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        <title>BioMedical Engineering OnLine - Latest Articles</title>
        <link>http://www.biomedical-engineering-online.com</link>
        <description>The latest research articles published by BioMedical Engineering OnLine</description>
        <dc:date>2010-03-09T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/16" />
                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/15" />
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                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/12" />
                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/11" />
                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/10" />
                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/9" />
                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/8" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/16">
        <title>Motion artifact cancellation in NIR spectroscopy using discrete Kalman filtering</title>
        <description>Background:
As a continuation of our earlier work, we present in this study a Kalman filtering based algorithm for the elimination of motion artifacts present in Near Infrared spectroscopy (NIR) measurements. Functional NIR measurements suffer from head motion especially in real world applications where movement cannot be restricted such as studies involving pilots, children, etc. Since head movement can cause fluctuations unrelated to metabolic changes in the blood due to the cognitive activity, removal of these artifacts from NIR signal is necessary for reliable assessment of cognitive activity in the brain for real life applications.
Methods:
Previously, we had worked on adaptive and Wiener filtering for the cancellation of motion artifacts in NIR studies. Using the same NIR data set we have collected in our previous work where different speed motion artifacts were induced on the NIR measurements we compared the results of the newly proposed Kalman filtering approach with the results of previously studied adaptive and Wiener filtering methods in terms of gains in signal to noise ratio. Here, comparisons are based on paired t-tests where data from eleven subjects are used.
Results:
The preliminary results in this current study revealed that the proposed Kalman filtering method provides better estimates in terms of the gain in signal to noise ratio than the classical adaptive filtering approach without the need for additional sensor measurements and results comparable to Wiener filtering but better suitable for real-time applications.
Conclusions:
This paper presented a novel approach based on Kalman filtering for motion artifact removal in NIR recordings. The proposed approach provides a suitable solution to the motion artifact removal problem in NIR studies by combining the advantages of the existing adaptive and Wiener filtering methods in one algorithm which allows efficient real time application with no requirement on additional sensor measurements.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/16</link>
                <dc:creator>Meltem Izzetoglu</dc:creator>
                <dc:creator>Prabhakar Chitrapu</dc:creator>
                <dc:creator>Scott Bunce</dc:creator>
                <dc:creator>Banu Onaral</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:16</dc:source>
        <dc:date>2010-03-09T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-16</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>16</prism:startingPage>
        <prism:publicationDate>2010-03-09T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/15">
        <title>Factors that affect mass transport from drug eluting stents into the artery wall</title>
        <description>Coronary artery disease can be treated by implanting a stent into the blocked region of an artery, thus enabling blood perfusion to distal vessels. Minimally invasive procedures of this nature often result in damage to the arterial tissue culminating in the re-blocking of the vessel. In an effort to alleviate this phenomenon, known as restenosis, drug eluting stents were developed. They are similar in composition to a bare metal stent but encompass a coating with therapeutic agents designed to reduce the overly aggressive healing response that contributes to restenosis. There are many variables that can influence the effectiveness of these therapeutic drugs being transported from the stent coating to and within the artery wall, many of which have been analysed and documented by researchers. However, the physical deformation of the artery substructure due to stent expansion, and its influence on a drugs ability to diffuse evenly within the artery wall have been lacking in published work to date. The paper highlights previous approaches adopted by researchers and proposes the addition of porous artery wall deformation to increase model accuracy.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/15</link>
                <dc:creator>Barry O'Connell</dc:creator>
                <dc:creator>Tim McGloughlin</dc:creator>
                <dc:creator>Michael Walsh</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:15</dc:source>
        <dc:date>2010-03-09T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-15</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>15</prism:startingPage>
        <prism:publicationDate>2010-03-09T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/14">
        <title>A novel method for blood vessel detection from retinal images</title>
        <description>Background:
The morphological changes of the retinal blood vessels in retinal images are important indicators for diseases like diabetes, hypertension and glaucoma. Thus the accurate segmentation of blood vessel is of diagnostic value.
Methods:
In this paper, we present a novel method to segment retinal blood vessels to overcome the variations in contrast of large and thin vessels. This method uses adaptive local thresholding to produce a binary image then extract large connected components as large vessels. The residual fragments in the binary image including some thin vessel segments (or pixels), are classified by Support Vector Machine (SVM). The tracking growth is applied to the thin vessel segments to form the whole vascular network.
Results:
The proposed algorithm is tested on DRIVE database, and the average sensitivity is over 77% while the average accuracy reaches 93.2%.
