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  3. Electrophysiological differences of randomized deep sedation with dexmedetomidine versus propofol.
 

Electrophysiological differences of randomized deep sedation with dexmedetomidine versus propofol.

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BORIS DOI
10.48350/199427
Publisher DOI
10.1186/s12871-024-02647-x
PubMed ID
39085782
Description
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

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

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

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

ClinicalTrials.gov number NCT03844841, 19/02/2019.
Date of Publication
2024-07-31
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
Atrial fibrillation Catheter ablation Dexmedetomidine Propofol Sedation
Language(s)
en
Contributor(s)
Servatius, Helge Simon
Universitätsklinik für Kardiologie
Küffer, Thomasorcid-logo
Universitätsklinik für Kardiologie
Erdoes, Gabor
Universitätsklinik für Anästhesiologie und Schmerztherapie
Seiler, Jens
Universitätsklinik für Kardiologie
Tanner, Hildegard
Universitätsklinik für Kardiologie
Noti, Fabian
Universitätsklinik für Kardiologie
Häberlin, Andreas David Heinrichorcid-logo
Universitätsklinik für Kardiologie
Madaffari, Antonio
Universitätsklinik für Kardiologie
Branca, Mattia
Department of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
Clinical Trials Unit Bern (CTU) - Statistics & Methodology (Bütikofer)
Dütschler, Sophie
Theiler, Lorenz
Reichlin, Tobias Romanorcid-logo
Universitätsklinik für Kardiologie
Roten, Laurentorcid-logo
Universitätsklinik für Kardiologie
Additional Credits
Department of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
Universitätsklinik für Kardiologie
Universitätsklinik für Anästhesiologie und Schmerztherapie
Series
BMC anesthesiology
Publisher
BioMed Central
ISSN
1471-2253
Access(Rights)
open.access
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