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1.
Sci Rep ; 8(1): 1418, 2018 01 23.
Artículo en Inglés | MEDLINE | ID: mdl-29362423

RESUMEN

In recent years, additive manufacturing has been evolving towards flexible substrates for the fabrication of printable electronic devices and circuits. Generally polymer-based, these emerging substrates suffer from their heat sensitivity and low glass-transition temperatures. As such they require new highly-localized sintering processes to treat the electronic inks without damaging the polymer-based substrate. Laser-based sintering techniques have shown great promises to achieve high-quality sintering locally, while controlling the heat penetration to preserve the polymer substrates integrity. In this report, we explore new optimization pathways for dynamic laser-based sintering of conductive silver inks. Multiple passes of a pulsed laser are first performed while varying pulse train frequencies and pulse energies as an attempt to optimize the properties of the silver inks. Then, time-domain pulse shaping is performed to alter the properties of the conductive inks. Together, these pathways allow for the careful control of the time-domain laser energy distribution in order to achieve the best electronic performances while preserving the substrate's integrity. Sheet resistance values as low as 0.024Ω/□ are achieved, which is comparable to conventional 1-hour oven annealing, with the processing time dramatically reduced to the milisecond range. These results are supported by finite element modeling of the laser-induced thermal dynamics.

2.
Nanoscale ; 9(28): 9893-9901, 2017 Jul 20.
Artículo en Inglés | MEDLINE | ID: mdl-28678235

RESUMEN

Graphene inks are becoming widely popular. However the vast majority of these inks are formulated in polar solvents with high-boiling points. Their slow evaporation is a bottleneck factor in roll-to-roll printing processes. Here, we developed a highly-conductive fast-drying graphene ink in isooctane, a non-polar and low-boiling solvent. For this purpose, a diblock copolymer containing pendant cholesterol groups was used during the exfoliation of natural graphite in isooctane. The polymer develops non-covalent supramolecular interactions with the graphene conjugated system, resulting in the formation of stable graphene dispersions (up to c = 4 mg mL-1). These dispersions were used for direct writing on a variety of substrates, and were shown to dry instantly after application. The influence of polymer concentration on graphene characteristics, on colloidal stability and on electrochemical characteristics has been studied. The lowest sheet resistance (80 Ω â–¡-1) was obtained when 23% of the graphene surface was covered by the polymer. In this case, the flakes were constituted of 2-5 graphene layers. More extensive exfoliation, down to single-layer graphene, was achieved at greater surface coverage, but led to inks with higher sheet resistance. Thus, by combining a tailored polymeric dispersant, a smooth exfoliation process and a low-boiling non-polar ink solvent, we were able to prepare highly-conductive fast-drying graphene inks which should have a high potentital for the development of roll-to-roll printed electronics.

3.
Clin Otolaryngol ; 35(6): 462-7, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21199406

RESUMEN

OBJECTIVES: To assess the correlation between acoustic rhinometry and visual analogue scale endpoints in the context of nasal challenge with occupational agents. DESIGN: Prospective controlled study. SETTING: University teaching hospital. PARTICIPANTS: Sixty-seven subjects with a history of work-related rhinitis and asthma symptoms. MAIN OUTCOMES MEASURES: Subjects underwent nasal challenge with control and specific agent on consecutive days. Nasal congestive response to challenge was monitored by acoustic rhinometry and visual analogue scale. RESULTS: Results showed no correlation between visual analogue scale and acoustic rhinometry measurements at baseline on the control (r=-0.13, P=0.3) and active (r=0.14, P=0.2) challenge days. No correlation was found between acoustic rhinometry and visual analogue scale when analysing all measurements obtained at all times after challenge with the control and active agent (control: r=0.09, P=0.04; active: r=0.001, P=0.9). The correlation between acoustic rhinometry and visual analogue scale was good and significant (r=-0.62, P=<0.01) when the analysis was restricted to cases showing a decrease in nasal volume>40% from baseline values. CONCLUSIONS: We showed that the correlation between acoustic rhinometry and subjective nasal patency was poor on steady conditions. However, a significant correlation was observed in those cases showing a greater nasal congestive response after challenge measured by acoustic rhinometry.


