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An automated method for analysis of microcirculation videos for accurate assessment of tissue perfusion
© Demir et al.; licensee BioMed Central Ltd. 2012
Received: 16 November 2011
Accepted: 17 December 2012
Published: 21 December 2012
Imaging of the human microcirculation in real-time has the potential to detect injuries and illnesses that disturb the microcirculation at earlier stages and may improve the efficacy of resuscitation. Despite advanced imaging techniques to monitor the microcirculation, there are currently no tools for the near real-time analysis of the videos produced by these imaging systems. An automated system tool that can extract microvasculature information and monitor changes in tissue perfusion quantitatively might be invaluable as a diagnostic and therapeutic endpoint for resuscitation.
The experimental algorithm automatically extracts microvascular network and quantitatively measures changes in the microcirculation. There are two main parts in the algorithm: video processing and vessel segmentation. Microcirculatory videos are first stabilized in a video processing step to remove motion artifacts. In the vessel segmentation process, the microvascular network is extracted using multiple level thresholding and pixel verification techniques. Threshold levels are selected using histogram information of a set of training video recordings. Pixel-by-pixel differences are calculated throughout the frames to identify active blood vessels and capillaries with flow.
Sublingual microcirculatory videos are recorded from anesthetized swine at baseline and during hemorrhage using a hand-held Side-stream Dark Field (SDF) imaging device to track changes in the microvasculature during hemorrhage. Automatically segmented vessels in the recordings are analyzed visually and the functional capillary density (FCD) values calculated by the algorithm are compared for both health baseline and hemorrhagic conditions. These results were compared to independently made FCD measurements using a well-known semi-automated method. Results of the fully automated algorithm demonstrated a significant decrease of FCD values. Similar, but more variable FCD values were calculated using a commercially available software program requiring manual editing.
An entirely automated system for analyzing microcirculation videos to reduce human interaction and computation time is developed. The algorithm successfully stabilizes video recordings, segments blood vessels, identifies vessels without flow and calculates FCD in a fully automated process. The automated process provides an equal or better separation between healthy and hemorrhagic FCD values compared to currently available semi-automatic techniques. The proposed method shows promise for the quantitative measurement of changes occurring in microcirculation during injury.
Understanding the distribution and circulation of blood in capillaries has been considered a key aspect for assessment of tissue perfusion . Visualization and quantification of changes in microcirculation has been proposed as a potential tool in diagnosis and treatment of illnesses and diseases such as sepsis , sickle cell disease [3, 4], chronic ulcers, diabetes mellitus and hypertension [5, 6]. In each of these diseases, several characteristics of the microcirculation such as the structure of capillaries and quality of blood flow in the capillaries change over time [7–11]. A recent study suggests there is value in monitoring the microcirculation for titrating vasodilators in perioperative use . Monitoring microcirculation during resuscitation could also be envisioned as a tool to prevent over and under resuscitation of victims of hemorrhage and other critical illness and injuries such as sepsis. Therefore, quantitative and accurate analysis of the microcirculation is likely to be essential if microcirculatory imaging is to be adopted as useful tool in clinical monitoring .
Orthogonal polarization spectral (OPS) imaging [1, 2, 5] and side-stream dark field (SDF) imaging [13, 14] have been extensively employed in the field of clinical microcirculatory research. OPS and SDF imaging are both non-invasive imaging modalities and have been used to track changes in the microcirculation on mucosal surfaces. Most studies have used the sublingual surfaces of the oral cavity. These imaging techniques use green polarized light with wavelength of 550 nm which is absorbed by hemoglobin and makes red blood cells visible [15, 16].
To analyze microcirculatory images and videos, several software tools have been developed. However currently available software is unable to perform real or near real time analysis of the videos and require manual intervention to ensure accurate results. Researchers in the field have stated the need for improvements of current software to expedite clinical bedside use . The computer-assisted image analysis system CapImage (Zeintl, Heidelberg, Germany) was originally developed for traditional intravital microscopy , but is capable of analysis of SDF and OPS images . It uses a Line Shift Diagram Method for measurement of velocity and real-time movement correlation. This software tool is capable of measuring different properties of the microcirculation such as blood cell velocity and capillary density. However, it is only capable of detecting straight blood vessels which limits its efficacy since the microvascular geometry is complex. Expert users of CapImage claim that analysis of microcirculation with CapImage is time consuming and may only be performed off-line .
