The Joint Commission: New R3 Report on reducing healthcare disparities
Editor's Note The Joint Commission on June 22 announced a new “R3 Report—Issue 36: New Requirements to Reduce Health Care Disparities,” which examines the rationale and references behind new and revised requirements to reduce healthcare disparities in accredited organizations, effective January 1, 2023. Among the new and revised requirements: A…
FDA: Class I recall of one lot of Draeger SafeStar 55 Breathing System Filters
Editor's Note The Food and Drug Administration (FDA) on June 21 identified the recall by Draeger, Inc, of one lot (LT2103) of its SafeStar 55 Breathing System Filters as Class I, the most serious. The Breathing System Filter is used as part of a ventilator when a patient is under…
Study: Best way to test for COVID-19 is nasopharyngeal swab
Editor's Note This study by researchers from Cornell University finds that nasopharyngeal swabs taken from back inside the nostril were more effective at detecting COVID-10 than saliva tests or swabs just inside the nostril or under the tongue. Comparing different samples from 77 patients, the researchers found that: Nasopharyngeal samples…
FDA: Class I recall of Medtronic HVAD Pump Implant Kit
Editor's Note The Food and Drug Administration (FDA) on June 8 identified the recall by Medtronic of its HeartWare Ventricular Assist Device (HVAD) Pump Implant Kit as Class I, the most serious. The HVAD System is used as a bridge to cardiac transplants. The Kit was recalled because of a…
Protection, waning of immunity to COVID-19 after infection, vaccination
Editor's Note This Israeli study finds that individuals previously infected with COVID-19, regardless of whether they had been vaccinated, had more protection against reinfection than those who were vaccinated (Pfizer-BioNTech vaccine) but previously uninfected. Among the findings for the number of COVID-19 cases per 100,000 person days since vaccination or…
FDA: Class I recall of Philips Respironics V60, V60 Plus Ventilators
Editor's Note The Food and Drug Administration on June 3 identified the recall by Philips Respironics of all V60 and V60 Plus Ventilators as Class I, the most serious. The recall was initiated because an internal power fluctuation may cause the ventilator to shut down unintentionally with or without any…
FDA: Class I recall of Atrium Medical’s iCast Covered Stent
Editor's Note The Food and Drug Administration (FDA) on June 2 identified the recall by Atrium Medical Corporation of its iCast Covered Stent System as Class I, the most serious. The recall was initiated because of increased complaints about the separation of the balloon or catheter hub from the delivery…
Changes in cancer screening during COVID-19
Editor's Note This study from the American Cancer Society, Atlanta, finds that the prevalence of breast, cervical, and colorectal cancer screening decreased during COVID-19. A total of 479,248 patients were included in the analysis for breast cancer screening, 301,453 for cervical cancer screening, and 854,210 for colorectal cancer screening. Between…
Effect of COVID-19 disruptions to in-person care after TKA
Editor's Note This study from the Hospital for Special Surgery, New York City, finds that halting in-person office visits and physical therapy (PT) after total knee arthroplasty (TKA) because of COVID-19 did not affect complication rates or outcomes. A total of 624 study patients who had a TKA between January…
FDA: Class I recall of Arjo Sara Plus lift
Editor's Note The Food and Drug Administration (FDA) on May 27 identified the recall of the ArjoHuntleigh Polska Sara Plus floor lift as Class I, the most serious. The recall was initiated because of the risk of smoke or fire if the lift is used when the battery is low.…
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