Association of Oral Anticoagulation Prescription with Clinical Events in Patients with an Asymptomatic Unrepaired Abdominal Aortic Aneurysm.

abdominal aortic aneurysm rupture and anticoagulation surgical repair

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
29 Aug 2022
Historique:
received: 16 08 2022
revised: 25 08 2022
accepted: 27 08 2022
entrez: 23 9 2022
pubmed: 24 9 2022
medline: 24 9 2022
Statut: epublish

Résumé

Most abdominal aortic aneurysms (AAA) have large volumes of intraluminal thrombus which has been implicated in promoting the risk of major adverse events. The aim of this study was to examine the association of therapeutic anticoagulation with AAA-related events and major adverse cardiovascular events (MACE) in patients with an unrepaired AAA. Patients with an asymptomatic unrepaired AAA were recruited from four sites in Australia. The primary outcome was the combined incidence of AAA repair or AAA rupture-related mortality (AAA-related events). The main secondary outcome was MACE (the combined incidence of myocardial infarction, stroke, or cardiovascular death). The associations of anticoagulation with these outcomes were assessed using Cox proportional hazard analyses (reporting hazard ratio, HR, and 95% confidence intervals, CI) to adjust for other risk factors. A total of 1161 patients were followed for a mean (standard deviation) of 4.9 (4.0) years. Of them, 536 (46.2%) patients had a least one AAA-related event and 319 (27.5%) at least one MACE. In the sample, 98 (8.4%) patients were receiving long-term therapeutic anticoagulation using warfarin (84), apixaban (7), rivaroxaban (6), or dabigatran (1). Prescription of an anticoagulant was associated with a reduced risk of an AAA-related event (adjusted HR 0.61; 95% CI 0.42, 0.90, These findings suggest that AAA-related events but not MACE may be reduced in patients prescribed an anticoagulant medication. Due to the inherent biases of observational studies, a randomized controlled trial is needed to assess whether anticoagulation reduces the risk of AAA-related events.

Sections du résumé

BACKGROUND BACKGROUND
Most abdominal aortic aneurysms (AAA) have large volumes of intraluminal thrombus which has been implicated in promoting the risk of major adverse events. The aim of this study was to examine the association of therapeutic anticoagulation with AAA-related events and major adverse cardiovascular events (MACE) in patients with an unrepaired AAA.
METHODS METHODS
Patients with an asymptomatic unrepaired AAA were recruited from four sites in Australia. The primary outcome was the combined incidence of AAA repair or AAA rupture-related mortality (AAA-related events). The main secondary outcome was MACE (the combined incidence of myocardial infarction, stroke, or cardiovascular death). The associations of anticoagulation with these outcomes were assessed using Cox proportional hazard analyses (reporting hazard ratio, HR, and 95% confidence intervals, CI) to adjust for other risk factors.
RESULTS RESULTS
A total of 1161 patients were followed for a mean (standard deviation) of 4.9 (4.0) years. Of them, 536 (46.2%) patients had a least one AAA-related event and 319 (27.5%) at least one MACE. In the sample, 98 (8.4%) patients were receiving long-term therapeutic anticoagulation using warfarin (84), apixaban (7), rivaroxaban (6), or dabigatran (1). Prescription of an anticoagulant was associated with a reduced risk of an AAA-related event (adjusted HR 0.61; 95% CI 0.42, 0.90,
CONCLUSIONS CONCLUSIONS
These findings suggest that AAA-related events but not MACE may be reduced in patients prescribed an anticoagulant medication. Due to the inherent biases of observational studies, a randomized controlled trial is needed to assess whether anticoagulation reduces the risk of AAA-related events.

Identifiants

pubmed: 36140213
pii: biomedicines10092112
doi: 10.3390/biomedicines10092112
pmc: PMC9495845
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Health and Medical Research Council
ID : 1180736

Références

Cardiovasc Res. 2011 Apr 1;90(1):18-27
pubmed: 21037321
Eur Heart J. 2011 Feb;32(3):354-64
pubmed: 20530504
Nat Rev Cardiol. 2019 Apr;16(4):225-242
pubmed: 30443031
Eur J Vasc Endovasc Surg. 2021 Oct;62(4):643-650
pubmed: 34507892
Eur J Vasc Endovasc Surg. 2019 Jan;57(1):8-93
pubmed: 30528142
J Vasc Surg. 2018 Jan;67(1):2-77.e2
pubmed: 29268916
Lancet. 2015 Jan 10;385(9963):117-71
pubmed: 25530442
Sci Rep. 2017 Feb 21;7:43079
pubmed: 28220880
Life Sci. 2020 Jan 1;240:117069
pubmed: 31751582
Thromb Haemost. 2019 May;119(5):807-820
pubmed: 30822810
Vasc Endovascular Surg. 2008 Aug-Sep;42(4):329-34
pubmed: 18728038
J Vasc Surg. 2017 Mar;65(3):616-625.e4
pubmed: 27460909
Ann Vasc Surg. 2020 Aug;67:482-489
pubmed: 32173474
J Vasc Surg. 2021 Oct;74(4):1183-1192.e5
pubmed: 33940069
J Vasc Interv Radiol. 2022 Feb;33(2):113-119
pubmed: 34742897
Br J Clin Pharmacol. 2017 Dec;83(12):2661-2670
pubmed: 28735510
Eur J Vasc Endovasc Surg. 2021 Dec;62(6):960-968
pubmed: 34740532
Cardiovasc Res. 2020 Feb 1;116(2):450-456
pubmed: 31135888
Vascul Pharmacol. 2021 Feb;136:106818
pubmed: 33227452
Interact Cardiovasc Thorac Surg. 2017 Apr 1;24(4):615-618
pubmed: 28108574
Eur J Vasc Endovasc Surg. 2019 Jan;57(1):94-101
pubmed: 30174271
Thromb J. 2021 Dec 18;19(1):102
pubmed: 34922573
Radiology. 2020 Mar;294(3):707-713
pubmed: 31990263
J Vasc Surg. 2011 Jan;53(1):28-35
pubmed: 20934838
J Am Coll Cardiol. 2020 Apr 7;75(13):1609-1610
pubmed: 32241378
Eur Radiol. 2008 Sep;18(9):1987-94
pubmed: 18414871
Blood. 2018 Dec 20;132(25):2619-2628
pubmed: 30228233

Auteurs

Jonathan Golledge (J)

Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD 4811, Australia.
The Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, QLD 4812, Australia.
The Australian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD 4811, Australia.

Jason Jenkins (J)

Royal Brisbane and Women's Hospital, Herston, QLD 4006, Australia.

Michael Bourke (M)

Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD 4811, Australia.
Gosford Vascular Clinic, Gosford, NSW 2250, Australia.

Bernard Bourke (B)

Gosford Vascular Clinic, Gosford, NSW 2250, Australia.

Tejas P Singh (TP)

Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD 4811, Australia.
The Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, QLD 4812, Australia.

Classifications MeSH