CapiScope, a system for the measurement of capillary morphology and capillary blood cell velocity, requires stable images, but lacks a stabilization function . JavaCap and Capilap Toolbox are two other available software tools which use triangulation methods to calculate intercapillary distance [22, 23].
Automated Vascular Analysis (AVA)—also known as MAS (Microvascular Analysis Software, Microvision Medical BV)—is the most current commercial software tool developed by Dobbe et al  for analysis of microcirculation videos. The method is the most accurate among the existing systems and performs a semi-automated process based on image stabilization, centerline detection and space time diagram. Despite all the capabilities provided by AVA, it does not provide full automation which leaves the burden of selecting the areas of interest, configuration, initialization, filtering of many false positives, dealing with many false negatives, and addressing of connectivity to the user. In addition, according to the developers of AVA, the software provides neither automatic vessel detection nor vessel diameter and blood flow calculation . The system, while an improvement, requires manual editing which can take over 20 minutes for a typical video sequence.
The aim of this study is to automate the analysis of microcirculatory video recordings and the derivation of Functional Capillary Density (FCD). FCD is defined as the ratio of the area of functionally active capillaries to the entire area of the image. FCD has been considered an important measurement of the microcirculation to indicate the quality of tissue perfusion . Image processing algorithms are designed for this study to automatically detect capillaries and small blood vessels in order to derive diagnostically useful information that may assist clinicians and medical researchers in the future.
The microcirculatory videos are captured by a commercially available hand-held SDF device (Microscan, Microvision Medical, BV). Because it is hand-held and is highly susceptible to motion artifacts due to movement of subject and/or device, we developed a stabilization algorithm to eliminate these motion artifacts. A block matching algorithm is developed that calculates cross-correlation coefficients to measure the similarity of the blocks. Block matching algorithms use a predefined size of windows-blocks or even entire images to estimate motion vectors. One of the disadvantages of block matching methods is defined as 'remarkableness' of the window content . If a window does not contain distinctive details, there is a high probability of mismatch. To avoid errors caused by ‘remarkableness’ issues, i.e. using points for matching that have no significant image-processing values (e.g. regular pixels inside the background) the processed blocks are checked to ensure they include blood vessels using Laplacian of Gaussian filtering. The stabilization process is described in detail in a previously published study . Gradients of the frames are calculated using the first order derivative of the Gaussian function. Gradient of the Gaussian enhances images and improves visibility of blood vessels. Distinctive features of the images, which are typically the branching points of blood vessels, are selected and assigned as control points to overcome remarkableness issues. Control points are selected which are known to belong to capillaries to calculate the transformation between two consecutive frames. For this purpose, a 3-by-3 Laplacian filter which calculates second order derivatives is applied to the output of the Gaussian Gradient.
The maximum values from seven areas of the frame are selected as control points. Then, around the control points, 25 × 25 pixel windows are selected as sub-regions. The cross-correlation is calculated between these sub-regions in the current frame and a 40 × 40 pixel window around these sub-regions in the following frame. The size of the windows discussed above was optimized based on a previous visual empirical assessment of the algorithm over a set of microcirculation videos. The frames are registered according to the results of correlation calculations. Since the control points are defined for the first frame and they are tracked through adjacent frames, Laplacian filtering is not repeated throughout the algorithm. If any of the defined control points leaves the current frame due to excessive motion, new control points are defined using the same method.
Preprocessing, multi-thresholding, and segmentation
After the stabilization of the video recordings, the weighted mean of five consecutive frames is calculated to improve connectivity of the blood vessels. The frame in the middle has the highest weight in this process. Averaging the frames is followed by preprocessing algorithms. The vessel extraction algorithm is based on multiple level thresholding. Preprocessing is repeated at each threshold with different parameters.
Video contrast and clarity vary widely from source to source and necessitate preprocessing in order to generate images that will yield accurate results. To enhance the local contrast, Contrast Limited Adaptive Histogram Equalization (CLAHE) is performed on microcirculation images. CLAHE partitions the image into small regions, called ‘tiles’, and applies histogram equalization to each tile in order to even out the overall gray level distribution of the image . Histogram equalization is followed by median filtering. To remove noise, median filtering is a widely preferred method in the literature . In this application, the purpose of applying median filtering is smoothing.
