Key result
Severe mobility impairment in AF linked to ~2.9-fold higher risk of death and MACE.
Why the study?
Although mobility impairment is associated with lower quality of life, higher healthcare expenditures, and a greater risk of adverse outcomes, little data existed regarding its impact in patients with AF.
Does mobility impairment increase the risk of a composite of all-cause death and major adverse cardiovascular events in European patients with atrial fibrillation?
Observational (n=8,954)
Yes
Does mobility impairment increase the risk of a composite of all-cause death and major adverse cardiovascular events in European patients with atrial fibrillation?
Mobility impairment affects half of European atrial fibrillation patients and is independently associated with lower oral anticoagulant prescription rates and a progressively higher risk of all-cause death and major adverse cardiovascular events.
Mobility status may refine AF risk stratification; leaves open whether targeted interventions improve outcomes or OAC use.
Introduction Atrial fibrillation (AF) is common in older adults and can be considered as part of a clinical geriatric syndrome model. Similarly, mobility impairment is associated with lower quality of life, higher healthcare expenditures, and a greater risk of adverse outcomes. Nonetheless, little data exist regarding the impact of mobility impairment in patients with AF. Methods Data for the present analysis were derived from a European observational study enrolling AF patients across 250 centres in 27 European countries from 2013 to 2016. Data on mobility impairment were derived from the mobility item in the EQ-5D-5L questionnaire, collected at baseline. Complete clinical and pharmacological data were collected at baseline. The primary outcome was a composite of all-cause death and major adverse cardiovascular events. Results Among the original 11,096 patients enrolled, data on 8,954 (80.7%) were available for this analysis (median [IQR] age 71 [62-77] years; 39.8% female). Of these, 3,686 (41.2%) presented with mild/moderate mobility impairment, while 775 (8.7%) had severe mobility impairment or were unable to walk. Patients with increasing mobility impairment were progressively older, more likely female, and overweight/ obese. Both baseline thromboembolic and bleeding risk were increasingly higher with increasing severity of mobility impairment (Table). At baseline, when compared to patients with no impairment or mild/moderate mobility impairment, those with more severe mobility impairment/unable to walk had greater multimorbidity (70.3% vs 86.5% vs 90.3%, respectively), frailty (9.1% vs 29.9% vs 51.8%), and polypharmacy (43.2% vs 61.5% vs 69.7%) (all p<0.001). After adjustments, when compared with no impairment, the mild/moderate mobility impairment and severe mobility impairment/unable to walk groups had a lower likelihood of oral anticoagulant prescription (ORs 0.75, 95% CI 0.65-0.86, and 0.55, 95% CI 0.44-0.69, respectively). During follow-up, there was an increasing cumulative incidence of the primary composite outcome across the three groups [Figure]. After full adjustments, compared with no impairment, mild/moderate mobility impairment and severe mobility impairment/unable to walk groups were associated with an increased risk of the composite outcome (HRs 1.93, 95% CI 1.67-2.23, and 2.86, 95% CI 2.36-3.46, respectively). Conclusions Mobility impairment affects a substantial proportion of AF patients, and influences both clinical management and clinical course, with a progressively higher risk of adverse outcomes as the severity of mobility impairment increases.
No takes yet. Share an insight, caveat, or question.
Proietti et al. (2026) conducted an observational in Atrial fibrillation (n=8,954). Mobility impairment (mild/moderate and severe/unable to walk) vs. No mobility impairment was evaluated on Composite of all-cause death and major adverse cardiovascular events (HR 2.86 (severe); HR 1.93 (mild/moderate), 95% CI 2.36-3.46). Mobility impairment in AF patients increased risk of death and MACE (mild/moderate: HR 1.93, 95% CI 1.67-2.23; severe: HR 2.86, 95% CI 2.36-3.46 vs no impairment).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: