Key result
STROKESTOP II tests whether NT-proBNP-directed AF screening reduces stroke or systemic embolus.
Why the study?
Atrial fibrillation is often paroxysmal and asymptomatic, making diagnosis challenging, and the value of NT-proBNP as an adjunct in population-based AF screening is hypothesized.
Does stepwise mass screening for atrial fibrillation using NT-proBNP reduce the incidence of stroke or systemic embolus in adults aged 75-76 years?
RCT (n=28,712)
1:1
Does stepwise mass screening for atrial fibrillation using NT-proBNP reduce the incidence of stroke or systemic embolus in adults aged 75-76 years?
The STROKESTOP II trial is designed to determine if a stepwise AF screening strategy using NT-proBNP to guide ambulatory ECG monitoring reduces stroke or systemic embolus in older adults.
Will test NT-proBNP-guided AF screening for stroke reduction in older adults; extends prior trials with biomarker-stratified randomization.
AIM: Atrial fibrillation (AF) is the most prevalent clinical arrhythmia and a major risk factor for ischaemic stroke. Treatment with oral anticoagulants (OACs) reduces the risk of stroke by two thirds in AF patients with risk factors. Due to its often paroxysmal and asymptomatic presentation, AF is sometimes challenging to diagnose. So far, AF screening studies have applied opportunistic or systematic screening, most often using a single 12-lead electrocardiogram (ECG) recording or ambulatory ECG. We hypothesise that the biomarker N-terminal pro b-type natriuretic peptide (NT-proBNP) is a valuable adjunct in population based AF screening. METHODS: We are conducting a randomized population-based study on AF screening using ambulatory ECG recording where the decision to use prolonged intermittent ECG recording is directed by NT-proBNP levels, the STROKESTOP II trial. The entire population of inhabitants 75 or 76 years of age (n = 28 712) in the capital region of Sweden will be randomized 1:1 to intervention or control group. In the intervention group NT-proBNP will be analysed in all without previously known AF. Those with NT-proBNP ≤ 125 pg/L will make a single one lead ECG recording, participants with NTproBNP ≥ 125 np/L will be instructed to record ECG for 30 s at least twice daily for 2 weeks with a handheld ambulatory ECG recorder. Participants with newly diagnosed or undertreated AF will be referred to a cardiologist and offered OAC treatment. Primary endpoint is incidence of stroke or systemic embolus, during a 5 year follow-up period in the control group vs the group invited to screening.
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Engdahl et al. (2016) conducted an RCT in Atrial fibrillation (n=28,712). Stepwise mass screening for atrial fibrillation using NT-proBNP vs. Control group was evaluated on Incidence of stroke or systemic embolus. The STROKESTOP II trial will randomize 28,712 adults aged 75-76 years to evaluate whether NT-proBNP-directed screening for atrial fibrillation reduces stroke or systemic embolus over 5 years.
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