- |||||||||| Percutaneous Rebuttal (109AB) - Aug 11, 2022 - Abstract #AHA2022AHA_3709;
Abstract is embargoed at this time. There is no abstract associated with this presentation.
- |||||||||| Q&A (Moderated Digital Posters 4) - Aug 11, 2022 - Abstract #AHA2022AHA_3492;
There is no abstract associated with this presentation. There is no abstract associated with this presentation.
- |||||||||| rivaroxaban / Generic mfg., clopidogrel / Generic mfg.
Review, Journal: Conservative treatment of peripheral arterial disease (Pubmed Central) - Aug 10, 2022 In patients with intermittent claudication exercise therapy is highly recommended. Despite the high risk, in particular patients with PAD are often undertreated in clinical practice.
- |||||||||| rivaroxaban / Generic mfg., apixaban / Generic mfg.
Review, Journal: Deep vein thrombosis and pulmonary embolism : Diagnosis and treatment (Pubmed Central) - Aug 10, 2022 In cancer-associated thromboembolism (CAT), the previous guideline recommendation to use low molecular weight heparin (LMWH) for 3-6 months is now broadened with the recommendation for factor Xa inhibitors, with the caveat for gastrointestinal and urothelial cancer or expected drug-drug interactions with the anticancer treatment. Here, and in unstable clinical situations, LMWH is preferred.
- |||||||||| rivaroxaban / Generic mfg.
Preclinical, Journal: Evaluation of Herb-Drug Interaction Between Danshen and Rivaroxaban in Rat and Human Liver Microsomes. (Pubmed Central) - Aug 7, 2022 Danshen tablet inhibits the metabolism of rivaroxaban, which may be because its lipid-soluble components such as dihydrotanshinone I strongly inhibit the activities of CYP enzymes, especially CYP3A and CYP2J. Therefore, when Danshen tablet and rivaroxaban are used simultaneously in the clinic, it is necessary to strengthen the drug monitoring of rivaroxaban and adjust the dosage.
- |||||||||| rivaroxaban / Generic mfg., enoxaparin sodium / Generic mfg.
Journal: Heparin-induced thrombocytopenia post-cardiovascular interventional therapy: a case report. (Pubmed Central) - Aug 6, 2022 This case emphasizes the significance of suspecting HIT in patients with unexplained rapid thrombocytopenia after frequent heparin exposure. Decision-making regarding alternative anticoagulation and platelet transfusion in HIT with hemorrhage must be based on unique patient characteristics.
- |||||||||| rivaroxaban / Generic mfg.
Journal: Determinants of label non-adherence to non-vitamin K oral anticoagulants in patients with newly diagnosed atrial fibrillation. (Pubmed Central) - Aug 4, 2022 In the 336 (10.3%) patients with a reduced dose NOAC recommendation, 22.9% were overdosed, most often with rivaroxaban...In newly diagnosed Dutch AF patients, off-label dosing of NOACs was seen in only 6.6% of patients, most often underdosing. In this study, determinants of off-label dosing were age, renal function, weight, anaemia, active malignancy, and concomitant use of antiplatelets.
- |||||||||| rivaroxaban / Generic mfg., dabigatran etexilate / Generic mfg., warfarin / Generic mfg.
Trial completion: A Study Based on Japanese Medical Records That Looks at Bleeding Events in People With Atrial Fibrillation and Coronary Artery Disease Who Start Taking Either Dabigatran, Rivaroxaban, or Warfarin (clinicaltrials.gov) - Aug 4, 2022 P=N/A, N=32000, Completed, In this study, determinants of off-label dosing were age, renal function, weight, anaemia, active malignancy, and concomitant use of antiplatelets. Active, not recruiting --> Completed
- |||||||||| rivaroxaban / Generic mfg., aspirin / Generic mfg., dabigatran etexilate / Generic mfg.
Review, Journal: Review and update of the concept of embolic stroke of undetermined source. (Pubmed Central) - Aug 4, 2022 The neutral results of the trials of anticoagulation and insights into ESUS from research conducted since the concept was introduced warrant reassessment of the ESUS construct as a research concept and a treatment target. In this Review, we discuss the evidence produced since the concept of ESUS was introduced, and propose updates to the criteria and diagnostic algorithm in light of the latest knowledge.
- |||||||||| rivaroxaban / Generic mfg.
