Atrial fibrillation and QT corrected. What is the best formula to use?


Journal

European journal of clinical investigation
ISSN: 1365-2362
Titre abrégé: Eur J Clin Invest
Pays: England
ID NLM: 0245331

Informations de publication

Date de publication:
Sep 2023
Historique:
revised: 15 04 2023
received: 12 02 2023
accepted: 27 04 2023
medline: 21 8 2023
pubmed: 5 5 2023
entrez: 5 5 2023
Statut: ppublish

Résumé

QT interval varies with the heart rate (HR), so a correction in QT calculation is needed (QTc). Atrial fibrillation (AF) is associated with elevated HR and beat-to-beat variation. To find best correlation between QTc in atrial fibrillation (AF) versus restored sinus rhytm (SR) after electrical cardioversion (ECV) (primary end point) and to determine which correction formula and method are the best to determine QTc in AF (secondary end point). During a 3-month period, we considered patients who underwent 12-lead ECG recording and received an AF diagnosis with indication for ECV. Exclusion criteria were as follows: QRS duration >120 ms, therapy with QT-prolonging drugs, a rate control strategy and a nonelectrical cardioversion. The QT interval was corrected using Bazzett's, Framingham, Fridericia and Hodges formulas during the last ECG during AF and the first one immediately after ECV. QTc mean was calculated as mQTc (average of 10 QTc calculated beat per beat) and as QTcM (QTc calculated from the average of 10 raw QT and RR for each beat). Fifty consecutive patients were enrolled in the study. Bazett's formula showed a significant change in mean QTc value between the two rhythms (421.5 ± 33.9 vs. 446.1 ± 31.9; p < 0.001 for mQTc and 420.9 ± 34.1 vs. 441.8 ± 30.9; p = 0.003 for QTcM). On the contrary, in patients with SR, QTc assessed by the Framingham, Fridericia, and Hodges formulas was similar to that in AF. Furthermore, good correlations between mQTc and QTcM are present for each formula, even in AF or SR. During AF, Bazzett's formula, seems to be the most imprecise in QTc estimation.

Sections du résumé

BACKGROUND BACKGROUND
QT interval varies with the heart rate (HR), so a correction in QT calculation is needed (QTc). Atrial fibrillation (AF) is associated with elevated HR and beat-to-beat variation.
AIM OBJECTIVE
To find best correlation between QTc in atrial fibrillation (AF) versus restored sinus rhytm (SR) after electrical cardioversion (ECV) (primary end point) and to determine which correction formula and method are the best to determine QTc in AF (secondary end point).
METHODS METHODS
During a 3-month period, we considered patients who underwent 12-lead ECG recording and received an AF diagnosis with indication for ECV. Exclusion criteria were as follows: QRS duration >120 ms, therapy with QT-prolonging drugs, a rate control strategy and a nonelectrical cardioversion. The QT interval was corrected using Bazzett's, Framingham, Fridericia and Hodges formulas during the last ECG during AF and the first one immediately after ECV. QTc mean was calculated as mQTc (average of 10 QTc calculated beat per beat) and as QTcM (QTc calculated from the average of 10 raw QT and RR for each beat).
RESULTS RESULTS
Fifty consecutive patients were enrolled in the study. Bazett's formula showed a significant change in mean QTc value between the two rhythms (421.5 ± 33.9 vs. 446.1 ± 31.9; p < 0.001 for mQTc and 420.9 ± 34.1 vs. 441.8 ± 30.9; p = 0.003 for QTcM). On the contrary, in patients with SR, QTc assessed by the Framingham, Fridericia, and Hodges formulas was similar to that in AF. Furthermore, good correlations between mQTc and QTcM are present for each formula, even in AF or SR.
CONCLUSIONS CONCLUSIONS
During AF, Bazzett's formula, seems to be the most imprecise in QTc estimation.

Identifiants

pubmed: 37144525
doi: 10.1111/eci.14013
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14013

Informations de copyright

© 2023 Stichting European Society for Clinical Investigation Journal Foundation. Published by John Wiley & Sons Ltd.

Références

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Auteurs

Francesco Luzza (F)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Rosalba De Sarro (R)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Roberto Licordari (R)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Pasquale Crea (P)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Pietro Pugliatti (P)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Giuseppe Certo (G)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Lorenzo Pistelli (L)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Francesca Campanella (F)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Maria Claudia Lo Nigro (MC)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Matteo Casale (M)

Operative Unit of ICCU and Cardiology, Hospital "S. Maria della Misericordia", Urbino, Italy.

Michele Correale (M)

Cardiothoracic Department, Policlinico Riuniti University Hospital, Foggia, Italy.

Giuseppe Dattilo (G)

Department of Biomedical and Dental Sciences and Morphofunctional Imaging, Section of Cardiology, University of Messina, Messina, Italy.

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