BACKGROUND:Delay in seeking care is a major impediment to effective management of tuberculosis (TB) in China. To elucidate factors that underpin patient and diagnostic delays in TB management, we conducted a systematic review and meta-analysis of factors that are associated with delays in TB care-seeking and diagnosis in the country.METHODS:This review was prepared following standard procedures of the Cochrane Collaboration and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement and checklist. Relevant studies published up to November 2012 were identified from three major international and Chinese literature databases: Medline/PubMed, EMBASE and CNKI (China National Knowledge Infrastructure).RESULTS:We included 29 studies involving 38,947 patients from 17 provinces in China. Qualitative analysis showed that key individual level determinants of delays included socio-demographic and economic factors, mostly poverty, rural residence, lack of health insurance, lower educational attainment, stigma and poor knowledge of TB. Health facility determinants included limited availability of resources to perform prompt diagnosis, lack of qualified health workers and geographical barriers.Quantitative meta-analysis indicated that living in rural areas was a risk factor for patient delays (pooled odds ratio (OR) (95% confidence interval (CI)): 1.79 (1.62, 1.98)) and diagnostic delays (pooled OR (95% CI): 1.40 (1.23, 1.59)). Female patients had higher risk of patient delay (pooled OR (95% CI): 1.94 (1.13, 3.33)). Low educational attainment (primary school and below) was also a risk factor for patient delay (pooled OR (95% CI): 2.14 (1.03, 4.47)). The practice of seeking care first from Traditional Chinese Medicine (TMC) providers was also identified as a risk factor for diagnostic delay (pooled OR (95% CI): 5.75 (3.03, 10.94)).CONCLUSION:Patient and diagnostic delays in TB care are mediated by individual and health facility factors. Population-based interventions that seek to reduce TB stigma and raise awareness about the benefits of early diagnosis and prompt treatment are needed. Policies that remove patients' financial barriers in access to TB care, and integration of the informal care sector into TB control in urban and rural settings are central factors in TB control.

Background: Endometriosis is a disease which, though it impacts one of ten women, has a lack of knowledge in the society and among healthcare professionals. The lack of knowledge causes delays in diagnosis and a lack of comprehension for the women. Aim: The aim of this study was to describe women's experiences of living with endometriosis. Method: The method used in this study was a method to contribute to evidence-based nursing with ground in analysis of qualitative research. Through the similarities and contradictions in the analyzed studies, themes and under-themes were created. Result: Findings showed that the women's experiences often were negative. Friends, family and healthcare professionals normalized the pain and the women often endured the pain in belief that it was normal. The lack of knowledge in endometriosis caused misdiagnosis and diagnostic delays. The endometriosis limited the women's daily living, work and social life by decreasing their activity because of symptoms as pain, nausea, fatigue, heavy bleeding and diarrhea. The disease also affected the women's relationships and the feeling of being a woman. Conclusion: The lack of knowledge in endometriosis caused an unnecessarily suffering among the women with the disease. If the awareness of endometriosis would increase in the society and among healthcare professionals the time for diagnosis and the encounters with patients suffering from endometriosis could improve.

Background: Historically the identification of ACL injuries upon initial presentation is low and considerable diagnostic delays have been reported. However, specific evidence on the individual elements of, and factors which influence delay, is lacking. Aims: The overarching aim was to provide a comprehensive picture of delay to diagnosis and specialist consultation, including factors which influence delay. An additional aim was to determine whether the approach to examining acute knee injuries varied as a consequence of varying patient presentation or experience of the assessing clinician. Methods: Study 1: Cross -sectional survey. Study 2: Non-participant direct observation methodology. Results: Data from 194 patients were analysed in the survey. Only 15.5% of patients were given a correct diagnosis of ACL rupture at the initial consultation. Median delay to diagnosis was 67.5 days (IQR= 15 to 178 days) and specialist consultation 108 days (IQR= 38 to 292 days). The factors most influential on delay were whether a follow-up appointment was arranged after attending A&E, whether the site of attendance operated an acute knee clinic and whether MRI was performed. The direct observation study showed wide variation in approach to injury assessment. Specialist clinicians performed the most comprehensive examination. A&E clinicians were more likely to assess for bony, neurovascular and gross tendon injuries as opposed to ligamentous or meniscal injury. Conclusions: The diagnostic rate of ACL injury at initial presentation remains low. Considerable delays to diagnosis and specialist consultation are apparent following ACL injury, the majority of which is attributable to health system delay.