The window sizes of adaptive histogram equalization and median filtering are subject to change at each threshold level. At low threshold levels, in order to include only wide and clear vessels, histogram equalization is applied in smaller windows. The median filter size is kept large at these low threshold levels. As the threshold level increases, the result of the process is a darker binary image with almost all vessels and background included. Window size of adaptive histogram equalization is increased and median filter size is reduced to enhance the thinner vessels. Without these steps results will suffer as vessels may not be fully segmented and flow correctly detected. This preprocessing is followed by thresholding.
Vessel segmentation is based on verifying each pixel at multiple threshold levels as vessel. The method is modified from a pixel verification method proposed by Jiang et al. using retinal images . The pre-processed images are converted to binary images using multiple threshold levels resulting in multiple binary images. Euclidean Distance Transform (EDT) is created for each binary image. EDT calculates the distance of nearest background pixel for each object pixel. The coordinates of the nearest background pixel is the second output of the transform. For each pixel of each binary image, three different features are calculated using the outputs of the EDT and the gray-level intensity values of the pixels. Two of these parameters are the diameter P d and the angle P θ of the vessel, which are considered as geometrical features. The gray level intensity values of pre-processed images are used to calculate the third feature, P C , which is the contrast ratio identifying the ratio of intensity across background and blood vessel pixels. These three features serve to determine if a pixel in the image is indeed a vessel pixel. Pd limits the size of the vessel to ensure it is a capillary. P θ ensures curvilinear structure to the pixel, and excludes any anomalous pixels because of physiological improbabilities. Pc, ensures contrast between background and vessel pixels.
where GL(p) is the gray-level intensity value of current pixel ’p’. To calculate contrast ratio, images with enhanced contrast are used. Therefore, GL in Equation 3 stands for the gray level of the output of the CLAHE.
To verify the vessel candidate pixel, ’d’ needs to be less than pre-defined P d to avoid large vessels, ’θ’ needs to be larger than P θ to assure curvilinear structure and the calculated contrast ratio needs to be higher than P C to remove background noise. If the pixel in the binary image is black and it meets the criteria defined by three parameters P d , P θ and P C , it is verified to be a vessel pixel. After repeating the same procedure for all threshold levels, the segmented images of each threshold level are combined resulting in one segmented binary image for each frame.
The parameters, P d , P θ and P C were selected from multiple experiments using a set of training videos. P d controls the maximum diameter of the blood vessels to accept. It is determined based on the diameter of blood vessels and capillaries to be included in the microcirculation. P θ is another geometric parameter to ensure curvilinear structure of the vessels and is empirically derived.
Since the segmentation algorithm is based on pixel verification, it is possible to have isolated pixels in the result. To prevent that, binary morphological operators are used before region growing. The morphological operators include filling the isolated interior pixels and opening.
The region growing algorithm is developed to overcome disconnectivity of blood vessels. First, the final segmented image is divided into 35∗35 windows to determine the orientation of segmented vessel within the window. The vessel is allowed to grow in the computed direction if the gray level is within the range of average gray level of vessel pixels in the window ±0.5∗standard deviation.
Segmentation processes described up until this stage detect all blood vessels at each frame of the video recording. To provide quantitative information on blood flow, the vessels through which blood is flowing must be identified. To that end, the difference of consecutive segmented frames is calculated pixel by pixel. If the summation of difference for twenty segmented frames is higher than a threshold value, the pixel is assigned as an active blood vessel.
FCD is currently one of the main parameters used to evaluate the microcirculation. FCD can be calculated using two different approaches: one is completely manual by gridding the frame and counting the number of vessels crossing the grid lines; the second approach calculates the ratio of perfused vessels to the total surface using a software tool . FCD is calculated automatically in this study by dividing the area of active vessels to the total area of interest. It is much easier to form the skeleton of the network of active capillaries and calculate the length of this skeleton to form the density measure. However, since the width/thickness of capillaries along this network would be inconsistent (on the actual sublingual surface, the captured video, and in the processed image), the density measure calculated on this length would be the least reliable measure, as it does not incorporate the changes in the thickness of the capillary and therefore the true extent of circulation inside the capillary. The area-based density measure, on the other hand, since it incorporates the thickness of the capillaries into the calculation, is not susceptible to this issue. We have also included the length-based FCD calculation in this paper for comparison with the output from AVA.