Asunto(s)
Pruebas de Provocación Nasal/métodos , Enfermedades Profesionales/diagnóstico , Exposición Profesional/efectos adversos , Rinitis/diagnóstico , Rinometría Acústica/métodos , Humanos , Estudios Prospectivos , Índice de Severidad de la Enfermedad
4.
Eur J Clin Nutr ; 64(2): 194-202, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19935818

RESUMEN

BACKGROUND/OBJECTIVES: To compare the effects of two dietary approaches on changes in dietary intakes and body weight: (1) an approach emphasizing nonrestrictive messages directed toward the inclusion of fruits and vegetables (HIFV) and (2) another approach using restrictive messages to limit high-fat foods (LOFAT). SUBJECTS/METHODS: A total of 68 overweight-obese postmenopausal women were randomly assigned to one of the two dietary approaches. The 6-month dietary intervention included three group sessions and ten individual sessions with a dietitian. Dietary food intake and anthropometric variables were measured at baseline, at 3 months and at 6 months. RESULTS: Energy density decreased in both groups after the intervention compared with baseline (HIFV, -0.3+/-0.2 kcal/g; LOFAT, -0.3+/-0.3 kcal/g; P<0.0001). Although body weight decreased significantly in both groups after the intervention compared with baseline (HIFV, -1.6+/-2.9 kg; LOFAT, -3.5+/-2.9 kg; P<0.0001), women in the LOFAT group lost significantly more body weight than women in the HIFV group (P=0.01). In the HIFV group, the decrease in energy density was found to be an independent predictor of body weight loss. CONCLUSIONS: The LOFAT approach induces more weight loss than does the HIFV approach in our sample of overweight-obese postmenopausal women.


Asunto(s)
Dieta Reductora , Ingestión de Energía , Promoción de la Salud/métodos , Obesidad/dietoterapia , Pérdida de Peso , Peso Corporal , Grasas de la Dieta/administración & dosificación , Femenino , Frutas , Humanos , Persona de Mediana Edad , Posmenopausia , Verduras
5.
Thorax ; 64(1): 50-4, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18835961

RESUMEN

BACKGROUND: The links between asthma and rhinitis are now referred to as united airways disease (UAD). Current evidence shows that the UAD model seems to be applicable to occupational rhinitis (OR) and occupational asthma (OA). A study was undertaken to objectively assess, in the context of specific inhalation challenge (SIC) testing, the concomitance of bronchial and nasal reaction in the investigation of OR and OA. METHODS: 43 subjects with a history of work-related asthma symptoms underwent SIC for confirmation of OA and investigation of OR. Changes in bronchial calibre were measured by spirometry and nasal patency and airway inflammation were assessed by acoustic rhinometry and nasal lavage. RESULTS: A positive nasal challenge was observed in 25 SIC tests and a positive bronchial challenge was observed in 17 SIC tests. A concomitant positive nasal and bronchial challenge was observed in 13 instances. This association was significant (risk ratio = 1.7; 95% CI 1.0 to 2.4; p = 0.04) and more frequent in subjects challenged with high molecular weight agents (n = 11/22) than with low molecular weight agents (n = 2/21). In subjects with a positive nasal challenge, nasal lavage showed a significant increase in eosinophils 30 min after exposure which correlated with changes in nasal patency. CONCLUSION: The results of this study provide objective evidence to support the concept of UAD using OR and OA as a model to demonstrate a significant concomitant physiological reaction of the nose and lungs after challenge. This study shows that OR can be assessed by objective means; it often coexists with OA but can be present without OA.


