<?xml version="1.0" encoding="UTF-8" standalone="yes"?><oembed><version><![CDATA[1.0]]></version><provider_name><![CDATA[TBI Rehabilitation]]></provider_name><provider_url><![CDATA[https://tbirehabilitation.wordpress.com]]></provider_url><author_name><![CDATA[Kostas Pantremenos]]></author_name><author_url><![CDATA[https://tbirehabilitation.wordpress.com/author/onganalop/]]></author_url><title><![CDATA[[ARTICLE] Visual processing speed in hemianopia patients secondary to acquired brain injury: a new assessment methodology &#8211; Full&nbsp;Text]]></title><type><![CDATA[link]]></type><html><![CDATA[<section lang="en" aria-labelledby="Abs1">
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<h2 id="Abs1" class="c-article-section__title u-h2 js-section-title js-c-reading-companion-sections-item">Abstract</h2>
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<h3 class="c-article__sub-heading u-h3">Background</h3>
<p>There is a clinical need to identify diagnostic parameters that objectively quantify and monitor the effective visual ability of patients with homonymous visual field defects (HVFDs). Visual processing speed (VPS) is an objective measure of visual ability. It is the reaction time (RT) needed to correctly search and/or reach for a visual stimulus. VPS depends on six main brain processing systems: auditory-cognitive, attentional, working memory, visuocognitive, visuomotor, and executive. We designed a new assessment methodology capable of activating these six systems and measuring RTs to determine the VPS of patients with HVFDs.</p>
<h3 class="c-article__sub-heading u-h3">Methods</h3>
<p>New software was designed for assessing subject visual stimulus search and reach times (S-RT and R-RT respectively), measured in seconds. Thirty-two different everyday visual stimuli were divided in four complexity groups that were presented along 8 radial visual field positions at three different eccentricities (10<sup>o</sup>, 20<sup>o</sup>, and 30<sup>o</sup>). Thus, for each HVFD and control subject, 96 S- and R-RT measures related to VPS were registered. Three additional variables were measured to gather objective data on the validity of the test: eye-hand coordination mistakes (ehcM), eye-hand coordination accuracy (ehcA), and degrees of head movement (dHM, measured by a head-tracker system). HVFD patients and healthy controls (30 each) matched by age and gender were included. Each subject was assessed in a single visit. VPS measurements for HFVD patients and control subjects were compared for the complete test, for each stimulus complexity group, and for each eccentricity.</p>
<h3 class="c-article__sub-heading u-h3">Results</h3>
<p>VPS was significantly slower (<i>p</i> &lt; 0.0001) in the HVFD group for the complete test, each stimulus complexity group, and each eccentricity. For the complete test, the VPS of the HVFD patients was 73.0% slower than controls. They also had 335.6% more ehcMs, 41.3% worse ehcA, and 189.0% more dHMs than the controls.</p>
<h3 class="c-article__sub-heading u-h3">Conclusions</h3>
<p>Measurement of VPS by this new assessment methodology could be an effective tool for objectively quantifying the visual ability of HVFD patients. Future research should evaluate the effectiveness of this novel method for measuring the impact that any specific neurovisual rehabilitation program has for these patients.</p>
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<section aria-labelledby="Sec1">
<div id="Sec1-section" class="c-article-section">
<h2 id="Sec1" class="c-article-section__title u-h2 js-section-title js-c-reading-companion-sections-item">Background</h2>
<div id="Sec1-content" class="c-article-section__content">
<p>Vision is the dominant sensory function in humans because visual search and reach tasks are crucial to efficient performance of the main activities of daily life [<a id="ref-link-section-d71843e780" title="Jan JE, Heaven RK, Matsuba C, Langley B, Roman-Lantzy C, Anthony T. Windows into the visual brain : new discoveries about the visual system, its functions, and implications for practitioners. J Vis Impair Blind. 2013;107:256–61." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR1" aria-label="Reference 1">1</a>, <a id="ref-link-section-d71843e783" title="Graven T. Aspects of object recognition: when touch replaces vision as the dominant sense modality. Vis Impair Res. 2003;5:101–12." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR2" aria-label="Reference 2">2</a>]. The term visual processing speed (VPS), an important variable of visual sensory function, is the <i>amount of time</i> needed to make a <i>correct interaction</i> with a visual stimulus [<a id="ref-link-section-d71843e792" title="Thorpe S, Fize D, Marlot C. Speed of processing in the human visual system. Nature. 1996;381:520–2." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR3" aria-label="Reference 3">3</a>, <a id="ref-link-section-d71843e796" title="Owsley C. Visual processing speed. Vis Res. 2013;90:52–6. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR4" aria-label="Reference 4">4</a>]. The term <i>correct interaction</i> is the effective realization of a complete executive action of visual search and reach [<a id="ref-link-section-d71843e802" title="Braddick O, Atkinson J. Development of human visual function. Vis Res. 2011;51:1588–609." