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Paediatric asthma
P83 Is a single intramuscular dose of triamcinolone and acute bronchodilator sufficient to determine optimal lung function in children with severe therapy resistant asthma?
  1. N Cartledge,
  2. S Brown,
  3. C Bossley,
  4. A Gupta,
  5. L Fleming,
  6. S Saglani,
  7. A Bush
  1. Department of Respiratory Paediatrics, Imperial College of Science, Technology and Medicine at the Royal Brompton Hospital and National Heart and Lung Institute, London, UK

Abstract

Background A small proportion of patients with long standing severe asthma develop irreversible airway obstruction (persistent airflow limitation (PAL)). There is no agreed definition of PAL in children, but pragmatically, most would define it as post steroid, post-bronchodilator FEV1 percent predicted <80% or Z score less than −1.96, with normative data from appropriate reference populations despite optimal therapy. However, there is no agreement on the dose, duration or route of administration of steroids to determine the optimal spirometry that a child can achieve.

Hypothesis A single intramuscular dose of triamcinolone and acute bronchodilator are insufficient to determine optimal lung function and reliably diagnose PAL. The aim of this study was to determine whether forced expired volume in 1 second (FEV1) 2–4 weeks after a single dose of triamcinolone and acute bronchodilator administration reflect the best obtained in the following year in patients with severe, therapy resistant asthma.

Patients and Methods 39 children age 5–16 received triamcinolone; the FEV1 was measured before the treatment, after triamcinolone and during the 12-month period. The highest follow-up FEV1 was compared with post-steroid post-post-bronchodilator FEV1.

Results In the year following the 1st dose of triamcinolone 25 (64%) of 39 patients exceeded their immediate post-steroid trial target lung function by >9% predicted. 13 out of 39 patients (33.3%) achieved FEV1 of >80% predicted at the 1st follow-up. If the diagnosis of PAL had been made just on the steroid trial, 16 patients would have been wrongly given this label; only 10 children were ultimately diagnosed with PAL. 13 of 39 patients received multiple (2–4) doses in 4 weeks intervals and only in 9 of them only the data was analysable. In this small group, the median and interquartile range of FEV1 were significantly higher (75 vs 68 and 38.75 vs 17) following the 3rd dose of triamcinolone than after the 1st.

Conclusion Reliance on a single dose of triamcinolone plus acute administration of ß-2 agonist will lead to an overdiagnosis of PAL in children with severe asthma.

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