| 1. |
- Fredriksson, Ingemar, 1980-, et al.
(författare)
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Model-based quantification of skin microcirculatory perfusion
- 2015. - 1
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Ingår i: Computational biophysics of the skin. - Boca Raton : CRC Press. - 9789814463843 - 9789814463850 ; , s. 395-418
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- During the last decades new tools, such as magnetic resonance imaging and Doppler ultra sound imaging, have rapidly been taken into clinical practice for studying the flow dynamics of the macrocirculation. M eanw hile, techniques for quantifying the microcirculation have struggled to become clinically accepted. This includes the use of laser Doppler flow metry (LDF), an optical technique that is capable of monitoring either spatial or temporal changes in the microcirculation by analyzing the backscattered Doppler shifted light from a laser illuminated tissue. Until now , LDF has only been capable of producing non-absolute relative measures, w hich has limited its cl inical acceptance. With a model based analysis approach, as presented here, this can be overcome, and objective diagnosis of the microcirculation may finally be a part of everyday clinical praxis. The most important advantages w ith the proposed method are that a quantitative perfusion estimate (% RBC × mm/ s) can be extracted, and that this measure can be resolved into different speed regions.
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| 2. |
- Fredriksson, Ingemar, 1980-, et al.
(författare)
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On the equivalence and differencesbetween laser Doppler flowmetry andlaser speckle contrast analysis
- 2016
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Ingår i: Journal of Biomedical Optics. - : SPIE - International Society for Optical Engineering. - 1083-3668 .- 1560-2281. ; 21:12
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Tidskriftsartikel (refereegranskat)abstract
- Laser Doppler flowmetry (LDF) and laser speckle contrast analysis (LASCA) both utilize the spatiotemporalproperties of laser speckle patterns to assess microcirculatory blood flow in tissue. Although the techniquesanalyze the speckle pattern differently, there is a close relationship between them. We present atheoretical overview describing how the LDF power spectrum and the LASCA contrast can be calculatedfrom each other, and how both these can be calculated from an optical Doppler spectrum containing variousdegrees of Doppler shifted light. The theoretical relationships are further demonstrated using time-resolvedspeckle simulations. A wide range of Monte Carlo simulated tissue models is then used to show how perfusionestimates for LDF and LASCA are affected by changes in blood concentration and speed distribution, as well asby geometrical and optical properties. We conclude that perfusion estimates from conventional single exposuretime LASCA are in general more sensitive to changes in optical and geometrical properties and are less accuratein the prediction of real perfusion changes, especially speed changes. Since there is a theoretical one-to-onerelationship between Doppler power spectrum and contrast, one can conclude that those drawbacks with theLASCA technique can be overcome using a multiple exposure time setup.
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| 3. |
- Hultman, Martin, et al.
(författare)
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A 15.6 frames per second 1 megapixel Multiple Exposure Laser Speckle Contrast Imaging setup
- 2018
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Ingår i: Journal of Biophotonics. - : Wiley-VCH Verlagsgesellschaft. - 1864-063X .- 1864-0648. ; 11:2
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Tidskriftsartikel (refereegranskat)abstract
- A multiple exposure laser speckle contrast imaging (MELSCI) setup for visualizing blood perfusion was developed using a field programmable gate array (FPGA), connected to a 1000 frames per second (fps) 1-megapixel camera sensor. Multiple exposure time images at 1, 2, 4, 8, 16, 32 and 64 milliseconds were calculated by cumulative summation of 64 consecutive snapshot images. The local contrast was calculated for all exposure times using regions of 4 × 4 pixels. Averaging of multiple contrast images from the 64-millisecond acquisition was done to improve the signal-to-noise ratio. The results show that with an effective implementation of the algorithm on an FPGA, contrast images at all exposure times can be calculated in only 28 milliseconds. The algorithm was applied to data recorded during a 5 minutes finger occlusion. Expected contrast changes were found during occlusion and the following hyperemia in the occluded finger, while unprovoked fingers showed constant contrast during the experiment. The developed setup is capable of massive data processing on an FPGA that enables processing of MELSCI data in 15.6 fps (1000/64 milliseconds). It also leads to improved frame rates, enhanced image quality and enables the calculation of improved microcirculatory perfusion estimates compared to single exposure time systems.