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR5" aria-label="Reference 5">5</a>], e.g., visualizing a glass of water placed on a table and then grasping it by precise eye-hand coordination (EHC). Accordingly, the VPS variable defines the global reaction time (RT) that is composed of two additive RT sub-variables: search reaction time (S-RT) and reach reaction time (R-RT) [<a id="ref-link-section-d71843e805" title="Orban GA, Dupont P, Vogels R, DeBruyn B, Bormans G, Mortelmans L. Task dependency of visual processing in the human visual system. Behav Brain Res. 1996;76:215–23." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR6">6</a>,<a id="ref-link-section-d71843e805_1" title="Kirchner H, Thorpe SJ. Ultra-rapid object detection with saccadic eye movements: visual processing speed revisited. Vis Res. 2006;46:1762–76." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR7">7</a>,<a id="ref-link-section-d71843e808" title="Lobier M, Dubois M, Valdois S. The role of visual processing speed in reading speed development. PLoS One. 2013;8:e58097. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR8" aria-label="Reference 8">8</a>]. Furthermore, VPS is mainly interdependent on intrinsic visual cognitive processing mechanisms, the complexity of the determined stimulus to be recognized (defined principally in terms of size, contrast, semantic content, and number of traces or interior angles [<a id="ref-link-section-d71843e811" title="Palumbo L, Ogden R, Makin ADJ, Bertamini M. Examining visual complexity and its influence on perceived duration. J Vis. 2014;14:1–18. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR9" aria-label="Reference 9">9</a>, <a id="ref-link-section-d71843e815" title="Donderi DC. Visual complexity: a review. Psychol Bull. 2006;132:73–97. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR10" aria-label="Reference 10">10</a>]), the number of distractor stimuli surrounding it, and the distance from the point of fixation to the particular stimulus that the person is tasked to identify (eccentricity) [<a id="ref-link-section-d71843e818" title="Owsley C. Visual processing speed. Vis Res. 2013;90:52–6. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR4" aria-label="Reference 4">4</a>, <a id="ref-link-section-d71843e821" title="Lamme V, Roelfsema P. The distinct modes of vision offered by feedforward and recurrent processing. Trends Neurosci. 2000;23:571–9." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR11">11</a>,<a id="ref-link-section-d71843e821_1" title="Mancebo-Azor R, Sáez-Moreno JA, Domínguez-Hidalgo I, Castillo JDL, Del Rodríguez-Ferrer JM. Efectos del contraste, excentricidad y posición en la detección de estímulos visuales en humanos. Rev Neurol. 2009;48:129–33." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR12">12</a>,<a id="ref-link-section-d71843e824" title="Land MF. Eye movements and the control of actions in everyday life. Prog Retin Eye Res. 2006;25:296–324." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR13" aria-label="Reference 13">13</a>]. Thus, VPS is a quantifiable parameter that objectively reflects a subject’s global visual ability.</p>
<p>Recent findings in the field of visual psychophysics show that having adequate VPS is necessary and dependent upon the proper functioning of six main brain-processing systems: auditory-cognitive, attentional, working-memory, visuocognitive, visuomotor, and executive [<a id="ref-link-section-d71843e830" title="Lewis JW, Beauchamp MS, DeYoe EA. A comparison of visual and auditory motion processing in human cerebral cortex. Cereb Cortex. 2000;10:873–88. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR14">14</a>,<a id="ref-link-section-d71843e830_1" title="Takeuchi H, Taki Y, Sassa Y, Hashizume H, Sekiguchi A, Fukushima A, et al. Brain structures associated with executive functions during everyday events in a non-clinical sample. Brain Struct Funct. 2013;218:1017–32." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR15">15</a>,<a id="ref-link-section-d71843e830_2" title="Petersen S, Posner M. The attention system of the human brain: 20 years after. Annu Rev Neurosci. 2012;21:73–89." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR16">16</a>,<a id="ref-link-section-d71843e830_3" title="Bleckley MK, Foster JL, Engle RW. Working memory capacity accounts for the ability to switch between object-based and location-based allocation of visual attention. Mem Cogn. 2015;43:379–88." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR17">17</a>,<a id="ref-link-section-d71843e833" title="Le-Hoa Võ M, Wolfe JM. The role of memory for visual search in scenes. Ann N Y Acad Sci. 2015;1339:72–81. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR18" aria-label="Reference 18">18</a>]. Consequently, an acquired brain injury (ABI) that affects any of these cerebral processing systems could decrease the VPS.</p>
<p>ABI is one of the most important and disabling public health problems of our era due to the high incidence and prevalence [<a id="ref-link-section-d71843e839" title="Brewer L, Horgan F, Hickey A, Williams D. Stroke rehabilitation: recent advances and future therapies. QJM. 2013;106:11–25. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR19" aria-label="Reference 19">19</a>]. Following an ABI, between 30 and 85% of patients will experience some type of visual dysfunction [<a id="ref-link-section-d71843e842" title="Khan S, Leung E, Jay WM. Stroke and visual rehabilitation. Top Stroke Rehabil. 2008;15:27–36. 