Results and discussion
Calculated FCD values using the automated MCA algorithm, including both area and length based results
Baseline (PPV = 1)
Hemorrhagic (PPV < 1)
FCD (Area) %
FCD (Length) mm/mm2
FCD (Area) %
FCD (Length) mm/mm2
FCD (Area) %
FCD (Length) mm/mm2
2.35 × 10-5
1.42 × 10-5
9.28 × 10-6
3.35 × 10-5
1.48 × 10-5
1.87 × 10-5
3.10 × 10-5
3.26 × 10-5
-1.54 × 10-6
2.56 × 10-5
1.97 × 10-5
5.91 × 10-6
3.10 × 10-5
2.02 × 10-5
1.08 × 10-5
3.75 × 10-5
2.12 × 10-5
1.63 × 10-5
4.01 × 10-5
1.65 × 10-5
2.36 × 10-5
4.04 × 10-5
1.77 × 10-5
2.28 × 10-5
3.11 × 10-5
2.26 × 10-5
8.52 × 10-6
3.26 × 10-5
1.99 × 10-5
1.27 × 10-5
Calculated FCD values using semi-automated software, AVA
Baseline (PPV = 1)
Hemorrhagic (PPV < 1)
FCD (Area) %
FCD (Length) mm/mm2
FCD (Area) %
FCD (Length) mm/mm2
FCD (Area) %
FCD (Length) mm/mm2
1.63 × 10-5
9.52 × 10-6
6.73 × 10-6
2.15 × 10-5
1.47 × 10-5
6.80 × 10-6
1.72 × 10-5
1.62 × 10-5
9.75 × 10-7
2.41 × 10-5
1.91 × 10-5
5.00 × 10-6
2.18 × 10-5
9.65 × 10-6
1.22 × 10-5
1.00 × 10-5
8.29 × 10-6
1.72 × 10-6
1.75 × 10-5
1.43 × 10-5
3.15 × 10-6
1.23 × 10-5
8.22 × 10-6
4.08 × 10-6
8.18 × 10-6
8.04 × 10-6
1.35 × 10-7
1.65 × 10-5
1.20 × 10-5
4.53 × 10-6
It should be pointed out that even though AVA allows manual interaction, the version we had access to does not allow the user to draw the capillaries to be included. If the user sees that a capillary has not been identified, the user must define an area that the vessel resides in and then have the program outline the vessel. However, in some instances, the program will still not outline the vessel for inclusion in the FCD calculations. The user cannot manually force the outlining of vessels.
This study presents an entirely automated method, MCA, to derive quantitative information from microcirculatory videos in near real-time. Currently available techniques for analysis of the microcirculation, in their present state, do not appear to be practical in the clinical setting due to the need for significant manual interaction with the software in order to process the image and determine FCD. The significant difference in calculated FCD values across healthy baseline and hemorrhage shows that MCA has the potential for analyzing microcirculation videos in the clinical settings. Although the sample size of this study is relatively small, the algorithm demonstrates promise in its ability to rapidly provide quantitative information. Future studies will test the MCA algorithm on larger datasets—including human microcirculation videos—and improved accordingly. To overcome the variance among different video recordings, machine learning techniques, in particular neural networks and support vector machines that show superior performance in detection of elongated vessel-like objects in both biomedical image processing applications [32, 33] as well as other image processing applications , will be applied and algorithm parameters adjusted accordingly. The use of machine learning techniques provide for a means to compensate for variations due to differences in factors such as lighting, pressure, video quality and specific machine/camera used for imaging. Notwithstanding the small sample size, the results show promise for an automated system that derives diagnostically important information from microcirculation videos.
