FREE CBIC Trivia Question and Answers
The ideal method for instructing a group of nurses, both experienced and inexperienced, is to:
Explanation:
The ideal strategy for training a group of nurses with varying levels of experience is to encourage the experienced nurses to share their experiences with the rookie nurses rather than dividing the group or reminding the experienced nurses to be patient. It may be challenging to strike a balance between what new nurses need to know and what seasoned nurses have acquired through practical work experience, so trying to utilize the same technique may be unsuccessful. Adult learners also like taking an active role in their education.
The IP's main area of attention should be:
Explanation:
Infection control should be the IP's first priority. In order to emphasize the roles that the infection preventionist (IP) has in ensuring that facilities and staff follow infection control procedures in order to prevent infections among patients and staff, the Association for Professionals in Infection Control and Epidemiology (APIC) has changed the professional's focus from the control of infection to prevention and recommended the title of infection prevention (IP) instead of infection control professional (IP).
The just-in-time inventory concept's main goal is to:
Explanation:
The just-in-time inventory concept's main goal is to reduce inventory costs. Due to the fact that supplies are ordered based on their intended usage rather than being kept in a huge stock, just-in-time inventory helps to bridge some of the gap between expenditures and reimbursements. This decreased the expense of replacing or re-sterilizing outdated materials that had to be returned or disposed of. The space needed for suppliers as well as the personnel costs related to maintaining supplies are both decreased with just-in-time inventory.
The first step in reviewing products with the product assessment committee is to:
Explanation:
The first phase in the product review process with the evaluation committee is to determine the need for the items, introduce them, and describe their use and purpose. The committee should study background material, consumer studies, and market surveys, produce functional product specifications, and analyze expenses related to the items. The IP should take into account how the items may affect infection and safety. The committee should create a protocol for product trials, carry them out, and assess their results.
Which of the following indicators is most likely to take the most time for surveillance data collection?
Explanation:
Since VRSA infections are relatively uncommon, the longest term of monitoring data collection will likely be needed for this indication. The IP must take into account the typical patterns of occurrence when defining the time period needed for monitoring because longer time periods are required to calculate infection rates for operations or infections that happen infrequently. Data are often gathered for durations of a month to a year.
The term that denotes the typical occurrence of a particular disease within a particular geographic area over a particular time period is:
Explanation:
the typical occurrence of a particular disease in a particular location within a particular time frame. Epidemic: Increased occurrence of a certain disease within a particular geographic area over a given time period above what is anticipated. Epizootic: Increased occurrence of a specific disease in an animal population in a particular location at a particular time period. A pandemic is a widespread epidemic that spreads across several continents or countries.
Most facilities will need the following when contemplating reprocessing medical devices:
Explanation:
Most facilities will need a contract with a third-party reprocessing company in order to reprocess medical equipment. This is advised as the lack of industrial-grade sterilization and processing procedures in facilities like hospitals increases the danger of infection and liability. The FDA regulates third-party reprocessing businesses, and they are subject to tight regulations. The medical devices that can be reprocessed and the steps to get the equipment ready for reprocessing should be specified by any facility that is thinking about doing so.