He was known for the "Allotey Formalism" which arose from his work on soft X-ray spectroscopy. He was the 1973 recipient of the UK Prince Philip Golden Award for his work in this area.
Source - Wikipedia
Answer:
The nurse knows the written instructions for healthcare when a person is incapacitated is called an advance directive. This includes instructions about CPR, death, resuscitation, or prolonging life beyond consciousness.
The caregiver must be authorized to make healthcare decisions for a person who is deemed incapable of giving consent. The advance directive may be in any form written, electronic or oral.
The nurse will help families to create an advance directive that can guide their healthcare needs without having to address those issues.
Explanation:
An advance directive is a document that a person places in physical or electronic form in order to express his or her preferences regarding medical care at the time of incapacitation.
Advance Directives are legal documents written by the incapacitated, living, or deceased. These directives allow families and doctors to abide by their wishes when making healthcare decisions for them.
The nurse takes care of the patient’s life by providing them with the best care possible and should make sure that there is an advance directive on file.
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Answer:
Benefits and Advantages of encoder:
Highly reliable and accurate.
Higher resolution.
Low-cost feedback.
Integrated electronics.
Compact in size.
Fuses optical and digital technology.
It can be incorporated into existing applications.
Drawback and Disadvantages of an encoder:
The subject of magnetic radio interference.
Susceptible to dirt, oil and dust contaminate.
Direct light source interference.
Explanation:
The Director of nursing would be most concerned with the safety standards established by the clinical laboratories’ improvement amendments or CLIA.
<h3>What is CLIA?</h3>
The Public Health Services Act was amended by the Clinical Laboratory Improvement Amendments of 1988 law, in which Congress altered the federal scheme for accreditation and oversight of clinical laboratory testing.
Federal standards that apply to all U.S. facilities or locations that test human specimens for health assessment or to diagnose, prevent, or treat disease are included in the Clinical Laboratory Improvement Amendments of 1988 (CLIA) rules.
Testing performed for forensic reasons (criminal investigations), testing carried out on human specimens for research or surveillance, and testing carried out on human specimens when patient-specific results are not reported are all exempt from the CLIA regulations.
These tests include employment-related drug testing by SAMSHA-certified laboratories.
To know more about CLIA, visit:
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