MCA and semi-automated AVA both show a significant decrease in FCD values for the hemorrhagic subjects. Even though FCD values calculated using semi-automated AVA are statistically different for the healthy and hemorrhagic cases (μ=3.78, σ=2.267, t8=5.0, p-value = 1.1 × 10−3), the difference is not consistent (Figure 7). As noted in Figure 9, the overlay of analyzed results demonstrates very close performance between the automated MCA algorithm and that of the heavily edited AVA method. FCD values during hemorrhage generated by MCA were consistently lower than FCD values from the healthy baseline state (Figure 8). Visual inspection of the videos confirmed the ability of MCA to identify more vessels without flow and thus not include them in the determination of FCD. A potential limitation to this finding is new version of AVA that reportedly allows users to add missed vessels by manual drawing. We did not have access to this version. While use of this newer version may have reduced the differences between semi-automated AVA and the fully automated MCA, this improved version of AVA still requires editing and interaction of the user with the software.
While the approach taken with MCA cannot be considered actual real-time, the 20 second wait for results versus the 20-40 minutes of manual interaction required with semi-automated AVA makes the use of MCA near real-time and may thus be appropriate in the future for bedside point-of-care decision making. Additionally, the use of MCA would negate the considerable training that must be provided to the AVA user in order for them to be able to properly identify the active vessels in the results. This is in contrast to the proposed automated system, which incorporates that knowledge in the algorithm.
In the future, the automated method could be easily integrated into existing SDF or OPSI hardware systems which would allow real-time bedside determinations of FCD and potentially other microcirculatory parameters such as flow quantification. It is likely that in order to use SDF or OPSI derived FCD measures to affect care, an automated and reproducible software approach to analysis will be required for regulatory approval of such an approach.
Recent automated capillary detection methods such as Bezemer et al.  demonstrated impressive speed in its analysis. The authors of this method, however, indicate that performance is limited by high cell densities and velocities, which severely impede the applicability of this method in real SDF images. We believe this is due to the fact that many factors and thresholds in this method were set to fixed numbers and that they require adjustment from one video to another (just as in AVA). Again, these issues form the basis for the MCA approach as a means of reaching true automation. While we used a binary assessment of flow (flow or no-flow) in identifying functional capillaries, improvements in assessing flow beyond this simple method may be helpful. This might result in improved accuracy and compensation for some of the mechanical shortcomings of image acquisition using the camera technology, which, is capable of producing pressure related flow artifacts.
A suggested algorithm to analyze microcirculation video recordings based on advanced machine learning is proposed which is capable of identifying active capillaries and calculating FCD parameters automatically. The approach is capable of detecting significant changes in FCD produced by hemorrhage and are comparable to a heavily manually edited commercially available software product. Future work will focus on adjusting the algorithm parameters on larger datasets and improving accuracy as well as developing improved methods of quantifying blood flow. It is hoped that these expanded methods and analyses will lead to the ability to derive diagnostically important decisions from the microcirculatory video recordings as well as to guide therapeutic interventions.
This material is based upon work supported by the National Science Foundation under Grant No. 1046521. All authors equally contributed to this work. The dataset used in this research was provided by Virginia Commonwealth University, Department of Emergency Medicine. In addition, the authors would like to thank Dr. Hakam Tiba and Gerard Draucker from the Virginia Commonwealth University Reanimation Engineering Science Center (VCURES) for their participation in sample preparation, data collection and verification of the results.
