Evidence map›Paper›PMID 33206300›Full record

Observational studyCardiovascular drugs and therapy2021

Vernakalant for Rapid Cardioversion of Recent-Onset Atrial Fibrillation: Results from the SPECTRUM Study.

Samuel Lévy, Juha Hartikainen, Beate Ritz, Tord Juhlin, José Carbajosa-Dalmau, Hans Domanovits

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cardiovascular drugs and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Review
  9. Management of atrial fibrillation: two decades of progress - a scientific statement from the European Cardiac Arrhythmia Society.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2022
    Review
  10. Observational
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

6 authors at 5 institutions in 5 countries.

Samuel LévyMarseille School of Medicine, Aix-Marseille University, bd Charles Livon, Marseille Cedex 07, 13284, Marseille, France. samuel@samuel-levy.com.ORCID 0000-0001-7753-1043
Juha HartikainenKuopio University Hospital, Kuopio, Finland.
Beate RitzCorrevio International Sàrl, Geneva, Switzerland.
Tord JuhlinSkåne University Hospital, Lund, Sweden.
José Carbajosa-DalmauISABIAL-Fundación FISABIO, Hospital General Universitario de Alicante, Alicante, Spain.
Hans DomanovitsVienna General Hospital, Medical University of Vienna, Vienna, Austria.
Aix-Marseille Université · FRFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESKuopio University Hospital · FISkåne University Hospital · SEVienna General Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsRapid restoration of sinus rhythm using pharmacological cardioversion is commonly indicated in patients with symptomatic recent-onset atrial fibrillation (AF). The objectives of this large, international, multicenter observational study were to determine the safety and effectiveness of intravenous (IV) vernakalant for conversion of AF to sinus rhythm in daily practice. METHODS AND

resultsConsenting patients with symptomatic recent-onset AF (< 7 days) treated with IV vernakalant were enrolled and followed up to 24 h after the last infusion or until discharge, in order to determine the incidence of predefined serious adverse events (SAEs) and other observed SAEs and evaluate the conversion rate within the first 90 min. Overall, 2009 treatment episodes in 1778 patients were analyzed. The age of patients was 62.3 ± 13.0 years (mean ± standard deviation). Median AF duration before treatment was 11.1 h (IQR 5.4-27.0 h). A total of 28 SAEs occurred in 26 patients including 19 predefined SAEs, i.e., sinus arrest (n = 4, 0.2%), significant bradycardia (n = 11, 0.5%), significant hypotension (n = 2, 0.1%), and atrial flutter with 1:1 conduction (n = 2, 0.1%). There were no cases of sustained ventricular arrhythmias or deaths. All patients who experienced SAEs recovered fully (n = 25) or with sequelae (n = 1). Conversion rate to sinus rhythm was 70.2%, within a median of 12 min (IQR 8.0-28.0 min).

conclusionsThis large multicenter, international observational study confirms the good safety profile and the high effectiveness of vernakalant for the rapid cardioversion of recent-onset AF in daily hospital practice.

Indexed as

AdolescentAdultAgedAged, 80 and overAnisolesAnti-Arrhythmia AgentsAtrial FibrillationFemaleHumansInfusions, IntravenousMaleMiddle AgedPyrrolidinesTime FactorsYoung AdultAnisolesAnti-Arrhythmia AgentsPyrrolidinesvernakalantAtrial ArrhythmiasAtrial fibrillationPharmacological cardioversionVernakalant

Identifiers

PMID33206300
PMCPMC7994211
OpenAlexW3099667714

What OpenQuestion holds

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LicenceCC BY
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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.