Asunto(s)
Asma/diagnóstico , Enfermedades Profesionales/diagnóstico , Rinitis/diagnóstico , Adulto , Femenino , Humanos , Masculino , Lavado Nasal (Proceso)/métodos , Rinometría Acústica/métodos
6.
Hum Gene Ther ; 12(13): 1673-80, 2001 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-11535170

RESUMEN

The enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT) expressed by the parasite Trypanosoma brucei (Tb) can convert allopurinol, a purine analogue, to corresponding nucleotides with greater efficiency than its human homologue. We have developed a retroviral system that expresses the parasitic enzyme and tested its capacity to activate the prodrug allopurinol to a cytotoxic metabolite. Cytotoxicity assays demonstrated that five non-small cell lung carcinoma cell lines transduced with the construct were sensitized to the prodrug by 2.1- to 7.6-fold compared with control values. This selectivity was not observed in seven other cell lines also expressing the construct, such as breast carcinoma. Assays indicated that enhanced cytotoxicity to allopurinol correlated with induction of apoptosis in lung cancer cells. The selectivity of this suicide gene was not explained either by the TbHGPRT expression or by the allopurinol accumulation. Our study shows that this novel system may represent a therapeutic tool for gene prodrug targeting of lung cancer, considering the fact that allopurinol is well tolerated in humans.


Asunto(s)
Genes Letales/genética , Terapia Genética/métodos , Hipoxantina Fosforribosiltransferasa/metabolismo , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/terapia , Trypanosoma brucei brucei/enzimología , Trypanosoma brucei brucei/genética , Alopurinol/metabolismo , Alopurinol/toxicidad , Animales , Apoptosis/efectos de los fármacos , Western Blotting , Neoplasias de la Mama/genética , Neoplasias de la Mama/metabolismo , Carcinoma de Pulmón de Células no Pequeñas/genética , Carcinoma de Pulmón de Células no Pequeñas/metabolismo , Carcinoma de Pulmón de Células no Pequeñas/patología , Carcinoma de Pulmón de Células no Pequeñas/terapia , Genes Protozoarios/genética , Humanos , Hipoxantina Fosforribosiltransferasa/genética , Hipoxantina Fosforribosiltransferasa/uso terapéutico , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/patología , Microscopía Fluorescente , Especificidad de Órganos , Profármacos/metabolismo , Factores de Tiempo , Transducción Genética , Células Tumorales Cultivadas , Virus de la Estomatitis Vesicular Indiana/genética
7.
J Allergy Clin Immunol ; 106(6): 1163-70, 2000 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11112901

RESUMEN

BACKGROUND: Little is known about the comparative kinetics of eosinophil recruitment after exposure to low- and high-molecular-weight sensitizers in subjects with occupational asthma (OA). OBJECTIVES: The aims of the study were to investigate the kinetics of changes in inflammatory mediators associated with eosinophil infiltration (IL-5 and eotaxin) and to examine the nature of the airway inflammation induced in response to different types of occupational agents. METHODS: We investigated 15 subjects with OA caused by high- and low-molecular-weight agents. The subjects were exposed to increasing doses of the relevant occupational agent over 3 to 4 days until a 20% fall in FEV(1) occurred. Methacholine challenge and sputum induction were performed at the end of each day of exposure. Sputum samples were assessed for differential cell counts, including eosinophils, IL-5, and eotaxin messenger RNA. RESULTS: There was an increase in sputum eosinophils, eotaxin, and IL-5 on the day preceding the occurrence of asthmatic reaction, although there was no change in functional parameters (FEV(1) and PC(20)). Increase in sputum eosinophils was more prominent in subjects exposed to low-molecular-weight agents than to high-molecular-weight agents. CONCLUSION: Changes in eosinophils, IL-5, and eotaxin precede functional changes after exposure to occupational agents in subjects with OA. Eosinophil inflammation is a feature of exposure to both high- and low-molecular-weight agents. Induced sputum may be a useful tool in the early diagnosis of OA.


Asunto(s)
Asma/fisiopatología , Hiperreactividad Bronquial/inmunología , Quimiocinas CC , Inflamación/inmunología , Exposición Profesional , Adulto , Quimiocina CCL11 , Factores Quimiotácticos Eosinófilos/análisis , Citocinas/análisis , Femenino , Humanos , Interleucina-5/análisis , Masculino , Persona de Mediana Edad , Peso Molecular , Exposición Profesional/estadística & datos numéricos , Esputo/química , Esputo/citología
8.
Am J Respir Crit Care Med ; 161(5): 1508-12, 2000 May.
Artículo en Inglés | MEDLINE | ID: mdl-10806146

