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Effectiveness and safety of direct oral anticoagulants versus vitamin K antagonists in patients on chronic dialysis: a nationwide registry study.
Laville, Solène M; Couchoud, Cécile; Bauwens, Marc; Coponat, Henri Vacher; Choukroun, Gabriel; Liabeuf, Sophie.
Afiliação
  • Laville SM; Pharmacology Department, Amiens University Hospital, Amiens, France.
  • Couchoud C; MP3CV Laboratory, EA7517, Jules Verne University of Picardie, Amiens, France.
  • Bauwens M; Renal Epidemiology and Information Network (REIN) registry, Agence de la biomédecine, Saint Denis La Plaine, France.
  • Coponat HV; Department of Nephrology and Haemodialysis, Poitiers University Hospital, Poitiers, France.
  • Choukroun G; Department of Nephrology and Kidney Transplantation, Felix Guyon Hospital, Saint-Denis, La Réunion, France.
  • Liabeuf S; MP3CV Laboratory, EA7517, Jules Verne University of Picardie, Amiens, France.
Article em En | MEDLINE | ID: mdl-38366954
ABSTRACT
BACKGROUND AND

HYPOTHESIS:

Clinical trials of direct oral anticoagulants (DOAC) are scarce and inconclusive in patients who are receiving dialysis, for whom DOAC are not labelled in Europe. In a French nationwide registry study of patients on chronic dialysis, we compared the effectiveness and safety of off-label DOAC use vs. approved vitamin K antagonist (VKA).

METHODS:

Data on patients on dialysis were extracted from the French Renal Epidemiology and Information Network (REIN) registry and merged with data from the French national healthcare system database (Système National des Données de Santé, SNDS). Patients on dialysis who had initiated treatment with an oral anticoagulant between January 1st, 2012, and December 31st, 2020, were eligible for inclusion. The primary safety outcome was the occurrence of major bleeding events and the primary effectiveness outcome was the occurrence of thrombotic events. Using propensity-score-weighted cause-specific Cox regression, we compared the safety and effectiveness outcomes for DOAC and VKA.

RESULTS:

8,954 patients received an oral anticoagulant (483 DOAC and 8,471 VKA) for the first time after the initiation of dialysis. Over a median [interquartile range] follow-up period of 1.7 [0.8-3.2] years, 2,567 patients presented a first thromboembolic event and 1,254 patients had a bleeding event. After propensity score adjustment, the risk of a thromboembolic event was significantly lower in patients treated with a DOAC than in patients treated with a VKA (weighted hazard ratio (wHR) [95% confidence interval (CI)] 0.66 [0.46; 0.94]. A non-significant trend toward a lower risk of major bleeding events was found in DOAC-treated patients, relative to VKA-treated patients (wHR [95%CI] 0.68 [0.41; 1.12]). The results were consistent across subgroups and in sensitivity analyses.

CONCLUSIONS:

In a large group of dialysis patients initiating an oral anticoagulant, the off-label use of DOACs was associated with a significantly lower risk of thromboembolic events and a non-significantly lower risk of bleeding, relative to VKA use. This provides reassurance regarding the off-label use of DOACs in people on dialysis.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article