107 research outputs found

    The Effects Of Nurse\u27s Mental Health On Quality Patient Outcomes: A Quality Improvement Study

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    Morale among nurses is declining rapidly, this could be due to the rising mental illnesses like anxiety, depression, chronic fatigue, stress, worry and post-traumatic stress disorder. Not to mention the rate of suicide in female nurses is 11.97/ 100,000 compared to non-nurse females having a rate of 7.58/ 100,000. Also, male nurses have an incidence of suicide at a rate of 39.8/ 100,000 compared to non-nurse males at 28.2/ 100,000. A thorough literature review was conducted and a total of 40 studies were reviewed. Common themes that emerged were A decrease in nursing staff retention related to low satisfaction, lack of resources, unfair compensation, and lack of communication,” the higher that staffing levels are, the better clinical outcomes and the better the patient\u27s experience is, frontline health care workers are at an increased risk for suffering from mental illness which directly affects work performance, patient care and outcomes, and life outside of work. An important conclusion showed that a nurse\u27s mental health status affects the quality of patient care and positive outcomes. As a result of this literature review an intervention was developed in the form of workshops for different coping strategies, stress and other information for support/ discussion groups that could be provided to nursing staff.https://scholarworks.moreheadstate.edu/celebration_posters_2021/1039/thumbnail.jp

    Behavioral Differences among Eastern Bluebird Populations Could Be a Consequence of Tree Swallow Presence: A Pilot Study

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    Aggressive interference competition for limited resources is frequently observed among animals. However, these behavioral interactions within (intraspecific) and between (interspecific) species are costly as they can be energetically expensive and cause injury or death. To avoid these agonistic interactions, numerous species alter their behaviors and resource requirements. Spatial variation in nest site competition allows for investigation of concurrent variation in territorial defense behavior. Further, among species with bi-parental nest defense, behavioral similarity in territorial defense may benefit pairs. Here, we studied territorial aggression between two eastern bluebird (Sialia sialis) populations (North Carolina and Alabama, USA) that differ in avian community structure; those in North Carolina have recently begun to experience strong interspecific competition for nesting cavities by tree swallows (Tachycineta bicolor), a competitive pressure that is relatively new for North Carolina bluebirds (~35–40 years) and is absent in Alabama populations. We found that bluebirds in North Carolina are more aggressive to simulated territorial intrusions compared to their Alabama counterparts. Behavioral similarity (here, in aggression) between partners is strong and similar in both populations. These results suggest that bluebirds in North Carolina may have to maintain higher baseline aggression during territory establishment and nest construction to co-occur with highly aggressive tree swallows, but that, in both populations, behavioral similarity between partners may be adaptive. Finally, we acknowledge the preliminary nature of this study and the need for expanding the behavioral studies to other sites in the southeastern United States. Greater regional coverage would exclude the possibility of alternative drivers of the observed behavioral differences between the North Carolina and Alabama populations

    Right to Serve, Right to Lead: Lives and Legacies of the USCT

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    This is a catalog for an exhibit that follows the evolution of African-American participation in the Civil War, from slaves, to contrabands, to soldiers of the United States Colored Troops (USCT), as well as the lives of black veterans beyond the war, and their ultimate military and social legacy. Using a variety of period items, it creates a narrative that stretches from the Antebellum Period to the current day. In doing so, the exhibit shows how black sacrifice on the battlefield redefined the war\u27s purpose throughout the divided nation, how Jim Crowe suppressed the memory of black participation after Reconstruction, and how the illustrious African-American military tradition left by the USCT endures to this day in their modern heirs

    The Vaccinia Virus (VACV) B1 and Cellular VRK2 Kinases Promote VACV Replication Factory Formation through Phosphorylation-Dependent Inhibition of VACV B12

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    Comparative examination of viral and host protein homologs reveals novel mechanisms governing downstream signaling effectors of both cellular and vi- ral origin. The vaccinia virus B1 protein kinase is involved in promoting multiple facets of the virus life cycle and is a homolog of three conserved cellular enzymes called vaccinia virus-related kinases (VRKs). Recent evidence indicates that B1 and VRK2 mediate a com- mon pathway that is largely uncharacterized but appears independent of previous VRK substrates. Interestingly, separate studies described a novel role for B1 in inhibiting vac- cinia virus protein B12, which otherwise impedes an early event in the viral lifecycle. Herein, we characterize the B1/VRK2 signaling axis to better understand their shared functions. First, we demonstrate that vaccinia virus uniquely requires VRK2 for viral repli- cation in the absence of B1, unlike other DNA viruses. Employing loss-of-function analy- sis, we demonstrate that vaccinia virus’s dependence on VRK2 is only observed in the presence of B12, suggesting that B1 and VRK2 share a pathway controlling B12. More- over, we substantiate a B1/VRK2/B12 signaling axis by examining coprecipitation of B12 by B1 and VRK2. Employing execution point analysis, we reveal that virus replication proceeds normally through early protein translation and uncoating but stalls at replica- tion factory formation in the presence of B12 activity. Finally, structure/function analyses of B1 and VRK2 demonstrate that enzymatic activity is essential for B1 or VRK2 to inhibit B12. Together, these data provide novel insights into B1/VRK signaling coregulation and support a model in which these enzymes modulate B12 in a phosphorylation-depen- dent manner

    The Vaccinia Virus (VACV) B1 and Cellular VRK2 Kinases Promote VACV Replication Factory Formation through Phosphorylation-Dependent Inhibition of VACV B12