Submitted by MARCIA ROVADOSCHI (marciar@unifra.br) on 2018-08-22T13:22:10Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_PaulaKielingRies.pdf: 3167125 bytes, checksum: 098524a661311a798864532206adad42 (MD5) / Made available in DSpace on 2018-08-22T13:22:10Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_PaulaKielingRies.pdf: 3167125 bytes, checksum: 098524a661311a798864532206adad42 (MD5) Previous issue date: 2017-06-08 / Childhood and adolescent cancer is a group of malignant diseases with a multifactorial origin that, despite the low incidence and despite advances in diagnosis and treatment, remains the second cause of infant mortality in developed countries aged from one to 14 years. Currently, early diagnosis is considered the best policy for improving prognosis and reducing treatment intensity. Knowing the factors related to the late diagnosis allows establishing strategies for early diagnosis of cancer in childhood and adolescence. Few studies related to this topic have been carried out in developing countries. Objectives: Report clinical and epidemiological data on cases of childhood and juvenile cancer, know the factors related to the late diagnosis of pediatric tumors; measure the intervals of the initial clinical presentation at diagnosis and treatment and correlate these intervals with larger clinical outcomes. Methods: A retrospective cohort study in which clinical and epidemiological data were collected from 198 patients aged zero to 18 years old, attended at a referral center in a public hospital in the central region of Rio Grande do Sul from January 2008 to December 2015. Results: Of the 198 patients, 56.1% were male, the age group with the highest frequency of diagnosis was from zero to four years. The most frequent diagnosis was leukemia, followed by lymphoma. Most of them, that is, 94.6% of the patients presented specific symptoms of the neoplasia, and yet 67.2% of the cases of solid tumors presented with locally invasive or metastatic disease. The median time for the diagnosis of 31 days, the delay of the parents was of 12 days and the one of the doctors was of six days. Tumor type was the only factor with relevance that interfered in time for the diagnosis (p <0.01). Event-free survival and overall 5-year survival were 73.6% and 80.9%, respectively. When comparing the survival curves for patients with late and non-late diagnosis, there was no significant difference (log-rank = 0.604). Conclusion: The time for diagnosis of childhood and juvenile neoplasms is among the lowest published. The results may reflect the parents difficulty in recognizing the signs and symptoms of childhood neoplasms, since the parents delay in seeking care is superior to that of the physicians in the oncologist. Corroborating, the great majority of patients have specific symptoms at diagnosis and yet they present with advanced disease, indicating the need for educational campaigns, familiarizing the population with the signs and symptoms of neoplasms. / O câncer infanto-juvenil é um grupo de doenças malignas com origem multifatorial que, apesar da baixa incidência e a despeito dos avanços obtidos no diagnóstico e tratamento, permanece como segunda causa de mortalidade infantil nos países desenvolvidos. Atualmente, considera-se o diagnóstico precoce como a melhor política para a melhora no prognóstico e redução da intensidade do tratamento. Conhecer os fatores relacionados ao diagnóstico tardio permite estabelecer estratégias para diagnóstico precoce do câncer na infância e adolescência. Poucos estudos relacionados a esse tema têm sido realizados em países em desenvolvimento. Objetivos: Relatar dados clínicos e epidemiológicos dos casos de câncer infanto-juvenil, conhecer os fatores relacionados ao diagnóstico tardio dos tumores pediátricos; mensurar os intervalos da apresentação clínica inicial ao diagnóstico e tratamento e correlacionar esses intervalos com desfechos clínicos maiores. Método: Estudo de coorte retrospectivo em que foram avaliados dados clínicos e epidemiológicos de 198 pacientes de zero a 18 anos, atendidos em um centro de referência de um hospital público da região central no Rio Grande do Sul, no período de janeiro de 2008 a dezembro de 2015. Resultados: Dos 198 pacientes, 56,1% pacientes eram do sexo masculino, a faixa etária com maior frequência de diagnóstico foi a de zero a quatro anos. O diagnóstico mais frequente foi o de leucemia, seguido pelo linfoma. A maioria, ou seja, 94,6% dos pacientes apresentaram sintomas específicos da neoplasia e, ainda assim, 67,2% dos casos de tumores sólidos apresentaram-se com doença localmente invasiva ou metastática. A mediana de tempo para o diagnóstico de 31 dias, a demora dos pais foi de 12 dias e a dos médicos foi de seis dias. O tipo de tumor foi o único fator com relevância que interferiu no tempo para o diagnóstico (p< 0,01). A sobrevida livre de eventos e a sobrevida global em cinco anos foram de 73,6% e 80,9%, respectivamente. Ao comparar as curvas de sobrevida dos pacientes com diagnóstico tardio e não tardio, não houve diferença significativa (log- rank = 0,604). Conclusão: O tempo para o diagnóstico das neoplasias infanto-juvenis está entre os menores publicados. Os resultados podem refletir a dificuldade dos pais em reconhecer os sinais e sintomas das neoplasias na infância, tendo em vista que a demora dos pais em procurar atendimento é superior à dos médicos em acionarem o oncologista. Corroborando, a grande maioria dos pacientes tem sintomas específicos ao diagnóstico e, mesmo assim, apresentam-se com doença avançada, indicando a necessidade de campanhas educativas, familiarizando a população quanto aos sinais e sintomas das neoplasias.

