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Due to harsh chemicals, medical device manufacturers need a solution to the problems caused by regular cleaning of healthcare equipment.
April 29, 2021
By: Ryan Hoobler, VP of Engineering, Code Corporation
One of the most fundamental lessons the general public learned from COVID-19 is that cleanliness can be serious business. The public was continuously urged to not only wash their hands and use hand sanitizers, but to also disinfect their homes, cars, and anywhere else subjected to physical contact. This wave of activity and awareness was intended as a widespread infection control campaign waged against the global pandemic. What most people are not aware of, however, is there have been fierce infection control battles waged for decades in healthcare facilities. While there is always collateral damage, some of the most surprising casualties emerged in the form of medical equipment and electronic devices that are used in hospitals and clinics. The majority of these patient-care tools are housed in plastic. In 2003, the U.S. Center for Disease Control (CDC) published Guidelines for Environmental Infection Control in Health-Care Facilities. The guidelines, which are still used today, explained that microorganisms, such as viruses and bacteria, are transferred from environmental surfaces to patients mostly by hand contact with a surface. Although properly washing hands is important to limit such transfers, appropriately cleaning and disinfecting environmental surfaces is, “fundamental in reducing their potential contribution to the incidence of healthcare-associated infections.” The early 2000s also saw a burst of innovation with clinics and hospital rooms seeing more wired and wireless devices used in monitoring and diagnosing patients as well as in the organization and hospital workflow to reduce errors and increase efficiencies, such as barcode scanners, computers, tablets, and smartphones. This is where the tech industry learned some hard lessons. Many companies found that even after spending millions of dollars on research and development to ensure their devices would solve critical issues for physicians and nurses, they would see their products shipped back to them in as little as a few months in little more than piles of scrap. The harsh chemicals—which have evolved over the years—that the healthcare staff was using would literally destroy the plastics and often corrode the metals that the devices were made of. Rational Approach to Disinfection The 2008 CDC Healthcare Infection Control Practices Advisory Committee Guideline for Disinfection and Sterilization in Healthcare Facilities states, “…more than 30 years ago, Earle H. Spaulding devised a rational approach to disinfection and sterilization of patient-care items and equipment. This classification scheme is so clear and logical that it has been retained, refined and successfully used by infection control professionals and others when planning methods for disinfection or sterilization.” Aside from items such as surgical instruments that are required to be sterilized due to a high risk for infection if they are contaminated with any microorganism, there are three levels of disinfection for devices and surfaces for safe use. These disinfection levels are “low-level,” “intermediate-level,” and “high-level.” The CDC’s basis for these levels is microorganisms can usually be grouped according to their innate resistance to a spectrum of physical or chemical germicidal agents. This information, coupled with the instrument/surface classification, determines the appropriate level of “terminal disinfection” needed for a device. The guidelines outline general cleaning strategies for patient-care areas, which depend on the number and types of microorganisms present on environmental surfaces, and are influenced by the following factors:
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