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    Comparative examination of viral and host protein homologs reveals novel mechanisms governing downstream signaling effectors of both cellular and viral origin. The vaccinia virus B1 protein kinase is involved in promoting multiple facets of the virus life cycle and is a homolog of three conserved cellular enzymes called vaccinia virus-related kinases (VRKs). Recent evidence indicates that B1 and VRK2 mediate a common pathway that is largely uncharacterized but appears independent of previous VRK substrates. Interestingly, separate studies described a novel role for B1 in inhibiting vaccinia virus protein B12, which otherwise impedes an early event in the viral lifecycle. Herein, we characterize the B1/VRK2 signaling axis to better understand their shared functions. First, we demonstrate that vaccinia virus uniquely requires VRK2 for viral replication in the absence of B1, unlike other DNA viruses. Employing loss-of-function analysis, we demonstrate that vaccinia virus’s dependence on VRK2 is only observed in the presence of B12, suggesting that B1 and VRK2 share a pathway controlling B12. Moreover, we substantiate a B1/VRK2/B12 signaling axis by examining coprecipitation of B12 by B1 and VRK2. Employing execution point analysis, we reveal that virus replication proceeds normally through early protein translation and uncoating but stalls at replication factory formation in the presence of B12 activity. Finally, structure/function analyses of B1 and VRK2 demonstrate that enzymatic activity is essential for B1 or VRK2 to inhibit B12. Together, these data provide novel insights into B1/VRK signaling coregulation and support a model in which these enzymes modulate B12 in a phosphorylation-dependent manner

    The Grizzly, February 4, 2016

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    Ursinus to Host Popular Author • Clearing the Path to a Career • Companies and Grad Schools Seek Out Ursinus Alumni • International Perspective: Cultural Differences in Parties • Businesses Offer Student Discounts • Talking About Depression with Nuance • Fighting Off the Freshman Fifteen • Ups and Downs of Being an RA in Reimert • New Face on Campus • Opinion: The Elephants Aren\u27t in the Room: Poll Probes Pupils on Pressing Politics • From Across the Atlantic • Dynamic Duohttps://digitalcommons.ursinus.edu/grizzlynews/1681/thumbnail.jp

    Increase of Direct C-C Coupling Reaction Yield by Identifying Structural and Electronic Properties of High-Spin Iron Tetra-azamacrocyclic Complexes

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    Macrocyclic ligands have been explored extensively as scaffolds for transition metal catalysts for oxygen and hydrogen atom transfer reactions. C–C reactions facilitated using earth abundant metals bound to macrocyclic ligands have not been well-understood but could be a green alternative to replacing the current expensive and toxic precious metal systems most commonly used for these processes. Therefore, the yields from direct Suzuki–Miyaura C–C coupling of phenylboronic acid and pyrrole to produce 2-phenylpyrrole facilitated by eight high-spin iron complexes ([Fe3+L1(Cl)2]+, [Fe3+L4(Cl)2]+, [Fe2+L5(Cl)]+, [Fe2+L6(Cl)2], [Fe3+L7(Cl)2]+, [Fe3+L8(Cl)2]+, [Fe2+L9(Cl)]+, and [Fe2+L10(Cl)]+) were compared to identify the effect of structural and electronic properties on catalytic efficiency. Specifically, catalyst complexes were compared to evaluate the effect of five properties on catalyst reaction yields: (1) the coordination requirements of the catalyst, (2) redox half-potential of each complex, (3) topological constraint/rigidity, (4) N atom modification(s) increasing oxidative stability of the complex, and (5) geometric parameters. The need for two labile cis-coordination sites was confirmed based on a 42% decrease in catalytic reaction yield observed when complexes containing pentadentate ligands were used in place of complexes with tetradentate ligands. A strong correlation between iron(III/II) redox potential and catalytic reaction yields was also observed, with [Fe2+L6(Cl)2] providing the highest yield (81%, −405 mV). A Lorentzian fitting of redox potential versus yields predicts that these catalysts can undergo more fine-tuning to further increase yields. Interestingly, the remaining properties explored did not show a direct, strong relationship to catalytic reaction yields. Altogether, these results show that modifications to the ligand scaffold using fundamental concepts of inorganic coordination chemistry can be used to control the catalytic activity of macrocyclic iron complexes by controlling redox chemistry of the iron center. Furthermore, the data provide direction for the design of improved catalysts for this reaction and strategies to understand the impact of a ligand scaffold on catalytic activity of other reactions

    Single-Cell Profiling Reveals Inflammatory Polarization of Human Carotid Versus Femoral Plaque Leukocytes

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    Femoral atherosclerotic plaques are less inflammatory than carotid plaques histologically, but limited cell-level data exist regarding comparative immune landscapes and polarization at these sites. We investigated intraplaque leukocyte phenotypes and transcriptional polarization in 49 patients undergoing femoral (n = 23) or carotid (n = 26) endarterectomy using single-cell RNA-Seq (scRNA-Seq; n = 13), flow cytometry (n = 24), and IHC (n = 12). Comparative scRNA-Seq of CD45+-selected leukocytes from femoral (n = 9; 35,265 cells) and carotid (n = 4; 30,655 cells) plaque revealed distinct transcriptional profiles. Inflammatory foam cell-like macrophages and monocytes comprised higher proportions of myeloid cells in carotid plaques, whereas noninflammatory foam cell-like macrophages and LYVE1-overexpressing macrophages comprised higher proportions of myeloid cells in femoral plaque (P \u3c 0.001 for all). A significant comparative excess of CCR2+ macrophages in carotid versus plaque was observed by flow cytometry in a separate validation cohort. B cells were more prevalent and exhibited a comparatively antiinflammatory profile in femoral plaque, whereas cytotoxic CD8+ T cells were more prevalent in carotid plaque. In conclusion, human femoral plaques exhibit distinct macrophage phenotypic and transcriptional profiles as well as diminished CD8+ T cell populations compared with human carotid plaques
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