A Multi-site Feasibility and Validation Study of Visual Signs and Symptoms Screen (V-SASS)

Research. Objectives: To investigate the feasibility and validity of the V-SASS, a tool for clinicians to easily identify vision function and functional visual deficits and facilitate appropriate referrals and intervention. Design: Prospective, multi-site study conducted across four states (Californ...

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Veröffentlicht in:Archives of physical medicine and rehabilitation 2022-12, Vol.103 (12), p.e120
Hauptverfasser: Wertheimer, Jeffrey, Roberts, Pamela, Hreha, Kimberly, Oullette, Debra, Fielder, Jaimee, Graf, Min Jeong, Watters, Kelsey, Stants, Holly, Rizzo, John Ross
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container_end_page
container_issue 12
container_start_page e120
container_title Archives of physical medicine and rehabilitation
container_volume 103
creator Wertheimer, Jeffrey
Roberts, Pamela
Hreha, Kimberly
Oullette, Debra
Fielder, Jaimee
Graf, Min Jeong
Watters, Kelsey
Stants, Holly
Rizzo, John Ross
description Research. Objectives: To investigate the feasibility and validity of the V-SASS, a tool for clinicians to easily identify vision function and functional visual deficits and facilitate appropriate referrals and intervention. Design: Prospective, multi-site study conducted across four states (California, Texas, Illinois, and Minnesota) and six facilities. Setting: Acute care hospital (22%), inpatient rehabilitation (36.9%), and outpatient rehabilitation (41.1%).Participants141 participants with new onset stroke, average age 61.8 years old, 51.4% male, 48.6% female; 56.4% white, 28.6% Black/African American, 9% Hispanic and 6% Asian/Pacific Islander. Interventions: N/A.Main Outcome MeasuresValidation and feasibility of the V-SASS. Results: The three domains of the V-SASS, inclusive of visual complaints, and static and functional observations, were assessed respectively. In the vision complaint domain, 70.5% of participants identified vision symptoms. 52.6% of the participants were observed to have vision symptoms in the static observation domain. In the final domain, functional observations, 31.9% of the participants exhibited signs of visual dysfunction. Each domain is further subdivided by chief signs and symptoms relative to the topic.Nineteen individuals were confirmed to have been seen by a vision specialist. Of these, 100% had either a vision function (60.0%) or functional vision (80.0%) deficit. 52.6% were found to have both a vision function and functional vision deficit.Feasibility of the V-SASS addressed by various elements, including ease of administration, likability of screen arrangement, confidence in use, and overall recommendations of the V-SASS. All areas addressed were in favor of the V-SASS (all above 75%). Frustration while using the V-SASS was also captured with 24.8% indicating some level of frustration. Conclusions: The three domains of the V-SASS identified vision signs and symptoms, with prevalence rates (70.5%) consistent with the literature (Rowe et al. 2019). Validity of the V-SASS was confirmed (100% of participants who screened positive were found to have vision deficits by a vision specialist). The V-SASS demonstrates feasibility in multiple clinical and geographic settings, though future research to further investigate robustness is warranted.Author(s) DisclosuresN/A.
doi_str_mv 10.1016/j.apmr.2022.08.749
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Objectives: To investigate the feasibility and validity of the V-SASS, a tool for clinicians to easily identify vision function and functional visual deficits and facilitate appropriate referrals and intervention. Design: Prospective, multi-site study conducted across four states (California, Texas, Illinois, and Minnesota) and six facilities. Setting: Acute care hospital (22%), inpatient rehabilitation (36.9%), and outpatient rehabilitation (41.1%).Participants141 participants with new onset stroke, average age 61.8 years old, 51.4% male, 48.6% female; 56.4% white, 28.6% Black/African American, 9% Hispanic and 6% Asian/Pacific Islander. Interventions: N/A.Main Outcome MeasuresValidation and feasibility of the V-SASS. Results: The three domains of the V-SASS, inclusive of visual complaints, and static and functional observations, were assessed respectively. In the vision complaint domain, 70.5% of participants identified vision symptoms. 52.6% of the participants were observed to have vision symptoms in the static observation domain. In the final domain, functional observations, 31.9% of the participants exhibited signs of visual dysfunction. Each domain is further subdivided by chief signs and symptoms relative to the topic.Nineteen individuals were confirmed to have been seen by a vision specialist. Of these, 100% had either a vision function (60.0%) or functional vision (80.0%) deficit. 