Other bulletins in this series include:

Breast Surgery

Showing posts with label atrial fibrillation. Show all posts
Showing posts with label atrial fibrillation. Show all posts

Wednesday, 24 May 2023

 

Atrial Fibrillation (AFIB) in the ICU: Incidence, Risk Factors, and Outcomes: The International AFIB-ICU Cohort Study

Critical Care Medicine, April 20, 2023

Objectives: To assess the incidence, risk factors, and outcomes of atrial fibrillation (AF) in the ICU and to describe current practice in the management of AF.

Design: Multicenter, prospective, inception cohort study.

Setting: Forty-four ICUs in 12 countries in four geographical regions.

Subjects: Adult, acutely admitted ICU patients without a history of persistent/permanent AF or recent cardiac surgery were enrolled; inception periods were from October 2020 to June 2021.

Interventions: None.

Measurements and Main Results: We included 1,423 ICU patients and analyzed 1,415 (99.4%), among whom 221 patients had 539 episodes of AF. Most (59%) episodes were diagnosed with continuous electrocardiogram monitoring. The incidence of AF was 15.6% (95% CI, 13.8–17.6), of which newly developed AF was 13.3% (11.5–15.1). A history of arterial hypertension, paroxysmal AF, sepsis, or high disease severity at ICU admission was associated with AF. Used interventions to manage AF were fluid bolus 19% (95% CI 16–23), magnesium 16% (13–20), potassium 15% (12–19), amiodarone 51% (47–55), beta-1 selective blockers 34% (30–38), calcium channel blockers 4% (2–6), digoxin 16% (12–19), and direct current cardioversion in 4% (2–6). Patients with AF had more ischemic, thromboembolic (13.6% vs 7.9%), and severe bleeding events (5.9% vs 2.1%), and higher mortality (41.2% vs 25.2%) than those without AF. The adjusted cause-specific hazard ratio for 90-day mortality by AF was 1.38 (95% CI, 0.95–1.99).

Conclusions: In ICU patients, AF occurred in one of six and was associated with different conditions. AF was associated with worse outcomes while not statistically significantly associated with 90-day mortality in the adjusted analyses. We observed variations in the diagnostic and management strategies for AF.

Wednesday, 5 January 2022

 

Automated left atrial strain analysis for predicting atrial fibrillation in severe COVID-19 pneumonia: a prospective study

by Christophe Beyls, Alexis Hermida, Yohann Bohbot, Nicolas Martin, Christophe Viart, Solenne Boisgard, Camille Daumin, Pierre Huette, HervĂ© Dupont, Osama Abou-Arab and Yazine Mahjoub 

Annals of Intensive Care volume 11, Article number: 168 (2021) Published: 07 December 2021

Background

Atrial fibrillation (AF) is the most documented arrhythmia in COVID-19 pneumonia. Left atrial (LA) strain (LAS) analysis, a marker of LA contractility, have been associated with the development of AF in several clinical situations. We aimed to assess the diagnostic ability of LA strain parameters to predict AF in patients with severe hypoxemic COVID-19 pneumonia. We conducted a prospective single center study in Amiens University Hospital intensive care unit (ICU) (France). Adult patients with severe or critical COVID-19 pneumonia according to the World Health Organization definition and in sinus rhythm were included. Transthoracic echocardiography was performed within 48 h of ICU admission. LA strain analysis was performed by an automated software. The following LA strain parameters were recorded: LA strain during reservoir phase (LASr), LA strain during conduit phase (LAScd) and LA strain during contraction phase (LASct). The primary endpoint was the occurrence of AF during ICU stay.

Results

From March 2020 to February of 2021, 79 patients were included. Sixteen patients (20%) developed AF in ICU. Patients of the AF group were significantly older with a higher SAPS II score than those without AF. LAScd and LASr were significantly more impaired in the AF group compared to the other group (− 8.1 [− 6.3; − 10.9] vs. − 17.2 [− 5.0; − 10.2] %; P < 0.001 and 20.2 [12.3;27.3] % vs. 30.5 [23.8;36.2] %; P = 0.002, respectively), while LASct did not significantly differ between groups (p = 0.31). In a multivariate model, LAScd and SOFA cv were significantly associated with the occurrence of AF. A LAScd cutoff value of − 11% had a sensitivity of 76% and a specificity of 75% to identify patients with AF. The 30-day cumulative risk of AF was 42 ± 9% with LAScd > − 11% and 8 ± 4% with LAScd ≤ − 11% (log rank test P value < 0.0001).

Conclusion

For patients with severe COVID-19 pneumonia, development of AF during ICU stay is common (20%). LAS parameters seem useful in predicting AF within the first 48 h of ICU admission.

Thursday, 28 February 2019

Risk Factors for New-Onset Atrial Fibrillation in Patients With Sepsis: A Systematic Review and Meta-Analysis



 by Bosch, Nicholas A.; Cohen, David M.; Walkey, Allan J.  


