Tag Archives: AAMI

Standards, Guidelines and Recommended Practice Crosswalks

Writing new or updating established policies and procedures or preparing for the next accreditation’s survey are both daunting tasks. With all the published standards, guidelines and recommended practices around reprocessing Sterile Processing (SP) managers may be baffled on which ones to follow. However, there are many ways to help interpret how these published documents relate […]

AORN’s Current Guideline for Sterilization

The Association of periOperative Registered Nurses (AORN) published their updated “Guideline for sterilization” last September. The guideline covers recommendations for sterilization reusable medical devices by steam, dry heat, as well as, low temperature methods including ethylene oxide, hydrogen peroxide gas plasma or vapor, ozone combined with hydrogen peroxide and peracetic acid. In addition to addressing […]

Guidelines for Table Top Sterilizers

Medical advances have led to an increased use of unconventional health care sites, such as offices, ambulatory-care centers, dental and other specialty clinical settings. Clinical or office-based practices may differ greatly from hospitals in their education and training of reprocessing employees and the physical design. ANSI/AAMI ST79:2017b Comprehensive guide to steam sterilization and sterility assurance […]

Sterilization and High-level Disinfection Guidelines: Should be Based on Current Evidence

Recently, physician societies have published their own guidelines for reprocessing instruments and equipment (e.g., gastroenterology and ophthalmology). These guidelines are very confusing and somewhat disconcerting to expert reprocessing professionals for the following reasons:   Those physician created guidelines did not go out for public comments, leaving no chance of input from reprocessing experts. Some recommendations […]

Point of Use Care for Surgical Instruments: A Hot Button for Surveyors

Care and handling of surgical instruments is a shared responsibility between the Operating Room (OR) and Sterile Processing (SP) personnel. Research has proven that preparation for decontamination must begin at the point of use (POU). However, many facilities are not following the guidelines. Surveyors from accreditation organizations such as The Joint Commission are citing facilities […]

Don’t Process What You Can’t Clean

It has been proven repeatedly that if an item is not properly cleaned it cannot be effectively reprocessed.  Healthcare professionals know, “If it isn’t clean it can’t be sterilized or high-level disinfected”.  The first and most important step in reprocessing reusable medical devices is thorough cleaning and rinsing. So how is cleaning defined? Let’s look […]

Standards, Guidelines or Recommendations: Do We Really Need to Follow Them?

There are many published standards guidelines and recommendations related to reprocessing reusable medical devices. As evidence becomes available, these publications are often updated to reflect most current best practices. So, does that mean we must follow them? Let’s start by discussing what the Association for the Advancement of medical instrumentation (AAMI), the Association of periOperative […]

Managing SPD Requires Critical Thinking Skills

Sterile Processing Department (SPD) managers have multiple responsibilities with big impacts on their department, the facility and even more important the patients. Therefore, SPD leaders must have critical thinking skills founded on published evidence based guidelines, education and experience. Critical thinking is disciplined thinking that is clear, rational, open-minded, and informed by evidence.  It also […]

Every Facility Needs a Processing Subject Matter Expert

There are many reasons why issues with sterilization or high-level disinfection of reusable medical devices are in the news headlines, as well as, a large focus in an accreditation survey.  There have been numerous reports of inadequate knowledge or competency, poor documentation, lack of following specific instructions for use (IFU) and not complying with current […]

Joint Commission: High-Level Disinfection (HLD) and Sterilization BoosterPakTM

  The Joint Commission (TJC) has created several Standards BoosterPaks.  These are searchable documents that provide specific information about TJC standards associated with a high volume of non-compliance scores in the health care field. The BoosterPaks were created for accredited organizations and staff within TJC to improve the understanding and consistency of standards interpretation. BoosterPaks […]

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