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| 4. |
- Hultman, Martin, 1992-, et al.
(författare)
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Evaluation of a high framerate multi-exposure laser speckle contrast imaging setup
- 2018
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Ingår i: High-Speed Biomedical Imaging and Spectroscopy III. - : SPIE - International Society for Optical Engineering. - 9781510614963
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Konferensbidrag (refereegranskat)abstract
- We present a first evaluation of a new multi-exposure laser speckle contrast imaging (MELSCI) system for assessing spatial variations in the microcirculatory perfusion. The MELSCI system is based on a 1000 frames per second 1-megapixel camera connected to a field programmable gate arrays (FPGA) capable of producing MELSCI data in realtime. The imaging system is evaluated against a single point laser Doppler flowmetry (LDF) system during occlusionrelease provocations of the arm in five subjects. Perfusion is calculated from MELSCI data using current state-of-the-art inverse models. The analysis displayed a good agreement between measured and modeled data, with an average error below 6%. This strongly indicates that the applied model is capable of accurately describing the MELSCI data and that the acquired data is of high quality. Comparing readings from the occlusion-release provocation showed that the MELSCI perfusion was significantly correlated (R=0.83) to the single point LDF perfusion, clearly outperforming perfusion estimations based on a single exposure time. We conclude that the MELSCI system provides blood flow images of enhanced quality, taking us one step closer to a system that accurately can monitor dynamic changes in skin perfusion over a large area in real-time
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| 5. |
- Strömberg, Tomas, 1966-, et al.
(författare)
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Spatial frequency domain imaging using a snap-shot filter mosaic camera with multi-wavelength sensitive pixels
- 2018
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Ingår i: Proceedings Volume 10467, Photonics in Dermatology and Plastic Surgery 2018; 104670D (2018). - : SPIE - International Society for Optical Engineering.
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Konferensbidrag (refereegranskat)abstract
- Spatial frequency domain imaging (SFDI) utilizes a digital light processing (DLP) projector for illuminating turbid media with sinusoidal patterns. The tissue absorption (μa) and reduced scattering coefficient (μ,s) are calculated by analyzing the modulation transfer function for at least two spatial frequencies. We evaluated different illumination strategies with a red, green and blue light emitting diodes (LED) in the DLP, while imaging with a filter mosaic camera, XiSpec, with 16 different multi-wavelength sensitive pixels in the 470-630 nm wavelength range. Data were compared to SFDI by a multispectral camera setup (MSI) consisting of four cameras with bandpass filters centered at 475, 560, 580 and 650 nm. A pointwise system for comprehensive microcirculation analysis was used (EPOS) for comparison. A 5-min arterial occlusion and release protocol on the forearm of a Caucasian male with fair skin was analyzed by fitting the absorption spectra of the chromophores HbO2, Hb and melanin to the estimatedμa. The tissue fractions of red blood cells (fRBC), melanin (/mel) and the Hb oxygenation (S02 ) were calculated at baseline, end of occlusion, early after release and late after release. EPOS results showed a decrease in S02 during the occlusion and hyperemia during release (S02 = 40%, 5%, 80% and 51%). The fRBC showed an increase during occlusion and release phases. The best MSI resemblance to the EPOS was for green LED illumination (S02 = 53%, 9%, 82%, 65%). Several illumination and analysis strategies using the XiSpec gave un-physiological results (e.g. negative S02 ). XiSpec with green LED illumination gave the expected change in /RBC , while the dynamics in S02 were less than those for EPOS. These results may be explained by the calculation of modulation using an illumination and detector setup with a broad spectral transmission bandwidth, with considerable variation in μa of included chromophores. Approaches for either reducing the effective bandwidth of the XiSpec filters or by including their characteristic in a light transport model for SFDI modulation, are proposed.
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