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Databases
- a repository of published scientific studies including peer reviewed research
- Box 5-1
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Institutional Review Board (IRB)
- scientists and laypersons who review all studies conducted in the institution to ensure that ethical principles are followed
- before conducting any study with human subjects the researcher must obtain approval from IRB
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National Institute of Nursing Research
supports clinical and basic research to establish a scientific basis for the care of individuals across the life span
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performance improvement
an organization analyzes and evaluates current performance to use results to develop focused improvement actions
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quality improvement
an approach to the continuous study and improvement of the processes of providing health care services to meet the needs of clients and others
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examples of nursing sensitive outcomes
- cental line bacteremia rate
- compliance/adherence to actions(eg diet, medication, activity restrictions)
- failure to rescue
- fall rate
- nosocomial infection rate
- nosocomial pressure ulcer rate
- symptom reduction
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Nursing research
- a way to identify new knowledge, improve professional education and practice and use resources effectively
- Box 5-3
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PICO question
- P= patient population of interest ( age, gender, ethnicity and disease or health problem)
- I= intervention of interest (e.g. treatment, diagnostic test, prognostic factor)
- C= comparison of interest ( what is the usual standard of care or current intervention currently used)
- O= Outcome ( what result do you wish to achieve or observe)
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Informed consent
- research subjects:
- are given full and complete info about the pupose of the study, procedure, data collection, potential harm and benifits and alternative methods of treatment
- are capable of fully understanding the research and the implications of participation
- have the power of free choice to voluntarily consent or decline participation
- understand how the researcher maintains confidentiality or anonymity
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Evidence based practice (EBP)
a problem solving approach to clinical practice that integrates the conscientious use of best evidence in combination with a clinician's expertise and client preferences and values in making decisions about client care
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Clinical Guidelines
rules, policies
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Anonymity
- unknown
- even the researcher cannot link the subject to the data
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