ABSTRACT
Oral corticosteroids are powerful relatively nonspecific antiinflammatory agents with
a range of well-characterized side effects. There is good evidence to show that they
accelerate the rate of resolution of exacerbations of COPD and relapse is less likely
if patients receive these drugs. Maintenance therapy with oral preparations is associated
with worse mortality and skeletal muscle myopathy is a particular problem.
Corticosteroids have little effect on biopsy proven inflammation or its surrogates
in COPD and did not change the rate of decline of FEV1 over a range of spirometric disease severity in a number of trials each lasting 3
years. However, meta-analysis of the data suggests that a small effect (up to 10ml
/year) might be present. There is more consistent evidence for an effect on postbronchodilator
FEV1 with both fluticasone propionate and budesonide. In patients with a postbronchodilator
FEV1 < 50% predicted where self-reported exacerbations become more common, inhaled corticosteroids
can reduce the number of attacks. This effect is the major factor accounting for the
reduction in deterioration in health status seen in patients who receive inhaled corticosteroids.
Inhaled corticosteroids are much safer than oral therapy, although they do have a
predictably higher incidence of candidiasis and hoarseness of the voice. Skin bruising
is seen in patients with better lung function who use these drugs. Triamcinolone use
is associated with reduction in bone density but this was not seen with budesonide.
Combining an inhaled corticosteroid and a long-acting beta-agonist in the same inhaler
increases the efficacy of the latte drug in COPD patients, with a significantly larger
improvement in FEV1, a larger reduction in reported breathlessness, and a reduction in exacerbation numbers
in those with severe disease where beta-agonists appear to be less effective. Inhaled
corticosteroids are not suitable for monotherapy in COPD but can be helpfully combined
with an inhaled bronchodilator in patients with symptomatic disease.
KEYWORDS
Chronic obstructive pulmonary disease - corticosteroid - exacerbation - lung function
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Peter M. A CalverleyM.D.
Department of Medicine, Clinical Sciences Centre
University Hospital Aintree, Liverpool L9 7AL, UK
Email: pmacal@liverpool.ac.uk