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t duration is decided, patients have been offered with every day videos employing push notifications. Outcomes were assessed by way of on the net, self-reported questionnaires at baseline, 1 days ahead of and 1 day immediately after the consultation. Information had been analyzed working with t-tests and linear mixed models for COX-1 Inhibitor custom synthesis repeated measurements. Benefits: The trial was terminated early as the inclusion prices dropped resulting from the COVID-19 pandemic. Data of 56 sufferers have been analyzed (imply age 573; 27 female). Satisfaction with received FIGURE 1 Change of satisfaction with received facts over time stratified by intervention group. Measured at baseline, 1 days prior to consultation (“pre”) and 1 day just after consultation (“post”). Colored lines indicate person patients; blue thick line and self-assurance band indicate imply and 95 confidence interval918 of|ABSTRACTTABLE 1 Intention to treat analysis of key and secondary outcomes in 26 sufferers getting the app (intervention) and 30 CaMK II Inhibitor custom synthesis individuals receiving regular of care only (manage). All data are shown as mean SD. All scores are positively associated with all the outcome (e.g. larger decisional conflict scale means extra decisional conflict). Abbreviation: CI self-assurance interval. indicates p-valueBefore consultation Intervention Satisfaction with received facts (range 10) Satisfaction with information (range 10) Perceived degree of information (variety 55) Decisional Conflict Scale (variety 000) Shared decision-making (doctor) (range 05) 6.7 1.7 six.7 2.two 13.8 three.0 n.a. n.a. Control 5.9 two.four six.2 2.4 13.1 3.8 n.a. n.a. Just after consultation Intervention 7.eight 1.five eight.0 1.3 17.1 three.3 29.8 15.2 31.8 9.five Control 7.1 two.0 7.2 2.0 15.2 4.3 46.2 22.5 31.six 9.0 Model estimated difference (intervention vs. control) (95 CI) 0.9 (0.0 to 1.7) 0.7 (- 0.three to 1.five) 1.0 (- 0.6 to two.six) n.a. n.a.P-value 0.04 0.11 0.22 0.01 0.Conclusions: An educational app about VTE and anticoagulation increases patients’ satisfaction and reduces decisional conflict when deciding to stop or continue anticoagulation immediately after initial treatment for VTE.Solutions: A cohort study applying prospectively collected administrative data identified treatment-na e, newly diagnosed adult VTE patients dispensed apixaban, dabigatran, edoxaban, rivaroxaban, or warfarin between 1 January 2013 and 30 September 2018 using Swedish nationwide registries. Patient demographics, clinical traits, and subgroups (deep vein thrombosis [DVT] or pulmo-PB1252|Real-world Data around the Use of Oral Anticoagulants for the Treatment of Venous Thromboembolism in Sweden: Oral Anticoagulant Use and Baseline Qualities in the Venous Thromboembolism Remedy Study A. Gotts er1; H. Pohjant ti-Maaroos2; K. Bokenberger3; S. Graham ; A. Jenkins ; D. Lambrelli ; K. Mercaldi ; M. Raluy ; W. Ghanima1 four 5 4 6nary embolism [PE]; diagnostic setting and etiology) are described per remedy cohort. This study was authorized by the Swedish Ethical Critique Authority (20194722). Results: A total of 33,979 patients from Sweden had been incorporated, with the vast majority getting rivaroxaban (38.eight ), warfarin (33.two ) or apixaban (26.eight ); few had been treated with dabigatran (1.1 ) or edoxaban (0.1 ). There was a marked boost in NOAC use and reduce in warfarin use in the course of the follow-up period (Figure 1). Nearly half (47.2 ) of all patients have been diagnosed with PEs (with or without a DVT). Over half (62.2 ) of VTE was unprovoked. The mean age for each the total and apixaban cohorts was 64.6 years; the warfarin cohort was slightly older (65.9

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