Background: Objective structured clinical examinations (OSCEs) are considered the most psychometrically robust form of clinical skills assessment in the health professions. In 2014, the College of Pharmacy at Qatar University (CoP-QU) piloted the first cumulative OSCE for graduating students in collaboration with the Supreme Council of Health and the University of Toronto. Since then, interest has grown in measuring the psychometric properties of this examination to ensure adequate reliability, validity and defensibility. Objectives: This study aimed to evaluate the psychometric properties of the OSCE conducted in 2015 at the CoP-QU. A secondary objective of this study was to identify quality improvement opportunities for design, implementation, and evaluation of the OSCE. Methods: The psychometric analysis occurred as follows: We calculated cut scores and pass rates of the 10 stations being used in the OSCE assessment using borderline regression method. Predictive validity of undergraduate courses grades with OSCE grades were calculated using correlation and regression statistics. Concurrent validity of similar cumulative exams were evaluated using Pearson correlation. Risk of bias was calculated using Spearman correlation between assessors' analytical (checklist sheet of required tasks to be performed in a station) and global (the score of whole performance including communication skills on a scale from 1 to 5) scoring. Content validity was assessed quantitatively using 18 student-feedback forms and qualitatively through focus groups with OSCE participants and contributors (total of 5 assessors, 3 students, 3 administrators, 3 standardized patients). Interrater reliability was assessed using intra-class correlation coefficients (ICCs). Construct validity was evaluated by comparing interrater reliability between the first and second OSCE cycles. Cronbach's alpha was used to determine internal consistency of students' performance in all stations in terms of global and total scores. Correlation statistics were conducted at α level < 0.05. Results: Out of 50% allocated for global score and 50% for analytical score per station, and based on the cut scores calculated for every station, average pass rate per analytical checklist grades in all stations was 70.4%, while average pass rate calculated for total scores in all stations was 79.2%. Four courses simulating professional skills of OSCE, two adapted undergraduate formative OSCEs, and a Medicinal Chemistry course, the control, correlated with the OSCE grades as follow, 0.72 (P < 0.01), 0.47 (P < 0.05), 0.43 (P>0.05), 0.65 (P < 0.01), 0.78 (P < 0.01), 0.61 (P < 0.01), and 0.36 (P>0.05) respectively. OSCE grades can be moderately predicted by Professional skills course grades (52.3%) and its practical assessment (61.2%). Average correlation between analytical and global grades for all assessors was 0.52. A total of 90% of the stations were deemed to reflect practice, according to student perceptions. The average ICC of analytical checklists scores, global scores, and total scores were 0.88 (0.71-0.95), 0.61 (0.19-0.82), and 0.75 (0.45-0.88) respectively. Cronbach's alpha of students' performance in global scores across stations was 0.87, and 0.93 in terms of total scores. Conclusion: The cumulative OSCE conducted in 2015 showed acceptable validity and reliability as a high stakes examination and therefore is suitable to be implemented as a mandatory core curriculum component for student pharmacist assessment in Qatar.
Background: Pathological cardiac hyper trophy is a wor ldwide problem and an independent risk factor that predisposes the hear t to failure. Enhanced activit y or expression of the sodium proton exchanger isoform 1 (NHE1) has been implicated in conditions of cardiac hyper trophy. Induction of cGMP has previousl y been demonstrated to reduce NHE1 activit y and expression, which could be through the expression of heme oxygenase isoform 1 (HO-1), a stress-induced enz yme that shows cardioprotective proper ties. In our study, we aimed to investigate the role of inducing HO-1 in a cardiac hyper trophy model that expresses active NHE1 to determine whether HO-1 could protect against NHE1 induced cardiomyoc yte hyper trophy.Methods: H9c2 cardiomyoc ytes were infected with the active form of the NHE1 adenovir us in the presence and absence of protopor phyrin (CoPP). W hich was used to induce HO-1. Protein and mRNA expression of HO-1 were invested in H9c2 cardiomyoc ytes in the presence and absence of the expression of the active form of the NHE1 adenovir us. The effects of HO-1 induction on NHE1 protein expression and cardiomyoc yte hyper trophic markers were measured respectivel y by western blotting and anal y zing the cell surface area of H9c2.Results: O ur results showed a significant decrease in HO-1 mRNA expression in cardiomyoc ytes expressing active NHE1 (74.84 ± 9.19 % vs. 100 % normal NHE1 expression, p<0.05). However, we did not see any changes in NHE1 protein expression following HO-1 induction. A trend towards decrease in cardiomyoc yte hyper trophy was obser ved in H9c2 cardiomyoblasts infected with the active form of NHE1 following stimulation with HO-1 (NHE1, 154.93 ± 14.87 % vs. NHE1 + CoPP, 109 ± 16.44 %).Conc lusion: In our model, HO-1 maybe a useful means to reduce NHE1 induced cardiomyoc yte hyper trophy, although the mechanism by which it does that requires fur ther investigation. Health and Biomedical
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