The first trial accusing Olympus Corp. of wrongdoing associated with contaminated duodenoscopes in US hospitals has recently concluded. The jury ultimately decided that the Olympus duodenoscope’s design was not to blame for the death of a patient – though its lack of proper warning was determined to be partially responsible, as well as the actions […]
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On July 21, 2017, Fujifilm Medical Systems USA issued an Urgent Medical Device Correction and Removal notification to inform customers of a recall of its ED-530XT duodenoscopes. This voluntary recall includes the replacement of the ED-530XT forceps elevator mechanism including the O-ring seal, replacement of the distal end cap, and the provision of new Operation
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Kaiser Permanente’s Largo Medical Center in Maryland has issued a notice to 23 patients that they should undergo testing following the use of an improperly disinfected flexible endoscope in their cases. This recall, coupled with the recent issue at an armed forces facility in Qatar, continues to remind us of the risks that improperly reprocessed
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The recent revelation of a potential endoscope-related outbreak at the Al Udeid Air Base in Qatar reminds us once again of the risks that improperly reprocessed scopes represent to our patients. This unfortunate episode potentially exposed 135 airmen to such diseases as HIV, hepatitis B and C and other potentially fatal bugs. The most disturbing
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The recent issues surrounding scope-related infections continue to gather media attention. A recent article by the Pittsburgh-Post Gazette follows the story of how UPMC in Pittsburgh, PA has managed its endoscope reprocessing since a scope-related outbreak in 2012. In the article, UPMC points to its adoption of additional steps added to its reprocessing guidelines since
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Hospitals and healthcare providers are under increased scrutiny by The Joint Commission (TJC), the FDA, DNV and even Congress to improve the documentation practices around flexible endoscope usage. There are articles are in the media seemingly every day about how a hospital was cited, sued or otherwise put in a negative light around their endoscope
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The first trial accusing Olympus Corp. of wrongdoing associated with contaminated duodenoscopes in US hospitals is underway. The case surrounds the death of Richard Bigler, a 57 year-old patient who underwent a scope procedure while battling pancreatic cancer in 2013. It’s alleged that during the procedure, a tainted duodenoscope at Virginia Mason Medical Center passed
First Olympus Superbug Trial Underway And What It Means For All Hospitals Read More »
All successful endoscopy practices within private practices and hospitals face the same dilemma – how do I track down scopes that have gone missing? With numerous docs, interns, techs and nurses all having access to all the scopes in your facility, it’s a near impossibility to keep track of all of your scopes with 100%
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There has been a lot of discussion lately about the number of days a flexible endoscope can safely be in storage before another cleaning is required. Different medical societies like SGNA, ASGE, AORN and APIC have come out with guidance on what the appropriate hang-time limits are. Some hospitals that we’ve talked to have listened
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A recent incident in the Philadelphia area reminds us of the dangers that can result from improperly trained staff in the endoscopy area of a hospital. In the incident, an elderly patient undergoing a surgical procedure had an improperly cleaned endoscope used on them during their procedure. The incident occurred at Crozer-Chester Medical Center, outside
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