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a 26Vo lower total serum IgE than men, which is surprising when asthma tends to be more<br />

prevalent in women in adulthood. <strong>The</strong>re was a lack <strong>of</strong> association between the prevalence <strong>of</strong><br />

atopy (defined as a positive response to any <strong>of</strong> the four specific allergens used in skin prick<br />

testing in all centres) and the geometric mean <strong>of</strong> total serum IgE. It is probable that the total<br />

and specific IgE are influenced differently and while raised IgE is associated both with atopy<br />

and with asthma, the relationship is not clear (Burney, Malmberg et al. 1997). Furthermore,<br />

IgE antibody production is T cell dependent, and the immune response to allergens can also<br />

include other immunoglobulins such as immunoglobulin Ga (IgG+) and immunoglobulin A<br />

(IgA) which may give further variations (Platts-Mills and Heyman 2006).It is true to say that<br />

if a child is thought to have bad asthma, but is non-atopic, then the search for an alternative<br />

diagnosis should be undertaken immediately.<br />

Pulmonary function tests have been one <strong>of</strong> the mainstays <strong>of</strong> assessing respiratory disease in<br />

older children and adults. A measurement in forced expiratory volume in I second (FEVI)<br />

alone can miss small airway obstruction in patients and the forced expiratory flow rate over<br />

25-75Vo <strong>of</strong> forced vital capacity (FEF25 -tsw) may well be a more sensitive indicator,<br />

particularly in children and/or in mild disease; however, the measurement may be very<br />

variable. Subjects can have a reduction in this parameter <strong>of</strong> more than two standard deviations<br />

below predicted norms even with no clinical symptoms (Kercsmar 2006). <strong>The</strong>re is a<br />

significant overlap with measurements between healthy children and those with episodes <strong>of</strong><br />

wheeze (if not current), and the diagnostic value <strong>of</strong> baseline lung function tests is generally<br />

thought to be poor (Dundas and McKenzie 2006). <strong>The</strong> guidelines suggest a test <strong>of</strong><br />

bronchodilator responsiveness for asthma either clinically and/or utilising improvement in<br />

lung function (usually FEVr) by an arbitrary amount, sometimes 157o. Despite this, the SIGN<br />

guideline states "a definitive diagnosis <strong>of</strong> asthma can be difficult to obtain in young children.<br />

It is <strong>of</strong>ten not possible to measure ainvay function in order to confirm the presence <strong>of</strong> variable<br />

airway obstruction" (SIGN 2005).<br />

<strong>The</strong> other option for possible diagnosis and monitoring <strong>of</strong> asthma is to use peak expiratory<br />

flow (PEF). This is defined as the largest expiratory flow achieved with a maximal forced<br />

effort from a position <strong>of</strong> maximum inspiration sustained for longer than l0 milliseconds<br />

(Wright and McKerrow 1959). PEF reflects a range <strong>of</strong> physiological characteristics including<br />

lung elastic recoil, large airway calibre and lung volume (Ruffin Z0O4). <strong>The</strong> original .peak<br />

Flow Meter' was pioneered by Martin Wright in 1959 (Wright and McKenow 1959) and is<br />

now supplanted by newer models but these have retained the advantages <strong>of</strong> the original in<br />

being low cost and easily portable. In the late 1970s the use <strong>of</strong> PEF recordings was first<br />

13

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