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Association of Dose of Inhaled Corticosteroids and Frequency of Adverse Events.
Bloom, Chloë I; Yang, Freda; Hubbard, Richard; Majeed, Azeem; Wedzicha, Jadwiga A.
Affiliation
  • Bloom CI; Imperial College London, National Heart and Lung Institute, London, United Kingdom of Great Britain and Northern Ireland; chloe.bloom06@imperial.ac.uk.
  • Yang F; Imperial College London, National Heart and Lung Institute, London, United Kingdom of Great Britain and Northern Ireland.
  • Hubbard R; Nottingham University, Nottingham, United Kingdom of Great Britain and Northern Ireland.
  • Majeed A; Imperial College London, School of Public Health, London, United Kingdom of Great Britain and Northern Ireland.
  • Wedzicha JA; Imperial College London, National Heart and Lung Institute, London, United Kingdom of Great Britain and Northern Ireland.
Article in En | MEDLINE | ID: mdl-39088770
ABSTRACT

BACKGROUND:

Inhaled corticosteroids (ICS) are the cornerstone of asthma treatment and significantly improve morbidity and mortality. Adverse effects of oral corticosteroids are well documented, but less is known about ICS.

METHODS:

We conducted observational studies in adults with asthma using two different UK nationwide datasets Clinical Practice Research Datalink (CPRD) Aurum and CPRD GOLD. The exposure was incident ICS; the outcomes were major adverse cardiac events (MACE), arrhythmia, pulmonary embolism (PE) and pneumonia over 12-months. Our main analyses used a cohort method with stabilized inverse probability treatment weighting to balance confounding between exposed and unexposed patients. Secondary analyses included nested case-control studies, and self-controlled case series. ICS was treated both as a categorical and continuous variable. Absolute risk was estimated using weighted flexible parametric models.

FINDINGS:

From 162,202 patients in our main cohort, there was an association with all outcomes at medium daily ICS dose or higher (HR, 95%CI at 201-599mcg MACE=2.63, 1.66-4.15, arrhythmia=2.21, 1.60-3.04, PE=2.10, 1.37-3.22, pneumonia=2.25, 1.77-2.85; at ≥600mcg MACE=4.63, 2.62-8.17, arrhythmia=2.91, 1.72-4.91, PE=3.32, 1.69-6.50, pneumonia=4.09, 2.98-5.60). There were no associations with lower doses of ICS. Secondary analyses produced similar results. The number needed to harm (95%CI) using 12-months of ICS 201-599mcg MACE=473 (344-754), arrhythmia=567 (395-1006), PE=1221 (744-3388) and pneumonia=230 (177-327) and using ICS ≥600mcg MACE=224 (148-461), arrhythmia=396 (228-1523), PE=577 (309-4311), pneumonia=93 (69-141).

INTERPRETATION:

Short-term use of low dose ICS was not associated with adverse effects. Moderate-high daily ICS doses were associated with an increased risk, but low-frequency, of cardiovascular events, pulmonary embolism and pneumonia. It is important for clinicians to adhere to guideline recommendations to use the lowest effective ICS dose. This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License (https//creativecommons.org/licenses/by/4.0/).
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Full text: 1 Database: MEDLINE Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2024 Type: Article