Anesthetists

Latest Issue of OR Manager
May 2024
Home Anesthesia > Anesthetists

Wildfire smoke linked to adverse events in pediatric patients under anesthesia

Editor's Note This study from the University of California San Francisco finds that pediatric patients with risk factors for respiratory complications had a greater incidence of adverse events under general anesthesia during periods of unhealthy air quality caused by wildfire smoke. A total of 625 pediatric patients were included in…

Read More

By: Judy Mathias
November 2, 2022
Share

FDA issues Safety Communication on tracheostomy tube shortages

Editor's Note The Food and Drug Administration (FDA) on October 31 issued a Medical Device Safety Communication on tracheostomy tube shortages. Included in the shortages are Bivona tracheostomy tubes manufactured by ICU Medical, which are more likely to affect pediatric patients. Also on the shortage list are JOH Tube Tracheostomy…

Read More

By: Judy Mathias
November 2, 2022
Share

FDA: Five companies are having amoxicillin shortages

Editor's Note As of November 1, the Food and Drug Administration (FDA) listed 26 amoxicillin products on its current drug shortages site. The FDA says increased demand is the largest cause of the shortage. The FDA does not list resupply dates, but the American Society of Health-System Pharmacists (ASHP) estimates…

Read More

By: Judy Mathias
November 1, 2022
Share

Reducing noise in the OR improves children’s postop behavior

Editor's Note Reducing noise in the OR positively affects children’s postoperative behavior, according to research presented October 24 at the Anesthesiology 2022 annual meeting in New Orleans. The study, led by researchers at Nationwide Children’s Hospital, Columbus, Ohio, included 64 preschool children (ages 4 to 5 years old) having general…

Read More

By: Judy Mathias
October 27, 2022
Share

Sponsored Message

FDA: Philips Respironics recalls certain BiPAP, CPAP masks

Editor's Note The Food and Drug Administration (FDA) on October 19 identified the recall by Philips Respironics of certain masks for BiPAP and CPAP machines as Class I, the most serious. The recall was initiated because magnetic headgear clips that hold the masks in place can cause injury or death…

Read More

By: Judy Mathias
October 24, 2022
Share

Postop effect of vaccination status, mode of anesthesia on COVID-19 patients

Editor's Note This study by researchers at Kaiser Permanente and the University of California, San Francisco-East Bay, Oakland, finds that having a surgical procedure shortly after COVID-19 infection was not associated with higher risks in fully vaccinated patients or those who did not have general anesthesia. The analysis included 228,913…

Read More

By: Judy Mathias
October 13, 2022
Share

Sponsored Message

ACS comments on colonoscopy study

Editor's Note The American College of Surgeons (ACS) on October 11 issued comments on a European study examining colonoscopies that was published October 9 in the New England Journal of Medicine. The study, which looked at colonoscopies in Sweden, Poland, Norway, and the Netherlands, seemed to question the effectiveness of…

Read More

By: Judy Mathias
October 12, 2022
Share

Disposition, outcomes of patients after day-of-surgery case cancellation

Editor's Note In this study from Rutgers New Jersey Medical School, researchers find that nearly a fifth of cases canceled on the day of surgery are never rescheduled, and, if they are rescheduled, the delay can be substantial. During the 2-year study period, 4,472 cases were canceled on the day…

Read More

By: Judy Mathias
October 6, 2022
Share

Study: Routine use of anesthesia personnel in cataract surgery questioned

Editor's Note This study led by researchers from the University of California, San Francisco, finds that it may be reasonable to consider performing cataract surgery without routine anesthesia support. Medicare claims for 36,652 patients who had cataract surgery were analyzed. Among the findings: 89.8% had an anesthesia provider, compared to…

Read More

By: Judy Mathias
October 4, 2022
Share

FDA: Class I recall of certain Philips Respironics BiPAP machines

Editor's Note The Food and Drug Administration (FDA) on September 23 identified the recall by Philips Respironics of certain models of its BiPAP machines as Class I, the most serious. The recall was initiated because certain machines may contain a plastic contaminated with a noncompatible material. If the plastic is…

Read More

By: Judy Mathias
September 26, 2022
Share
Live chat by BoldChat