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Background: The Juniper Asthma Specific Quality of Life Questionnaire (AQLQ(S)) is a questionnaire that allows measurement of disease specific quality of life. We wanted to examine correlations between the (AQLQ(S)) general and different subscale scores and both psychiatric morbidity and levels of psychological distress in individuals with occupational asthma (OA) and to determine if results in the emotional function subscale allow identification of individuals with clinically significant psychological distress or current psychiatric disorders., Methods: This was a cross-sectional study of individuals with OA who were assessed during a re-evaluation for permanent disability, after they were no longer exposed to the sensitizing agent. Patients underwent a general sociodemographic and medical history evaluation, a brief psychiatric interview (Primary Care Evaluation of Mental Disorders, PRIME-MD) and completed a battery of questionnaires including the AQLQ(S), the St-Georges Respiratory Questionnaire (SGRQ), and the Psychiatric Symptom Index (PSI)., Results: There was good internal consistency (Cronbach alpha = 0.936 for the AQLQ(S) total score) and construct validity for the AQLQ(S) (Spearman rho = -0.693 for the SGRQ symptom score and rho = -0.650 for the asthma severity score). There were medium to large correlations between the total score of the AQLQ(S) and the SGRQ symptom score (r = -.693), and PSI total (r = -.619) and subscale scores (including depression, r = -.419; anxiety, r = -.664; anger, r = -.367; cognitive disturbances, r = -.419). A cut-off of 5.1 on the AQLQ(S) emotional function subscale (where 0 = high impairment and 7 = no impairment) had the best discriminative value to distinguish individuals with or without clinically significant psychiatric distress according to the PSI, and a cut-off of 4.7 best distinguished individuals with or without a current psychiatric disorder according to the PRIME-MD., Conclusions: Impaired quality of life is associated with psychological distress and psychiatric disorders in individuals with OA. Findings suggest that the AQLQ(S) questionnaire may be used to identify patients with potentially clinically significant levels of psychological distress.

We assessed the prevalence of occupational asthma among current (n = 29/31, 94%) and former (n = 13/49, 27%) employees of a sawmill in which eastern white cedar has been made into shingles during the past 3 yr. All participants answered a respiratory questionnaire, and all except one underwent spirometry and methacholine inhalation tests. All those with bronchial hyperresponsiveness (PC20 methacholine < or = 19 mg/ml) were invited to undergo specific inhalation challenges. Mean duration of exposure was 13 mo (19 workers > 12 mo). Twenty-eight workers (65%) reported a history compatible with asthma, and 25 (58%) had symptoms that were suggestive of occupational asthma. Only two subjects had significant airway obstruction (FEV1 < 80% pred) (mean value = 98% pred). Eighteen subjects (42%) had a PC20 < or = 16 mg/ml. Specific inhalation tests with plicatic acid and/or western red cedar (which contains twice as much plicatic acid as eastern white cedar), were done on 12 subjects who had a PC20 < or = 16 mg/ml when they were assessed. Three subjects were considered to have positive tests (one had an isolated immediate reaction, one had a late reaction, and one had significant changes in PC20 each time he was exposed but no changes in FEV1). Environmental monitoring showed concentrations of total dusts above 2 mg/m3 in half of the samples. The prevalence of occupational asthma in this workplace was three of 42 participants (7%) or at least three of 80 (3.8%) of all current or ex-workers. This is comparable to the prevalence of occupational asthma in subjects exposed to western red cedar.

Repeated exposure to chlorine in pulp mills and paper can induce persistent asthma-like symptoms such as bronchial hyperresponsiveness and variable changes in airway caliber. The long-term time course of bronchial hyperresponsiveness has not been examined. We studied 20 of 29 subjects (69% participation rate) who demonstrated bronchial hyperresponsiveness to methacholine when they were first assessed, 18 to 24 mo after repeatedly inhaling "puffs" of high concentrations of chlorine in a paper mill over a 3-mo period. Each subject answered a respiratory questionnaire and underwent spirometry and a methacholine inhalation test 12 mo after the initial survey, 30 to 36 mo after the chlorine inhalations. Three subjects required inhaled steroids at the time of the initial survey and three at the time of the second, including two who carried on using these preparations. Only one subject changed smoking habits. There were no significant overall changes in FEV1 on the two occasions, nine subjects having a FEV1 < 80% on the first occasion and eight on the second. Six of the 18 subjects (33%) who underwent a methacholine inhalation test on both occasions had significantly improved PC20 results, including five for whom the PC20 value was within the normal range. All six subjects had normal FEV1 values on both assessments. Although changes in spirometry induced by repeated exposure to chlorine seem to persist, bronchial hyperresponsiveness can improve significantly in those with normal airway caliber. This suggests that less pronounced bronchial alterations induced by repeated exposures to chlorine may be reversible.