Electrophysiological differences of randomized deep sedation with dexmedetomidine versus propofol.


Journal

BMC anesthesiology
ISSN: 1471-2253
Titre abrégé: BMC Anesthesiol
Pays: England
ID NLM: 100968535

Informations de publication

Date de publication:
31 Jul 2024
Historique:
received: 13 02 2024
accepted: 18 07 2024
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 31 7 2024
Statut: epublish

Résumé

Dexmedetomidine and propofol are common sedatives in intensive care units and for interventional procedures. Both may compromise sinus node function and atrioventricular conduction. The objective of this prospective, randomized study is to compare the effect of dexmedetomidine with propofol on sinus node function and atrioventricular conduction. In a tertiary care center in Switzerland we included from September 2019 to October 2020 160 patients (65 ± 11 years old; 32% female) undergoing first ablation for atrial fibrillation by cryoballoon ablation or by radiofrequency ablation. Patients were randomly assigned to deep sedation with dexmedetomidine (DEX group) versus propofol (PRO group). A standard electrophysiological study was performed after pulmonary vein isolation with the patients still deeply sedated and hemodynamically stable. Eighty patients each were randomized to the DEX and PRO group. DEX group patients had higher baseline sinus cycle length (1022 vs. 1138 ms; p = 0.003) and longer sinus node recovery time (SNRT400; 1597 vs. 1412 ms; p = 0.042). However, both corrected SNRT and normalized SNRT did not differ. DEX group patients had longer PR interval (207 vs. 186 ms; p = 0.002) and AH interval (111 vs. 95 ms, p = 0.008), longer Wenckebach cycle length of the atrioventricular node (512 vs. 456 ms; p = 0.005), and longer atrioventricular node effective refractory period (390 vs. 344 ms; p = 0.009). QRS width and HV interval were not different. An arrhythmia, mainly atrial fibrillation, was induced in 33 patients during the electrophysiological study, without differences among groups (20% vs. 15%, p = 0.533). Dexmedetomidine has a more pronounced slowing effect on sinus rate and suprahissian AV conduction than propofol, but not on infrahissian AV conduction and ventricular repolarization. These differences need to be taken into account when using these sedatives. ClinicalTrials.gov number NCT03844841, 19/02/2019.

Sections du résumé

BACKGROUND BACKGROUND
Dexmedetomidine and propofol are common sedatives in intensive care units and for interventional procedures. Both may compromise sinus node function and atrioventricular conduction. The objective of this prospective, randomized study is to compare the effect of dexmedetomidine with propofol on sinus node function and atrioventricular conduction.
METHODS METHODS
In a tertiary care center in Switzerland we included from September 2019 to October 2020 160 patients (65 ± 11 years old; 32% female) undergoing first ablation for atrial fibrillation by cryoballoon ablation or by radiofrequency ablation. Patients were randomly assigned to deep sedation with dexmedetomidine (DEX group) versus propofol (PRO group). A standard electrophysiological study was performed after pulmonary vein isolation with the patients still deeply sedated and hemodynamically stable.
RESULTS RESULTS
Eighty patients each were randomized to the DEX and PRO group. DEX group patients had higher baseline sinus cycle length (1022 vs. 1138 ms; p = 0.003) and longer sinus node recovery time (SNRT400; 1597 vs. 1412 ms; p = 0.042). However, both corrected SNRT and normalized SNRT did not differ. DEX group patients had longer PR interval (207 vs. 186 ms; p = 0.002) and AH interval (111 vs. 95 ms, p = 0.008), longer Wenckebach cycle length of the atrioventricular node (512 vs. 456 ms; p = 0.005), and longer atrioventricular node effective refractory period (390 vs. 344 ms; p = 0.009). QRS width and HV interval were not different. An arrhythmia, mainly atrial fibrillation, was induced in 33 patients during the electrophysiological study, without differences among groups (20% vs. 15%, p = 0.533).
CONCLUSIONS CONCLUSIONS
Dexmedetomidine has a more pronounced slowing effect on sinus rate and suprahissian AV conduction than propofol, but not on infrahissian AV conduction and ventricular repolarization. These differences need to be taken into account when using these sedatives.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov number NCT03844841, 19/02/2019.

Identifiants

pubmed: 39085782
doi: 10.1186/s12871-024-02647-x
pii: 10.1186/s12871-024-02647-x
doi:

Substances chimiques

Dexmedetomidine 67VB76HONO
Propofol YI7VU623SF
Hypnotics and Sedatives 0

Banques de données

ClinicalTrials.gov
['NCT03844841']

Types de publication

Journal Article Randomized Controlled Trial Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

263

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Helge Servatius (H)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Thomas Kueffer (T)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Gabor Erdoes (G)

Department of Anaesthesiology and Pain Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Jens Seiler (J)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Hildegard Tanner (H)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Fabian Noti (F)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Andreas Haeberlin (A)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Antonio Madaffari (A)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Mattia Branca (M)

CTU Bern, University of Bern, Bern, Switzerland.

Sophie Dütschler (S)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Lorenz Theiler (L)

Department of Anaesthesiology, Kantonsspital Aarau, Aarau, Switzerland.

Tobias Reichlin (T)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Laurent Roten (L)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. laurent.roten@insel.ch.

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