RESUMEN

To determine whether specific immunological sensitization (SIS) and symptoms of allergy are associated with quitting apprenticeships with exposure to high-molecular-weight (HMW) agents. In a cohort study of 769 apprentices starting career programs in animal health technology (AHT), pastry-making (PM), and dental hygiene technology (DHT), health status was assessed at baseline and yearly for up to 44 mo. Subjects who quit the apprenticeship were contacted and offered a last series of measurements as if they pursued. The effect of various factors-at baseline and during the career program-on quitting was examined. Eighty-nine of 769 subjects (11.6%) quit, of whom 74 participated in this study. In multivariate analysis, a history of hay fever (OR = 1.66, 95% CI = 1.0 to 2.75) and attending the pastry-making program (OR = 2.33, 95% CI = 1.11 to 4.91) were significant determinants for quitting. In the subgroup of AHT, SIS to laboratory animals, hay fever, and shortness of breath were significant determinants by univariate analysis; in PM, the only determinant was age; and in DHT, hay fever. Work-related symptoms during training were not associated with quitting. In a multivariate logistic regression analysis in AHT, including characteristics at baseline and at follow-up, baseline SIS (OR = 2.8, 95% CI = 0.94 to 8.38) and symptoms of asthma in general during follow-up (OR = 2.2, 95% CI = 0.94 to 5.38) were the main determinants for quitting, though they were of borderline significance. We conclude that health-related self-selection out of an apprenticeship with exposure to HMW agents is likely to occur and to cause an attrition bias.


Asunto(s)
Alérgenos , Asma/inducido químicamente , Enfermedades Profesionales/inducido químicamente , Reorganización del Personal , Adulto , Técnicos de Animales , Asma/diagnóstico , Higienistas Dentales , Femenino , Manipulación de Alimentos , Humanos , Hipersensibilidad/diagnóstico , Hipersensibilidad/etiología , Masculino , Peso Molecular , Enfermedades Profesionales/diagnóstico , Exposición Profesional , Factores de Riesgo
9.
Vet Parasitol ; 82(4): 297-303, 1999 May.
Artículo en Inglés | MEDLINE | ID: mdl-10384905

RESUMEN

Two studies were conducted to determine the persistent efficacy of doramectin pour-on against an artificial, trickle challenge of mixed nematodes in calves. In each study, 42, 4-8 months old calves were randomly assigned into four groups of 10 animals each (T1-T4), plus two larval-viability monitor animals. All animals were treated with fenbendazole (10 mg kg(-1)) 14 days prior to the start of the study to clear any existing infection. Doramectin pour-on at 500 microg kg(-1) was used on each animal in Groups T2, T3, and T4 with intervals of 1 week (Day 0, 7, and 14, respectively). Calves in Group T1 were treated with saline solution on Day 0 and at the same volumetric rate (1 ml 10 kg(-1)) as the doramectin treated animals. All treatments were applied in a single passage along the midline of the back, from the withers to the tailhead. Subsequently, trickle inoculations with infective larvae were administered to all calves for 22 consecutive days (Days 14-35). Doramectin pour-on provided > or = 91.9% efficacy against challenge with Dictyocaulus viviparus, Haemonchus spp., and Ostertagia ostertagi for up to 35 days post-treatment and against challenge with Cooperia oncophora, Cooperia punctata, and Oesophagostomum radiatum for up to 28 days post-treatment.


Asunto(s)
Antihelmínticos/uso terapéutico , Enfermedades de los Bovinos/tratamiento farmacológico , Ivermectina/análogos & derivados , Nematodos/efectos de los fármacos , Infecciones por Nematodos/prevención & control , Infecciones por Nematodos/veterinaria , Abomaso/parasitología , Administración Tópica , Animales , Antihelmínticos/administración & dosificación , Antihelmínticos/normas , Bovinos , Enfermedades de los Bovinos/parasitología , Dictyocaulus/efectos de los fármacos , Femenino , Haemonchus/efectos de los fármacos , Intestino Grueso/parasitología , Intestino Delgado/parasitología , Ivermectina/administración & dosificación , Ivermectina/normas , Ivermectina/uso terapéutico , Pulmón/parasitología , Masculino , Infecciones por Nematodos/tratamiento farmacológico , Infecciones por Nematodos/parasitología , Oesophagostomum/efectos de los fármacos , Ostertagia/efectos de los fármacos , Distribución Aleatoria , Trichostrongyloidea/efectos de los fármacos
10.
Am J Respir Crit Care Med ; 158(3): 827-32, 1998 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9731012

