scholarly journals At‐home assessment of cognitive performance: Establishing norm scores for the Cognitive Online Self‐Test Amsterdam (COST‐A)

2021 ◽  
Vol 17 (S6) ◽  
Author(s):  
Leonie N.C. Visser ◽  
Mark A. Dubbelman ◽  
Merike Verrijp ◽  
Lisa Wanders ◽  
Sophie Pelt ◽  
...  
Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 1935-1935
Author(s):  
Alicia Rovo ◽  
Claudia Baierlein-Leimbach ◽  
Cesare Medri ◽  
Ioannis Chanias ◽  
Loreen Errass ◽  
...  

Abstract Introduction: Patients with polycythemia vera (PV) have an increased risk of morbidity and mortality from thromboembolic events and cardiovascular disease, particularly for hematocrit (Hct) levels > 45% (Marchioli et al., 2013). Maintaining Hct < 45% is therefore important to reduce these risks. A device that patients can use to frequently monitor their own Hct levels could provide a detailed picture of the change in Hct over time, enable timely clinical visits and disease management, reduce disease burden, and increase patients' quality of life (QoL). A meter to measure hemoglobin (Hb) and Hct that has been approved for medical professional use (StatStrip Xpress ® 2 Hb/Hct meter, Nova Biomedical Corporation) has potential as an at-home, self-testing device. Purpose: To carry out a proof-of-concept study in clinical practice to test the accuracy of the StatStrip Xpress 2 Hb/Hct meter, to evaluate its feasibility for patient self-testing, and to assess its impact on patient-reported outcomes. Methods: Adults (aged > 18 years) who had PV (according to the World Health Organization 2016 criteria), or conditions with Hct < 35% or Hct > 50%, who required monitoring of Hct/Hb values in clinical practice and who provided informed consent were enrolled from two Swiss centers in this observational study. During each routine visit, patients collected and analyzed a finger-prick blood sample using StatStrip Xpress 2 Hb/Hct (self-test) without guidance or intervention from healthcare professionals (HCPs); HCPs then repeated this test (professional test). At each visit, HCPs also collected and analyzed a venous blood sample using a laboratory hematology analyzer (Sysmex), and patients completed a 15-minute questionnaire about use of the self-test device. The primary endpoint was mean difference in absolute percentage points between Hct values from the professional test and the analyzer (mdiff, 90% confidence interval [CI]; Spearman correlation [r]). Secondary endpoints included mdiff for Hct (%) and Hb (g/dl) between values obtained from the self-test and professional test, and the self-test and analyzer. Other endpoints included the correlation between the professional test Hct values and other blood cell counts. The study was approved by local ethics committees. Results: Blood measurements from 68 visits for 60 patients (PV = 32; other conditions with Hct < 35% or > 50% = 28) were included in the analysis. For the primary endpoint, Hct values were very similar for the analyzer and professional test (66 data points after removal of 1 outlier; mdiff = 0.1% [CI: ‒0.5-0.8]; r = 0.95, p < 0.001). Importantly, Hct results were also similar for the self-test and professional test (63 data points after removal of 2 outliers; mdiff = -0.2% [CI: ‒0.98-0.5]; r = 0.93, p < 0.001) and the analyzer and self-test (64 data points after removal of 2 outliers; mdiff = 0.1% [CI: ‒0.6-0.8]; r = 0.93, p < 0.001). Similar results were obtained for Hb measurements across the tests. There was no correlation between the accuracy of Hct values from the professional test (vs the analyzer) and blood cell counts, but this should be interpreted with caution because there was a limited number of patients with extreme white blood cell and platelet counts. There was no influence of sex (male/female), age (≤ 75 years/> 75 years) or, in the case of patients with PV, time from diagnosis on the results. Responses to the patient questionnaire showed that 92% of patients were satisfied or very satisfied with the self-test device, 100% found it easy to use, and 97% were willing to start using it at home. Of patients with PV, 71% stated that using a self-testing device would make them feel safer and 56% felt that it would have a positive effect on their QoL. Conclusions: This study demonstrates the accuracy of the StatStrip Xpress 2 Hct/Hb meter vs a laboratory analyzer for measuring Hct and Hb levels. Importantly, it shows that measurements taken by patients are as accurate as those taken by HCPs. These findings highlight the potential benefits of introducing an instrument for at-home self-testing to the management of patients with PV or other hematological conditions that require regular Hct/Hb monitoring. Benefits to patients may include increased QoL, improved clinical outcomes, and reduced morbidity and mortality through timely clinical action. In addition, fewer outpatient appointments may mean reduced healthcare costs. Figure 1 Figure 1. Disclosures Rovo: Novartis: Honoraria; BMS: Honoraria; Amgen: Other: Financial support for congresses and conference travel; AstraZeneca: Other; Swedish Orphan Biovitrum AG: Honoraria; AG Alexion: Honoraria; OrPhaSwiss GmbH: Honoraria; AstraZeneca: Honoraria; BMS: Other; Sanofi: Other; Roche: Other; Novartis: Research Funding; CSL Behring: Research Funding; AG Alexion: Research Funding. Baierlein-Leimbach: Novartis Pharma Schweiz AG: Current Employment. Triemer: Novartis Pharma Schweiz AG: Current Employment. McCarthy-Pontier: Novartis Pharma Schweiz AG: Current Employment. Lehmann: AbbVie: Honoraria; Novartis: Research Funding; Janssen: Honoraria; Swedish Orphan Biovitrum AG: Honoraria; Janssen: Other; Roche: Other; Abbvie: Other: Financial support for congress and conference travel ; Amgen: Other: Financial support for congress and conference travel ; Celgene: Research Funding; Incyte: Honoraria; BMS: Honoraria; Amgen: Honoraria.


