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DOI 10.1093/eurheartj/ehae596

Медицинская библиотека · European heart journal · 2024

Anticoagulation in device-detected atrial fibrillation with or without vascular disease: a combined analysis of the NOAH-AFNET 6 and ARTESiA trials.

Schnabel Renate B, Benezet-Mazuecos Juan, Becher Nina, McIntyre William F, Fierenz Alexander, Lee Shun Fu, Goette Andreas, Atar Dan, Bertaglia Emanuele, Benz Alexander P, Chlouverakis Gregory, Birnie David H, Dichtl Wolfgang, Blomstrom-Lundqvist Carina, Camm A John, Erath Julia W, Simantirakis Emmanuel, Kutyifa Valentina, Lip Gregory Y H, Mabo Philippe, Marijon Eloi, Rivard Lena, Schotten Ulrich, Alings Marco, Sehner Susanne, Toennis Tobias, Linde Cecilia, Vardas Panos, Granger Christopher B, Zapf Antonia, Lopes Renato D, Healey Jeff S, Kirchhof Paulus

СтатьяМетаанализПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND AND AIMS: The optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation.

METHODS

These pre-specified analyses of the NOAH-AFNET 6 (n = 2534 patients) and ARTESiA (n = 4012 patients) trials compared anticoagulation with no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischaemic attack, coronary or peripheral artery disease. Efficacy outcomes were the primary outcomes of both trials, a composite of stroke, systemic arterial embolism (SE), myocardial infarction, pulmonary embolism or cardiovascular death, and stroke or SE. Safety outcomes were major bleeding or major bleeding and death.

RESULTS

In patients with vascular disease (NOAH-AFNET 6, 56%; ARTESiA, 46%), stroke, myocardial infarction, systemic or pulmonary embolism, or cardiovascular death occurred at 3.9%/patient-year with and 5.0%/patient-year without anticoagulation (NOAH-AFNET 6), and 3.2%/patient-year with and 4.4%/patient-year without anticoagulation (ARTESiA). Without vascular disease, outcomes were equal with and without anticoagulation (NOAH-AFNET 6, 2.7%/patient-year; ARTESiA, 2.3%/patient-year in both randomized groups). Meta-analysis found consistent results across both trials (I2heterogeneity = 6%) with a trend for interaction with randomized therapy (pinteraction = .08). Stroke/SE behaved similarly. Anticoagulation equally increased major bleeding in vascular disease patients [edoxaban, 2.1%/patient-year; no anticoagulation, 1.3%/patient-year; apixaban, 1.7%/patient-years; no anticoagulation, 1.1%/patient-year; incidence rate ratio 1.55 (1.10-2.20)] and without vascular disease [edoxaban, 2.2%/patient-year; no anticoagulation, 0.6%/patient-year; apixaban, 1.4%/patient-year; no anticoagulation, 1.1%/patient-year; incidence rate ratio 1.93 (0.72-5.20)].

CONCLUSIONS

Patients with DDAF and vascular disease are at higher risk of stroke and cardiovascular events and may derive a greater benefit from anticoagulation than patients with DDAF without vascular disease.

Для цитирования: Schnabel Renate B, Benezet-Mazuecos Juan, Becher Nina, McIntyre William F, Fierenz Alexander, Lee Shun Fu, Goette Andreas, Atar Dan, Bertaglia Emanuele, Benz Alexander P, Chlouverakis Gregory, Birnie David H, Dichtl Wolfgang, Blomstrom-Lundqvist Carina, Camm A John, Erath Julia W, Simantirakis Emmanuel, Kutyifa Valentina, Lip Gregory Y H, Mabo Philippe, Marijon Eloi, Rivard Lena, Schotten Ulrich, Alings Marco, Sehner Susanne, Toennis Tobias, Linde Cecilia, Vardas Panos, Granger Christopher B, Zapf Antonia, Lopes Renato D, Healey Jeff S, Kirchhof Paulus. Anticoagulation in device-detected atrial fibrillation with or without vascular disease: a combined analysis of the NOAH-AFNET 6 and ARTESiA trials.. European heart journal. 2024. DOI: 10.1093/eurheartj/ehae596.

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