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Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?

BACKGROUND: Isolated distal deep vein thrombosis (IDDVT), a disease frequently detected in hospitalized patients, can progress to proximal deep vein thrombosis (PDVT) and pulmonary embolism (PE). Here, we evaluated the effects of anticoagulation in hospitalized IDDVT patients. METHODS: We conducted...

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Autores principales: Luo, Xiaolin, Zhang, Liying, Hou, Changchun, Li, Pengda, Wu, Shaofa, Wang, Zebi, Yang, Enpu, Cui, Yun, Sun, Ning, Yu, Yang, An, Zhixia, Jin, Jun, Qin, Zhexue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472408/
https://www.ncbi.nlm.nih.gov/pubmed/36100922
http://dx.doi.org/10.1186/s12959-022-00410-1
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author Luo, Xiaolin
Zhang, Liying
Hou, Changchun
Li, Pengda
Wu, Shaofa
Wang, Zebi
Yang, Enpu
Cui, Yun
Sun, Ning
Yu, Yang
An, Zhixia
Jin, Jun
Qin, Zhexue
author_facet Luo, Xiaolin
Zhang, Liying
Hou, Changchun
Li, Pengda
Wu, Shaofa
Wang, Zebi
Yang, Enpu
Cui, Yun
Sun, Ning
Yu, Yang
An, Zhixia
Jin, Jun
Qin, Zhexue
author_sort Luo, Xiaolin
collection PubMed
description BACKGROUND: Isolated distal deep vein thrombosis (IDDVT), a disease frequently detected in hospitalized patients, can progress to proximal deep vein thrombosis (PDVT) and pulmonary embolism (PE). Here, we evaluated the effects of anticoagulation in hospitalized IDDVT patients. METHODS: We conducted a retrospective study in our hospital and enrolled hospitalized IDDVT patients diagnosed by compression ultrasonography (CUS) from January to December 2020. Participants were divided into anticoagulation (AC) and non-anticoagulation (non-AC) groups. After propensity score matching (PSM), multivariate Cox regression analyses were performed to assess whether anticoagulation was associated with PDVT/PE, and all-cause mortality. RESULTS: A total of 426 IDDVT inpatients with CUS follow-up were screened from 1502 distal DVT patients and finally enrolled. The median age was 67 years with 51.4% males and 15.5% cancer patients. The median follow-up was 11.6 months. There were 288 and 138 patients treated with or without anticoagulants, respectively. Patients in the non-AC group had less body mass index and more comorbidities. Patients in the AC group were treated with rivaroxaban or dabigatran (52.1%), low molecular weight heparin (42.7%), and warfarin (5.2%). The PSM generated 111 pairs of well-matched IDDVT patients with or without anticoagulation. The Kaplan–Meier analysis demonstrated that neither the incidence of PDVT/PE (5.4% vs. 2.7%, log-rank p = 0.313) nor all-cause mortality (27.9% vs. 18.9%, log-rank p = 0.098) was significant different between groups. Anticoagulation was not associated with PDVT/PE and all-cause mortality in the multivariable Cox regression analyses using the matched cohorts. The main risk factors for all-cause mortality were age, malignancy history, BMI, sepsis, heart failure, and white blood cell (WBC) count. CONCLUSIONS: In hospitalized IDDVT patients, the thrombosis extension rate to PDVT/PE was low. Anticoagulation did not reduce the incidence of thrombosis extension of IDDVT and was not associated with all-cause mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12959-022-00410-1.
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spelling pubmed-94724082022-09-15 Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not? Luo, Xiaolin Zhang, Liying Hou, Changchun Li, Pengda Wu, Shaofa Wang, Zebi Yang, Enpu Cui, Yun Sun, Ning Yu, Yang An, Zhixia Jin, Jun Qin, Zhexue Thromb J Research BACKGROUND: Isolated distal deep vein thrombosis (IDDVT), a disease frequently detected in hospitalized patients, can progress to proximal deep vein thrombosis (PDVT) and pulmonary embolism (PE). Here, we evaluated the effects of anticoagulation in hospitalized IDDVT patients. METHODS: We conducted a retrospective study in our hospital and enrolled hospitalized IDDVT patients diagnosed by compression ultrasonography (CUS) from January to December 2020. Participants were divided into anticoagulation (AC) and non-anticoagulation (non-AC) groups. After propensity score matching (PSM), multivariate Cox regression analyses were performed to assess whether anticoagulation was associated with PDVT/PE, and all-cause mortality. RESULTS: A total of 426 IDDVT inpatients with CUS follow-up were screened from 1502 distal DVT patients and finally enrolled. The median age was 67 years with 51.4% males and 15.5% cancer patients. The median follow-up was 11.6 months. There were 288 and 138 patients treated with or without anticoagulants, respectively. Patients in the non-AC group had less body mass index and more comorbidities. Patients in the AC group were treated with rivaroxaban or dabigatran (52.1%), low molecular weight heparin (42.7%), and warfarin (5.2%). The PSM generated 111 pairs of well-matched IDDVT patients with or without anticoagulation. The Kaplan–Meier analysis demonstrated that neither the incidence of PDVT/PE (5.4% vs. 2.7%, log-rank p = 0.313) nor all-cause mortality (27.9% vs. 18.9%, log-rank p = 0.098) was significant different between groups. Anticoagulation was not associated with PDVT/PE and all-cause mortality in the multivariable Cox regression analyses using the matched cohorts. The main risk factors for all-cause mortality were age, malignancy history, BMI, sepsis, heart failure, and white blood cell (WBC) count. CONCLUSIONS: In hospitalized IDDVT patients, the thrombosis extension rate to PDVT/PE was low. Anticoagulation did not reduce the incidence of thrombosis extension of IDDVT and was not associated with all-cause mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12959-022-00410-1. BioMed Central 2022-09-13 /pmc/articles/PMC9472408/ /pubmed/36100922 http://dx.doi.org/10.1186/s12959-022-00410-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Luo, Xiaolin
Zhang, Liying
Hou, Changchun
Li, Pengda
Wu, Shaofa
Wang, Zebi
Yang, Enpu
Cui, Yun
Sun, Ning
Yu, Yang
An, Zhixia
Jin, Jun
Qin, Zhexue
Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title_full Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title_fullStr Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title_full_unstemmed Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title_short Hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
title_sort hospitalized patients with isolated distal deep vein thrombosis: anticoagulation therapy or not?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472408/
https://www.ncbi.nlm.nih.gov/pubmed/36100922
http://dx.doi.org/10.1186/s12959-022-00410-1
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