Effectiveness of Maintenance and Reliever Therapy Using Inhaled Corticosteroid-Formoterol in Asthmatics.


Journal

The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220

Informations de publication

Date de publication:
10 2022
Historique:
received: 23 11 2021
revised: 08 05 2022
accepted: 06 06 2022
pubmed: 26 6 2022
medline: 13 10 2022
entrez: 25 6 2022
Statut: ppublish

Résumé

Real-world evidence on the effectiveness of maintenance and reliever therapy (MART) using inhaled corticosteroids plus long-acting beta-2 agonist (ICS-LABA) is sparse. This study aimed to evaluate the clinical effectiveness of MART (ICS-formoterol) by comparing its effectiveness with that of ICS-LABA plus as-needed short-acting beta-2 agonist (SABA) in adult asthmatics. We retrospectively retrieved data from the medical records of the Ajou University Medical Center, Korea, to compare clinical outcomes between patients treated with MART (the MART group) and those treated with ICS-LABA plus SABA (the non-MART group). Propensity score matching was performed and hazard ratios (HRs) with 95% confidence intervals were calculated using the Cox proportional hazards model. Severe asthma exacerbation (SAEx) was the primary end point, and asthma exacerbation (AEx), hospitalization, and pneumonia were secondary end points. Corticosteroid requirement was also analyzed. After propensity score matching, the MART and the non-MART groups included 231 and 512 adult asthmatics, respectively. The risk of SAEx and AEx was significantly lower in the MART group than in the non-MART group (HR [95% CI] 0.39 [0.18-0.77] and 0.61 [0.37-0.99], respectively). There was no significant difference in hospitalization and pneumonia risk between the 2 groups (HR [95% CI] 0.88 [0.55-1.37] and 0.63 [0.03-4.51], respectively). Corticosteroid requirements were lower in the MART group than in the non-MART group (median [interquartile range], 190.0 [97.9-420.0] and 411.0 [143.0-833.0] mg/person-year, respectively; P < .01). The MART strategy of ICS-formoterol was associated with lower risk of AEx and reduced corticosteroid requirement.

Sections du résumé

BACKGROUND
Real-world evidence on the effectiveness of maintenance and reliever therapy (MART) using inhaled corticosteroids plus long-acting beta-2 agonist (ICS-LABA) is sparse.
OBJECTIVE
This study aimed to evaluate the clinical effectiveness of MART (ICS-formoterol) by comparing its effectiveness with that of ICS-LABA plus as-needed short-acting beta-2 agonist (SABA) in adult asthmatics.
METHODS
We retrospectively retrieved data from the medical records of the Ajou University Medical Center, Korea, to compare clinical outcomes between patients treated with MART (the MART group) and those treated with ICS-LABA plus SABA (the non-MART group). Propensity score matching was performed and hazard ratios (HRs) with 95% confidence intervals were calculated using the Cox proportional hazards model. Severe asthma exacerbation (SAEx) was the primary end point, and asthma exacerbation (AEx), hospitalization, and pneumonia were secondary end points. Corticosteroid requirement was also analyzed.
RESULTS
After propensity score matching, the MART and the non-MART groups included 231 and 512 adult asthmatics, respectively. The risk of SAEx and AEx was significantly lower in the MART group than in the non-MART group (HR [95% CI] 0.39 [0.18-0.77] and 0.61 [0.37-0.99], respectively). There was no significant difference in hospitalization and pneumonia risk between the 2 groups (HR [95% CI] 0.88 [0.55-1.37] and 0.63 [0.03-4.51], respectively). Corticosteroid requirements were lower in the MART group than in the non-MART group (median [interquartile range], 190.0 [97.9-420.0] and 411.0 [143.0-833.0] mg/person-year, respectively; P < .01).
CONCLUSIONS
The MART strategy of ICS-formoterol was associated with lower risk of AEx and reduced corticosteroid requirement.

Identifiants

pubmed: 35752435
pii: S2213-2198(22)00594-3
doi: 10.1016/j.jaip.2022.06.009
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Anti-Asthmatic Agents 0
Budesonide 51333-22-3
Ethanolamines 0
Formoterol Fumarate W34SHF8J2K

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2638-2645.e3

Informations de copyright

Copyright © 2022 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Chungsoo Kim (C)

Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon, South Korea.

Youngsoo Lee (Y)

Department of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea.

Eunyoung Lee (E)

Department of Biomedical Informatics, Ajou University School of Medicine, Suwon, South Korea; Office of Biostatistics, Medical Research Collaboration Center, Ajou Research Institute for Innovative Medicine, Ajou University Medical Center, Suwon, South Korea.

Seng Chan You (S)

Department of Preventive Medicine and Public Health, Yonsei University College of Medicine, Seoul, South Korea.

Jae-Hyuk Jang (JH)

Department of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea.

Rae Woong Park (RW)

Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon, South Korea; Department of Biomedical Informatics, Ajou University School of Medicine, Suwon, South Korea. Electronic address: veritas@ajou.ac.kr.

Hae-Sim Park (HS)

Department of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea. Electronic address: hspark@ajou.ac.kr.

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Classifications MeSH