Severe renal impairment and risk of bleeding during anticoagulation for venous thromboembolism.


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:
07 2020
Historique:
received: 26 11 2019
revised: 31 03 2020
accepted: 06 04 2020
pubmed: 17 4 2020
medline: 15 5 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

Detection of severe renal impairment in patients with venous thromboembolism (VTE) is mandatory both for selecting anticoagulant therapy and for evaluating major bleeding risk, increased by severe renal impairment. To determine whether the Cockcroft and Gault (CG) and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formulas identify severe renal impairment in the same VTE patients presenting the same risk of major bleeding. We compared clinical characteristics and outcomes during the first 3 months of anticoagulation between VTE patients in the RIETE registry with severe renal impairment according to the CG and/or CKD-EPI formula (estimated glomerular filtration rate <30 mL/min and <30 mL/min/1.73 m Up to October 2017, 41 796 patients were included in RIETE. Among the 4676 patients with severe renal impairment according to at least one of the formulas, this was not confirmed by the other formula in 1904 (40.7%). Major bleeding risk was increased in every patient subgroup with severe renal impairment vs patients without this condition (CG or CKD-EPI < 30: odds ratio [OR] = 2.26, 95% confidence interval [CI 2.01-2.53], only CG < 30: OR = 1.72, 95% CI [1.37-2.13], only CKD-EPI < 30: OR = 2.34, 95% CI [1.77-3.05], CG+CKD-EPI < 30: OR = 2.47, 95% CI [2.16-2.83], all vs CG+CKD-EPI > 30). The CG and CKD-EPI formulas identify different subgroups of patients with severe renal impairment, leading to discordant results in 40.7% of these patients. Irrespective of the formula used for their identification, patients with severe renal impairment have a higher risk of major bleeding under anticoagulant therapy.

Sections du résumé

BACKGROUND
Detection of severe renal impairment in patients with venous thromboembolism (VTE) is mandatory both for selecting anticoagulant therapy and for evaluating major bleeding risk, increased by severe renal impairment.
OBJECTIVES
To determine whether the Cockcroft and Gault (CG) and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formulas identify severe renal impairment in the same VTE patients presenting the same risk of major bleeding.
PATIENTS/METHODS
We compared clinical characteristics and outcomes during the first 3 months of anticoagulation between VTE patients in the RIETE registry with severe renal impairment according to the CG and/or CKD-EPI formula (estimated glomerular filtration rate <30 mL/min and <30 mL/min/1.73 m
RESULTS
Up to October 2017, 41 796 patients were included in RIETE. Among the 4676 patients with severe renal impairment according to at least one of the formulas, this was not confirmed by the other formula in 1904 (40.7%). Major bleeding risk was increased in every patient subgroup with severe renal impairment vs patients without this condition (CG or CKD-EPI < 30: odds ratio [OR] = 2.26, 95% confidence interval [CI 2.01-2.53], only CG < 30: OR = 1.72, 95% CI [1.37-2.13], only CKD-EPI < 30: OR = 2.34, 95% CI [1.77-3.05], CG+CKD-EPI < 30: OR = 2.47, 95% CI [2.16-2.83], all vs CG+CKD-EPI > 30).
CONCLUSION
The CG and CKD-EPI formulas identify different subgroups of patients with severe renal impairment, leading to discordant results in 40.7% of these patients. Irrespective of the formula used for their identification, patients with severe renal impairment have a higher risk of major bleeding under anticoagulant therapy.

Identifiants

pubmed: 32299150
doi: 10.1111/jth.14837
pii: S1538-7836(22)01340-X
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1728-1737

Informations de copyright

© 2020 International Society on Thrombosis and Haemostasis.

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Auteurs

Judith Catella (J)

Service de Médecine Vasculaire et Thérapeutique, CHU de St-Etienne, Saint-Etienne, France.

Laurent Bertoletti (L)

Service de Médecine Vasculaire et Thérapeutique, CHU de St-Etienne, Saint-Etienne, France.
INSERM, UMR1059, Equipe Dysfonction Vasculaire et Hémostase, Université Jean-Monnet, Saint-Etienne, France.
INSERM, CIC-1408, CHU Saint-Etienne, Saint-Etienne, France.
F-CRIN INNOVTE network, Saint-Etienne, France.

Patrick Mismetti (P)

Service de Médecine Vasculaire et Thérapeutique, CHU de St-Etienne, Saint-Etienne, France.
INSERM, UMR1059, Equipe Dysfonction Vasculaire et Hémostase, Université Jean-Monnet, Saint-Etienne, France.
INSERM, CIC-1408, CHU Saint-Etienne, Saint-Etienne, France.
F-CRIN INNOVTE network, Saint-Etienne, France.

Edouard Ollier (E)

INSERM, UMR1059, Equipe Dysfonction Vasculaire et Hémostase, Université Jean-Monnet, Saint-Etienne, France.
URCIP, CHU de St-Etienne, Saint-Etienne, France.

Angel Samperiz (A)

Department of Internal Medicine, Hospital Reina Sofía, Tudela, Spain.

Silvia Soler (S)

Department of Internal Medicine, Hospital Olot i Comarcal de la Garrotxa, Gerona, Spain.

José Maria Suriñach (JM)

Department of Internal Medicine, Hospital Universitario Vall d'Hebron, Barcelona, Spain.

Isabelle Mahé (I)

F-CRIN INNOVTE network, Saint-Etienne, France.
Department of Internal Medicine, Hôpital Louis Mourier (APHP), University Paris 7, Colombes, France.

Manuel Alejandro Lorente (MA)

Department of Internal Medicine, Hospital Vega Baja de Orihuela, Alicante, Spain.

Andrei Braester (A)

Department of Haematology, Galilee Medical Center, Nahariya, Israel.
Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel.

Manuel Monreal (M)

Department of Internal Medicine, Hospital Germans Trias i Pujol, Badalona, Spain.

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