Retrospective data, Journal: Neutrophil-to-Lymphocyte Ratio Predicts Restenosis After Drug-Coated Balloon Therapy for Femoropopliteal Artery Lesions: A Retrospective Study. (Pubmed Central) - Aug 3, 2022 Logistic univariate and multivariate analysis showed that baseline hs-CRP level (OR = 1.10, 95%CI: 1.05-1.34), lesion length (OR = 1.04, 95%CI: 1.02-1.27), use of rivaroxaban (OR = 1.08, 95%CI: 1.05-1.39), NLR (OR = 1.47, 95%CI: 1.13-2.48), LDL-C level (OR = 1.25, 95%CI: 1.05-1.52), and diabetes (OR = 1.25, 95%CI: 1.05-1.52) = 1.18, 95%CI: 1.06-1.66) were predictors of restenosis. Baseline NLR before DCB can predict the risk of restenosis after surgery.
- |||||||||| Savaysa (edoxaban) / Daiichi Sankyo
Retrospective data, Review, Journal: Safety of direct oral anticoagulants in patients with liver disease: a systematic review and meta-analysis. (Pubmed Central) - Aug 2, 2022 Furthermore, the pooled estimates of the Child-Turcotte-Pugh (CTP) class indicated that DOACs reduced the incidence of all bleeding (RR: 0.61; 95%CI: 0.45 to 0.82), gastrointestinal bleeding (RR 0.55; 95%CI: 0.37 to 0.83), and all-cause death (RR: 0.62; 95%CI: 0.49 to 0.79) in patients with mild to moderate cirrhosis. Our study demonstrates that DOACs significantly reduce the risk of bleeding in patients with liver disease compared with warfarin/LMWH.
- |||||||||| rivaroxaban / Generic mfg., aspirin / Generic mfg.
Enrollment open, Trial completion date, Trial primary completion date: EPCATIII: VTE Prevention Following Total Hip and Knee Arthroplasty (clinicaltrials.gov) - Aug 1, 2022 P3, N=5400, Recruiting, Our study demonstrates that DOACs significantly reduce the risk of bleeding in patients with liver disease compared with warfarin/LMWH. Not yet recruiting --> Recruiting | Trial completion date: Apr 2024 --> Jan 2025 | Trial primary completion date: Jan 2024 --> Jan 2025
- |||||||||| Savaysa (edoxaban) / Daiichi Sankyo
Observational data, Journal: Prothrombinase-Induced Clotting Time to Measure Drug Concentrations of Rivaroxaban, Apixaban, and Edoxaban in Clinical Practice: A Cross-Sectional Study. (Pubmed Central) - Jul 29, 2022 The sensitivity to detect clinically relevant drug concentrations was 85.1% in the case of 30 µg L (95% CI 82.0, 87.7; specificity 77.9; 72.1, 82.7), 85.7% in the case of 50 µg L (82.4, 88.4; specificity 77.3; 72.5, 81.5), and 85.1% in the case of 100 µg L (80.9, 88.4; specificity 73.2%; 69.1, 76.9). In conclusion, the association of PiCT with DOAC concentrations was fair, and the majority of clinically relevant drug concentrations were correctly predicted.
- |||||||||| diltiazem / Generic mfg.
Retrospective data, Journal: Concomitant Use of Diltiazem With Direct Oral Anticoagulants and Bleeding Risk in Atrial Fibrillation. (Pubmed Central) - Jul 29, 2022 Conclusions Concomitant use of diltiazem with DOACs was associated with a higher bleeding risk in patients with atrial fibrillation, consistently in both subgroups of chronic kidney disease and non-chronic kidney disease. For DOAC users, concomitant diltiazem should be prescribed only when the benefit outweighs the risk, with close monitoring for signs of bleeding.
- |||||||||| rivaroxaban / Generic mfg.
Enrollment open, Trial completion date, Trial primary completion date: ACCOG: AntiCoagulants and COGnition (clinicaltrials.gov) - Jul 27, 2022 P4, N=48, Recruiting, For DOAC users, concomitant diltiazem should be prescribed only when the benefit outweighs the risk, with close monitoring for signs of bleeding. Unknown status --> Recruiting | Trial completion date: Mar 2021 --> Feb 2023 | Trial primary completion date: Mar 2021 --> Feb 2023
- |||||||||| rivaroxaban / Generic mfg., apixaban / Generic mfg.
Enrollment closed, Real-world evidence, Head-to-Head, Real-world: An Observational Study Called H2H-OSCAR-US to Learn More About How Well Rivaroxaban Works and How Safe it is Compared to Apixaban Under Real World Conditions in People in the US With Cancer Who Have Problems Due to Formation of Blood Clots in the Veins (Venous Thromboembolism) (clinicaltrials.gov) - Jul 27, 2022 P=N/A, N=2000, Active, not recruiting, Unknown status --> Recruiting | Trial completion date: Mar 2021 --> Feb 2023 | Trial primary completion date: Mar 2021 --> Feb 2023 Not yet recruiting --> Active, not recruiting
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