2017
DOI: 10.1016/j.thromres.2017.10.012
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Exploring the impact of route of administration on medication acceptance in hospitalized patients: Implications for venous thromboembolism prevention

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Cited by 26 publications
(19 citation statements)
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“…If pharmacological prophylaxis is contraindicated, mechanical VTE prophylaxis (intermittent pneumatic compression) should be considered in immobilized patients (64,65). Missed doses of pharmacologic VTE prophylaxis are common and are likely associated with worse outcomes (66). Therefore, every effort should be made to ensure that patients receive all scheduled doses of pharmacologic VTE prophylaxis.…”
Section: Risk Stratification and In-hospital Prophylaxismentioning
confidence: 99%
“…If pharmacological prophylaxis is contraindicated, mechanical VTE prophylaxis (intermittent pneumatic compression) should be considered in immobilized patients (64,65). Missed doses of pharmacologic VTE prophylaxis are common and are likely associated with worse outcomes (66). Therefore, every effort should be made to ensure that patients receive all scheduled doses of pharmacologic VTE prophylaxis.…”
Section: Risk Stratification and In-hospital Prophylaxismentioning
confidence: 99%
“…10,11,25) In another study, 66.9% of patients who experienced DVT and/or PE events were diagnosed within the first month after hospital discharge, with 19.9% between months 1 and 2, and 13.2% between months 2 and 3. 26) In the International Medical Prevention Registry on Venous Thromboembolism (IMPROVE) registry of 15,156 patients, the median time for all VTE events was 17 days (interquartile range 6-43 days), and the median time for post-discharge VTE events was 44 days (interquartile range 25-68 days). 27) In an effort to increase compliance and safety in preventing VTEs post-hospitalization, multiple randomized control trials have been performed examining the utility and safety of several novel oral anticoagulants in the use of extended duration VTE prophylaxis.…”
Section: Extended Prophylaxis After Dischargementioning
confidence: 99%
“…Additionally, use of an oral agent should reduce nonadherence often seen with subcutaneous VTE thromboprophylaxis regimens. 26 However, betrixaban has additional bleed risk without a FDA-approved antidote to reverse betrixaban-related bleeding. Currently, andexanet alfa is being studied as an antidote for other FXa inhibitors in the ongoing ANNEXA-4 trial, and its protocol may be amended to incorporate betrixaban users.…”
Section: Discussionmentioning
confidence: 99%