Key Terms
Key Terms
Key Terms
Key Terms
100

1: An obligation to do or not do something
2:An obligation that may result, or has resulted, from a negligent act.

Liability

100

Professional misconduct that results in harm to another; negligence of a health care professional

Malpractice

100

affidavit

voluntary statement of facts sworn before an authority to be true

100

Advance Directive

written instructions expressing the patients wishes concerning the types and amount of medical treatment to be rendered in the event the patient can no longer make those decisions

200

failure to act, or take an action, that a reasonable or prudent person would not take under the same circumstances

Negligence

200

branch of philosophy dealing with good conduct and moral values

ethics

200

tort law

a body of civil law that deals with private wrongs causing harm to individuals or their property

200

Accreditation 

process whereby businesses, educational institutions and programs, and health care organizations are determined to meet standards and performance criteria as established by an accrediting agency

300

mechanism for reporting an incident, usually by completing a document describing what happened

Incident report

300

a situation in which a patient gives voluntary permission to another party to perform procedures that have been explained

Informed consent

300

Scope of practice 

professional duty limits based on state and federal law and on an individuals education and experience

300

abandonment

to leave a patient who is still in need of care or observation

400

process by which an agency or organization establishes a minimum knowledge base for a given health care profession 

credentialing

400

Guidelines given in a series of statements that provide ethical standards of conduct for a profession

Code of ethics

400
Patient care partnership 

replaced the AHA patients' bill of rights, this informs patients about what they should expect during their hospital stay with regard to their rights and responsibilities 

500

established in 1990, this act requires medical device users to report to the manufacturer and/or FDA incidents that reasonably suggest there is a probability that a medical device has cause or contributed to harm, death, or illness of a patient

Safe Medical Device Act

500

efforts of a health care provider organization to collect and utilize data to decrease the chance of harm to patients or staff 

risk management 

500

moral principles

guides for ethical decision making that include the concern that individuals have for the well being of others, respect for individual autonomy, basic justice, and prevention of harm to others 

M
e
n
u