20 research outputs found

    PCI Choice: early prototype of benefits page.

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    <p>Used with permission of Mayo Foundation for Medical Education and Research; Creative Commons License does not apply.</p

    Encounter Decision Aid vs. Clinical Decision Support or Usual Care to Support Patient-Centered Treatment Decisions in Osteoporosis: The Osteoporosis Choice Randomized Trial II

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    <div><p>Purpose</p><p>Osteoporosis Choice, an encounter decision aid, can engage patients and clinicians in shared decision making about osteoporosis treatment. Its effectiveness compared to the routine provision to clinicians of the patient’s estimated risk of fracture using the FRAX calculator is unknown.</p><p>Methods</p><p>Patient-level, randomized, three-arm trial enrolling women over 50 with osteopenia or osteoporosis eligible for treatment with bisphosphonates, where the use of Osteoporosis Choice was compared to FRAX only and to usual care to determine impact on patient knowledge, decisional conflict, involvement in the decision-making process, decision to start and adherence to bisphosphonates.</p><p>Results</p><p>We enrolled 79 women in the three arms. Because FRAX estimation alone and usual care produced similar results, we grouped them for analysis. Compared to these, use of Osteoporosis Choice increased patient knowledge (median score 6 vs. 4, p = .01), improved understanding of fracture risk and risk reduction with bisphosphonates (p = .01 and p<.0001, respectively), had no effect on decision conflict, and increased patient engagement in the decision making process (OPTION scores 57% vs. 43%, p = .001). Encounters with the decision aid were 0.8 minutes longer (range: 33 minutes shorter to 3.0 minutes longer). There were twice as many patients receiving and filling prescriptions in the decision aid arm (83% vs. 40%, p = .07); medication adherence at 6 months was no different across arms.</p><p>Conclusion</p><p>Supporting both patients and clinicians during the clinical encounter with the Osteoporosis Choice decision aid efficiently improves treatment decision making when compared to usual care with or without clinical decision support with FRAX results.</p><p>Trial Registration</p><p>clinical trials.gov <a href="http://clinicaltrials.gov/show/NCT00949611" target="_blank">NCT00949611</a></p></div

    Decision and adherence.

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    <p><sup>1</sup>Counts (%),Chi-square test p-value, unless noted otherwise</p><p><sup>2</sup>Median (95% CI), Wilcoxon Rank Sum Test p-value</p><p><sup>3</sup>Decision Aid is the reference of relative risk where ‘Start Bisphosphonates’ is being compared to the combination of ‘Do not start’ and ‘Undecided/Other’</p><p><sup>4</sup>Fisher’s Exact Test p-value</p><p>Decision and adherence.</p

    Patient knowledge and decisional conflict.

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    <p><sup>1</sup>Median (IQR), Wilcoxon rank sum test p-value</p><p><sup>2</sup>Answered correctly (% Correct), Chi-square test p-value.</p><p><sup>3</sup>Decision Aid is the reference for Relative Risk.</p><p>Patient knowledge and decisional conflict.</p

    Patient and clinician characteristics.

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    <p><sup>1</sup>Values missing for patients</p><p><sup>2</sup>Bias assessment of prescribing rates assessed for stratifying patients</p><p><sup>3</sup>Number of encounters included in the study; SD = Standard deviation</p><p>Patient and clinician characteristics.</p
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