Evidence map›Paper›PMID 42232734›Full record

ArticleCritical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine2026

A prospective, multi-site, observational study assessing the treatment thresholds of new onset atrial fibrillation in the critically ill.

H G M Walker, N P Anthony, J Reeve, C McDermott, M Fogarty, P Emerson, J Walker, T Evans, J Holmes, K J Denny and 2 more

Abstract read
In one paragraph

Article in Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

H G M WalkerDepartment of Critical Care Medicine, St Vincent's Hospital, Melbourne, Victoria, Australia.
N P AnthonyIntensive Care Unit, Fiona Stanley Hospital, Western Australia, Australia.
J ReeveDepartment of Critical Care Medicine, St Vincent's Hospital, Melbourne, Victoria, Australia.
C McDermottIntensive Care Unit, Austin Hospital, Victoria, Australia.
M FogartyIntensive Care Unit, Bendigo Health, Victoria, Australia.
P EmersonDepartment of Intensive Care Medicine, Royal Adelaide Hospital, South Australia, Australia.
J WalkerIntensive Care Unit, Gold Coast University Hospital, Queensland, Australia.
T EvansDepartment of Critical Care, University of Melbourne, Victoria, Australia.
J HolmesDepartment of Critical Care Medicine, St Vincent's Hospital, Melbourne, Victoria, Australia.
K J DennyIntensive Care Unit, Gold Coast University Hospital, Queensland, Australia.
A BrownDepartment of Critical Care Medicine, St Vincent's Hospital, Melbourne, Victoria, Australia.
OPEN-ICU Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To define haemodynamic thresholds for pharmacological treatment of new-onset atrial fibrillation (NOAF) in critically ill patients and examine associations with short-term outcomes including reversion to sinus rhythm and in-hospital mortality. Design setting and participants: prospective multicentre observational cohort study conducted across six Australian intensive care units (ICUs) from December 2024 to September 2025. Adult patients (≥18 years) who developed NOAF during ICU admission were included. A Cox proportional hazards model treating time to treatment as a time-dependent covariate was used to assess associations between pharmacological therapy and secondary outcomes. Main outcome measures: The primary outcome was heart rate at initiation of the first pharmacological therapy for NOAF. Secondary outcomes included mean arterial pressure at time of treatment, reversion to sinus rhythm, haemodynamic deterioration, ICU length of stay, and in-hospital mortality. Results: Four hundred eighty-two patients were screened for eligibility and 210 met the inclusion criteria. One hundred fifty-four (73.3%) received pharmacological treatment for NOAF. The median heart rate at treatment initiation was 128 beats per minute (interquartile range [IQR]: 113-147) and median mean arterial pressure 76 mmHg (IQR: 70-87). Pharmacological treatment was not independently associated with sustained reversion to sinus rhythm (adjusted hazard ratio: 1.44, 95% confidence interval [CI]: 0.94-2.20) or in-hospital mortality (adjusted odds ratio: 0.96, 95% CI: 0.36-2.58). Pharmacological treatment was associated with prolonged ICU stay (multiplicative adjusted effect: 1.39, 95% CI: 1.06-1.82). Conclusions: Pharmacological treatment for NOAF is typically initiated at heart rates approximating 130 bpm. After accounting for time-dependent exposure, pharmacological treatment was not independently associated with reversion to sustained sinus rhythm. Given the methodological limitations encountered, these findings warrant validation in randomised trials to better define optimal treatment strategies for NOAF in critical illness.

Indexed as

AntiarrhythmicsAtrial fibrillationCritical illnessNew-onset atrial fibrillationRate control

Identifiers

PMID42232734
PMCPMC13223826

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.