Impact of tolvaptan add-on treatment on patients with heart failure requiring long-term congestion management: A retrospective cohort study using a medical claim database in Japan.


Journal

Journal of cardiology
ISSN: 1876-4738
Titre abrégé: J Cardiol
Pays: Netherlands
ID NLM: 8804703

Informations de publication

Date de publication:
07 2023
Historique:
received: 23 08 2022
revised: 29 11 2022
accepted: 08 12 2022
medline: 5 6 2023
pubmed: 2 1 2023
entrez: 1 1 2023
Statut: ppublish

Résumé

The impact of tolvaptan on the long-term outcomes of patients with heart failure (HF) remains inconclusive. We evaluated patients requiring long-term congestion management for the time to rehospitalization for HF (HF rehospitalization), the time to in-hospital death and explored the factors that may influence the outcomes. Using data (April 2008 to September 2019) from a medical claims database, patients with HF prescribed tolvaptan (tolvaptan cohort) and those prescribed loop diuretics before tolvaptan was introduced to the hospital (furosemide cohort) were compared. Patients with HF who experienced ≥2 HF hospitalizations and ≥1 tolvaptan or loop diuretic prescription during and after HF hospitalization were included. Data of patients with serum creatinine and estimated glomerular filtration rate were analyzed for time to HF rehospitalization and in-hospital death within 1 year after the second discharge and factors that may influence the outcomes. Among the 1931 and 631 tolvaptan and furosemide cohort patients, respectively, time to HF rehospitalization was not significantly different (p = 0.0921); time to in-hospital death was significantly longer in the tolvaptan cohort than in the furosemide cohort (p = 0.0005). Age, serum sodium, angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers were identified as factors for both outcomes (p < 0.05). Tolvaptan did not significantly affect time to HF rehospitalization. However, further worsening of the condition leading to death may be delayed, and time to in-hospital death may be prolonged in patients treated with tolvaptan, indicating its usefulness for long-term congestion management.

Sections du résumé

BACKGROUND
The impact of tolvaptan on the long-term outcomes of patients with heart failure (HF) remains inconclusive. We evaluated patients requiring long-term congestion management for the time to rehospitalization for HF (HF rehospitalization), the time to in-hospital death and explored the factors that may influence the outcomes.
METHODS
Using data (April 2008 to September 2019) from a medical claims database, patients with HF prescribed tolvaptan (tolvaptan cohort) and those prescribed loop diuretics before tolvaptan was introduced to the hospital (furosemide cohort) were compared. Patients with HF who experienced ≥2 HF hospitalizations and ≥1 tolvaptan or loop diuretic prescription during and after HF hospitalization were included. Data of patients with serum creatinine and estimated glomerular filtration rate were analyzed for time to HF rehospitalization and in-hospital death within 1 year after the second discharge and factors that may influence the outcomes.
RESULTS
Among the 1931 and 631 tolvaptan and furosemide cohort patients, respectively, time to HF rehospitalization was not significantly different (p = 0.0921); time to in-hospital death was significantly longer in the tolvaptan cohort than in the furosemide cohort (p = 0.0005). Age, serum sodium, angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers were identified as factors for both outcomes (p < 0.05).
CONCLUSIONS
Tolvaptan did not significantly affect time to HF rehospitalization. However, further worsening of the condition leading to death may be delayed, and time to in-hospital death may be prolonged in patients treated with tolvaptan, indicating its usefulness for long-term congestion management.

Identifiants

pubmed: 36587792
pii: S0914-5087(22)00323-9
doi: 10.1016/j.jjcc.2022.12.006
pii:
doi:

Substances chimiques

Tolvaptan 21G72T1950
Furosemide 7LXU5N7ZO5
Antidiuretic Hormone Receptor Antagonists 0
Benzazepines 0
Sodium Potassium Chloride Symporter Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

35-42

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Koichiro Kinugawa received consultancy fees, lecture fees, manuscript fees for writing of a leaflet and scholarship funds from Otsuka Pharmaceutical Co., Ltd. Miyuki Matsukawa, Yumiko Nakamura, Miki Aihara, and Hiromi Sano are employees of Otsuka Pharmaceutical Co., Ltd.

Auteurs

Koichiro Kinugawa (K)

Second Department of Internal Medicine, University of Toyama, Toyama, Japan. Electronic address: kinugawa@med.u-toyama.ac.jp.

Miyuki Matsukawa (M)

Medical Affairs, Otsuka Pharmaceutical Co., Ltd., Osaka, Japan.

Yumiko Nakamura (Y)

Medical Affairs, Otsuka Pharmaceutical Co., Ltd., Tokyo, Japan.

Miki Aihara (M)

Medical Affairs, Otsuka Pharmaceutical Co., Ltd., Tokyo, Japan.

Hiromi Sano (H)

Medical Affairs, Otsuka Pharmaceutical Co., Ltd., Osaka, Japan.

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Classifications MeSH