- Cĕrný V, Turek Z, Pařízková R: Orthogonal polarization spectral imaging: a review. Physiol Res. 2007, 56: 141-147.PubMedGoogle Scholar
- Bateman R, Sharpe M, Ellis C: Bench-to-bedside review: microvascular dysfunction in sepsis: hemodynamics, oxygen transport and nitric oxide. Crit Care Med. 2003, 7: 359-373. 10.1186/cc2353.Google Scholar
- Hebbel R, Osarogiagbon R, Kaul D: The endothelial biology of sickle cell disease; inflammation and chronic vasculopathy. Microcirculation. 2004, 11: 129-151.View ArticlePubMedGoogle Scholar
- Stuart M, Nagel R: Sickle cell disease. Lancet. 2004, 364: 1343-1360. 10.1016/S0140-6736(04)17192-4.View ArticlePubMedGoogle Scholar
- Levy B, Ambrosio G, Pries A, Struijker-Boudier H: Microcirculation in hypertension: a new target for treatment?. Circulation. 2001, 104: 735-740. 10.1161/hc3101.091158.View ArticlePubMedGoogle Scholar
- Verdant C, Backer DD: Monitoring of the microcirculation may help us at the bedside. Curr OpinCrit Care. 2005, 11 (3): 240-244. 10.1097/01.ccx.0000158849.94225.11.View ArticleGoogle Scholar
- Nath K, Katusic Z, Gladwin M: The perfusion paradox and instability in sickle cell disease. Microcirculation. 2004, 11: 179-193.View ArticlePubMedGoogle Scholar
- Kaul D, Farby M: In vivo studies of sickle red blood cells. Microcirculation. 2004, 11: 153-156.PubMedGoogle Scholar
- Touyz R: Intracellular mechanisms involved in vascular remodeling of resistance arteries in hypertension: role of angiotensin II. Exp Physiol. 2005, 90: 449-455. 10.1113/expphysiol.2005.030080.View ArticlePubMedGoogle Scholar
- Serne E, Gans R, ter Maaten J, Tangelder G, Donker A, Stehouwer C: Impaired skin capillary recruitment in essential hypertension is caused by both functional and structural capillary rarefaction. Hypertension. 2001, 38: 238-242. 10.1161/01.HYP.38.2.238.View ArticlePubMedGoogle Scholar
- Creager M, Luscher T, Cosentino F, Bechkman J: Diabetes and vascular disease: pathophysiology, clinical consequences, and medical therapy: part I. Circulation. 2003, 108: 1527-1532. 10.1161/01.CIR.0000091257.27563.32.View ArticlePubMedGoogle Scholar
- Atasever B, Boer C, van der Kuil M: Quantitative imaging of microcirculatory response during nitroglycerin-induced hypotension. J Cardiothorac Vasc Anesth. 2011, 25 (1): 140-144. 10.1053/j.jvca.2009.11.006.View ArticlePubMedGoogle Scholar
- Balestra G, Bezemer R, Boerma E, Yong Z, Sjauw K, Engstrom A, Koopmans M, Ince C: Improvement of sidestream dark field imaging with an image acquisition stabilizer. BMC Med Imaging. 2010, 10: 15-10.1186/1471-2342-10-15.View ArticlePubMedPubMed CentralGoogle Scholar
- Ince C: Sidestream dark field imaging: an improved technique to observe sublingual microcirculation. Crit Care. 2005, 9: 72-View ArticleGoogle Scholar
- Groner W, Winkelman JW, Harris AG, Ince C, Bouma GJ, Messmer K, Nadeau RG: Orthogonal polarization spectral imaging: a new method for study of the microcirculation. Natmed. 1999, 5: 1209-1212.Google Scholar
- Goedhart PT, Khalilzada M, Bezemer R, Merza J, Ince C: Sidestream dark field (SDF) imaging: a novel stroboscopic LED ring-based imaging modality for clinical assessment of the microcirculation. Opt Express. 2007, 15: 15101-15114. 10.1364/OE.15.015101.View ArticlePubMedGoogle Scholar
- Awan ZA, Wester T, Kvernebo K: Human microvascular imaging: a review of skin and tongue videomicroscopy techniques and analysing variables. Clin Physiol Funct Imaging. 2010, 30: 79-88. 10.1111/j.1475-097X.2009.00913.x.View ArticlePubMedGoogle Scholar
- Klyscz T, Junger M, Jung F, Zeintl H: Cap image: a new kind of computer-assisted video image analysis system for dynamic capillary microscopy. Biomed Tech (Berl). 1997, 42: 168-175.View ArticleGoogle Scholar
- Genzel-Boroviczeny O, Strotgen J, Harris AG, Messmer K, Christ F: Orthogonal polarization spectral imaging (OPS): a novel method to measure the microcirculation in term and preterm infants transcutaneously. Pediatr Res. 2002, 51: 386-391. 10.1203/00006450-200203000-00019.View ArticlePubMedGoogle Scholar