RESUMEN

Peak expiratory flow (PEF) monitoring is often used to establish the relationship between occupational exposure and asthma. FEV1 has been found to be a better physiologic index than PEF in the measurement of airflow obstruction. The aim of this study was to compare the accuracy of serial monitoring of PEF and FEV1 in the diagnosis of occupational asthma. Twenty consecutive subjects referred for possible occupational asthma were asked to perform serial monitoring of PEF and FEV1 using a portable ventilometer. Two sets of graphs were plotted for both PEF and FEV1: graphs with the best of all values and graphs with the best of two reproducible values. Three observers interpreted both PEF and FEV1 recordings by the visual method in a blind, randomized manner as either compatible with occupational asthma or not. Eleven of the subjects had a positive inhalation challenge test (high-molecular-weight agents, n = 6; low-molecular-weight agents, n = 5). In the case of analysis of the graphs plotted with the best of all values, the sensitivity of the PEF recording interpreted by the three observers was 82, 73, and 73%, and of the FEV1 recording as 55, 55, and 45%; specificity of PEF recording was 89, 100, and 100%, and of FEV1 was 56, 89, and 100%. When an agreement between two of the three readers was required to define occupational asthma, sensitivity and specificity were 73 and 100% for PEF and 55 and 89% for FEV1. Lower sensitivities were found when the same analyses were performed with the graphs plotted with the best of two reproducible values. It was concluded that unsupervised FEV1 is not more accurate than unsupervised PEF monitoring in the diagnosis of occupational asthma. Plotting graphs using the best value gives better diagnostic accuracy than plotting them with the best of two reproducible values.


Asunto(s)
Asma/diagnóstico , Volumen Espiratorio Forzado/fisiología , Enfermedades Profesionales/diagnóstico , Ápice del Flujo Espiratorio/fisiología , Adulto , Obstrucción de las Vías Aéreas/diagnóstico , Obstrucción de las Vías Aéreas/fisiopatología , Asma/fisiopatología , Pruebas de Provocación Bronquial , Femenino , Humanos , Mediciones del Volumen Pulmonar/instrumentación , Masculino , Registros Médicos , Persona de Mediana Edad , Peso Molecular , Variaciones Dependientes del Observador , Enfermedades Profesionales/fisiopatología , Exposición Profesional , Valor Predictivo de las Pruebas , Reproducibilidad de los Resultados , Fármacos del Sistema Respiratorio , Sensibilidad y Especificidad , Método Simple Ciego
11.
Vet Parasitol ; 72(1): 25-31, 1997 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9403974

RESUMEN

A study was conducted to investigate reinfection with nematodes in calves following treatment with doramectin or ivermectin administered subcutaneously at a dose rate of 200 micrograms kg-1 of body weight under conditions of natural challenge. Thirty calves were allocated to three groups of 10 calves each based on body weight, sex, breed and pre-treatment faecal egg counts (FEC) after grazing together on a common pasture for three months. Treatments were doramectin, ivermectin and no treatment. Calves were returned to the same pasture for 56 days, placed on dry lot from days 56 to 63 and then necropsied over days 64-66. Faecal egg counts were done at days -1 and 0, then bi-weekly from day 14 to 56 and day 63. Mean FEC in control calves continued to rise throughout the grazing period. Trichostrongyle FEC were significantly (P < 0.05) greater in the control group compared to either treated group at each sample time following treatment. At necropsy, a total geometric mean of 19,847 nematodes per calf was recovered from untreated controls, of which eight genera were identified. The predominant nematode genera were Ostertagia (8749), Nematodirus (3702) and Cooperia (1927). In the ivermectin-treated calves, geometric mean worm burden was similar to that of the untreated controls: A total of 20,349 nematodes per calf was present including the genera Nematodirus (8633), Ostertagia (4700) and Cooperia (1740). In contrast, the geometric mean worm burden in doramectin-treated calves was 12,173, including Ostertagia (4310), Cooperia (1141) and Nematodirus (1667). Doramectin was more effective than ivermectin in protecting calves from reinfection over a 56-day post-treatment grazing period under conditions of natural challenge as measured by accumulated mean worm burdens.