Conclusions:
In this paper, we distinguish large vessels by adaptive local thresholding for their good contrast. Then identify some thin vessel segments with bad contrast by SVM, which can be lengthened by tracking. This proposed method can avoid heavy computation and manual intervention.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/14</link>
                <dc:creator>Lili Xu</dc:creator>
                <dc:creator>Shuqian Luo</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:14</dc:source>
        <dc:date>2010-02-28T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-14</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>14</prism:startingPage>
        <prism:publicationDate>2010-02-28T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/13">
        <title>A statistical model for multidimensional irreversible electroporation cell death in tissue</title>
        <description>Background:
Irreversible electroporation (IRE) is a minimally invasive tissue ablation technique which utilizes electric pulses delivered by electrodes to a targeted area of tissue to produce high high amplitude electric fields, thus inducing irreversible damage to the cell membrane lipid bilayer.  An important application of this technique is for cancer tissue ablation. Mathematical modelling is considered important in IRE treatment planning. In the past, IRE mathematical modelling used a deterministic single value for the amplitude of the electric field required for causing cell death.  However, tissue, particularly cancerous tissue, is comprised of a population of different cells of different sizes and orientations, which in conventional IRE are exposed to complex electric fields; therefore, using a deterministic single value is overly simplistic.
Methods:
We introduce and describe a new methodology for evaluating IRE induced cell death in tissue. Our approach employs a statistical Peleg-Fermi model to correlate probability of cell death in heterogeneous tissue to the parameters of electroporation pulses such as the number of pulses, electric field amplitude and pulse length. For treatment planning, the Peleg-Fermi model is combined with a numerical solution of the multidimensional electric field equation cast in a dimensionless form.  This is the first time in which this concept is used for evaluating IRE cell death in multidimensional situations.
Results:
We illustrate the methodology using data reported in literature for prostate cancer cell death by IRE. We show how to fit this data to a Fermi function in order to calculate the critical statistic parameters. To illustrate the use of the methodology, we simulated 2-D irreversible electroporation protocols and produced 2-D maps of the statistical distribution of cell death in the treated region. These plots were compared to plots produced using a deterministic model of cell death by IRE and the differences were noted.
Conclusions:
In this work we introduce a new methodology for evaluation of tissue ablation by IRE using statistical models of cell death. We believe that the use of a statistical model rather than a deterministic model for IRE cell death will improve the accuracy of treatment planning for cancer treatment with IRE.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/13</link>
                <dc:creator>Alex Golberg</dc:creator>
                <dc:creator>Boris Rubinsky</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:13</dc:source>
        <dc:date>2010-02-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-13</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>13</prism:startingPage>
        <prism:publicationDate>2010-02-26T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/12">
        <title>Measurement of intrinsic optical backscattering characteristics of cells using fiber-guided near infrared light

</title>
        <description>Background:
Intrinsic optical signals (IOS), which reflect changes in transmittance and scattering light, have been applied to characterize the physiological conditions of target biological tissues. Backscattering approaches allow mounting of the source and detector on the same side of a sample which creates a more compact physical layout of device. This study presents a compact backscattering design using fiber-optic guided near-infrared (NIR) light to measure the amplitude and phase changes of IOS under different osmotic challenges.
Methods:
High-frequency intensity-modulated light was guided via optic fiber, which was controlled by micromanipulator to closely aim at a minimum cluster of cortical neurons. Several factors including the probe design, wavelength selection, optimal measuring distance between the fiber-optical probe and cells were considered. Our experimental setup was tested in cultured cells to observe the relationship between the changes in backscattered NIR light and cellular IOS, which is believed mainly caused by cell volume changes in hypo/hyperosmotic solutions (+/-20, +/-40 and +/-60 mOsm).
Results:
The critical parameters of the current setup including the optimal measuring distance from fiber-optical probe to target tissue and the linear relationship between backscattering intensity and cell volume were determined. The backscattering intensity was found to be inversely proportional to osmotic changes. However, the phase shift exhibited a nonlinear feature and reached a plateau at hyperosmotic solution.
Conclusions:
Our study indicated that the backscattering NIR light guided by fiber-optical probe makes it a potential alternative for continuous observation of intrinsic optical properties of cell culture under varied physical or chemical challenges.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/12</link>
                <dc:creator>Ching-Huang Hsu</dc:creator>
                <dc:creator>Gwo-Ching Chang</dc:creator>
                <dc:creator>En-Ting Li</dc:creator>
                <dc:creator>Yu-Jing Lin</dc:creator>
                <dc:creator>Jia-Jin Chen</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:12</dc:source>
        <dc:date>2010-02-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-12</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>12</prism:startingPage>
        <prism:publicationDate>2010-02-25T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/11">
        <title>A cardiorespiratory classifier of voluntary and involuntary electrodermal activity</title>
        <description>Background:
Electrodermal reactions (EDRs) can be attributed to many origins, including spontaneous fluctuations of electrodermal activity (EDA) and stimuli such as deep inspirations, voluntary mental activity and startling events.  In fields that use EDA as a measure of psychophysiological state, the fact that EDRs may be elicited from many different stimuli is often ignored.  This study attempts to classify observed EDRs as voluntary (i.e., generated from intentional respiratory or mental activity) or involuntary (i.e., generated from startling events or spontaneous electrodermal fluctuations).