Author(s):  
Huifang Liu ◽  
Thuy Nguyen Thi Dao ◽  
Bonhan Koo ◽  
Yoon Ok Jang ◽  
Yong Shin
Keyword(s):  

Author(s):  
Leonie N.C. Visser ◽  
Mark A. Dubbelman ◽  
Merike Verrijp ◽  
Lisa Wanders ◽  
Sophie Pelt ◽  
...  

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Morgan Braden ◽  
Steve Douglas ◽  
Michelle Kruse ◽  
Heather Leidy

Abstract Objectives This pilot, feasibility study examined the effects of implementing a free, egg-based ‘Breakfast in the Classroom’ program (BIC) on school breakfast participation, breakfast consumption, and snacking behavior compared to a Traditional School Breakfast Program (SBP) in middle-school adolescents. Cognitive performance was also assessed in a sub-set of participants based on BIC participation. Methods Ninety-two, 8th-grade students (age: 14 ± 0.1 y; BMI percentile based on weight for age: 73.1 ± 3.0%) participated in the following acute crossover study. School breakfast participation, breakfast consumption at school, and snacking behavior at home were assessed through questionnaires, at baseline, during SBP at the Center Middle School, Kansas City, MO. Following these assessments, a 2-wk BIC program was implemented that provided free, reimbursable breakfasts with the addition of two eggs/day using hallway kiosks to all students. During week 3, breakfast and snacking questionnaires were again completed. Cognitive performance using the CNS-Vital Signs program was also completed prior to lunch. Results School breakfast participation increased by approximately 57% following BIC (94.4 ± 0.8%) vs. SBP (37.2 ± 2.9%; P < 0.001). Grain (P < 0.05), dairy (P < 0.05), and protein (P < 0.001) consumption increased following BIC vs. SPB. With respect to afternoon/evening snacking behavior, BIC decreased consumption of salty snacks (P < 0.001), candy (P < 0.005), and baked sweets (P < 0.01) at home vs. SBP. Lastly, executive function (P < 0.05) and cognitive flexibility (P = 0.07, trend) improved in students who participated in BIC 3–5 times/wk vs. those who did not. Conclusions Implementation of an egg-based BIC improved school breakfast participation, consumption of higher-quality foods at school, cognitive performance, and unhealthy snacking at home in middle-school adolescents. Funding Sources American Egg Board supplied eggs.


2020 ◽  
pp. 147572572096476
Author(s):  
Astrid M. G. Poorthuis ◽  
Anouk van Dijk

Many students use ineffective learning strategies. They tend to start too late and learn in a superficial way, without integrating different parts of the study materials. To help students in Psychological Assessment in Youth overcome these problems, we designed online study-aids to spread their learning over the semester (distributed practice) and provide them with self-test questions (practice testing). Study-aids covered the last week’s course readings and consisted of 10 to 15 questions presented in several stimulating closed formats (e.g., connecting one theory with another, or filling out norm scores in a bell curve). Participation was voluntary and promoted using an incentive system. The study-aids were evaluated in two cohorts of students (2018: N = 94; 2019: N = 84). Participation was good: 79% of the students completed the study-aids (range 69–85%). Satisfaction was high: most students indicated that the study-aids supported their studies well (89%). Exam performance improved significantly upon introduction of the study-aids (comparison cohort 2017: N = 69), although more so for the midterm exam ( r = 0.47) than for the final exam ( r = 0.17). These findings suggest that online study-aids can stimulate effective learning by helping students distribute and self-test their learning.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Paula Iruzubieta ◽  
Tatiana Fernández-Lanas ◽  
Laura Rasines ◽  
Lorena Cayon ◽  
Ana Álvarez-Cancelo ◽  
...  

