FDA issues Unique Device Identification final rule
The Food and Drug Administration (FDA) on September 24 published the final rule for its Unique Device Identification (UDI) system to provide a consistent way to identify medical devices throughout their distribution and use. “A UDI system for medical devices is an important step towards increasing patient safety, modernizing postmarket…
Stryker's Neptune recall raises stakes for compliance
Strict requirements needed to comply with a recall for the Neptune brand of roving suction devices are raising questions and concern for ORs whose facilities continue to use the devices. The recall of the Neptune Waste Management System from Stryker, used to collect and dispose of fluid waste, was initiated…
Could technology lend a hand in cleaning of ORs?
Manual cleaning is performed by humans, and thus will always be imperfect. Could technology lend a hand? Some hospitals and a few ORs are adopting an extra disinfection step—employing robot-like machines that can disinfect an entire room. The machines are meant to augment—not replace—manual cleaning. These technologies have some compelling…
A checkup for your OR's value analysis process
How healthy is your value analysis process? A strong program for evaluating products and new technology is essential to the cost-effective management of resources. Characteristics of a good value analysis program are offered by Barbara Strain, MA, past president of the Association of Healthcare Value Analysis Professionals. She is director…
ORs could see benefits from FDA's UDI system
Your OR could see real benefits from the Food and Drug Administration’s (FDA) proposed unique device identification (UDI) system. But will your systems be ready to capture, record, and retrieve UDI information? Comments on the FDA’s UDI proposed rule are due by November 7, 2012. The proposal was published July…
RTLS yields new data for managing patient logistics
A patient arrives for surgery. As soon as she checks in, she receives a wristband with a small locator tag that monitors her progress as she moves through the surgical process. Behind the scenes, the tag is signaling the surgical department’s real-time locating system (RTLS), which sends notices to OR…
Smartphones, tablets in the OR: With benefits come distractions
Use of personal mobile devices is pervasive in surgery departments. As in the rest of life, they bring benefits but also risks, OR Manager found in an online survey. An overwhelming majority of respondents—86%—say they believe personal use of mobile devices in the OR sometimes distracts providers from patient care.…
Social media: Helping staff manage personal, professional boundaries
A 20-year-old nursing student, Emily, was excited to be on her pediatrics rotation and taking care of Tommy, a 3-year-old leukemia patient. One day, when Tommy’s mom was out of the room, Emily asked Tommy if she could take his picture. He readily agreed. When she got home, Emily excitedly…
A new "electronic etiquette" for surgical services
Nurses texting between—or even during—cases. Anesthesia providers playing games on their cell phones. A surgeon answering calls during surgery using his Bluetooth device. Mobile devices like smartphones and tablets have introduced a brand of constant communication—and a management challenge. Banning the devices isn’t the answer. Instead, health care needs to…
Capnography: New standard of care for sedation?
Capnography—is it the standard of care for patients having moderate sedation? Should capnographic monitoring be added for procedures performed under moderate sedation in areas like the preop holding area, GI endoscopy unit, and cath lab? The issue is generating discussion following an update in the American Society of Anesthesiologists (ASA)…
Free Daily News
- Legislation proposes to halt Medicare physician payment cuts
- Cigna ties executive pay to patient experience
- Proposed tax credit aims to bolster nurse preceptor ranks
- Study links financial conflicts of interest to favorable robotic bariatric surgery research
- Hospitals double down on ambulatory care expansion with major investments
- Study: Post-laparotomy incisional negative pressure wound therapy fails to reduce infection risk
- FDA announces multiple Class 1 recalls
- Study: ERAS protocol reduces opioid use after cardiac surgery
- Study: Prehabilitation reduces surgical complications, speeds recovery
- Commentary: Studies show how surgeon decisions follow the money