Background: Historically the identification of ACL injuries upon initial presentation is low and considerable diagnostic delays have been reported. However, specific evidence on the individual elements of, and factors which influence delay, is lacking. Aims: The overarching aim was to provide a comprehensive picture of delay to diagnosis and specialist consultation, including factors which influence delay. An additional aim was to determine whether the approach to examining acute knee injuries varied as a consequence of varying patient presentation or experience of the assessing clinician. Methods: Study 1: Cross -sectional survey. Study 2: Non-participant direct observation methodology. Results: Data from 194 patients were analysed in the survey. Only 15.5% of patients were given a correct diagnosis of ACL rupture at the initial consultation. Median delay to diagnosis was 67.5 days (IQR= 15 to 178 days) and specialist consultation 108 days (IQR= 38 to 292 days). The factors most influential on delay were whether a follow-up appointment was arranged after attending A&E, whether the site of attendance operated an acute knee clinic and whether MRI was performed. The direct observation study showed wide variation in approach to injury assessment. Specialist clinicians performed the most comprehensive examination. A&E clinicians were more likely to assess for bony, neurovascular and gross tendon injuries as opposed to ligamentous or meniscal injury. Conclusions: The diagnostic rate of ACL injury at initial presentation remains low. Considerable delays to diagnosis and specialist consultation are apparent following ACL injury, the majority of which is attributable to health system delay.

Le facteur le plus important de pronostic de l'asthme professionnel (AP) est la durée des symptômes avant le retrait de lʼexposition à lʼagent causant lʼAP. La qualité de vie réduite, la détresse psychologique et les maladies psychiatriques sont des conditions souvent associées à l'AP. Notre objectif était d'identifier les facteurs, incluant le statut socioéconomique, qui ont une influence sur lʼintervalle de temps nécessaire pour présenter une requête à une agence médicolégale à la suite de lʼapparition de symptômes dʼasthme et de confirmer qu'un tel délai est associé à un moins bon pronostic respiratoire et à des coûts directs plus élevés. En outre, nous avons examiné la relation entre les variables cliniques et socio-économiques dʼune part et leur influence sur les facteurs psychologiques et économiques dʼautre part chez des travailleurs atteints d'AP. Ensuite, nous avons voulu évaluer si les individus souffrant de détresse psychologique (DP) et de morbidité psychiatrique pourraient être identifiés en utilisant un instrument mesurant la qualité de vie (QV). Lʼétude a été effectuée auprès dʼindividus ayant déposé des demandes d'indemnisation pourʼAP auprès du Commission de la sécurité et de la santé du travail du Québec (CSST). Les données ont été recueillies au moment de la réévaluation, soit environ deux ans et demi après le diagnostic. Outre la collecte des marqueurs cliniques de l'asthme, les individus ont été soumis à une évaluation générale de leur histoire sociodémographique et médicale, à une brève entrevue psychiatrique (évaluation des soins primaires des troubles mentaux, PRIME-MD) et à un ensemble de questionnaires, incluant le Questionnaire sur la qualité de vie - AQLQ(S), le Questionnaire respiratoire de St. George (SGRQ) et le Psychiatric Symptom Index (PSI).Soixante personnes ont été incluses dans l'étude. Etre plus âgé, avoir un revenu supérieur à 30 000$ CA etêtre atteint dʼAP dû à un allergène de haut poids moléculaire ont une association positive avec le nombre dʼannées dʼexposition avec symptômes avant le retrait. Au cours de la période de suivi, le nombre dʼannées dʼexposition avec symptômes était plus grand chez les individus ayant une hyperréactivité bronchique persistante. Par ailleurs, la présence de symptômes au poste de travail pendant moins d'un an est associée à une réduction des coûts directs. Les paramètres de QV et de DP avaient des corrélations modérées avec les marqueurs cliniques de lʼAP. Les plus fortes associations avec ces variables ont pu être observées dans les cas de la sévérité de l'asthme, des statuts dʼemploi et matrimonial, du revenu et de la durée de la période de travail