Evidence map›Paper›PMID 36256594›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2023

Critical illness associated new onset atrial fibrillation: subsequent atrial fibrillation diagnoses and other adverse outcomes.

Daniel Lancini, Wei Lian Tan, Kristyan Guppy-Coles, Robert Boots, Sandhir Prasad, John Atherton, Paul Martin

Abstract read
In one paragraph

Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. A prospective, multi-site, observational study assessing the treatment thresholds of new onset atrial fibrillation in the critically ill.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. New-onset atrial fibrillation during critical illness: another piece of the puzzle.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Daniel LanciniCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.ORCID 0000-0002-2131-0628
Wei Lian TanCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.
Kristyan Guppy-ColesCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.ORCID 0000-0002-2928-2983
Robert BootsBurns, Trauma and Critical Care Research Centre, University of Queensland, Brisbane 4029, Australia.ORCID 0000-0002-2436-7654
Sandhir PrasadCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.ORCID 0000-0002-8681-9425
John AthertonCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.ORCID 0000-0003-2271-578X
Paul MartinCardiology Department, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia.ORCID 0000-0002-5151-2394

Funding

Investment and Research OfficeJunior Doctor Research FellowshipNational Health and Medical Research Council HREC/15/QRBW/510Queensland Healththe Health Innovation
6 · The paper itself

Abstract

aimsAmongst patients with critical illness associated new onset AF (CI-NOAF), the risk of subsequent atrial fibrillation (AF) diagnoses and other adverse outcomes is unknown, and the role for long-term anticoagulation is unclear. This study sought to determine the factors associated with subsequent AF diagnoses and other adverse outcomes in this cohort. METHODS AND

resultsAdmissions to a tertiary general intensive care unit (ICU) between December 2015 and September 2018 were screened for AF episodes through hourly analysis of continuous ECG monitoring. Patients with a prior history of AF were excluded. AF burden was defined as the percentage of monitored ICU hours in AF. The primary endpoint was subsequent AF diagnoses, as collated from the statewide electronic medical records. Secondary endpoints included mortality, embolic events, MACE and subsequent anticoagulation.

resultsOf 7030 admissions with 509 303 h of monitoring data, 309 patients with CI-NOAF were identified, and 235 survived to discharge. Subsequent AF diagnoses were identified in 75 (31.9%) patients after a median of 413 days. Increased AF burden had the strongest independent association with AF recurrence (OR = 15.03, P = 0.002), followed by increased left atrial area (OR = 1.12, P = 0.01). Only 128 (54.5%) patients had their AF diagnosis acknowledged at ICU discharge, and 50 (21.3%) received anticoagulation at hospital discharge.

conclusionCI-NOAF is often under-recognized, and subsequent AF diagnoses are common post-discharge. AF burden during ICU admission has a strong independent association with subsequent AF diagnoses. Left atrial size is also independently associated with subsequent AF.

Indexed as

Atrial FibrillationAftercareAnticoagulantsCritical IllnessHumansPatient DischargeRisk FactorsAnticoagulantsAtrial fibrillationAtrial fibrillation burdenAtriopathyCritical illness

Identifiers

PMID36256594
PMCPMC9935047

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.