Objective: Atrial fibrillation frequently develops in patients with sepsis and is associated with increased morbidity and mortality. Unfortunately, risk factors for new-onset atrial fibrillation in sepsis have not been clearly elucidated. Clarification of the risk factors for atrial fibrillation during sepsis may improve our understanding of the mechanisms of arrhythmia development and help guide clinical practice.
Data Sources: Medline, Embase, Web of Science, and Cochrane CENTRAL.
Study Selection: We conducted a systematic review and meta-analysis to identify risk factors for new-onset atrial fibrillation during sepsis.
Data Extraction: We extracted the adjusted odds ratio for each risk factor associated with new-onset atrial fibrillation during sepsis. For risk factors present in more than one study, we calculated pooled odds ratios (meta-analysis). We classified risk factors according to type and quantified the factor effect sizes. We then compared sepsis-associated atrial fibrillation risk factors with risk factors for community-associated atrial fibrillation.
Data Synthesis: Forty-four factors were examined as possible risk factors for new-onset atrial fibrillation in sepsis, 18 of which were included in meta-analyses. Risk factors for new-onset atrial fibrillation included demographic factors, comorbid conditions, and most strongly, sepsis-related factors. Sepsis-related factors with a greater than 50% change in odds of new-onset atrial fibrillation included corticosteroid use, right heart catheterization, fungal infection, vasopressor use, and a mean arterial pressure target of 80–85 mm Hg. Several cardiovascular conditions that are known risk factors for community-associated atrial fibrillation were not identified as risk factors for new-onset atrial fibrillation in sepsis.
Conclusions: Our study shows that risk factors for new-onset atrial fibrillation during sepsis are mainly factors that are associated with the acute sepsis event and are not synonymous with risk factors for community-associated atrial fibrillation. Our results provide targets for future studies focused on atrial fibrillation prevention and have implications for several key areas in the management of patients with sepsis such as glucocorticoid administration, vasopressor selection, and blood pressure targets.

Tuesday, 16 May 2017

New-Onset Atrial Fibrillation in the Critically Ill

New-Onset Atrial Fibrillation in the Critically Ill

Moss, T J et al
Critical Care Medicine: May 2017 - Volume 45 - Issue 5 - p 790–797

Objective: To determine the association of new-onset atrial fibrillation with outcomes, including ICU length of stay and survival. Design: Retrospective cohort of ICU admissions. We found atrial fibrillation using automated detection (≥ 90 s in 30 min) and classed as new-onset if there was no prior diagnosis of atrial fibrillation. We identified determinants of new-onset atrial fibrillation and, using propensity matching, characterized its impact on outcomes. Setting: Tertiary care academic center. Patients: A total of 8,356 consecutive adult admissions to either the medical or surgical/trauma/burn ICU with available continuous electrocardiogram data. Interventions: None. 
Measurements and Main Results: From 74 patient-years of every 15-minute observations, we detected atrial fibrillation in 1,610 admissions (19%), with median burden less than 2%. Most atrial fibrillation was paroxysmal; less than 2% of admissions were always in atrial fibrillation. New-onset atrial fibrillation was subclinical or went undocumented in 626, or 8% of all ICU admissions. Advanced age, acute respiratory failure, and sepsis were the strongest predictors of new-onset atrial fibrillation. In propensity-adjusted regression analyses, clinical new-onset atrial fibrillation was associated with increased hospital mortality (odds ratio, 1.63; 95% CI, 1.01–2.63) and longer length of stay (2.25 d; CI, 0.58–3.92). New-onset atrial fibrillation was not associated with survival after hospital discharge (hazard ratio, 0.99; 95% CI, 0.76–1.28 and hazard ratio, 1.11; 95% CI, 0.67–1.83, respectively, for subclinical and clinical new-onset atrial fibrillation). 
Conclusions: Automated analysis of continuous electrocardiogram heart rate dynamics detects new-onset atrial fibrillation in many ICU patients. Though often transient and frequently unrecognized, new-onset atrial fibrillation is associated with poor hospital outcomes.

Thursday, 18 December 2014

Incidence, risk factors and outcomes of new-onset atrial fibrillation in patients with sepsis

Incidence, risk factors and outcomes of new-onset atrial fibrillation in patients with sepsis: a systematic review. Critical Care 2014, 18: 688

Kuipers, S., et al.

http://ccforum.com/content/pdf/s13054-014-0688-5.pdf

Critically ill patients with sepsis are prone to develop cardiac dysrhythmias, most commonly
atrial fibrillation (AF). Systemic inflammation, circulating stress hormones, autonomic
dysfunction, and volume shifts are all possible triggers for AF in this setting. We conducted a
systematic review to describe the incidence, risk factors and outcomes of new-onset AF in
patients with sepsis. 

