A Randomized Controlled Trial of an Individualized PreoperativeEducation Intervention for Symptom Ma
A Randomized Controlled Trial of an Individualized PreoperativeEducation Intervention for Symptom Management After TotalKnee Arthroplasty Rosemary A. Wilson Judith Watt… Show more… Show moremanagement strategies, may result in better patient out- et al.,2004). Further, systematic reviews have recom- comes thaneducation focused on pathophysiology. mended indivi… Show more… Show moreCharacteristics of the Individual vidual areas of concern for patientswith TKA (Chang Age, sex, educational level et al., 2005). To ensureconcerns, found in the literature, were consistent with … Show more… Show moreQuestions asked by participants focused on (a) use of SAMPLESIZE the intravenous patient-controlled analgesia (PCA-IV) pump, (b)concerns about the adverse effects of opioid Sample si… Show more… Show moreResults PRIMARY RESEARCH QUESTION A total of 337 patientswere screened for participation in Day 3 measurements of the BPI-Iare presented in this trial (see Figure 3). Of these, 162… Show more… Show moreTABLE 2. BASELINE DEMOGRAPHICS OF PARTICIPANTS TABLE4. PAIN ON POSTOPERATIVE DAYS 1, 2, AND 3 InterventionStandard Care Intervention Standard Care (n = 73) (n … Show more… Show moreTABLE 5. TOTAL OPIOID ANALGESIC ADMINISTRATION FORwere intended to maximize pain relief and improve mo- ALLPARTICIPANTS IN MILLIGRAMS OF ORAL MORPHIN… Show more… Show moremanagement (e.g., Pain, the 5th Vital Sign). Other re- up was notsufficient to impact postoperative symptoms search has suggestedthat this is not an unusual finding; after TKA surgery, t… Show more… Show more1. If the study involved an intervention, where the intervention and control conditions adequately described? Was blinding used, and if so who was blinded? If not is there a good rationale for failure to use blinding?2. If the study was non-experimental, why did the researcher opt not to intervene? If the study was looking for a cause, which criteria for inferring causality were potentially compromised? Was a retrospective or prospective design used and was such a design appropriate?3. What did the researcher do to control confounding participant characteristics and were their procedures effective? What are the threats to a study’s internal validity? Did the design enable the researcher to draw causal inferences about the relationship between the independent variable and the outcome?Reference: Polit, D. F., & Beck, C. T. (2022). Essentials of Nursing Research CoursePoint Enhanced (10th ed). Lippincott WW. ISBN: 9781975177867 Health Science Science Nursing NUR 395 Share QuestionEmailCopy link Comments (0)
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