Sterile Processing Questions and Answers Latest Updated 2023 Rated A

What is the Area Temp & Humidity for Decontamination? 60 deg to 65 deg F, 30% to 60% Humidity What is the air exchange rate & pressure type for Decontamination? 10 air exchanges per hour under Negative Pressure What is the Area Temp & Humidity for the Sterile Storage Area? 68 deg to 75 deg F, 35% to 70% Humidity What is the air exchange rate & pressure type for Sterile Storage Area? 4 air exchanges per hour under Positive Pressure What is the Area Temp & Humidity for the Prep & Packaging Area? 68 deg to 73 deg F, Ideal Humidity 50% - not lower than 35% What is the air exchange rate & pressure type for the Prep & Packaging Area? 10 air exchanges per hour under Positive Pressure The main role of sterile processing is to: Provide dependable reliable services to enhance the quality of patient care. Instrument sets and patient care equipment must be processed and distributed in an accurate and timely manner so that: Patient care is not adversely affected. Ethics is the practice of: Doing the right thing. Compliance with OSHA is: Required by law. Which of the following establishes sterilization practice standards based on opinion, research, and/or theory: AAMI Recommended practices are: Statements of sound principals of practice that are based on scientific data and the opinions of experts. EPA, FDA, OSHA and state departments of health (DOH) primarily issue: Regulations. Standards for CS/SPD practice are written by: AAMI The Health Insurance Portability and Accountability Act provides for which ethical issue? Confidentiality A rule designed to govern behavior is called a: Regulation An established norm which is based on theory is called a: Standard Before a pesticide can be marketed and used in the United States, it must be evaluated and registered by which of the following? EPA Which of the following regulates and makes sure products are safe and effective before companies put them on the market? FDA If healthcare facilities reprocess single-use devices, the devices must be cleared by: FDA How often should cleaning and sterilization instructions be requested from device manufacturers? Each time the item is purchased