Key result
Phenylephrine in critically ill patients is linked to a ~29% higher risk of new-onset AF.
Why the study?
Vasopressors can cause irregular heartbeats, but existing studies have not definitively proven whether phenylephrine triggers new atrial fibrillation in critically ill patients.
Does phenylephrine increase the risk of new atrial fibrillation in critically ill patients?
Cohort (n=51,294)
Yes
Does phenylephrine increase the risk of new atrial fibrillation in critically ill patients?
Hazard Ratio: 1.29 (95% CI 1.05–1.58)
Absolute Event Rate: 10.5% vs 4.9%
p-value: p=0.017
Phenylephrine administration in critically ill patients is associated with a significantly increased risk of new-onset atrial fibrillation, highlighting the need for risk-aware vasopressor selection.
Background Vasopressors are vital for maintaining blood pressure in critically ill patients, though they carry risks like irregular heartbeats and impaired cardiac oxygen balance. Existing studies have not definitively proven that phenylephrine triggers new atrial fibrillation (AF). Aims This study was designed to assess pharmacological associations between phenylephrine utilization and new AF occurrence risk. Methods This multicenter retrospective study analyzed eICU database records. Propensity score matching (PSM) balanced baseline confounders. Cox regression models (unadjusted/adjusted) assessed phenylephrine-AF associations. Results In this cohort encompassing 51,294 critically ill adults (mean age 62.4 ± 16.6 years; 53.5% male), propensity score matching established comparable cohorts: 2,110 phenylephrine-exposed patients and 6,330 matched controls. The analysis revealed a clinically significant disparity in new AF incidence, with phenylephrine-exposed patients demonstrating a 10.5% event rate (282/2,673) versus 4.9% (2,395/48,621) in non-exposed counterparts (p < 0.001). Multivariable-adjusted Cox proportional hazards models identified a 29% elevated risk of new AF associated with phenylephrine administration (aHR, 1.29; 95%CI, 1.05–1.58). Notably, this association remained robust across multiple sensitivity analyses employing alternative matching methodologies and covariate adjustments. Conclusion This evidence positions phenylephrine as a modifiable new AF risk factor in critical care, supporting risk-aware vasopressor selection through benefit-harm analysis.
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Huang et al. (2025) conducted a cohort in Critically ill patients (n=51,294). Phenylephrine vs. Non-exposed controls was evaluated on New-onset atrial fibrillation within 30 days of ICU admission (aHR 1.29, 95% CI 1.05-1.58, p=0.017). Phenylephrine administration in critically ill patients was associated with a 29% increased risk of new-onset atrial fibrillation compared to non-exposed patients (aHR 1.29).
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