Sterile Processing Department Rotation:Your Central Processing experience will be two days Friday, November 18,and Friday, December 2, 2022 from 8 a.m. – noon. For these 2...

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Sterile Processing Department Rotation:






Your Central Processing experience will be two days Friday, November 18,








and Friday, December 2, 2022 from 8 a.m. – noon. For these 2 days you will








be in the Central Sterile Processing Department






Re-review Chapter 7 pp. 140-170 in your Surgical Technology textbook








prior to the days you are assigned this clinical rotation. You will be asked to








compare the AST Recommended Standards of Practice (RSOP)* with the








institution’s practices. (*visit




www.ast.org)








Complete the following objectives; turn in your written review to your








clinical instructor by Monday December11, 2020. Each paper will be








graded based on the comprehensive review of each of the 4 areas noted








below:






1. What methods were utilized in the sterile processing department as a








means of protective wear? How and why did the protective wear differ








from items utilized in the OR?









2. List the steps in the decontamination of used items received from the OR.








Include such things as where does sterilization start, the separation of clean








from dirty processes and the implementation of standard precautions.








Compare these processes with AST Recommended Standards of Practice for








decontamination of surgical instruments.






3. Review the methods of packaging used, and compare these to the AST








Recommended Standards of Practice for packaging material and preparing








items for sterilization. Be specific in terms of the type of sterilization








system, indicators that are included in and on the package to determine








exposure to the sterilization process, filters and how to interpret them.






4. Describe the steps in the steam sterilization process, beginning with








loading, starting the sterilizer, drying cycles, cooling cycles, and records











Surgical Technology Program








AHS 100/101









Central Processing Rotation




















































































maintained. Compare these to the information in Chapter 7 and the AST








RSOP








5. Select another sterilization system used in the central processing








department (other than steam) and give a description of the sterilization








process, the type of items sterilized by this process and why steam








sterilization is not utilized on these items. Describe the difference between








this process and steam sterilization.




































Answered 2 days AfterDec 07, 2022

Answer To: Sterile Processing Department Rotation:Your Central Processing experience will be two days...

Dr Insiyah R. answered on Dec 09 2022
39 Votes
Ans1: Certain tasks and situations necessitate using specialised personal protective equipment for sterile processing experts to keep them safe while doing their duties (PPE). Ralph Basile, vice president of Healthmark Industries, was asked by Healthcare Purchasing News to discuss the criteria for CS PPE, what CS or SPD personnel' top concerns are, what they must wear and why. PPE includes things like protective clothing, headgear, gloves, face shields, protective eyewear, facemasks, respiratory protection, and other things that shield the wearer from injury or the spread of illness (PPE). PPE is frequently used in medical facilities, such as hospitals, clinics, and doctor's offices. When worn properly, personal protective equipment (PPE) serves as a barrier separate your skin, mouths, nose, and eyes and infectious agents like bacteria and viruses (mucous membranes). The barrier has a slightest possibility to prevent the transmission of pollutants from blood, bodily fluids, or respiratory secretions. PPE can protect patients at high risk of infection during surgery or by a health condition like immunodeficiency from exposure to chemicals or other infectious material handled by visitors and healthcare professionals. The barrier may prevent the transmission of pollutants from blood, bodily fluids, or respiratory secretions. PPE can protect patients at high risk of infection during surgery or by a health condition like immunodeficiency from exposure to chemicals or other infectious material handled by visitors and healthcare professionals. To use PPE properly and prevent infecting the user and others, soiled PPE must be discarded and disposed of properly of. FDA regulations and the necessary voluntary consensus protection standards must be met by all protective equipment (PPE) meant to be utilised as a medical device. This includes surgical masks, gowns, gloves, and N95 respirators. Different FDA requirements and consensus standards apply depending on the precise kind of PPE. When these standards and laws are followed, the device's efficacy and safety can be regarded as substantially ensured.
Before they may be marketed lawfully in the US, several PPEs must pass FDA inspection. The producers must prove they satisfy specified requirements for performance, labelling, and intended use to establish significant equivalence in this evaluation, also referred to as Premarket Notification or 510(k) clearance. Adherence to generally accepted criteria for reliability tests was carried out, and resistance to rips and snags is one method substantial equivalency may be shown, at least in part. Additionally, utilising voluntary agreed-upon standards, sterility (where suitable), biological uses, liquid resistance, and thermal properties may be shown. The standards-based testing techniques must be verified by the manufacturers, and each product must be given the pertinent performance test results.
Ans 2: Standard precautions are the minimal infection prevention practises that are required to be followed in any setting where hospital care is provided, regardless of whether a person has a proven or suspected disease. These steps are designed to protect DHCP and prevent it from infecting health care workers. One typical safety measure is hand washing.
The next sections include details of each Standard Precaution, including the use of personal protective equipment, coughing etiquette, respiratory hygiene, Sharps security, safe injection procedures, such as utilising an aseptic way to administer parenteral medications, sterile instruments and equipment, and clean and sanitised surfaces. Education and training are crucial elements of Standard Precautions because they help DHCP make educated decisions and follow suggested practises. Transmission-Based Precautions are implemented when Increase The survival by themselves are inadequate to inhibit transmission. In addition to standard precautions, this second tier of infection protection is always employed when patients have...
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