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Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli

There is little reported on the efficacy and safety of direct oral anticoagulants (DOACs) in morbid obesity after venous thromboembolism (VTE). In this observational study, patients were followed up after intermediate- or high-risk pulmonary embolism (PE) at the University of Rochester Pulmonary Hyp...

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Autores principales: Lachant, Daniel J., Bach, Christina, Fe, Alexander, White, R. James, Lachant, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861033/
https://www.ncbi.nlm.nih.gov/pubmed/33569503
http://dx.doi.org/10.1183/23120541.00554-2020
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author Lachant, Daniel J.
Bach, Christina
Fe, Alexander
White, R. James
Lachant, Neil A.
author_facet Lachant, Daniel J.
Bach, Christina
Fe, Alexander
White, R. James
Lachant, Neil A.
author_sort Lachant, Daniel J.
collection PubMed
description There is little reported on the efficacy and safety of direct oral anticoagulants (DOACs) in morbid obesity after venous thromboembolism (VTE). In this observational study, patients were followed up after intermediate- or high-risk pulmonary embolism (PE) at the University of Rochester Pulmonary Hypertension Clinic 2–4 months after the initial event. All patients had echocardiography and V/Q imaging regardless of symptoms. Outcomes of interest were the rates of recurrent VTE, thrombus resolution and development of chronic thromboembolic pulmonary hypertension (CTEPH) in patients with morbid obesity treated with a DOAC compared to treatment with vitamin K antagonists and to non-morbidly obese patients after PE. Using the electronic medical record, recurrent events were assessed up to 12 months after the event. 107 patients (body mass index (BMI)>40 kg·m(−2), n=32; BMI 30–39.9 kg·m(−2), n=39; BMI<30 kg·m(−2), n=36) attended follow-up appointments after treatment for PE. A DOAC was used in 70 patients (BMI>40 kg·m(−2), n=19; BMI 30–39.9 kg·m(−2), n=27; BMI<30 kg·m(−2), n=24). There were no recurrent events within the first 12 months of initial diagnosis based on symptoms and imaging in any patient. There was no difference in rate of residual unmatched perfusion defect with DOACs or conventional anticoagulation (49% versus 49%). This finding remained in the subset of morbidly obese patients (47% versus 50%). For the overall cohort, there was no difference in the rate of CTEPH development based on anticoagulation with a DOAC (5% versus 8% with warfarin). There were no major bleeding complications with a DOAC. DOAC therapy appears to be effective and safe in morbid obesity even after intermediate- or high-risk PE. ​
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spelling pubmed-78610332021-02-09 Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli Lachant, Daniel J. Bach, Christina Fe, Alexander White, R. James Lachant, Neil A. ERJ Open Res Original Articles There is little reported on the efficacy and safety of direct oral anticoagulants (DOACs) in morbid obesity after venous thromboembolism (VTE). In this observational study, patients were followed up after intermediate- or high-risk pulmonary embolism (PE) at the University of Rochester Pulmonary Hypertension Clinic 2–4 months after the initial event. All patients had echocardiography and V/Q imaging regardless of symptoms. Outcomes of interest were the rates of recurrent VTE, thrombus resolution and development of chronic thromboembolic pulmonary hypertension (CTEPH) in patients with morbid obesity treated with a DOAC compared to treatment with vitamin K antagonists and to non-morbidly obese patients after PE. Using the electronic medical record, recurrent events were assessed up to 12 months after the event. 107 patients (body mass index (BMI)>40 kg·m(−2), n=32; BMI 30–39.9 kg·m(−2), n=39; BMI<30 kg·m(−2), n=36) attended follow-up appointments after treatment for PE. A DOAC was used in 70 patients (BMI>40 kg·m(−2), n=19; BMI 30–39.9 kg·m(−2), n=27; BMI<30 kg·m(−2), n=24). There were no recurrent events within the first 12 months of initial diagnosis based on symptoms and imaging in any patient. There was no difference in rate of residual unmatched perfusion defect with DOACs or conventional anticoagulation (49% versus 49%). This finding remained in the subset of morbidly obese patients (47% versus 50%). For the overall cohort, there was no difference in the rate of CTEPH development based on anticoagulation with a DOAC (5% versus 8% with warfarin). There were no major bleeding complications with a DOAC. DOAC therapy appears to be effective and safe in morbid obesity even after intermediate- or high-risk PE. ​ European Respiratory Society 2021-02-01 /pmc/articles/PMC7861033/ /pubmed/33569503 http://dx.doi.org/10.1183/23120541.00554-2020 Text en Copyright ©ERS 2021 http://creativecommons.org/licenses/by-nc/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Original Articles
Lachant, Daniel J.
Bach, Christina
Fe, Alexander
White, R. James
Lachant, Neil A.
Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title_full Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title_fullStr Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title_full_unstemmed Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title_short Direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
title_sort direct oral anticoagulant therapy in patients with morbid obesity after intermediate- or high-risk pulmonary emboli
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861033/
https://www.ncbi.nlm.nih.gov/pubmed/33569503
http://dx.doi.org/10.1183/23120541.00554-2020
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