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Nosocomial infections claim approximately 90,000 lives in the United States annually. When patients are hospitalized and identified as having methicillin-resistant Staphylococcus aureus or infections that can be spread to other patients, best practices isolate these patients in rooms that are subjected to terminal cleaning when the patient is discharged.
ISGOTT has its roots in the late 1960s and early 1970s when the shipping industry recognised the need for comprehensive guidelines to ensure the safety of oil tankers and terminals. During this time, there were increasing concerns about the safety and environmental risks associated with the transportation and handling of oil.
For example, medical device manufacturers design their sterilization processes for an extremely low SAL, such as 10 −6, which is a 1 in 1,000,000 chance of a non-sterile unit. SAL also describes the killing efficacy of a sterilization process. A very effective sterilization process has a very low SAL.
Equipment used in aseptic processing of food and beverages must be sterilized before processing and remain sterile during processing. [1] When designing aseptic processing equipment there are six basic requirements to consider: the equipment must have the capability of being cleaned thoroughly, it must be able to be sterilized with steam, chemicals, or high-temperature water, sterilization ...
Sterile dental instruments from hospital central supply (barcoded label indicating sterilization date, expiry date and contents). The central sterile services department (CSSD), also called sterile processing department (SPD), sterile processing, central supply department (CSD), or central supply, is an integrated place in hospitals and other health care facilities that performs sterilization ...
Microorganisms growing on an agar plate. Sterilization (British English: sterilisation) refers to any process that removes, kills, or deactivates all forms of life (particularly microorganisms such as fungi, bacteria, spores, and unicellular eukaryotic organisms) and other biological agents (such as prions or viruses) present in fluid or on a specific surface or object. [1]
Each country has their own strict legislation on single use medical devices. They all feature similar overall ideas, that focus on putting a patient’s health and safety first, with clear emphasis on sterilisation. In Australia the following legislation applies on medical devices, that includes single use medical devices.
In microbiology, in the context of a sterilization procedure, the D-value or decimal reduction time (or decimal reduction dose) is the time (or dose of an antimicrobial drug) required, at a given condition (e.g. temperature) or set of conditions, to achieve a one-log reduction, that is, to kill 90% of relevant microorganisms. [1]