Methods:
Eight able-bodied participants were subjected to conditions that would cause a change in EDA: music imagery, startling noises, and deep inspirations.  A user-centered cardiorespiratory classifier consisting of 1) an EDR detector, 2) a respiratory filter and 3) a cardiorespiratory filter was developed to automatically detect a participant&apos;s EDRs and to classify the origin of their stimulation as voluntary or involuntary.
Results:
Detected EDRs were classified with a positive predictive value of 78%, a negative predictive value of 81% and an overall accuracy of 78%.  Without the classifier, EDRs could only be correctly attributed as voluntary or involuntary with an accuracy of 50%.
Conclusions:
The proposed classifier may enable investigators to form more accurate interpretations of electrodermal activity as a measure of an individual&apos;s psychophysiological state.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/11</link>
                <dc:creator>Stefanie Blain</dc:creator>
                <dc:creator>Sarah Power</dc:creator>
                <dc:creator>Ervin Sejdic</dc:creator>
                <dc:creator>Alex Mihailidis</dc:creator>
                <dc:creator>Tom Chau</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:11</dc:source>
        <dc:date>2010-02-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-11</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>11</prism:startingPage>
        <prism:publicationDate>2010-02-25T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/10">
        <title>Towards treatment planning and treatment of deep-seated solid tumors by electrochemotherapy</title>
        <description>Background:
Electrochemotherapy treats tumors by combining specific chemotherapeutic drugs with an intracellular target and electric pulses, which increases drug uptake into the tumor cells. Electrochemotherapy has been successfully used for treatment of easily accessible superficial tumor nodules. In this paper, we present the first case of deep-seated tumor electrochemotherapy based on numerical treatment planning.
Methods:
The aim of our study was to treat a melanoma metastasis in the thigh of a patient. Treatment planning for electrode positioning and electrical pulse parameters was performed for two different electrode configurations: one with four and another with five long needle electrodes. During the procedure, the four electrode treatment plan was adopted and the patient was treated accordingly by electrochemotherapy with bleomycin. The response to treatment was clinically and radiographically evaluated. Due to a partial response of the treated tumor, the metastasis was surgically removed after 2 months and pathological analysis was performed.
Results:
A partial response of the tumor to electrochemotherapy was obtained. Histologically, the metastasis showed partial necrosis due to electrochemotherapy, estimated to represent 40-50% of the tumor. Based on the data obtained, we re-evaluated the electrical treatment parameters in order to correlate the treatment plan with the clinical response. Electrode positions in the numerical model were updated according to the actual positions during treatment. We compared the maximum value of the measured electric current with the current predicted by the model and good agreement was obtained. Finally, tumor coverage with an electric field above the reversible threshold was recalculated and determined to be approximately 94%. Therefore, according to the calculations, a small volume of tumor cells remained viable after electrochemotherapy, and these were sufficient for tumor regrowth.
Conclusions:
In this, the first reported clinical case, deep-seated melanoma metastasis in the thigh of the patient was treated by electrochemotherapy, according to a treatment plan obtained by numerical modeling and optimization. Although only a partial response was obtained, the presented work demonstrates that treatment of deep-seated tumor nodules by electrochemotherapy is feasible and sets the ground for numerical treatment planning-based electrochemotherapy.Trial registration: EudraCT:2008-008290-54</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/10</link>
                <dc:creator>Damijan Miklavcic</dc:creator>
                <dc:creator>Marko Snoj</dc:creator>
                <dc:creator>Anze Zupanic</dc:creator>
                <dc:creator>Bor Kos</dc:creator>
                <dc:creator>Maja Cemazar</dc:creator>
                <dc:creator>Mateja Kropivnik</dc:creator>
                <dc:creator>Matej Bracko</dc:creator>
                <dc:creator>Tjasa Pecnik</dc:creator>
                <dc:creator>Eldar Gadzijev</dc:creator>
                <dc:creator>Gregor Sersa</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:10</dc:source>
        <dc:date>2010-02-23T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-10</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>10</prism:startingPage>
        <prism:publicationDate>2010-02-23T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/9">
        <title>Influence of nanofibers on growth and gene expression of human tendon derived fibroblasts</title>
        <description>Background:
Rotator cuff tears are a common and frequent lesion especially in older patients. The mechanisms of tendon repair are not fully understood. Common therapy options for tendon repair include mini-open or arthroscopic surgery. The use of growth factors in experimental studies is mentioned in the literature. Nanofiber scaffolds, which provide several criteria for the healing process, might be a suitable therapy option for operative treatment. The aim of this study was to explore the effects of nanofiber scaffolds on human tendon derived fibroblasts (TDF&apos;s), as well as the gene expression and matrix deposition of these fibroblasts.
