Abbonarsi

Acute cardioversion vs a wait-and-see approach for recent-onset symptomatic atrial fibrillation in the emergency department: Rationale and design of the randomized ACWAS trial - 18/04/17

Doi : 10.1016/j.ahj.2016.09.009 
Elton Dudink, MD a, Brigitte Essers, MSc b, Wouter Holvoet, MD a, c, Bob Weijs, MD, PhD a, c, Justin Luermans, MD, PhD a, Hemanth Ramanna, MD, PhD d, Anho Liem, MD, PhD e, Jurren van Opstal, MD, PhD f, Lukas Dekker, MD, PhD g, Vincent van Dijk, MD, PhD h, Timo Lenderink, MD, PhD i, Otto Kamp, MD, PhD j, Lennert Kulker, MSc k, Michiel Rienstra, MD, PhD l, Bas Kietselaer, MD, PhD a, Marco Alings, MD, PhD m, Jos Widdershoven, MD, PhD n, Joan Meeder, MD, PhD c, Martin Prins, MD, PhD b, Isabelle van Gelder, MD, PhD l, Harry Crijns, MD, PhD a,
a Department of Cardiology, Maastricht University Medical Center and Cardiovascular Research Institute Maastricht, Maastricht, the Netherlands 
b Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Center, Maastricht, the Netherlands 
c Department of Cardiology, VieCuri Medical Center, Venlo, the Netherlands 
d Department of Cardiology, Haga Teaching Hospital, The Hague, the Netherlands 
e Department of Cardiology, Sint Franciscus Hospital, Rotterdam, the Netherlands 
f Department of Cardiology, Medisch Spectrum Twente, Enschede, the Netherlands 
g Department of Cardiology, Catharina Hospital, Eindhoven, the Netherlands 
h Department of Cardiology, St Antonius Hospital, Nieuwegein, the Netherlands 
i Department of Cardiology, Zuyderland Medical Center, Heerlen, the Netherlands 
j Department of Cardiology, VU University Medical Center, Amsterdam, the Netherlands 
k Department of Cardiology, Alrijne Hospital, Leiderdorp, the Netherlands 
l Department of Cardiology, University Medical Center Groningen, Groningen, the Netherlands 
m Department of Cardiology, Amphia Hospital, Breda, the Netherlands 
n Department of Cardiology, Elisabeth—TweeSteden Hospital, Tilburg, the Netherlands 

Reprint requests: H. J. G. M. Crijns, Department of Cardiology, Maastricht University Medical Center, PO Box 5800, 6202 AZ, Maastricht, the Netherlands.Department of CardiologyMaastricht University Medical CenterPO Box 5800Maastricht6202 AZthe Netherlands

Abstract

Background

Current standard of care for patients with recent-onset atrial fibrillation (AF) in the emergency department aims at urgent restoration of sinus rhythm, although paroxysmal AF is a condition that resolves spontaneously within 24 hours in more than 70% of the cases. A wait-and-see approach with rate-control medication only and when needed cardioversion within 48 hours of onset of symptoms is hypothesized to be noninferior, safe, and cost-effective as compared with current standard of care and to lead to a higher quality of life.

Design

The ACWAS trial (NCT02248753) is an investigator-initiated, randomized, controlled, 2-arm noninferiority trial that compares a wait-and-see approach to the standard of care. Consenting adults with recent-onset symptomatic AF in the emergency department without urgent need for cardioversion are eligible for participation. A total of 437 patients will be randomized to either standard care (pharmacologic or electrical cardioversion) or the wait-and-see approach, consisting of symptom reduction through rate control medication until spontaneous conversion is achieved, with the possibility of cardioversion within 48 hours after onset of symptoms. Primary end point is the presence of sinus rhythm on 12-lead electrocardiogram at 4 weeks; main secondary outcomes are adverse events, total medical and societal costs, quality of life, and cost-effectiveness for 1 year.

Conclusions

The ACWAS trial aims at providing evidence for the use of a wait-and-see approach for patients with recent-onset symptomatic AF in the emergency department.

Il testo completo di questo articolo è disponibile in PDF.

Mappa


 RCT No. NCT02248753.
 This trial is funded by a grant of Netherlands Organization for Health Research and Development – Health Care Efficiency Research program (Grant No. 837002524). No additional extramural funding was used to support this work.


© 2016  The Authors. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
Aggiungere alla mia biblioteca Togliere dalla mia biblioteca Stampare
Esportazione

    Citazioni Export

  • File

  • Contenuto

Vol 183

P. 49-53 - gennaio 2017 Ritorno al numero
Articolo precedente Articolo precedente
  • Baseline assessment and comparison of arterial anatomy, hyperemic flow, and skeletal muscle perfusion in peripheral artery disease: The Cardiovascular Cell Therapy Research Network “Patients with Intermittent Claudication Injected with ALDH Bright Cells” (CCTRN PACE) study
  • Bharath Ambale Venkatesh, Victor Nauffal, Chikara Noda, Tomoki Fujii, Phillip C. Yang, Judy Bettencourt, Erin P. Ricketts, Michael Murphy, Nicholas J. Leeper, Lem Moyé, Ray F. Ebert, Raja Muthupillai, David A. Bluemke, Emerson C. Perin, Alan T. Hirsch, João A.C. Lima, Cardiovascular Cell Therapy Research Network (CCTRN)
| Articolo seguente Articolo seguente
  • Interventional left atrial appendage closure vs novel anticoagulation agents in patients with atrial fibrillation indicated for long-term anticoagulation (PRAGUE-17 study)
  • Pavel Osmancik, Petr Tousek, Dalibor Herman, Petr Neuzil, Pavel Hala, Josef Stasek, Ludek Haman, Petr Kala, Martin Poloczek, Marian Branny, Jan Chovancik, Pavel Cervinka, Jiri Holy, Vlastimil Vancura, Richard Rokyta, Milos Taborsky, Tomas Kovarnik, David Zemanek, Petr Peichl, Sarka Haskova, Jiri Jarkovsky, Petr Widimsky, PRAGUE-17 Investigators

Benvenuto su EM|consulte, il riferimento dei professionisti della salute.
L'accesso al testo integrale di questo articolo richiede un abbonamento.

Già abbonato a @@106933@@ rivista ?

@@150455@@ Voir plus

Il mio account


Dichiarazione CNIL

EM-CONSULTE.COM è registrato presso la CNIL, dichiarazione n. 1286925.

Ai sensi della legge n. 78-17 del 6 gennaio 1978 sull'informatica, sui file e sulle libertà, Lei puo' esercitare i diritti di opposizione (art.26 della legge), di accesso (art.34 a 38 Legge), e di rettifica (art.36 della legge) per i dati che La riguardano. Lei puo' cosi chiedere che siano rettificati, compeltati, chiariti, aggiornati o cancellati i suoi dati personali inesati, incompleti, equivoci, obsoleti o la cui raccolta o di uso o di conservazione sono vietati.
Le informazioni relative ai visitatori del nostro sito, compresa la loro identità, sono confidenziali.
Il responsabile del sito si impegna sull'onore a rispettare le condizioni legali di confidenzialità applicabili in Francia e a non divulgare tali informazioni a terzi.


Tutto il contenuto di questo sito: Copyright © 2026 Elsevier, i suoi licenziatari e contributori. Tutti i diritti sono riservati. Inclusi diritti per estrazione di testo e di dati, addestramento dell’intelligenza artificiale, e tecnologie simili. Per tutto il contenuto ‘open access’ sono applicati i termini della licenza Creative Commons.