avec l'employeur. Un seuil de 5,1 au niveau de la sous-échelle de la fonction émotionnelle de lʼAQLQ(S) sʼest avéré avoir la meilleure valeur discriminante pour distinguer les individus avec ou sans détresse psychiatrique cliniquement significative selon le PSI. Nous avons été en mesure d'identifier les variables socio-économiques associées à un intervalle plus long dʼexposition professionnelle en présence de symptômes dʼasthme. De même, une plus longue période d'exposition a été associée à un moins bon pronostic de la maladie et à des coûts de compensation plus élevés. Ces résultats s'avèrent utiles pour la surveillance de lʼAP qui pourrait cibler ces sous-groupes d'individus. La QV et la PS sont fréquemment réduites chez les individus atteints d'AP qui perçoivent une compensation. Elles sont associées à des marqueurs cliniques de lʼasthme et à des facteurs socio-économiques. En outre, nos résultats suggèrent que le questionnaire de lʼAQLQ(S) peut être utilisé pour identifier les individus avec un niveau de détresse psychologique potentiellement significatif. / The most important factor in the prognosis of occupational asthma (OA) is the length of exposure with symptoms prior to removal from exposure. Impaired quality of life, psychological distress and psychiatric disease are conditions frequently associated with OA. Our goal was to identify factors, including socio-economic status, that can influence the delay in submitting a claim to a medicolegal agency after the onset of asthmatic symptoms, and to confirm that such a delay is associated with a worse respiratory prognosis and higher direct costs. Further, we examined the association between clinical and socio-economic variables and their influence on psychological and cost outcomes in individuals with OA. Next, we wanted to evaluate whether individuals with clinically significant psychological distress (PD) and psychiatric morbidity could be identified by using a quality of life (QOL) measurement instrument. This is a study of individuals who filed claims for compensation for occupational asthma from the Workersʼ Compensation Board of Quebec (the CSST). Data were collected at re-evaluation, approximately two and a half years after diagnosis. Besides collecting clinical markers of asthma, individuals underwent a general socio-demographic and medical history evaluation, a brief psychiatric interview (Primary Care Evaluation of Mental Disorders, PRIME-MD) and completed a battery of questionnaires, including the Asthma Quality of Life Questionnaire - AQLQ(S), the St. Georgeʼs Respiratory Questionnaire (SGRQ), and the Psychiatric Symptoms Index (PSI). Sixty individuals were included in the study. Being older, having a revenue of >$30,000 Can. (CAD$) and having OA due to high- molecular- weight agents were all positively associated with the number of years of exposure with symptoms before removal from exposure. Individuals with persistent airway hyperresponsiveness at follow-up had a higher number of years with symptoms. Experiencing symptoms in the workplace for less than one year generated lower direct costs. QOL and PD parameters had moderate correlations with clinical markers of OA. Asthma severity, employment and marital status, income and length of employment with the employer showed the strongest associations with QOL and PD. More impaired QOL was associated with higher direct costs for compensation. A cut-off of 5.1 on the AQLQ(S) emotional function subscale had the best discriminative value to distinguish individuals with or without clinically significant psychological distress according to the PSI. We were able to identify socio-economic variables that were associated with a longer interval during which individuals remained symptomatic in the workplace before being removed from exposure. This longer exposure time was associated with worse disease outcomes and higher compensation costs. These findings could prove to be useful in surveillance programs that could be preferentially targeted for these subgroups of individuals. Impaired QOL and PD are frequent among individuals with OA receiving compensation and are associated with clinical markers of OA and socio-economic factors. Further, our findings suggest that the AQLQ(S) questionnaire could be used to identify individuals with potentially clinically significant levels of psychological distress.

