Atomoxetine for suppression of vasovagal syncope.


Journal

Clinical autonomic research : official journal of the Clinical Autonomic Research Society
ISSN: 1619-1560
Titre abrégé: Clin Auton Res
Pays: Germany
ID NLM: 9106549

Informations de publication

Date de publication:
02 2023
Historique:
received: 24 08 2022
accepted: 26 10 2022
pubmed: 20 11 2022
medline: 8 3 2023
entrez: 19 11 2022
Statut: ppublish

Résumé

Vasovagal syncope (VVS) is a common clinical condition with few effective medical therapies. The study aimed to evaluate the effectiveness of atomoxetine in suppressing syncope in patients with recurrent VVS. This was a retrospective, open-label, observational case series of 12 patients taking atomoxetine for suppression of recurrent vasovagal syncope. We compared syncope frequency in the 1 year before atomoxetine and while subjects were taking atomoxetine. We used novel applications of the Poisson distribution to describe the results as a collection of n = 1 studies. There were 12 subjects, eight female, with a mean age 47 ± 22 years and a mean Calgary Syncope Symptom Score of 2 (diagnostic of vasovagal syncope). The patients received a mean dose of atomoxetine of 66 ± 16 mg (1.06 ± 0.21 mg/kg). The mean follow-up period was 1.21 ± 1.01 years. While taking atomoxetine, 11/12 patients appeared to improve and 7/12 had no syncope in follow-up (p = 0.0046). The annualized syncope frequency decreased from a median 5.5 (IQR 4, 6.75) syncope per year to 0 (IQR 0, 0.88) syncope per year (p = 0.002, Wilcoxon rank-sum test). According to the Poisson distribution, 7/12 subjects significantly improved with p values of < 0.0001 to 0.0235, 3/12 did not faint but had too brief follow-up times to detect significance, and 2/12 did not improve significantly. In this case series, atomoxetine was a promising oral agent for the prevention of vasovagal syncope. The Poisson distribution permits individual patient-level assessment of improvement and detects insufficient follow-up despite apparent improvement.

Identifiants

pubmed: 36401665
doi: 10.1007/s10286-022-00905-x
pii: 10.1007/s10286-022-00905-x
doi:

Substances chimiques

Atomoxetine Hydrochloride 57WVB6I2W0

Types de publication

Clinical Trial Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

23-28

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

Références

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Auteurs

Robert S Sheldon (RS)

Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, GAA02 HRIC Building, 3280 Hospital Drive NW AB, Calgary, T2N 4Z6, Canada. sheldon@ucalgary.ca.

Colette Seifer (C)

Cardiac Sciences Programme, University of Manitoba, Winnipeg, Canada.

Ratika Parkash (R)

Department of Medicine, Dalhousie University, Halifax, Canada.

Roopinder K Sandhu (RK)

Cedars-Sinai Medical Center, Smidt Heart Institute, Los Angeles, California, USA.

Rasha Hamzeh (R)

Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, GAA02 HRIC Building, 3280 Hospital Drive NW AB, Calgary, T2N 4Z6, Canada.

Satish R Raj (SR)

Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, GAA02 HRIC Building, 3280 Hospital Drive NW AB, Calgary, T2N 4Z6, Canada.

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