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1.9: Key Terms

  • Page ID
    111080
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    anonymity
    state of being unknown; refers to a participant in a study whose identity is not disclosed
    autonomy
    right to make one’s own decisions related to treatment and care
    beneficence
    responsibility to act in the patient’s best interest
    clinical decision-making
    application of both critical thinking and clinical judgment to make decisions about nursing care
    clinical judgment
    process by which nurses make decisions about patient care on the basis of observations, assessments, and interpretations of relevant information
    collaborative care model
    approach to health care in which a team of providers works together to manage patient care more effectively and improve patient outcomes
    critical thinking
    multidimensional, systematic, and organized way of reasoning
    data
    pieces of information that help researchers answer questions and draw relevant conclusions
    electronic health record (EHR)
    digital version of a patient’s medical history; enables providers to immediately access information about a patient’s health, including conditions, medications, and test results
    empirical evidence
    objective data gathered by the senses from observations or experiments
    ethics
    study of right and wrong actions
    evidence-based practice
    process of making clinical decisions on the basis of the best available evidence from the most up-to-date research
    full disclosure
    process of providing a complete description of a study or medical procedure, including the risks and possible benefits
    health equity
    condition in which everyone has the same fair opportunities to attain the highest level of health outcomes
    health inequities
    disparities created by socioeconomic systems and the status of different populations
    Health Insurance Portability and Accountability Act (HIPAA)
    federal law to protect sensitive patient health information from being disclosed without the patient’s consent or knowledge
    health policy
    laws and regulations that define the actions and decisions that promote a society’s health goals
    health-care delivery system
    individuals and organizations collectively responsible for providing and overseeing health care in an area
    informed consent
    legal document an individual signs to indicate a thorough understanding of a study, medical treatment, or procedure and to agree to participate
    intercollaborative care
    team-based approach that uses shared responsibilities, interactive planning, and collaborative decision-making to promote person-centered care and improve patient and health system outcomes
    ISBAR
    acronym that stands for Introduction, Safety, Background, Assessment, and Recommendation. The ISBAR format provides a structure of written communication that can be replicated by each team member to keep communication on track, create a workflow for the intercollaborative team, and promote patient safety
    justice
    principle that all patients should be treated fairly
    macrosystem
    culture or society that surrounds smaller systems and gives them structure
    microsystem
    relatively simple, localized system, such as the one in which a health-care provider directly works
    nonmaleficence
    responsibility to do no harm
    Nurse Practice Act
    law passed by a state’s legislature regulating nurses’ scope of practice
    nursing informatics
    specialty that uses information and technology to improve the efficiency of health care and its delivery
    nursing research
    inquiry that is systematically designed to provide knowledge for important issues relevant to the nursing profession
    patient-centered care (PCC)
    model of care that requires listening to patients to understand what they value most, then using the information as the catalyst for health-care decisions
    PICOT
    acronym based on the elements of a clinical research question: population or problem, intervention, comparison, outcome, time frame
    primary prevention
    health care intended to prevent disease before it occurs
    qualitative research
    inquiry that focuses on personal experiences obtained through observation and interaction with patients
    Quality and Safety Education for Nurses (QSEN)
    project focusing on the preparation of future nurses to promote the quality and safety of health-care systems
    quality improvement (QI)
    framework to improve patient care and outcomes systematically
    quantitative research
    inquiry that uses deduction and generalization from empirical evidence to draw conclusions
    scope of practice
    range of activities a licensed person is permitted to perform as part of their work
    secondary prevention
    health care that promotes early diagnosis and treatment to slow the progression of a disease or injury
    social determinants of health (SDOH)
    nonmedical factors that have an influence on health outcomes
    systems-based practice
    health care that considers the multiple systems involved in a patient’s condition and uses evidence about their interactions to develop a treatment plan that incorporates all the entities involved in the patient’s care
    telehealth
    use of digital communications technology to remotely provide health-care services
    tertiary prevention
    health care intended to decrease the impact of an ongoing illness or injury
    The Joint Commission
    independent, not-for-profit organization that sets standards for quality care, quality improvement, and patient safety for organizations and workers in the health-care industry
    theory–practice gap
    divide between theoretical knowledge acquired in academic settings and the practical application of that knowledge in real-world clinical settings
    whole-person care
    holistic care that focuses on all of a patient’s needs

    This page titled 1.9: Key Terms is shared under a CC BY 4.0 license and was authored, remixed, and/or curated by OpenStax.

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