Evidence map›Paper›PMID 35706899›Full record

ArticleEuropean heart journal supplements : journal of the European Society of Cardiology2022

Short acting intravenous beta-blocker as a first line of treatment for atrial fibrillation after cardiac surgery: a prospective observational study.

X Chapalain, J F Oilleau, L Henaff, P Lorillon PharmD, D Le Saout, P Kha, K Pluchon, E Bezon, O Huet

Open access · bronzeAbstract read
In one paragraph

Article in European heart journal supplements : journal of the European Society of Cardiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Observational
  2. Article
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

9 authors at 1 institution in 1 country.

X ChapalainDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
J F OilleauDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
L HenaffDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
P Lorillon PharmDDepartment of Pharmacy, Brest University Hospital, 29200 Brest, France.
D Le SaoutDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
P KhaDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
K PluchonDepartment of Cardiovascular and Thoracic Surgery, Brest University Hospital, 29200 Brest, France.
E BezonDepartment of Cardiovascular and Thoracic Surgery, Brest University Hospital, 29200 Brest, France.
O HuetDepartment of Anesthesiology and Surgical intensive care unit, Brest University Hospital, 29200 Brest, France.
Centre Hospitalier Régional Universitaire de Brest · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-operative atrial fibrillation (POAF) defined as a new-onset of atrial fibrillation (AF) following surgery occurs frequently after cardiac surgery. For non-symptomatic patients, rate control strategy seems to be as effective as rhythm control one in surgical patients. Landiolol is a new highly cardio-selective beta-blocker agent with interesting pharmacological properties that may have some interest in this clinical situation. This is a prospective, monocentric, observational study. All consecutive adult patients (age >18 years old) admitted in the intensive care unit following cardiac surgery with a diagnosed episode of AF were eligible. Success of landiolol administration was defined by a definitive rate control from the beginning of infusion to the 72th h. We also evaluated rhythm control following landiolol infusion. Safety analysis was focused on haemodynamic, renal and respiratory side effects. From 1 January 2020 to 30 June 2021, we included 54 consecutive patients. A sustainable rate control was obtained for 49 patients (90.7%). Median time until a sustainable rate control was 4 h (1, 22). Median infusion rate of landiolol needed for a sustainable rate control was 10 µg/kg/min (6, 19). Following landiolol infusion, median time until pharmacological cardioversion was 24 h. During landiolol infusion, maintenance of mean arterial pressure target requires a concomitant very low dose of norepinephrine. We did not find any other side effects. Low dose of landiolol used for POAF treatment was effective and safe for a rapid and sustainable rate and rhythm control after cardiac surgery.

Indexed as

Beta-blockerCardiac surgeryLandiololPost-operative atrial fibrillationRate control

Identifiers

PMID35706899
PMCPMC9190753
OpenAlexW4282594976

What OpenQuestion holds

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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.