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asthmatics at 8.6 microns, in 'cough variant asthmatic' subjects at7.l microns and both were<br />

significantly different than healthy controls at 5.0 microns (Niimi, Matsumoto et al. 2000).<br />

Others are less enthusiastic for this diagnostic category -<br />

given that cough is a very corlmon<br />

symptom. A diagnosis <strong>of</strong> cough variant asthma could result in a significant increased number<br />

<strong>of</strong> children being treated' "Isolated chronic cough in children is rarely asthma, and the term<br />

'cough-variant-asthma' should not be used" (Chang, Landau et al. 2006). Wheezing reported<br />

by children had a very good discriminating ability for asthma whereas cough less so in over<br />

1600 school children aged 8-12 years (Yu, Wong et aI.2004). In asthmatic children who had<br />

cough as a predominant symptom, the cough occurred early and heralded the onset <strong>of</strong> an<br />

exacerbation. Asthma scores did relate to cough scores, although neither cough receptor<br />

sensitivity nor cough scores related to any specific inflammatory marker (Chang, Harrhy et al.<br />

2002). In 1245 children 6-12 years <strong>of</strong> age comparing symptoms <strong>of</strong> persistent cough with<br />

symptoms <strong>of</strong> wheeze, the former had less demonstrable atopy and less morbidity. <strong>The</strong> authors<br />

concluded that while 'cough variant asthma' was not shown, there remained a significant<br />

number <strong>of</strong> children with persistent cough diagnosed and treated as having asthma @aniran,<br />

Peat et al. 1999). So in the presence <strong>of</strong> persistent cough, if history, examination, chest x-ray<br />

and spirometry are normal, the cough could be regarded as non-specific and the child<br />

regarded as in the category <strong>of</strong> 'normal', as opposed to heralding a morbid or pre-morbid<br />

condition (Chang and Powell 1998; Bush 2002).<br />

Finally, treatment trials for cough using inhaled corticosteroids (IHCS) (Dicpinigaitis 2006;<br />

Matsumoto, Niimi et aL.2006) and a leukotriene receptor antagonist (Spector and Tan 2004)<br />

showed an improvement in symptoms. However the natural history <strong>of</strong> post-viral cough is that<br />

most will have resolved in 3-4 weeks and only l\Vo will continue for more than 25 days, with<br />

gradual resolution. Improvement could therefore have erroneously been attributed to<br />

treatment. <strong>The</strong> Cochrane Systematic Review <strong>of</strong> the efficacy <strong>of</strong> IHCS for non-specific cough<br />

in children > two years <strong>of</strong> age evaluated two trials enrolling a total <strong>of</strong> 123 children. <strong>The</strong> first<br />

trial using beclomethasone dipropionate 4o0ltglday (metered dose inhaler via a spacer) found<br />

no difference from placebo in reducing cough frequency measured objectively or scored<br />

subjectively. <strong>The</strong> second trial using fluticasone propionate 2mglday for three days followed<br />

by I mg/day for 1l days (metered dose inhaler via a spacer) showed a significant<br />

improvement in nocturnal cough frequency after two weeks, but also with a significant<br />

(though smaller) improvement with placebo (Tomerak, McGlashan et al. 2005). <strong>The</strong>re was no<br />

difference between the use <strong>of</strong> inhaled salbutamol and placebo (Tomerak, Vyas et al. 2005) or<br />

ll

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