Editor's Note This study found a marked decline from 1998 to 2013 in surgical (open and laparoscopic) common bile duct exploration (CBDE) for choledocholithiasis (ie, bile duct stones). At the same time, the rate of endoscopic retrograde cholangiopancreatography (ERCP) increased and is becoming the predominant treatment strategy. The percentage of…
Editor's Note The Food and Drug Administration (FDA) on August 18 approved an expanded indication for the Sapien XT and Sapien 3 transcatheter heart valves for patients with aortic stenosis. The new indication is for patients who are at intermediate risk for death or complications associated with open-heart surgery. Previously,…
Editor's Note The Food and Drug Administration (FDA) on August 8 published draft guidance on when medical device manufacturers and software developers must obtain FDA clearance before making changes to existing products, the August 8 Modern Healthcare reports. The draft says if the “overall structure” of a device’s software is…
The interactive hybrid OR, which debuted at the annual OR Manager Conference in 2014, grows larger and more comprehensive each year. For 2016, representatives from more than 10 different companies will be on hand to answer questions, and product demonstrations will create a dynamic learning environment. The 2015 town hall…
More than 1,200 individuals from the US and abroad attended the 2016 annual conference of the International Association of Healthcare Central Service Materiel Management (IAHCSMM) in San Antonio, Texas. The conference, which covered sterile processing techniques, management skills, and regulations, also provided numerous networking opportunities. Preconference educational events included IAHCSMM’s…
Editor's Note A survey by Loftware, Inc (Portsmouth, New Hampshire), shows that only 15% of medical device companies are currently compliant with the next phase of the Food and Drug Administration's Unique Device Identification (UDI) regulation, the August 3 PRWEB reports. The deadline is September 24. Of 120 companies polled,…
Editor's Note The Food and Drug Administration (FDA) on July 26 issued a draft Unique Device Identification (UDI) guideline that requires most medical device labels and packages to bear a UDI in easily readable plain-text and automatic identification and data capture technology forms. UDIs must be issued under a system…
Editor's Note An automated text and voice messaging system improved communication about preventive steps orthopedic patients should take a week before surgery and the postoperative signs of infection to report in the 2 weeks after surgery. The system reminds patients to fill their prescriptions for antibiotic ointment and body wash…
Personal wearable technology, which covers the gamut from activity trackers such as Fitbit to e-textiles that monitor vital signs, have the potential to revolutionize healthcare. Like most innovations, however, the technology comes with risks. For OR leaders, those risks include possible security breaches, distractions, and violation of patient privacy and…
How do OR leaders enhance family members’ satisfaction with the communication they receive when their loved ones are in surgery? Thanks to advances in technology, many are turning to tools like mobile apps and text messaging. At Memorial Medical Center (MMC) in Springfield, Illinois, Lexanne Darwent, BSN, RN, helped implement…