Comparative effectiveness of torasemide versus furosemide in symptomatic therapy in heart failure patients: Preliminary results from the randomized TORNADO trial.


Journal

Cardiology journal
ISSN: 1898-018X
Titre abrégé: Cardiol J
Pays: Poland
ID NLM: 101392712

Informations de publication

Date de publication:
2019
Historique:
received: 09 07 2019
accepted: 23 11 2019
revised: 17 11 2019
pubmed: 8 1 2020
medline: 4 8 2020
entrez: 8 1 2020
Statut: ppublish

Résumé

Recent reports suggest that torasemide might be more beneficial than furosemide in patients with symptomatic heart failure (HF). The aim was to compare the effects of torasemide and furosemide on clinical outcomes in HF patients. This study pilot consisted of data from the ongoing multicenter, randomized, unblinded endpoint phase IV TORNADO (NCT01942109) study. HF patients in New York Heart Association (NYHA) II-IV class with a stable dose of furosemide were randomized to treatment with equipotential dose of torasemide (4:1) or continuation of unchanged dose of furosemide. On enrollment and control visit (3 months after enrollment) clinical examination, 6-minute walk test (6MWT) and assessment of fluid retention by ZOE Fluid Status Monitor were performed. The primary endpoint was a composite of improvement of NYHA class, improvement of at least 50 m during 6MWT and decrease in fluid retention of at least 0.5 W after 3-months follow-up. The study group included 40 patients (median age 66 years; 77.5% male). During follow-up 7 patients were hospitalized for HF worsening (3 in torasemide and 4 in furosemide-treated patients). The primary endpoint reached 15 (94%) and 14 (58%) patients on torasemide and furosemide, respectively (p = 0.03). In HF patients treated with torasemide fluid overload and symptoms improved more than in the furosemide group. This positive effect occurred already within 3-month observation.

Sections du résumé

BACKGROUND
Recent reports suggest that torasemide might be more beneficial than furosemide in patients with symptomatic heart failure (HF). The aim was to compare the effects of torasemide and furosemide on clinical outcomes in HF patients.
METHODS
This study pilot consisted of data from the ongoing multicenter, randomized, unblinded endpoint phase IV TORNADO (NCT01942109) study. HF patients in New York Heart Association (NYHA) II-IV class with a stable dose of furosemide were randomized to treatment with equipotential dose of torasemide (4:1) or continuation of unchanged dose of furosemide. On enrollment and control visit (3 months after enrollment) clinical examination, 6-minute walk test (6MWT) and assessment of fluid retention by ZOE Fluid Status Monitor were performed. The primary endpoint was a composite of improvement of NYHA class, improvement of at least 50 m during 6MWT and decrease in fluid retention of at least 0.5 W after 3-months follow-up.
RESULTS
The study group included 40 patients (median age 66 years; 77.5% male). During follow-up 7 patients were hospitalized for HF worsening (3 in torasemide and 4 in furosemide-treated patients). The primary endpoint reached 15 (94%) and 14 (58%) patients on torasemide and furosemide, respectively (p = 0.03).
CONCLUSIONS
In HF patients treated with torasemide fluid overload and symptoms improved more than in the furosemide group. This positive effect occurred already within 3-month observation.

Identifiants

pubmed: 31909470
pii: VM/OJS/J/65083
doi: 10.5603/CJ.a2019.0114
pmc: PMC8083045
doi:

Substances chimiques

Sodium Potassium Chloride Symporter Inhibitors 0
Furosemide 7LXU5N7ZO5
Torsemide W31X2H97FB

Types de publication

Clinical Trial, Phase IV Comparative Study Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

661-668

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Auteurs

Paweł Balsam (P)

I Katedra i Klinika Kardiologii, Poland.

Krzysztof Ozierański (K)

I Katedra i Klinika Kardiologii, Poland.

Michał Marchel (M)

I Katedra i Klinika Kardiologii, Poland. michal.marchel@wum.edu.pl.

Monika Gawałko (M)

I Katedra i Klinika Kardiologii, Poland.

Łukasz Niedziela (Ł)

I Katedra i Klinika Kardiologii, Poland.

Agata Tymińska (A)

I Katedra i Klinika Kardiologii, Poland.

Bartosz Sieradzki (B)

I Katedra i Klinika Kardiologii, Poland.

Maciej Sieradzki (M)

I Katedra i Klinika Kardiologii, Poland.

Anna Fojt (A)

I Katedra i Klinika Kardiologii, Poland.

Elwira Bakuła (E)

Cardiology Unit, John Paul II Western Hospital, ul. Daleka 11, 05-825 Grodzisk Mazowiecki, Poland.

Renata Główczyńska (R)

I Katedra i Klinika Kardiologii, Poland.

Michał Peller (M)

I Katedra i Klinika Kardiologii, Poland.

Maciej Markulis (M)

I Katedra i Klinika Kardiologii, Poland.

Janusz Bednarski (J)

Cardiology Unit, John Paul II Western Hospital, ul. Daleka 11, 05-825 Grodzisk Mazowiecki, Poland.

Robert Kowalik (R)

I Katedra i Klinika Kardiologii, Poland.

Andrzej Cacko (A)

I Katedra i Klinika Kardiologii, Poland.

Grzegorz Niewiński (G)

Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Banacha 1A, 02-677 Warsaw, Poland.

Krzysztof J Filipiak (KJ)

I Katedra i Klinika Kardiologii, Poland.

Grzegorz Opolski (G)

I Katedra i Klinika Kardiologii, Poland.

Marcin Grabowski (M)

I Katedra i Klinika Kardiologii, Poland.

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Classifications MeSH