Asunto(s)
Antihelmínticos/uso terapéutico , Enfermedades de los Bovinos , Ivermectina/análogos & derivados , Ivermectina/uso terapéutico , Infecciones por Nematodos/veterinaria , Animales , Bovinos , Heces/parasitología , Femenino , Larva , Masculino , Nematodos/aislamiento & purificación , Infecciones por Nematodos/tratamiento farmacológico , Infecciones por Nematodos/prevención & control , Ostertagiasis/tratamiento farmacológico , Ostertagiasis/prevención & control , Ostertagiasis/veterinaria , Recuento de Huevos de Parásitos , Recurrencia
12.
Eur Respir J ; 9(5): 880-5, 1996 May.
Artículo en Inglés | MEDLINE | ID: mdl-8793446

RESUMEN

Serial peak expiratory flow (PEF) assessment has been proposed in the clinical evaluation of asthma. In subjects attending the asthma clinic of a tertiary care hospital, we wanted to assess: 1) compliance in performing PEF; and 2) accuracy of a PEF-diary. Twenty adult asthmatic subjects, all using inhaled steroids, were asked to assess their PEF in the morning and evening with a VMX instrument (Clement Clarke Int., Colombus, OH, USA). This instrument, which incorporates a standard mini-Wright peak flow meter, stores PEF data on a computer chip. Subjects were not informed that the values were being stored. The mean duration of PEF monitoring was 89 days (range 44-131 days). For the total of 20 subjects, it was estimated that 3,482 values should have been written down and stored on the VMX computer chip. Whilst 1,897 values (54%) were written down, only 1,533 (44%) were stored, 425 values being invented. Morning and evening values were stored on 34% of days; and values were stored at least once a day on 55% of days. The values written down corresponded precisely to stored values 90% of the time, and were within +/- 20 L 94% of the time. We conclude that: 1) compliance with daily peak expiratory flow assessments is generally poor in chronic stable asthmatic subjects assessed on two visits separated by a 3 month period; and 2) a substantial percentage of values (22%) is invented. The unsatisfactory compliance with peak expiratory flow monitoring in this group of asthmatics on inhaled steroids underlines the need for similar studies on peak expiratory flow monitoring as part of an action treatment plan, and in more severe and brittle asthmatics.


Asunto(s)
Asma/tratamiento farmacológico , Monitoreo Fisiológico , Esteroides/uso terapéutico , Administración por Inhalación , Adulto , Asma/fisiopatología , Femenino , Humanos , Masculino , Registros Médicos , Persona de Mediana Edad , Monitoreo Fisiológico/métodos , Cooperación del Paciente , Ápice del Flujo Espiratorio , Pronóstico , Reproducibilidad de los Resultados , Esteroides/administración & dosificación
13.
Eur Respir J ; 9(3): 517-23, 1996 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8730013

RESUMEN

Fever is sometimes associated with asthmatic reactions following specific inhalation challenges with occupational agents. Our aims were to estimate the prevalence of fever in subjects with occupational asthma confirmed by specific inhalation challenge and to examine the characteristics and clinical correlates of subjects who develop fever on specific inhalation challenge. We performed a retrospective analysis of 317 subjects who had positive specific inhalation challenge to occupational agents and a comparison of subjects who developed fever after specific inhalation challenge with a random sample of those who did not. Fifteen subjects (5%) developed fever associated with positive specific inhalation challenge. They were compared with a random sample of 60 subjects who did not develop fever. The fever group: 1) showed a larger increase in absolute number of blood neutrophils, and a larger decrease both of blood lymphocytes and forced vital capacity after specific inhalation challenge; 2) included fewer atopics; 3) had been exposed more frequently to low rather than high molecular compounds; and 4) always experienced a late reaction and had more atypical reactions. We conclude that after positive specific inhalation challenge; fever occurs infrequently, and is associated with an increase in blood neutrophils and a decrease in blood lymphocytes and forced vital capacity. Such reactions seem more likely to occur in nonatopic subjects exposed to low molecular weight agents.