AbstractThe simplicity and low cost of rapid point-of-care tests greatly facilitate large-scale population testing, which can contribute to controlling the spread of the COVID-19 virus. We evaluated the applicability of a self-testing strategy for SARS-CoV2 in a population-based, cross-sectional study in Cantabria, Spain, between April and May 2020. For the self-testing strategy, participants received the necessary material for the self-collection of blood and performance of a rapid antibody test using lateral flow immunoassay at home without the supervision of healthcare personnel. A total of 1,022 participants were enrolled. Most participants correctly performed the COVID-19 self-test the first time (91.3% [95% CI 89.4–92.9]). Only a minority of the participants (0.7%) needed the help of healthcare personnel, while 6.9% required a second kit delivery, for a total valid test result in 96.9% of the participants. Incorrect use of the self-test was not associated with the educational level, age over 65, or housing area. Prevalence of IgG antibodies against SARS-CoV2 for subjects with a valid rapid test result was 3.1% (95% CI 2.2–4.4), similar to the seroprevalence result obtained using a conventional approach carried out by healthcare professionals. In conclusion, COVID-19 self-testing should be considered as a screening tool.


Author(s):  
Rachel E. Geyer ◽  
Jack Henry Kotnik ◽  
Victoria Lyon ◽  
Elisabeth Brandstetter ◽  
Monica Zigman Suchsland ◽  
...  

2021 ◽  
Author(s):  
Rachel E. Geyer ◽  
Jack Henry Kotnik ◽  
Victoria Lyon ◽  
Elisabeth Brandstetter ◽  
Monica Zigman Suchsland ◽  
...  

BACKGROUND Rapid diagnostic tests (RDT) for influenza used by individuals at home could potentially expand access to testing and reduce the impact of influenza on health systems. Improving access to testing could lead to earlier diagnosis following symptom onset, allowing more rapid interventions on those who test positive, including behavioral changes to minimize spread. However, the accuracy of RDTs for influenza has not been determined among self-testing populations. OBJECTIVE To assess the accuracy of an influenza RDT conducted at home by lay users with acute respiratory illness (ARI), compared to a self-collected sample conducted by the same individual mailed to a laboratory for reference testing. METHODS A comparative accuracy study of an at-home influenza RDT (Ellume, Brisbane, Qld, Australia) in a convenience sample of individuals experiencing ARI symptoms. Participants were enrolled in February and March 2020, from the greater Seattle region, Washington, USA. Participants were mailed the influenza RDT and reference sample collection materials, which they completed and returned for RT-qPCR influenza testing in a central laboratory. We explored the impact of age, influenza type, duration, and severity of symptoms on RDT accuracy, viral CT (cycle threshold), and a marker of human DNA (RNase P). RESULTS 605 participants completed all study steps and were included in our analysis, of whom 87 (14.4%) tested positive for influenza by RT-qPCR (70 influenza A, 17 influenza B). The overall sensitivity and specificity of the RDT compared to the reference test were 61% (95%CI 50-71) and 95% (95%CI 93-97), respectively. Among individuals with symptom onset ≤72 hours, sensitivity was 63% (95%CI 48-76) and specificity was 94% (95% CI 91-97), while for those with duration > 72 hours, sensitivity and specificity were 58% (95%CI 41-74) and 96% (95%CI 93-98), respectively. Viral load on reference swabs was negatively correlated with symptom onset, while quantities of the endogenous marker gene RNase P did not differ between PCR positive/negative groups, age groups, or influenza subtypes. The RDT did not have higher sensitivity or specificity among those who reported more severe illness. CONCLUSIONS The sensitivity and specificity of the self-test was comparable to that of influenza RDTs used in clinical settings. False negative self-test results were more common when the test was used after 72 hours of symptom onset, but were not related to inadequate swab collection, or severity of illness. Deployment of home tests may provide a valuable tool to support management of influenza and other respiratory infections.


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