.2% (diffuse SSc). Moreover, in SSc patients, FOI findings were significantly associated with a late capillaroscopic pattern, disseminated SSc features, a diffuse SSc subtype, and the presence of digital ulcers or pitting scars. Intra- and inter-reader reliability for FOI amounted to κ = 0.786 and κ = 0.834, respectively.ConclusionsFOI is able to detect areas of reduced microcirculation in patients with SSc with high association to capillaroscopic findings. The results pave the way for future FOI investigations into its role in the prediction of complications due to an impaired acral perfusion.

Highlights

  • Utilising fluorescence optical imaging (FOI), the distribution of an intravenously applied colouring agent indocyanine green (ICG) can be analysed with the potential to identify malperfusion by little to no tissue enhancement

  • Pathologic ICG accumulation is related to general presence of digital ulcers and/or pitting scars in Systemic sclerosis (SSc) patients We observed a strong (≥65% of maximum signal intensity) initial enhancement (IE) behaviour in both patients with (n = 37, group 1) and patients without (n = 26, group 2) current digital ulcers and/or pitting scars (DU/PS) at the time of the examination

  • Fingers with a strong IE more proximal than that, were more likely to belong to patients with current digital ulcers and/or pitting scars: between 63.5% and 100% of fingers with a strong IE in the areas between region 2 and region 8 belonged to patients of group 1

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Summary

Introduction

Utilising fluorescence optical imaging (FOI), the distribution of an intravenously applied colouring agent indocyanine green (ICG) can be analysed with the potential to identify malperfusion by little to no tissue enhancement. The objective was to investigate the potential of FOI in the detection of disturbed microcirculation in the hands and fingers of patients with SSc and to link FOI findings to clinical signs of ischemia such as digital ulcers and pitting scars. Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is a novel, fast and quantitative imaging method that is already used in the diagnostics of inflammatory arthritis with good agreement to other imaging modalities (magnetic resonance imaging [MRI], ultrasound [US]) and good reliability [1,2,3]. ICG fluorescence video angiography has been shown to help in the detection of compromised tissue perfusion as a perioperative tool in microsurgery [4]. Already since the 1970s, ICG has safely been used in ophthalmologic angiography and even proved its value in the evaluation of skin perfusion in plastic surgery [6]

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