Methods:
Nanofibers composed of PLLA and PLLA/Col-I were seeded with human tendon derived fibroblasts and cultivated over a period of 22 days under growth-inductive conditions, and analyzed during the course of culture, with respect to gene expression of different extra cellular matrix components such as collagens, bigylcan and decorin. Furthermore, we measured cell densities and proliferation by using fluorescene microscopy.
Results:
PLLA nanofibers possessed a growth inhibitory effect on TDF&apos;s. Furthermore, no meaningful influence on the gene expression of collagen I, collagen III and decorin could be observed, while the expression of collagen X increased during the course of cultivation. On the other hand, PLLA/Col-I blend nanofibers had no negative influence on the growth of TDF&apos;s. Furthermore, blending PLLA nanofibers with collagen had a positive effect on the gene expression of collagen I, III, X and decorin. Here, gene expression indicated that focal adherence kinases might be involved.
Conclusion:
This study indicates that the use of nanofibers influence expression of genes associated with the extra cellular matrix formation. The composition of the nanofibers plays a critical role. While PLLA/Col-I blend nanofibers enhance the collagen I and III formation, their expression on PLLA nanofibers was more comparable to controls. However, irrespective of the chemical composition of the fibres, the collagen deposition was altered, an effect which might be associated with a decreased expression of biglycanes.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/9</link>
                <dc:creator>Christina Theisen</dc:creator>
                <dc:creator>Susanne Fuchs-Winkelmann</dc:creator>
                <dc:creator>Karola Knappstein</dc:creator>
                <dc:creator>Turgay Efe</dc:creator>
                <dc:creator>Jan Schmitt</dc:creator>
                <dc:creator>Juergen Paletta</dc:creator>
                <dc:creator>Markus Schofer</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:9</dc:source>
        <dc:date>2010-02-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-9</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>9</prism:startingPage>
        <prism:publicationDate>2010-02-17T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/8">
        <title>Non-rigid registration of breast surfaces using the laplace and diffusion equations</title>
        <description>A semi-automated, non-rigid breast surface registration method is presented that involves solving the Laplace or diffusion equations over undeformed and deformed breast surfaces. The resulting potential energy fields and isocontours are used to establish surface correspondence. This novel surface-based method, which does not require intensity images, anatomical landmarks, or fiducials, is compared to a gold standard of thin-plate spline (TPS) interpolation. Realistic finite element simulations of breast compression and further testing against a tissue-mimicking phantom demonstrate that this method is capable of registering surfaces experiencing 6 - 36 mm compression to within a mean error of 0.5 - 5.7 mm.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/8</link>
                <dc:creator>Rowena Ong</dc:creator>
                <dc:creator>Jao Ou</dc:creator>
                <dc:creator>Michael Miga</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:8</dc:source>
        <dc:date>2010-02-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-8</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2010-02-12T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/7">
        <title>Effects of liquid stimuli on dual-axis swallowing accelerometry signals in a healthy population</title>
        <description>Background:
Dual-axis swallowing accelerometry has recently been proposed as a tool for non-invasive analysis of swallowing function. Although swallowing is known to be physiologically modifiable by the type of food or liquid (i.e., stimuli), the effects of stimuli on dual-axis accelerometry signals have never been thoroughly investigated. Thus, the objective of this study was to investigate stimulus effects on dual-axis accelerometry signal characteristics. Signals were acquired from 17 healthy participants while swallowing 4 different stimuli: water, nectar-thick and honey-thick apple juices, and a thin-liquid barium suspension. Two swallowing tasks were examined: discrete and sequential. A variety of features were extracted in the time and time-frequency domains after swallow segmentation and pre-processing. A separate Friedman test was conducted for each feature and for each swallowing task.
Results:
Significant main stimulus effects were found on 6 out of 30 features for the discrete task and on 5 out of 30 features for the sequential task. Analysis of the features with significant stimulus effects suggested that the changes in the signals revealed slower and more pronounced swallowing patterns with increasing bolus viscosity.
Conclusions:
We conclude that stimulus type does affect specific characteristics of dual-axis swallowing accelerometry signals, suggesting that associated clinical screening protocols may need to be stimulus specific.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/7</link>
                <dc:creator>Joon Lee</dc:creator>
                <dc:creator>Ervin Sejdic</dc:creator>
                <dc:creator>Catriona Steele</dc:creator>
                <dc:creator>Tom Chau</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:7</dc:source>
        <dc:date>2010-02-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-7</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2010-02-04T00:00:00Z</prism:publicationDate>
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