Publications by authors named "Joel Valencia"

Article Synopsis
  • This study explores how structural empowerment and work ethics impact work engagement in millennial Saudi clinical nurses, filling a gap in research for this demographic in Arab countries.
  • Utilizing a descriptive correlation quantitative design, 250 millennial nurses completed an online survey that assessed various dimensions of work ethics, empowerment, and engagement.
  • Findings indicate that factors like marital and employment status, along with ethics and empowerment, are significant for enhancing engagement, suggesting that nursing management should implement strategies like recognition and rewards to boost morale and productivity.
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Objective: We sought to compare the quick sequential organ failure assessment (qSOFA) to systemic inflammatory response syndrome (SIRS), severe sepsis criteria and lactate levels for their ability to identify ED patients with sepsis with critical illness.

Methods: We conducted this multicenter retrospective cohort study at five US hospitals, enrolling all adult patients admitted to these hospitals from their EDs with infectious disease-related illnesses from 1 January 2016 to 30 April 2016. We abstracted clinical variables for SIRS, severe sepsis and qSOFA scores, using values in the first 6 hours of ED stay.

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Bone is increasingly recognized as an endocrine organ that can regulate systemic hormones and metabolism through secreted factors. Although bone loss and increased adiposity appear to be linked clinically, whether conditions of increased bone formation can also change systemic metabolism remains unclear. In this study, we examined how increased osteogenesis affects metabolism by using an engineered G protein-coupled receptor, Rs1, to activate Gs signaling in osteoblastic cells in ColI(2.

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Centromeres control chromosome inheritance in eukaryotes, yet their DNA structure and primary sequence are hypervariable. Most animals and plants have megabases of tandem repeats at their centromeres, unlike yeast with unique centromere sequences. Centromere function requires the centromere-specific histone CENH3 (CENP-A in human), which replaces histone H3 in centromeric nucleosomes.

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