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So is induced sputum in adults and children safe? Particularly those with asthma? In 34<br />

asthmatic and normal subjects, a mean fall in FEVr <strong>of</strong> 5.3Vo was seen, but with a maximum <strong>of</strong><br />

20Vo (Pin, Gibson et al. 1992). Pre-treatment with a 9z agonist did not prevent<br />

bronchoconstriction in all the asthmatic subjects, especially in those with a baseline low FEVr<br />

(Wong and Fahy t997). Such pre{reatment in mild asthmatics resulted in an unchanged<br />

FEV1, but with a reduction observed in the normal subjects (Thomas, Yates et al. 1999). One<br />

group also documented that an overuse <strong>of</strong> F, agonists the day before sputum induction<br />

reduced the protective effect <strong>of</strong> the pre-medication (Pizzichini, Pizzichini et al. 1997). While<br />

samples were successfully obtained even in subjects with 'difficult to control' asthma, severe<br />

bronchoconstriction occurred in22Vo with development <strong>of</strong> symptoms and a reduction in FEVr<br />

<strong>of</strong> > l1%o (ten Brinke, de Lange et al. 2001). Another study noted that the procedure had to be<br />

stopped because <strong>of</strong> side effects in l2Vo overall and in 17-l8%o <strong>of</strong> those with severe asthma (de<br />

la Fuente, Romagnoli et al. 1998). When performed as part <strong>of</strong> their routine clinical visit, the<br />

procedure was well tolerated in over 300 asthmatics, even among those with more severe<br />

respiratory obstruction with an FEVr down to 60Vo predicted or one litre. However in patients<br />

with a baseline FEVr between 4OVo and 59Vo, there was a mean 8Vo reduction in FEVr and in<br />

patients with a baseline FEVr <strong>of</strong> < 40Vo predicted, 6Vo fellby 2OVo (Vlachos-Mayer, Leigh et<br />

al. 2000). A decrease in arterial oxygen saturations <strong>of</strong> 6Vo in asthmatic patients, 5.3Vo in<br />

smokers and 67o in healthy subjects has been reported suggesting that patients needed<br />

monitoring during this procedure (Castagnaro, Chetta et al. 1999).<br />

Reviewing the safety in children; in 53 sputum induction alone was tolerated in 98Vo, with<br />

94Vo completing the procedure,92To providing an adequate sample but 4Vo experienced a<br />

>l1vo fall in FEVr (Jones, Hankin et al. 2001). In 182 children who had combined sputum<br />

induction and bronchial provocation testing using hypertonic saline, the procedure was<br />

completed by 90Vo with a distressing cough in l3%o and mucosal irritation with wheeze in IVo<br />

and fewer, 70Vo, successful samples obtained. So while the two investigations can be<br />

combined, this was less well tolerated and resulted in less sampling success (Jones, Hankin et<br />

al. 2001). In 40 children with a baseline FEVr > 65Vo predicted, seven (l8vo) had symptoms<br />

<strong>of</strong> shortness <strong>of</strong> breath and wheezing and <strong>of</strong> these three (8Vo) had a significant fall in FEVr <strong>of</strong><br />

greater than 2O7o despite pre-treatment with a bronchodilator (Lex, Payne et al. 2005).In the<br />

CAMP study, nine (87o) <strong>of</strong> 117 children with mild to moderate asthma developed significant<br />

bronchospasm requiring treatment (Covar, Spahn et aI.2004).<br />

40

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