Safety and Prognostic Impact of Early Treatment with Angiotensin-Converting Enzyme Inhibitors or Angiotensin Receptor Blockers in Patients with Acute Heart Failure.


Journal

American journal of cardiovascular drugs : drugs, devices, and other interventions
ISSN: 1179-187X
Titre abrégé: Am J Cardiovasc Drugs
Pays: New Zealand
ID NLM: 100967755

Informations de publication

Date de publication:
Dec 2019
Historique:
pubmed: 21 6 2019
medline: 21 4 2020
entrez: 21 6 2019
Statut: ppublish

Résumé

Although angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) have been recommended for patients with heart failure, their clinical and prognostic impact in the very acute phase of acute heart failure (AHF) is unclear, mainly because data on their safety and efficacy are lacking. This study was a post hoc analysis of the REALITY-AHF trial. Patients with AHF who did not take an ACEI or ARB at admission were enrolled. Patients who received these medications within 48 h of admission were categorized as the ACEI/ARB group, and all other patients were categorized as the no ACEI/ARB group. The primary endpoint was a composite of all-cause death and heart failure readmission within 1 year of admission. Of the 1682 patients in the REALITY-AHF cohort, 900 were enrolled in this study, and 288 (32%) were included in the ACEI/ARB group. After propensity score matching, 152 pairs were evaluated, and no significant difference was found for in-hospital mortality, worsening renal function, or length of hospital stay. The ACEI/ARB group had significantly higher event-free survival (hazard ratio 0.51; 95% confidence interval 0.32-0.82; p = 0.006). Early initiation of ACEIs/ARBs within 48 h of admission for hospitalized patients with AHF was not associated with adverse events and correlated with improved outcomes at 1 year from admission.

Sections du résumé

BACKGROUND BACKGROUND
Although angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) have been recommended for patients with heart failure, their clinical and prognostic impact in the very acute phase of acute heart failure (AHF) is unclear, mainly because data on their safety and efficacy are lacking.
METHODS METHODS
This study was a post hoc analysis of the REALITY-AHF trial. Patients with AHF who did not take an ACEI or ARB at admission were enrolled. Patients who received these medications within 48 h of admission were categorized as the ACEI/ARB group, and all other patients were categorized as the no ACEI/ARB group. The primary endpoint was a composite of all-cause death and heart failure readmission within 1 year of admission.
RESULTS RESULTS
Of the 1682 patients in the REALITY-AHF cohort, 900 were enrolled in this study, and 288 (32%) were included in the ACEI/ARB group. After propensity score matching, 152 pairs were evaluated, and no significant difference was found for in-hospital mortality, worsening renal function, or length of hospital stay. The ACEI/ARB group had significantly higher event-free survival (hazard ratio 0.51; 95% confidence interval 0.32-0.82; p = 0.006).
CONCLUSIONS CONCLUSIONS
Early initiation of ACEIs/ARBs within 48 h of admission for hospitalized patients with AHF was not associated with adverse events and correlated with improved outcomes at 1 year from admission.

Identifiants

pubmed: 31218508
doi: 10.1007/s40256-019-00355-3
pii: 10.1007/s40256-019-00355-3
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

597-605

Auteurs

Kenji Yoshioka (K)

Department of Cardiology, Kameda Medical Center, Chiba, Japan.
Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

Yuya Matsue (Y)

Department of Cardiovascular Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan. yuya8950@gmail.com.
Cardiovascular Respiratory Sleep Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan. yuya8950@gmail.com.

Tetsuo Yamaguchi (T)

Department of Cardiology, Japanese Red Cross Musashino Hospital, Tokyo, Japan.

Takeshi Kitai (T)

Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.

Nobuyuki Kagiyama (N)

Department of Cardiology, The Sakakibara Heart Institute of Okayama, Okayama, Japan.

Takahiro Okumura (T)

Department of Cardiology, Nagoya University School of Medicine, Nagoya, Japan.

Keisuke Kida (K)

Department of Pharmacology, St. Marianna University School of Medicine, Kawasaki, Japan.

Shogo Oishi (S)

Department of Cardiology, Himeji Cardiovascular Center, Himeji, Japan.

Eiichi Akiyama (E)

Division of Cardiology, Yokohama City University Medical Center, Yokohama, Japan.

Satoshi Suzuki (S)

Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.

Masayoshi Yamamoto (M)

Cardiovascular Division, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.

Shunsuke Kuroda (S)

Department of Cardiology, Kameda Medical Center, Chiba, Japan.
Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

Akihiko Matsumura (A)

Department of Cardiology, Kameda Medical Center, Chiba, Japan.

Kenzo Hirao (K)

Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

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Classifications MeSH