Tuesday, 25 November 2008

Critical Care Vol 11 Number 6

Critical Care
VOL 11; NUMBER 6; 2007
ISSN 1364-8535

p. 423
A wise nurse can manage a paper protocol but prefers intelligent technology.
Vogelzang, M.; Zijlstra, F.; Nijsten, M. W.
http://zetoc.mimas.ac.uk/wzgw?db=etoc&terms=PM018086318&field=zid

p. 177
Alveolar microstrain and the dark side of the lung.
Oeckler, R. A.; Hubmayr, R. D.
http://zetoc.mimas.ac.uk/wzgw?db=etoc&terms=PM018036270&field=zid

p. 233
Clinical review: Treatment of new-onset atrial fibrillation in medical intensive care patients: a clinical framework.
Sleeswijk, M. E.; Van Noord, T.; Tulleken, J. E.; Ligtenberg, J. J.; Girbes, A. R.; Zijlstra, J. G.
http://zetoc.mimas.ac.uk/wzgw?db=etoc&terms=PM018036267&field=zid

Monday, 7 July 2008

Paroxysmal Atrial Fibrillation in Critically Ill Patients With Sepsis

Article Title: Paroxysmal Atrial Fibrillation in Critically Ill Patients With Sepsis
Author(s): Salman , S . ; Bajwa , A . ; Gajic , O . ; Afessa , B .
ISSUE: 2008 ; VOL 23 ; PART 3 (2008-May)
Journal Title: Journal of Intensive Care Medicine Journal of Intensive Care Medicine
Page: 178-183
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Tuesday, 3 June 2008

Sepsis articles:

Review of A Large Clinical Series : Paroxysmal Atrial Fibrillation in Critically Ill Patients With Sepsis
Author(s): Salam Salman
ISSUE: 2008 ; VOL 23 ; PART 3 (2008-May)
Journal Title: Journal of Intensive Care Medicine Journal of Intensive Care Medicine
Page: 178 - 183
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Resuscitating the Microcirculation in Sepsis : The Central Role of Nitric Oxide , Emerging Concepts for Novel Therapies , and Challenges for Clinical Trials
Author(s): Trzeciak , S . ; Cinel , I . ; Phillip Dellinger , R . ; Shapiro , N . I . ; Arnold , R . C . ; Parrillo , J . E . ; Hollenberg , S . M .
ISSUE: 2008 ; VOL 15 ; PART 5 (2008/05/01)
Journal Title: Academic Emergency Medicine From Proquest NHS (07/2001 - 04/2006)
Page: 399-413
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Sepsis syndrome and death in trauma patients are associated with variation in the gene encoding tumor necrosis factor
Author(s): Menges , T . ; Konig , I . R . ; Hossain , H . ; Little , S . ; Tchatalbachev , S . ; Thierer , F . ; Hackstein , H . ; Franjkovic , I . ; Colaris , T . ; Martens , F .
ISSUE: 2008 ; VOL 36 ; PART 5
Journal Title: Critical Care Medicine http://ovidsp.ovid.com/athens/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00003246-000000000-00000 [Full Text] (01/1995 - /) Customer Notes: 1997 v25/1 - Print Location: Macclesfield
Page: 1456-1462
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Combination of biphasic transmittance waveform with blood procalcitonin levels for diagnosis of sepsis in acutely ill patients
Author(s):
Zakariah , A . N . ; Cozzi , S . M . ; Van Nuffelen , M . ; Clausi , C . M . ; Pradier , O . ; et al
ISSUE: 2008 ; VOL 36 ; PART 5
Journal Title: Critical Care Medicine http://ovidsp.ovid.com/athens/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00003246-000000000-00000 [Full Text] (01/1995 - /) Customer Notes: 1997 v25/1 - Print Location: Macclesfield
Page: 1507-1512
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Alterations in intracellular Ca^ 2^ +-homeostasis of skeletal muscle fibers during sepsis
Author(s): Zink , W . ; Kaess , M . ; Hofer , S . ; Plachky , J . ; Zausig , Y . A . ; Sinner , B . ; et al
ISSUE: 2008 ; VOL 36 ; PART 5
Journal Title: Critical Care Medicine http://ovidsp.ovid.com/athens/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00003246-000000000-00000 [Full Text] (01/1995 - /) Customer Notes: 1997 v25/1 - Print Location: Macclesfield
Page: 1559-1563
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Genes and sepsis: How tight is the fit ?
Author(s): Gordon , A . ; Knight , J . C . ; Hinds , C . J .
ISSUE: 2008 ; VOL 36 ; PART 5
Journal Title: Critical Care Medicine http://ovidsp.ovid.com/athens/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00003246-000000000-00000 [Full Text] (01/1995 - /) Customer Notes: 1997 v25/1 - Print Location: Macclesfield
Page: 1652-1653
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