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If your ED patient is sedated, he or she may have an adverse reaction to medications used in the procedure, an allergic reaction, or become hypoxic from inadequate respiratory effort, warns Brad Guffin, BSN, RN-BC, CPEN, director of emergency services at Martin Memorial Medical Center in Stuart, FL.
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It's no secret that emergency medicine providers are frustrated by patients who inappropriately come to the ED for primary care, pharmaceuticals, and help with a wide range of social issues.
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With demand for ED beds surging as the nation's demographics, health care needs, and finances continue to change, a number of health systems across the country are opening stand-alone EDs freestanding centers that are staffed by emergency physicians and deliver emergency care, but are not attached to a main campus or hospital facility.
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Hospitals that want to distinguish themselves as centers of excellence in the care of heart failure (HF) have a new avenue to pursue.
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With our economy in shambles, and July unemployment at 9.2% nationally just short of the all-time high of 10.81% and way off the mark of the all-time low of 3.31% fewer and fewer ED patients are insured, and it's a significant challenge to manage the resulting uptick in ED visits.
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When it's typical for patients to wait four hours or more to see an emergency physician, and your leave-without-being-seen (LWBS) rate is pushing 10%, you know it's time to rethink the whole process.
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In this issue: Medication poisonings in children; rosuvastatin vs atorvastatin for atherosclerosis; saw palmetto for prostate symptoms; using atypical antipsychotics for off-label indications in adults; and FDA actions.
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Saddle pulmonary embolism (SPE) is defined as the presence of a thromboembolus located at the bifurcation of the main pulmonary artery.
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This was a prospective, randomized, controlled, multicenter trial that took place between 2007 and 2010 at seven ICUs in Belgium. Inclusion criteria were evidence of nutritional impairment or significant risk for it (measured using a validated and standardized nutritional risk screen questionnaire) and age > 18 years.
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To determine the risk of potentially unintended discontinuation of common, evidence-based medications for chronic disease, Bell and colleagues examined administrative records for 12 years (19972009) for all hospitalized patients and all outpatient prescriptions in Ontario, Canada.