L’objectif de cette thèse était d’étudier la distribution, les déterminants et les conséquences des délais diagnostiques des cancers de l’enfant, par une revue systématique de la littérature, une analyse des plaintes déposées en France et au Canada et par des études ad hoc en population sur les tumeurs ayant des délais particulièrement longs : le médulloblastome et le sarcome d’Ewing.La revue systématique n’a pas retrouvé de diminution significative de la longueur des délais au cours du temps. Les délais longs étaient associés à un âge élevé, au type histologique et à la localisation de la tumeur. Les relations entre délai et gravité de la maladie étaient variables. Seul un tiers des conclusions des expertises judiciaires (n = 56) étaient concordantes avec les données de la littérature.Le délai diagnostique médian des enfants atteints de médulloblastome en Ile-de-France (n = 166) était de 65 jours. Les délais longs étaient associés paradoxalement à des métastases moins fréquentes et à une histologie favorable, mais pas à la survie ni aux séquelles.Le délai diagnostique médian des enfants atteints de sarcome d’Ewing en France (n = 436) était de 70 jours. Les délais longs, liés à un âge élevé et à la localisation de la tumeur, n’étaient pas associés au volume tumoral, à la présence de métastases, à l’opérabilité ni à la survie.Pour certaines tumeurs, une association entre délais diagnostiques et gravité est établie (rétinoblastome) ou hautement probable. Pour d’autres, l’absence d’association démontrée permettrait de dédramatiser la perception de leurs conséquences, sans dispenser d’essayer de réduire ces délais, notamment pour en atténuer les conséquences psychologiques. / The aim of this thesis was to study the distribution, determinants and consequences of time to diagnosis of cancer in children, through a systematic review of the literature and an analysis of lawsuits in France and Canada, and two population-based studies of tumors with particularly long diagnosis delays: medulloblastoma and Ewing sarcoma.The systematic review did not identify any significant decreases in time to diagnosis during the studies. Long times to diagnosis were associated with older age, histological type and location of the tumor. Associations between time to diagnosis and severity of the disease varied. Only a third of the court-appointed experts (n = 56) provided testimony concordant with the available medical literature.The median time to diagnosis of children with medulloblastoma in the area of Paris (n = 166) was 65 days. Diagnosis delays were paradoxically associated with less frequent metastasis and favorable histology, but not with survival, or sequelae.The median time to diagnosis of children with Ewing sarcoma in France (n = 436) was 70 days. Diagnosis delays, related with older age and tumor location, were not associated with tumor size, presence of metastasis, surgical outcome, or survival.For some tumors, an association between time to diagnosis and severity of the disease is well established (e.g. retinoblastoma), or highly probable. For others, the lack of demonstrated associations could tone down the perception of the supposed consequences of diagnosis delays - but does not exempt from trying to reduce them, in order to alleviate their psychological consequences.

Le facteur le plus important de pronostic de l'asthme professionnel (AP) est la durée des symptômes avant le retrait de lʼexposition à lʼagent causant lʼAP. La qualité de vie réduite, la détresse psychologique et les maladies psychiatriques sont des conditions souvent associées à l'AP. Notre objectif était d'identifier les facteurs, incluant le statut socioéconomique, qui ont une influence sur lʼintervalle de temps nécessaire pour présenter une requête à une agence médicolégale à la suite de lʼapparition de symptômes dʼasthme et de confirmer qu'un tel délai est associé à un moins bon pronostic respiratoire et à des coûts directs plus élevés. En outre, nous avons examiné la relation entre les variables cliniques et socio-économiques dʼune part et leur influence sur les facteurs psychologiques et économiques dʼautre part chez des travailleurs atteints d'AP. Ensuite, nous avons voulu évaluer si les individus souffrant de détresse psychologique (DP) et de morbidité psychiatrique pourraient être identifiés en utilisant un instrument mesurant la qualité de vie (QV). Lʼétude a été effectuée auprès dʼindividus ayant déposé des demandes d'indemnisation pourʼAP auprès du Commission de la sécurité et de la santé du travail du Québec (CSST). Les données ont été recueillies au moment de la réévaluation, soit environ deux ans et demi après le diagnostic. Outre la collecte des marqueurs cliniques de l'asthme, les individus ont été soumis à une évaluation générale de leur histoire sociodémographique et médicale, à une brève entrevue psychiatrique (évaluation des soins primaires des troubles mentaux, PRIME-MD) et à un ensemble de questionnaires, incluant le Questionnaire sur la qualité de vie - AQLQ(S), le Questionnaire respiratoire de St. George (SGRQ) et le Psychiatric Symptom Index (PSI).Soixante personnes ont été incluses dans l'étude. Etre plus