Editor's Note Preoperative falls may be common and often injurious in surgical patients across all ages, and they are associated with preoperative functional dependence and quality of life, this study finds. The study included 15,060 adult patients undergoing elective surgery. In the 6 months before surgery, 26% fell at least…

Read More

Editor's Note The Food and Drug Administration (FDA) on February 25 issued a Safety Communication on neurosurgical head holders (skull clamps) and device slippage. From January 2009 to January 2016, the FDA received more than 1,000 reports of slippage or movement of skull clamps before and/or during surgical procedures. The slippage,…

Read More

Editor's Note The Food and Drug Administration (FDA) in partnership with the National Library of Medicine on October 19 announced the launch of three new features on AccessGUDID, the public portal to data submitted to the FDA’s Global Unique Device Identification Database (GUDID). Two new APIs (application program interface) and…

Read More

A highlight of this year’s OR Manager Conference in Nashville, Tennessee, was an interactive hybrid OR exhibit with products from 15 companies. During a special Town Hall on Thursday, October 8, members of the Hybrid OR Steering Committee answered questions from conference attendees seeking information about what’s involved in planning…

Read More

Editor's Note The Food and Drug Administration (FDA), on September 28, issued a safety alert for cranial perforators with an automatic clutch mechanism. Most cranial perforators are designed to automatically stop drilling after penetrating the skull to prevent the tip from unintentionally drilling into the brain. However this clutch mechanism…

Read More