PSH model improves postop outcomes
Editor's Note Implementing the Perioperative Surgical Home (PSH) model resulted in improved patient outcomes, patient satisfaction, and shorter hospital stays in this study presented October 22 at the Anesthesiology 2016 annual meeting. The study included 1,356 patients who had total knee, hip, or shoulder replacements. Half received care under the…
FDA: Class I recall of HeartWare Ventricular Assist Device Pumps
Editor's Note The Food and Drug Administration on October 24 categorized HeartWare Inc’s recall of its HeartWare Ventricular Assist Device Pumps as Class I, the most serious. The recall is because of a design problem with the driveline connector that connects the pump to the external controller and power source.…
FDA: Class I recall of Willy Rusch Tracheostomy Tube Set
Editor's Note The Food and Drug Administration (FDA) on October 20 categorized the recall by TeleFlex Medical of its Willy Rusch Tracheostomy Tube Set as Class I, the most serious. The recall was issued because of the possibility that the connector may disconnect from the tracheostomy tube during use on…
New tool predicts ICU readmission for surgical patients
Editor's Note Researchers from the University of Utah School of Medicine, Salt Lake City, have developed a risk prediction tool, called a “nomogram,” that uses a scoring system to determine a patient’s risk for returning to the surgical ICU within 72 hours after discharge. The study was presented October 20…
FDA: Medtronic recalls certain neurovascular products
Editor's Note The Food and Drug Administration (FDA) on October 18 announced the recall by Medtronic of certain lots of its Pipeline embolization device, Alligator retrieval device, and X-Celerator hydrophilic guidewire. The recall also includes the stylet containing UltraFlow flow directed micro catheters and Marathon flow directed micro catheters. The…
Fitness tracker monitors postop recovery
Editor's Note Monitoring patients’ postoperative functional recovery using a commercially available, wireless activity tracker is feasible and strongly correlates with complications reported by patients, finds a study presented October 17 at the 2016 Clinical Congress of the American College of Surgeons. The median number of steps that patients took on…
FDA: Class I recall of Skintact DF29N Multi-function Defibrillation Electrodes
Editor's Note The Food and Drug Administration (FDA) on October 14 categorized the recall by Leonhard Lang of its Skintact DF29N Multi-function Defibrillation Electrodes as Class I, the most serious. The electrode is being recalled because of a connector compatibility issue with the Welch Allyn automatic external defibrillator (AED), model…
Diagnosing SSIs with photography
Editor's Note The addition of patient-generated wound photographs to existing data significantly improved diagnostic accuracy of surgical site infections (SSIs) and prevented overtreatment in this study. When photographs were added, overall diagnostic accuracy improved from 67% to 76%, and specificity increased from 77% to 92%, but sensitivity did not significantly…
FDA, CDC issue alerts on Stӧckert 3T Heater-Cooler System
Editor's Note The Food and Drug Administration (FDA) on October 13 updated its Safety Alert on the Stӧckert 3T Heater-Cooler System by LivaNova to provide new information from the Centers for Disease Control and Prevention (CDC) about Mycobacterium chimaera infections associated with the use of the system in US patients…
Dirty scopes persist despite cleaning protocol compliance
Recent outbreaks of deadly infections linked to flexible endoscopes have made headlines, and the Food and Drug Administration has issued strict guidelines for reprocessing these devices. However, cleaning and disinfection may not be effective under the recommended protocols, says Cori L. Ofstead, MSPH, epidemiologist and president and chief executive officer,…
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