Asunto(s)
Asma/complicaciones , Asma/etiología , Fiebre/complicaciones , Leucocitosis/complicaciones , Exposición Profesional/efectos adversos , Adulto , Asma/fisiopatología , Pruebas de Provocación Bronquial , Femenino , Fiebre/etiología , Volumen Espiratorio Forzado , Humanos , Leucocitosis/etiología , Masculino , Persona de Mediana Edad , Enfermedades Profesionales/fisiopatología , Prevalencia , Pruebas de Función Respiratoria , Estudios Retrospectivos , Factores de Riesgo
14.
J Allergy Clin Immunol ; 96(5 Pt 1): 601-7, 1995 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-7499676

RESUMEN

BACKGROUND AND AIM: Serial assessment of peak expiratory flow (PEF) rates has been advocated as a sensitive and specific means of investigating occupational asthma. The possibility that, for several reasons, subjects do not accurately report their values has been raised. The availability of portable instruments that assess PEF and store timings and values now make it possible to estimate compliance and accuracy of results. METHODS: Twenty-one subjects consecutively investigated for occupational asthma were asked to assess their PEF every 2 hours during the day, both at work and away from work, with a VMX instrument (Clement Clarke International, Columbus, Ohio) and record the times and values on a sheet of paper. The subjects were not aware that the data were also being stored on a computer chip. The diagnosis was occupational asthma in eight subjects, personal asthma in four subjects, and neither condition in nine subjects. RESULTS: The mean duration of recording was 36 days (range, 14 to 79 days). At least 6048 values should have been recorded, but only 4839 (80%) were either recorded or stored. Reported values corresponded precisely to stored values in 2533 of 4839 recordings (52%). The timing of the recording was also examined in relation to the time at which the recording was solicited; values recorded within 1 hour of the solicited time were judged as acceptable. Of the total of 3342 recordings stored, 2375 (71%) satisfied this criterion. Compliance was significantly less satisfactory in those referred by the Workers' Compensation Board (n = 11). CONCLUSION: In this survey of 21 subjects investigated for possible occupational asthma, compliance with PEF recording, as assessed by comparing recorded and stored results and the time at which the recording was solicited, was poor.


Asunto(s)
Asma/diagnóstico , Enfermedades Profesionales/diagnóstico , Exposición Profesional , Adulto , Alérgenos/efectos adversos , Asma/etiología , Asma/fisiopatología , Femenino , Volumen Espiratorio Forzado , Humanos , Pulmón/fisiología , Masculino , Persona de Mediana Edad , Monitoreo Fisiológico , Enfermedades Profesionales/etiología , Enfermedades Profesionales/fisiopatología , Cooperación del Paciente , Ápice del Flujo Espiratorio/fisiología , Estudios Prospectivos , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
15.
Respir Med ; 89(8): 537-43, 1995 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-7480986

RESUMEN

The aim of this study was to compare the efficacy, compliance and side-effects of budesonide administered twice daily (b.d.) and four times a day (q.d.) with a Turbuhaler device in asthmatic subjects requiring < or = 1200 micrograms daily. The randomized, parallel group study design included a 2-week baseline period followed by a 6-12-month treatment period. Subjects were assessed at regular intervals in hospital through FEV1, PC20 methacholine, adrenal function and throat swabs. They were asked to record their symptoms and PEF values morning and evening at home. An asthmatic flare-up, which was the main outcome resulting in a patient's termination of the study, was defined beforehand as (a) 25% or greater diurnal variability in PEF for 2 consecutive days, and/or (b) nocturnal awakenings due to asthma symptoms 2 days or more in the same week and/or (c) an increase (doubling or more) in the need for inhaled bronchodilator 2 days in the same week. Fifty-eight adult asthmatic subjects (20 males and 38 females) entered the study, one-half being randomly assigned to the b.d. regimen and one half to the q.d. regimen. Fourteen subjects were on 400 micrograms, 15 subjects on 800 micrograms and 29 subjects on 1200 micrograms of budesonide daily. Seventeen flare-ups were recorded in the b.d. regimen group as opposed to 11 in the q.d. regimen (P = 0.05), significant differences being found in the 800 and 1200 micrograms groups (a total of 13 flare-ups in the b.d. group and eight flare-ups in the q.d. group for the two doses, P = 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Antiinflamatorios/administración & dosificación , Asma/tratamiento farmacológico , Pregnenodionas/administración & dosificación , Administración Tópica , Adulto , Antiinflamatorios/efectos adversos , Budesonida , Esquema de Medicación , Femenino , Glucocorticoides , Humanos , Masculino , Persona de Mediana Edad , Cooperación del Paciente , Pregnenodionas/efectos adversos
16.
Am J Respir Crit Care Med ; 150(6 Pt 1): 1697-701, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7952635

