Tag: Patient Safety

Aspirin use linked to improved outcomes in COVID-19 patients

Editor's Note This multicenter retrospective study led by researchers from George Washington University School of Medicine, Washington, DC, found that aspirin use by COVID-19 patients was associated with improved outcomes. Of 412 COVID-19 patients included in the study, 314 (76.3%) did not receive aspirin, and 98 (23.7%) received aspirin within…

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By: Judy Mathias
April 7, 2021
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CDC: Risk of getting COVID-19 from surfaces is low

Editor's Note In a science brief based on the Centers for Disease Control and Prevention’s (CDC’s) analysis of the latest available data, the agency says the risk of getting COVID-19 from surfaces “is generally considered to be low.” The CDC noted that: The risk of COVID-19 infection via surface transmission…

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By: Judy Mathias
April 6, 2021
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Use of telehealth by surgical specialties before, during COVID-19

Editor's Note This study led by the University of Michigan, Ann Arbor, finds that early in the COVID-19 pandemic, there was a substantial increase in telehealth use across all surgical specialties, with a slow decline after June 2020. Of 4,405 surgeons included in the study, 2,588 (58.8%) used telehealth in…

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By: Judy Mathias
April 5, 2021
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HHS report finds US hospitals in crisis

Editor's report A new report released by the Department of Health and Human Services (HHS) Office of Inspector General (OIG) on March 23 details how the COVID-19 pandemic has created new problems and worsened existing issues at US hospitals, leaving staff frustrated, exhausted, and burned out. Among the problems outlined…

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By: Judy Mathias
March 25, 2021
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FDA: Class I recall of Medtronic Affinity Pixie Oxygenator and Cardiotomy/Venous Reservoir with Balance Biosurface

Editor's Note The Food and Drug Administration (FDA), on March 24, identified the recall by Medtronic of its Affinity Pixie Oxygenator and Cardiotomy/Venous Reservoir with Balance Biosurface as Class I, the most serious. The recall was issued because of potentially elevated levels of harmful bacterial endotoxins. Use of a device…

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By: Judy Mathias
March 25, 2021
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The Joint Commission releases 2020 sentinel event statistics

Editor's Note The Joint Commission, on March 24, released its sentinel event statistics for 2020, which totaled 794. The top five most frequently reported events were: Falls: 170 Unintended retention of a foreign object: 106 Suicide: 81 Delay in treatment: 76 Wrong-site surgery: 68. The Joint Commission’s Office of Quality…

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By: Judy Mathias
March 25, 2021
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Protective effects of surgical masks, face shields, combination of both

Editor's Note In this study from Wayne State University School of Medicine, Detroit, researchers found that surgical masks alone surpassed protection by face shields, and a combination of both was similar to surgical masks alone. Researchers simulated human speaking to examine the transmission of aerosols using blood agar plates (simulating…

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By: Judy Mathias
March 24, 2021
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Kentucky is third state to enact legislation on surgical smoke evacuation

Editor's Note AORN announced on March 24 that Kentucky Governor Andy Beshear had signed into law new legislation that will require licensed hospitals and ambulatory surgery centers to adopt and implement policies to prevent human exposure to surgical smoke. AORN’s government affairs team and Kentucky AORN members worked closely with…

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By: Judy Mathias
March 24, 2021
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Survey: Healthcare workers’ intentions to receive COVID-19 vaccine

Editor's Note This survey by researchers at the Geisinger Health System, Danville, Pennsylvania, shows a trend of increased intention by healthcare workers to receive a COVID-19 vaccine. A total of 16,292 employees completed the survey, for a response rate of 68.5%. During the period of survey data collection, the researchers…

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By: Judy Mathias
March 23, 2021
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FDA: Class I recall of ACIST Kodama Intravascular Ultrasound Catheter

Editor's Note The Food and Drug Administration (FDA), on March 17, identified the recall by ACIST of its Kodama Intravascular Ultrasound Catheter as Class I, the most serious. The recall was initiated because the O-ring housing tubing may squeeze and damage the O-ring. If there is damage, broken O-ring pieces…

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By: Judy Mathias
March 23, 2021
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