https://doi.org/10.1310/tsr1501-27

." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR20" aria-label="Reference 20">20</a>, <a id="ref-link-section-d71843e845" title="Kerkhoff G. Neurovisual rehabilitation: recent developments and future directions. J Neurol Neurosurg Psychiatry. 2000;68:691–706. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR21" aria-label="Reference 21">21</a>], especially homonymous visual field defects (HVFDs) secondary to lesions involving the visual afferent pathways posterior to the chiasm [<a id="ref-link-section-d71843e848" title="Goodwin D. Homonymous hemianopia: challenges and solutions. Clin Ophthalmol. 2014;8:1919–27. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR22" aria-label="Reference 22">22</a>]. Eye tracking technology has shown that HVFDs prevent patients from having the appropriate control of their oculomotor systems [<a id="ref-link-section-d71843e851" title="Reinhard JI, Damm I, Ivanov IV, Trauzettel-Klosinski S. Eye movements during saccadic and fixation tasks in patients with homonymous hemianopia. J Neuroophthalmol. 2014;34:354–61." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR23">23</a>,<a id="ref-link-section-d71843e851_1" title="McDonald SA, Spitsyna G, Shillcock RC, WiseRichard JS, Leff AP. Patients with hemianopic alexia adopt an inefficient eye movement strategy when reading text. Brain. 2005;129:158–67 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR26" aria-label="Reference 26">26</a>]. This is especially apparent in the saccadic system, because it is interdependent with the covert attention mechanisms associated with peripheral vision [<a id="ref-link-section-d71843e858" title="Schall JD. Production, control, and visual guidance of saccadic eye movements. ISRN Neurol. 2013;2013:1–17. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR33" aria-label="Reference 33">33</a>, <a id="ref-link-section-d71843e886" title="Sand KM, Midelfart A, Thomassen L, Melms A, Wilhelm H, Hoff JM. Visual impairment in stroke patients - a review. Acta Neurol Scand. 2013;127:52–6." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR38">38</a>,<a id="ref-link-section-d71843e886_1" title="Warren M. Pilot study on activities of daily living limitations in adults with hemianopsia. Am J Occup Ther. 2009;63:626–33." href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound#ref-CR39">39</a>,<a id="ref-link-section-d71843e889" title="Mennem TA, Warren M, Yuen HK. Preliminary validation of a vision-dependent activities of daily living instrument on adults with homonymous hemianopia. Am J Occup Ther. 2012;66:478–82. 
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." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR40" aria-label="Reference 40">40</a>]. In this regard, in recent years the scientific community has joined efforts to develop increasingly effective neurovisual rehabilitation training programs (NVRTPs) for these patients [<a id="ref-link-section-d71843e893" title="Howard C, Rowe FJ. Adaptation to poststroke visual field loss: a systematic review. Brain Behav. 2018;8:e01041:1–21. 
https://doi.org/10.1002/brb3.1041

." href="https://link.springer.com/article/10.1186/s12984-020-0650-5#ref-CR41" aria-label="Reference 41">41</a>]. Different forms of NVRTPs have been developed, including compensatory NVRTP (C-NVRTP), restitution NVRTP (R-NVRTP), and substitution NVRTP (S-NVRTP) [<a id="ref-link-section-d71843e896" title="Howard C, Rowe FJ. Adaptation to poststroke visual field loss: a systematic review. Brain Behav. 2018;8:e01041:1–21. 
https://doi.org/10.1002/brb3.1041

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<p>via <a href="https://link.springer.com/article/10.1186/s12984-020-0650-5?utm_source=researcher_app&amp;utm_medium=referral&amp;utm_campaign=RESR_MRKT_Researcher_inbound">Visual processing speed in hemianopia patients secondary to acquired brain injury: a new assessment methodology | SpringerLink</a></p>
<div style="width: 1191px" class="wp-caption alignnone"><img src="https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs12984-020-0650-5/MediaObjects/12984_2020_650_Fig2_HTML.png" alt="Fig. 2" width="1181" height="832" /><p class="wp-caption-text"><b id="Fig2" class="c-article-section__figure-caption">Fig. 2 </b>Head Tracker System incorporated in the new software to measure the number of degrees of absolute head movements (dHM) performed by the study subjects, along the coordinate axes “X” and “Y”, while they performed the test. It consisted of specific software capable of detecting human faces (<b>a</b>), a fluorescent light (<b>b</b>), and a web camera (<b>c</b>) that registered the specific movement of a green point placed on a human mask positioned on the back of the subject’s head and neck (<b>d</b>.1 and <b>d</b>.2). The subject had to remain seated in front of the digital resistive-touch whiteboard at a distance of 40 cm (15.7 in.) and at 70 cm (27.5 in.) from the webcam</p></div>
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