52.6% were found to have both a vision function and functional vision deficit.Feasibility of the V-SASS addressed by various elements, including ease of administration, likability of screen arrangement, confidence in use, and overall recommendations of the V-SASS. All areas addressed were in favor of the V-SASS (all above 75%). Frustration while using the V-SASS was also captured with 24.8% indicating some level of frustration. Conclusions: The three domains of the V-SASS identified vision signs and symptoms, with prevalence rates (70.5%) consistent with the literature (Rowe et al. 2019). Validity of the V-SASS was confirmed (100% of participants who screened positive were found to have vision deficits by a vision specialist). 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Objectives: To investigate the feasibility and validity of the V-SASS, a tool for clinicians to easily identify vision function and functional visual deficits and facilitate appropriate referrals and intervention. Design: Prospective, multi-site study conducted across four states (California, Texas, Illinois, and Minnesota) and six facilities. Setting: Acute care hospital (22%), inpatient rehabilitation (36.9%), and outpatient rehabilitation (41.1%).Participants141 participants with new onset stroke, average age 61.8 years old, 51.4% male, 48.6% female; 56.4% white, 28.6% Black/African American, 9% Hispanic and 6% Asian/Pacific Islander. Interventions: N/A.Main Outcome MeasuresValidation and feasibility of the V-SASS. Results: The three domains of the V-SASS, inclusive of visual complaints, and static and functional observations, were assessed respectively. In the vision complaint domain, 70.5% of participants identified vision symptoms. 52.6% of the participants were observed to have vision symptoms in the static observation domain. In the final domain, functional observations, 31.9% of the participants exhibited signs of visual dysfunction. Each domain is further subdivided by chief signs and symptoms relative to the topic.Nineteen individuals were confirmed to have been seen by a vision specialist. Of these, 100% had either a vision function (60.0%) or functional vision (80.0%) deficit. 52.6% were found to have both a vision function and functional vision deficit.Feasibility of the V-SASS addressed by various elements, including ease of administration, likability of screen arrangement, confidence in use, and overall recommendations of the V-SASS. All areas addressed were in favor of the V-SASS (all above 75%). Frustration while using the V-SASS was also captured with 24.8% indicating some level of frustration. Conclusions: The three domains of the V-SASS identified vision signs and symptoms, with prevalence rates (70.5%) consistent with the literature (Rowe et al. 2019). Validity of the V-SASS was confirmed (100% of participants who screened positive were found to have vision deficits by a vision specialist). 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Objectives: To investigate the feasibility and validity of the V-SASS, a tool for clinicians to easily identify vision function and functional visual deficits and facilitate appropriate referrals and intervention. Design: Prospective, multi-site study conducted across four states (California, Texas, Illinois, and Minnesota) and six facilities. Setting: Acute care hospital (22%), inpatient rehabilitation (36.9%), and outpatient rehabilitation (41.1%).Participants141 participants with new onset stroke, average age 61.8 years old, 51.4% male, 48.6% female; 56.4% white, 28.6% Black/African American, 9% Hispanic and 6% Asian/Pacific Islander. Interventions: N/A.Main Outcome MeasuresValidation and feasibility of the V-SASS. Results: The three domains of the V-SASS, inclusive of visual complaints, and static and functional observations, were assessed respectively. In the vision complaint domain, 70.5% of participants identified vision symptoms. 52.6% of the participants were observed to have vision symptoms in the static observation domain. In the final domain, functional observations, 31.9% of the participants exhibited signs of visual dysfunction. Each domain is further subdivided by chief signs and symptoms relative to the topic.Nineteen individuals were confirmed to have been seen by a vision specialist. Of these, 100% had either a vision function (60.0%) or functional vision (80.0%) deficit. 52.6% were found to have both a vision function and functional vision deficit.Feasibility of the V-SASS addressed by various elements, including ease of administration, likability of screen arrangement, confidence in use, and overall recommendations of the V-SASS. All areas addressed were in favor of the V-SASS (all above 75%). Frustration while using the V-SASS was also captured with 24.8% indicating some level of frustration. Conclusions: The three domains of the V-SASS identified vision signs and symptoms, with prevalence rates (70.5%) consistent with the literature (Rowe et al. 2019). Validity of the V-SASS was confirmed (100% of participants who screened positive were found to have vision deficits by a vision specialist). The V-SASS demonstrates feasibility in multiple clinical and geographic settings, though future research to further investigate robustness is warranted.Author(s) DisclosuresN/A.</abstract><doi>10.1016/j.apmr.2022.08.749</doi></addata></record>
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