âgé, avoir un revenu supérieur à 30 000$ CA etêtre atteint dʼAP dû à un allergène de haut poids moléculaire ont une association positive avec le nombre dʼannées dʼexposition avec symptômes avant le retrait. Au cours de la période de suivi, le nombre dʼannées dʼexposition avec symptômes était plus grand chez les individus ayant une hyperréactivité bronchique persistante. Par ailleurs, la présence de symptômes au poste de travail pendant moins d'un an est associée à une réduction des coûts directs. Les paramètres de QV et de DP avaient des corrélations modérées avec les marqueurs cliniques de lʼAP. Les plus fortes associations avec ces variables ont pu être observées dans les cas de la sévérité de l'asthme, des statuts dʼemploi et matrimonial, du revenu et de la durée de la période de travail avec l'employeur. Un seuil de 5,1 au niveau de la sous-échelle de la fonction émotionnelle de lʼAQLQ(S) sʼest avéré avoir la meilleure valeur discriminante pour distinguer les individus avec ou sans détresse psychiatrique cliniquement significative selon le PSI. Nous avons été en mesure d'identifier les variables socio-économiques associées à un intervalle plus long dʼexposition professionnelle en présence de symptômes dʼasthme. De même, une plus longue période d'exposition a été associée à un moins bon pronostic de la maladie et à des coûts de compensation plus élevés. Ces résultats s'avèrent utiles pour la surveillance de lʼAP qui pourrait cibler ces sous-groupes d'individus. La QV et la PS sont fréquemment réduites chez les individus atteints d'AP qui perçoivent une compensation. Elles sont associées à des marqueurs cliniques de lʼasthme et à des facteurs socio-économiques. En outre, nos résultats suggèrent que le questionnaire de lʼAQLQ(S) peut être utilisé pour identifier les individus avec un niveau de détresse psychologique potentiellement significatif. / The most important factor in the prognosis of occupational asthma (OA) is the length of exposure with symptoms prior to removal from exposure. Impaired quality of life, psychological distress and psychiatric disease are conditions frequently associated with OA. Our goal was to identify factors, including socio-economic status, that can influence the delay in submitting a claim to a medicolegal agency after the onset of asthmatic symptoms, and to confirm that such a delay is associated with a worse respiratory prognosis and higher direct costs. Further, we examined the association between clinical and socio-economic variables and their influence on psychological and cost outcomes in individuals with OA. Next, we wanted to evaluate whether individuals with clinically significant psychological distress (PD) and psychiatric morbidity could be identified by using a quality of life (QOL) measurement instrument. This is a study of individuals who filed claims for compensation for occupational asthma from the Workersʼ Compensation Board of Quebec (the CSST). Data were collected at re-evaluation, approximately two and a half years after diagnosis. Besides collecting clinical markers of asthma, individuals underwent a general socio-demographic and medical history evaluation, a brief psychiatric interview (Primary Care Evaluation of Mental Disorders, PRIME-MD) and completed a battery of questionnaires, including the Asthma Quality of Life Questionnaire - AQLQ(S), the St. Georgeʼs Respiratory Questionnaire (SGRQ), and the Psychiatric Symptoms Index (PSI). Sixty individuals were included in the study. Being older, having a revenue of >$30,000 Can. (CAD$) and having OA due to high- molecular- weight agents were all positively associated with the number of years of exposure with symptoms before removal from exposure. Individuals with persistent airway hyperresponsiveness at follow-up had a higher number of years with symptoms. Experiencing symptoms in the workplace for less than one year generated lower direct costs. QOL and PD parameters had moderate correlations with clinical markers of OA. Asthma severity, employment and marital status, income and length of employment with the employer showed the strongest associations with QOL and PD. More impaired QOL was associated with higher direct costs for compensation. A cut-off of 5.1 on the AQLQ(S) emotional function subscale had the best discriminative value to distinguish individuals with or without clinically significant psychological distress according to the PSI. We were able to identify socio-economic variables that were associated with a longer interval during which individuals remained symptomatic in the workplace before being removed from exposure. This longer exposure time was associated with worse disease outcomes and higher compensation costs. These findings could prove to be useful in surveillance programs that could be preferentially targeted for these subgroups of individuals. Impaired QOL and PD are frequent among individuals with OA receiving compensation and are associated with clinical markers of OA and socio-economic factors. Further, our findings suggest that the AQLQ(S) questionnaire could be used to identify individuals with potentially clinically significant levels of psychological distress.