Periprocedural bridging anticoagulation in patients with venous thromboembolism: A registry-based cohort study.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
08 2020
Historique:
received: 27 02 2020
revised: 06 05 2020
accepted: 08 05 2020
pubmed: 20 5 2020
medline: 15 5 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Use of bridging anticoagulation increases a patient's bleeding risk without clear evidence of thrombotic prevention among warfarin-treated patients with atrial fibrillation. Contemporary use of bridging anticoagulation among warfarin-treated patients with venous thromboembolism (VTE) has not been studied. We identified warfarin-treated patients with VTE who temporarily stopped warfarin for a surgical procedure between 2010 and 2018 at six health systems. Using the 2012 American College of Chest Physicians guideline, we assessed use of periprocedural bridging anticoagulation based on recurrent VTE risk. Recurrent VTE risk and 30-day outcomes (bleeding, thromboembolism, emergency department visit) were each assessed using logistic regression adjusted for multiple procedures per patient. During the study period, 789 warfarin-treated patients with VTE underwent 1529 procedures (median, 2; interquartile range, 1-4). Unadjusted use of bridging anticoagulation was more common in patients at high risk for VTE recurrence (99/171, 57.9%) than for patients at moderate (515/1078, 47.8%) or low risk of recurrence (134/280, 47.86%). Bridging anticoagulation use was higher in high-risk patients compared with low- or moderate-risk patients in both unadjusted (P = .013) and patient-level cluster-adjusted analyses (P = .031). Adherence to American College of Chest Physicians guidelines in high- and low-risk patients did not change during the study period (odds ratio, 0.98 per year; 95% confidence interval, 0.91-1.05). Adverse events were rare and not statistically different between the two treatment groups. Bridging anticoagulation was commonly overused among low-risk patients and underused among high-risk patients treated with warfarin for VTE. Adverse events were rare and not different between the two treatment groups.

Sections du résumé

BACKGROUND
Use of bridging anticoagulation increases a patient's bleeding risk without clear evidence of thrombotic prevention among warfarin-treated patients with atrial fibrillation. Contemporary use of bridging anticoagulation among warfarin-treated patients with venous thromboembolism (VTE) has not been studied.
METHODS
We identified warfarin-treated patients with VTE who temporarily stopped warfarin for a surgical procedure between 2010 and 2018 at six health systems. Using the 2012 American College of Chest Physicians guideline, we assessed use of periprocedural bridging anticoagulation based on recurrent VTE risk. Recurrent VTE risk and 30-day outcomes (bleeding, thromboembolism, emergency department visit) were each assessed using logistic regression adjusted for multiple procedures per patient.
RESULTS
During the study period, 789 warfarin-treated patients with VTE underwent 1529 procedures (median, 2; interquartile range, 1-4). Unadjusted use of bridging anticoagulation was more common in patients at high risk for VTE recurrence (99/171, 57.9%) than for patients at moderate (515/1078, 47.8%) or low risk of recurrence (134/280, 47.86%). Bridging anticoagulation use was higher in high-risk patients compared with low- or moderate-risk patients in both unadjusted (P = .013) and patient-level cluster-adjusted analyses (P = .031). Adherence to American College of Chest Physicians guidelines in high- and low-risk patients did not change during the study period (odds ratio, 0.98 per year; 95% confidence interval, 0.91-1.05). Adverse events were rare and not statistically different between the two treatment groups.
CONCLUSIONS
Bridging anticoagulation was commonly overused among low-risk patients and underused among high-risk patients treated with warfarin for VTE. Adverse events were rare and not different between the two treatment groups.

Identifiants

pubmed: 32428998
doi: 10.1111/jth.14903
pmc: PMC7415673
mid: NIHMS1605830
pii: S1538-7836(22)01623-3
doi:

Substances chimiques

Anticoagulants 0
Heparin, Low-Molecular-Weight 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2025-2030

Subventions

Organisme : NHLBI NIH HHS
ID : K01 HL135392
Pays : United States

Informations de copyright

© 2020 International Society on Thrombosis and Haemostasis.

Références

N Engl J Med. 2015 Aug 27;373(9):823-33
pubmed: 26095867
JAMA. 2015 Jul 7;314(1):72-3
pubmed: 26151268
Chest. 2012 Feb;141(2 Suppl):e326S-e350S
pubmed: 22315266
JAMA Intern Med. 2019 Aug 5;:
pubmed: 31380891
Am J Med. 2019 Jun;132(6):722-732.e7
pubmed: 30659809
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354
JAMA Intern Med. 2015 Jul;175(7):1163-8
pubmed: 26010033
J Thromb Thrombolysis. 2015 Apr;39(3):403-9
pubmed: 25772116
Am J Cardiol. 2019 Nov 15;124(10):1549-1553
pubmed: 31543215
JAMA. 2015 Jul 7;314(1):31-40
pubmed: 26151264
Clin Appl Thromb Hemost. 2017 Nov;23(8):961-966
pubmed: 28468510
Am J Med. 2019 Jan;132(1):109.e1-109.e7
pubmed: 30076828

Auteurs

Geoffrey D Barnes (GD)

Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Yun Li (Y)

School of Public Health, University of Michigan, Ann Arbor, MI, USA.

Xiaokui Gu (X)

Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Brian Haymart (B)

Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Eva Kline-Rogers (E)

Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Mona A Ali (MA)

Department of Pharmacy, Beaumont Hospital, Royal Oak, MI, USA.

Jay Kozlowski (J)

Department of Internal Medicine, Huron Valley Sinai Hospital, Commerce Township, MI, USA.

Gregory Krol (G)

Department of Internal Medicine, Henry Ford Health System, Detroit, MI, USA.

James B Froehlich (JB)

Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Scott Kaatz (S)

Division of Hospital Medicine, Henry Ford Hospital, Detroit, MI, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH