FDA Clears First Duodenoscope With Disposable Elevator Component To Reduce Infection Risk

The United States Food and Drug Administration (FDA) has cleared the first duodenoscope on the market with a disposable elevator piece. The industry believes that a move to disposable parts, like the elevator, will help reduce infection risks. The elevators of duodenoscopes have been identified in numerous instances as a difficult to clean component that […]

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Unnecessary Healthcare Supply Chain Spend Tops $25 Billion

According to a recent survey, unnecessary hospital supply chain spending increased over 10% from 2017 to 2018. The total unnecessary spend across US hospitals reached $25.7 billion in 2018, up $2.7 billion from 2017. The survey, conducted by Navigant, surveyed over 2,000 hospitals. The study also found that the average savings opportunity by reducing unnecessary

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FDA Discussion Of Duodenoscopes Points To Several Causes For Safety Issues

The United States Food and Drug Administration (FDA) recently held a panel discussion to review the causes and possible solutions to safety issues arising from the use of duodenoscopes. Participants in the FDA’s General Hospital and Personal Use Panel of the Medical Devices Advisory Committee discussed how particular aspects of duodenoscopes have led to recent

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How Community Hospitals and ASCs Can Keep Up With Endoscope Documentation Requirements

When community hospitals and ambulatory surgery centers (ASCs) are visited by accreditation agencies like The Joint Commission (TJC) or DNV, they are held to the same strict endoscope documentation requirements as academic medical centers. While it may seem unfair for these smaller facilities with access to fewer resources to be held to the same strict

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Survey: Health System Profit Margins Up, But Still Below 2015 Levels

According to a recent survey, health system operating margins improved in 2018, but still remained significantly below 2015 levels. The analysis, conducted by Navigant, looked at the financial performance of over 100 large health systems that together own 44% of total hospitals in the US. The survey revealed that the average health system improved its

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How To Determine When To Sterilize Flexible Endoscopes

As the major endoscope manufacturers continue to work with regulators such as The United States Food and Drug Administration (FDA) to improve the safety of their endoscopes, many possible long-term solutions have been raised for discussion. Some thought leaders say that improving current high-level disinfection (HLD) processes will improve safety significantly, while many other experts

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New Study Puts Price Tag of US Healthcare Waste At Nearly $1 Trillion

A new study published in the Journal of the American Medical Association (JAMA) estimated the annual cost of waste in the US healthcare system between $760 billion to $935 billion. The study, conducted by researchers at Humana and UPMC, looked at 54 published reports that explored the costs of waste in US healthcare. As this

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ECRI Top Health Technology Hazards List Includes Poor Sterilization Practices

The ECRI Institute, based in Philadelphia, has just released its annual list of health technology hazards for 2020.  This year’s list includes an entry at number 3 for poor sterilization practices, echoing prior year concerns about sub-standard disinfection practices for flexible endoscopes. ECRI’s list is the result of extensive research by its own engineers, scientists

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A Scope Tracking Solution That Can Grow With Your Hospital

The Joint Commission (TJC), the United States Food & Drug Administration (FDA) and several other regulatory and accreditation agencies have recently put more focus on flexible endoscopes in their guidance to US hospitals and surgery centers. It comes as no surprise, as over the last decade the number of reported outbreaks based on inadequately reprocessed

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Why Channel Drying Is So Crucial To Endoscope Infection Control

Because endoscopes are reusable medical instruments, one of their biggest risks is the very real possibility of passing diseases to patients through contact with inadequately disinfected scopes. Though the risk of passing diseases through scopes is relatively low, the danger is always there, especially when high-level disinfection (HLD) protocols aren’t closely followed. One area where

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