Editor's Note The American College of Surgeons (ACS) on July 12 announced their new cross-specialty ACS Quality Verification Program (ACS QVP) at the 2021 ACS Quality and Safety Conference. The program provides the tools for hospitals to have a standardized approach to surgical care for all surgical patients. It is…

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Editor's Note The Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) issued a joint statement on July 8 saying that fully vaccinated Americans do not need COVID-19 booster shots at this time. The statement says the CDC, FDA, and National Institutes of Health are engaged…

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Editor's Note Since listing the hospitals and health systems mandating COVID-19 vaccination for its employees on June 29 ( https://www.ormanager.com/briefs/growing-number-of-hospitals-healthcare-systems-mandating-covid-19-vaccinations-for-hcws/ ), Becker’s Hospital Review has added five more, bringing the number to 26. In chronological order, the five additional organizations that have added mandates as of July 8 are: Trinity Health, Livonia,…

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Editor's Note The Joint Commission announced on July 7 that second quarter Accelerate PI Dashboard Reports are available for accredited organizations. The reports reflect the most recent data from the Centers for Medicare & Medicaid Compare website and electronic clinical quality measure (eCQM) data reported under The Joint Commission's ORYX…

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Editor's Note This randomized controlled clinical trial led by German researchers finds a concern of mask-wearing causing hypercapnia (excessive carbon dioxide in the bloodstream) in children. In this analysis of 45 children, carbon dioxide levels were measured at baseline without a face mask and during inhalation and exhalation under surgical…

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Editor's Note The Food and Drug Administration (FDA) on July 2 identified the recall by Medtronic Vascular of its angiographic guidewire component as Class I, the most serious. The recall was initiated because the devices were not sterilized before being shipped to hospitals. The guidewire is used during angiography or other interventional…

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Editor's Note The Food and Drug Administration (FDA) on June 30 announced that it is revoking the Emergency Use Authorizations (EUAs) for non-NIOSH-approved disposable respirators (including N95s), effective July 6. The announcement also revokes EUAs for decontamination and bioburden reduction systems for disposable respirators, effective immediately. The FDA says the…

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Editor's Note The Food and Drug Administration on June 25 identified the recall by Avid Medical of its convenience kits for medical-surgical procedures as Class I, the most serious. The company is recalling those kits that contain BD/Carefusion’s Chloraprep 3 mL applicator because of the risk of contamination of the…

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Editor's Note This study from Austria finds a high prevalence of mental disorders in high school students 1 year after the COVID-19 pandemic began. Of 3,052 adolescents who participated in the study: 55% had clinically relevant depressive symptoms 47% had clinically relevant anxiety symptoms 22.8% had clinically relevant moderate insomnia…

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Editor's Note The number of hospitals and healthcare systems mandating COVID-19 vaccinations for their healthcare workers (HCWs) is growing, the June 29 Becker’s Hospital Review reports. In chronological order, the organizations that have announced mandates as of June 29 are: Henry Ford Health System, Detroit, will require its workforce of…

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