- Bauer A, Kofler S, Thiel M, Elfert S, Christ F: Monitoring of the sublingual microcirculation in cardiac surgery using orthogonal polarization spectral imaging. The American Society of Anesthesiologists. 2007, 107 (6): 939-945.Google Scholar
- Schaudig S, Dadasch B, Kellam K, Christ F: Validation of an analysis software for OPS-imaging used in humans. Proceedings of the 7th World Congress for Microcirculation. 2001, Sydney: Australian and New Zealand Microcirculation Society, 2-59.Google Scholar
- Zhong J, Asker C, Salerud E: Imaging, image processing and pattern analysis of skin capillary ensembles. Skin Res Technol. 2000, 6: 45-57. 10.1034/j.1600-0846.2000.006002045.x.View ArticlePubMedGoogle Scholar
- Sainthillier J, Gharbi T, Muret P, Humbert P: Skin capillary network recognition and analysis by means of neural algorithms. Skin Res Technol. 2005, 11: 9-16. 10.1111/j.1600-0846.2005.00087.x.View ArticlePubMedGoogle Scholar
- Dobbe J, Streekstra G, Atasever B, van Zijderveld R, Ince C: The measurement of functional microcirculatory density and velocity distributions using automated image analysis. Med BiolEngComput. 2008, 46 (7): 659-670.Google Scholar
- Nolte D, Zeintl H, Steinbauer M, Pickelmann S, Messmer K: Functional capillary density: an indicator of tissue perfusion?. Int J MicrocircClinExp. 1995, 15: 244-249. 10.1159/000179025.View ArticleGoogle Scholar
- Zitov_a B, Flusser J: Image registration methods: a survey. Image and Vision Computing. 2003, 21 (11): 977-1000. 10.1016/S0262-8856(03)00137-9.View ArticleGoogle Scholar
- Demir S, Mirshahi N, Tiba M, Draucker G, Ward K, Hobson R, Najarian K: Image processing and machine learning for diagnostic analysis of microcirculation. ICME International Conference on Complex Medical Engineering (CME 2009): 9-11 April 2009; Tempe. 2009, IEEE, 1-5.View ArticleGoogle Scholar
- Zuiderveld K: Contrast limited adaptive histogram equalization. Graphics Gems IV. Edited by: Heckbert PS. 1994, San Francisco: Morgan Kaufmann, 474-485.View ArticleGoogle Scholar
- Najarian K, Splinter R: Biomedical Signal and Image Processing. 2005, Boca Raton: The CRC PressGoogle Scholar
- Jiang X, Mojon D: Adaptive local thresholding by verification-based multithreshold probing with application to vessel detection in retinal images. IEEE Trans Pattern Anal Mach Intell. 2003, 25: 131-137. 10.1109/TPAMI.2003.1159954.View ArticleGoogle Scholar
- Backer DD, Hollenberg S, Boerma C, Goedhart P, Büchele G, Ospina-Tascon G, Dobbe I, Ince C: How to evaluate the microcirculation: report of a round table conference. Crit Care. 2007, 11 (5): R101-10.1186/cc6118.View ArticlePubMedPubMed CentralGoogle Scholar
- Chen W, Smith R, Ji SY, Ward K, Najarian K: Automated ventricular systems segmentation in brain CT images by combining low-level segmentation and high level template matching. BMC Med Inform Decis Mak. 2009, 9 (Suppl 1): S4-10.1186/1472-6947-9-S1-S4.View ArticlePubMedPubMed CentralGoogle Scholar
- Ji SY, Smith R, Huynh T, Najarian K: A comparative analysis of multi-level computer-assisted decision making systems for traumatic brain injuries. BMC Med Inform Decis Mak. 2009, 9: 2-10.1186/1472-6947-9-2.View ArticlePubMedPubMed CentralGoogle Scholar
- Muralikrishnan B, Najarian K, Raja J: Surface wavelength based clustering using neural networks for manufacturing process mapping. Int J Mach Tool Manuf. 2003, 43 (4): 369-477. 10.1016/S0890-6955(02)00272-9.View ArticleGoogle Scholar
- Bezemer R, Dobbe J, Bartels S, Boerma C, Elbers P, Heger M, Ince C: Rapid automatic assessment of microvascular density in sidestream dark field images. Med Biol Eng Comput. 2011, 49: 1269-1278. 10.1007/s11517-011-0824-1.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2342/12/37/prepub
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