Minimum respiratory function for breath alcohol testing in South Australia.

The aim of this study was to determine if inability to complete a breath alcohol test successfully, using a Lion Alcolmeter SD-2 or Drager Alcotest 7110, was related to any of the standard parameters obtained from the lung function spirometry test. A total of 153 subjects referred to a clinical laboratory for routine lung function testing were tested using the Alcolmeter, 158 using the Alcotest, with 69 subjects completing tests on both instruments. Of the 153 patients who volunteered to use the Alcolmeter, 49 (32%) were unable to produce a valid test effort on this instrument. One subject failed to complete a satisfactory test using the Alcotest, and one was unable to master the technique. There was considerable overlap of the minimum value for each of the lung function parameters of those subjects who could or could not successfully complete the breath alcohol test. It is recommended that changes are made to both of the instruments, the techniques used and the legislation, to minimize the number of breath alcohol testing failures and to reduce the variability of the results.

Longitudinal study of near fatal asthma.

The effect of careful follow-up and treatment modification for 45 patients with an admission for NFA has been studied. In 24 of 45, inciting events were recognized. BDP was used by 14 patients pre-NFA. In the mean follow-up of 863 days, there have been no deaths and seven patients have been readmitted with asthma. Six of the 45 patients have attained normal FEV1 and PC20H. Blunted perception of breathlessness, change in VAS ratio/change in FEV1, was found when first measured, but normalized to be no different than that of other asthmatic subjects as airway responsiveness became milder. The CO2 ventilatory responses did not differentiate individual NFA patients from non-NFA asthmatic or normal subjects. Comparison of the NFA cohort with the 1985 asthma admission cohort showed that an asthma admission within the last five years was a risk factor for a NFA episode.

Bronchial hyperresponsiveness in two populations of South Australian rural schoolchildren.

This report describes the cross-sectional analyses of the results obtained from the first year of a longitudinal study designed to investigate the natural history of bronchial hyperresponsiveness in association with reported respiratory symptoms in children attending the Burra and Kingston Community Schools. Bronchial hyperresponsiveness to methacholine was measured using a modified Yan technique. Prevalence rates of respiratory symptoms were obtained using the Tasmanian Asthma Foundation Questionnaire. Considerable overlap of reported symptoms of asthma and/or wheezy breathing and bronchitis and/or loose and productive cough was observed suggesting that a clear distinction between such symptoms in childhood may not be possible. Analyses of data showed the prevalence of reactive airways in children to be 21.3% in Burra and 22.0% in Kingston. These values were the same as results obtained from an earlier pilot study in Burra and similar to results from Wagga Wagga (19.6%) and Auckland (20.1%) but higher than from Belmont (15.5%) and Villawood (15.3%). Increased bronchial hyperresponsiveness was associated with the reporting of symptoms of asthma and/or wheezy breathing (odds ratio, 5.04; 95% confidence interval, 2.18-11.74) and bronchitis and/or loose and productive cough (odds ratio, 2.28; 95% confidence interval, 1.02-5.13), at any time in the child's life. Of children with no reported symptoms 10% also had demonstrable bronchial hyperresponsiveness.

Biochemical studies of N-methyltransferase in human and guinea-pig lung: no apparent role in the pathogenesis of asthma.

1. N-Methyltransferase activity was measured in surgical specimens of human lung using phenylethanolamine as substrate. Thirty-three male and seven female patients, age range 19-78 (median 62.5) years were studied. The activity in lung homogenates was 0.59 x 10(-6) units/mg of protein (SEM 0.03, n = 40), with a range of 0.16-1.16 x 10(-6) units/mg of protein. There was no difference (P = 0.97) in activity between males and females. 2. Non-specific N-methyltransferase activity was estimated in 17 of the surgical specimens using beta-phenylethylamine as substrate. This activity was 38.9% (SEM 5.3) of that with phenylethanolamine. Comparative studies with rabbit lung, which has a well-characterized non-specific N-methyltransferase, showed significant differences in substrate specificity between the two species. 3. The apparent Km and Vmax for phenylethanolamine in seven human lung homogenates was 22.0 (SEM 4.6).mmol/l and 1.82 x 10(-6) units/mg of protein (SEM 0.36). The noradrenaline N-methyltransferase (NMT; EC 2.1.1.28) inhibitors SKF 64139-A and LY 134046 did not inhibit this activity up to a concentration of 100 mumol/l. This activity was inhibited 51.4% (SEM 8.6, n = 6) by 100 mumol/l S-adenosyl-L-homocysteine. Immunohistochemistry did not reveal immunoreactive NMT in human lung sections. 4. Comparative studies with guinea-pig lung homogenates demonstrated non-specific N-methyltransferase activity in this species which is similar to the human lung.(ABSTRACT TRUNCATED AT 250 WORDS)

The prevalence rate of respiratory symptoms in school children from two South Australian rural communities.

The respiratory symptoms and respiratory function of 680 schoolchildren from two rural area of South Australia were studied. The initial results of this prospective, longitudinal study showed that the cumulative prevalence of asthma and/or wheezy breathing was 27.4% in the Burra population and 23.1% in the Kingston population. The cumulative prevalence of one or more attacks of asthma/wheezy breathing amongst Burra (38.8%) and Kingston (23%) children aged up to 8 years was significantly higher than that reported for urban Melbourne children (11%, p less than 0.01). The combined South Australian group reported a cumulative prevalence of asthma/wheezy breathing alone of 10% which was significantly higher than the cumulative prevalence rates in three previous studies reported in Australia (1.8%, 2.6%, 2.7%, p less than 0.01). The highest overall cumulative prevalence of bronchitis/loose or productive cough occurred in the 12 year old Burra children (41.5%). Burra girls had the highest prevalence of bronchitis/loose or productive cough (36.8%) compared to other groups studied at both locations. The parental smoking rate (60.4% in Burra, 57.4% in Kingston) is much higher than the national figure reported by the Bureau of Statistics in 1977 (35.9%). The prevalence of asthma/wheezy breathing is much higher in the South Australian cohort compared to the Queensland and Tasmanian cohorts studied using the same questionnaire. Predicted respiratory function parameters using initial algorithms are similar to those reported for urban Australian children.