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Real-world association between systemic corticosteroid exposure and complications in US patients with severe asthma.
Casale, Thomas B; Corbridge, Thomas; Germain, Guillaume; Laliberté, François; MacKnight, Sean D; Boudreau, Julien; Duh, Mei S; Deb, Arijita.
Afiliação
  • Casale TB; Division of Allergy/Immunology, University of South Florida, Tampa, FL, USA.
  • Corbridge T; US Medical Affairs, GSK, Durham, NC, USA.
  • Germain G; Health Economics and Outcomes Research, Groupe d'analyse, Montréal, QC, Canada.
  • Laliberté F; Health Economics and Outcomes Research, Groupe d'analyse, Montréal, QC, Canada.
  • MacKnight SD; Health Economics and Outcomes Research, Groupe d'analyse, Montréal, QC, Canada.
  • Boudreau J; Health Economics and Outcomes Research, Groupe d'analyse, Montréal, QC, Canada.
  • Duh MS; Health Economics and Outcomes Research, Analysis Group Inc, Boston, MA, USA.
  • Deb A; Value Evidence and Outcomes, GSK, Upper Providence, PA, USA. arijita.x.deb@gsk.com.
Allergy Asthma Clin Immunol ; 20(1): 25, 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38532489
ABSTRACT

BACKGROUND:

Systemic corticosteroid (SCS) use remains widespread among patients with severe asthma, despite associated complications.

OBJECTIVE:

Evaluate the association between cumulative SCS exposure and SCS-related complications in severe asthma.

METHODS:

This retrospective, longitudinal study used claims data from the Optum Clinformatics Data Mart database (GSK ID 214469). Eligible patients (≥ 12 years old) had an asthma diagnosis and were divided into two cohorts SCS use and non/burst-SCS use. Patients in the SCS use cohort had a claim for a daily prednisone-equivalent dose ≥ 5 mg SCS following ≥ 6 months of continuous SCS use; those in the non/burst-SCS cohort had no evidence of continuous SCS use and had a non-SCS controller/rescue medication initiation claim. For each cohort, the date of the qualifying claim was the index date. SCS users were further stratified by SCS use during each quarter of follow-up low (≤ 6 mg/day), medium (> 6-12 mg/day), high (> 12 mg/day), and continuous high (≥ 20 mg/day for 90 days). SCS-related complications were evaluated in the quarter following SCS exposure. The adjusted odds ratios (OR) of experiencing SCS-related complications during follow-up in each of the SCS use groups versus the non/burst SCS cohort were calculated using generalized estimating equations models.

RESULTS:

SCS and non/burst-SCS use cohorts included 7473 and 89,281 patients (mean follow-up 24.6 and 24.2 months), respectively. Compared with the non/burst-SCS use cohort, medium, high, and continuous high SCS use was associated with greater odds of any SCS-related complication (adjusted OR [95% confidence interval] 1.30 [1.21, 1.39], 1.49 [1.35, 1.64] and 1.63 [1.40, 1.89], respectively) including increased acute gastrointestinal, cardiovascular, and immune system-related complications, and chronic cardiovascular, metabolic/endocrine, central nervous system, bone-/muscle-related, ophthalmologic, and hematologic/oncologic complications. Low-dose SCS use was also associated with significantly increased odds of acute gastrointestinal and immune system-related complications, and chronic bone-/muscle-related and hematologic/oncologic complications versus the non/burst-SCS use cohort.

CONCLUSION:

SCS use, even at low doses, is associated with increased risk of SCS-related complications among patients with severe asthma.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article