RESUMEN

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.


Asunto(s)
Asma/epidemiología , Polvo/efectos adversos , Enfermedades Profesionales/epidemiología , Madera , Adulto , Asma/diagnóstico , Asma/etiología , Femenino , Humanos , Masculino , Enfermedades Profesionales/diagnóstico , Enfermedades Profesionales/etiología , Prevalencia , Quebec/epidemiología , Pruebas de Función Respiratoria/estadística & datos numéricos , Encuestas y Cuestionarios
17.
J Allergy Clin Immunol ; 93(2): 437-45, 1994 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-8120271

RESUMEN

AIMS: The aims of the study conducted on lawn cutters were: (1) to evaluate exposure to pollens and molds; and (2) to assess the prevalence rate of IgE sensitization and symptoms in relation to exposure to pollens and molds. METHODS: Environmental assessment was done with the use of personal samplers on eight workers. Our population consisted of 181 municipal park workers, including 128 lawn cutters and 67 control subjects (blue-collar workers in the hospital). A questionnaire was administered, as well as skin prick tests with seven common inhalants including pollens and eight grass molds. The main outcome variables were grass or mold sensitization (at least one of eight molds) and work-related rhinitis, conjunctivitis, and rhinoconjunctivitis. Atopy and exposure to park-related allergens, as well as sensitization to grass pollens, were considered as explanatory factors. Smoking was taken into consideration as a covariant. Both presence and duration of occupational exposure to park-related allergens were considered as parameters of exposure. Duration of exposure (months x years of exposure as lawn cutters) was used as a continuous or as a categorical variable. RESULTS: Environmental monitoring showed that the concentration of pollens and molds decreased in magnitude from samples collected close to lawn cutters faces, short distance away in parks, and in the general environment. There was no difference in the prevalence rates for atopy between lawn cutters (32%) and control subjects (37%). Sensitization rates to grass pollen were also similar in lawn cutters (18%) and in control subjects (22%). However, there was a tendency for prevalence rates of sensitization to molds to be greater among lawn cutters (12% to Alternaria) compared with control subjects (5%). In the logistic model atopy was significantly related to grass sensitization (odds ratio [OR] = 7.2), mold sensitization (OR = 9.3), and sensitization to Alternaria (OR = 5.8). Grass sensitization was a significant risk factor for park-related rhinitis (OR = 5.8), conjunctivitis (OR = 5.0), and rhinoconjunctivitis (OR = 9.4). Exposure for 12 years or more was associated with rhinoconjunctivitis with an OR of 4.1 (95% confidence interval, 1.0-16.7). Smoking was not significantly related to any outcome. CONCLUSION: We conclude that among lawn cutters exposure to pollens and molds is higher than in the general population, atopy is the main determinant of sensitization to these aeroallergens, and sensitization and, to a much lesser extent, exposure to grass are determinants of symptoms.


Asunto(s)
Alérgenos , Hipersensibilidad/etiología , Inmunoglobulina E/metabolismo , Exposición Profesional , Adulto , Alérgenos/aislamiento & purificación , Femenino , Hongos/inmunología , Hongos/aislamiento & purificación , Humanos , Hipersensibilidad/inmunología , Hipersensibilidad Inmediata/etiología , Hipersensibilidad Inmediata/inmunología , Inmunización , Masculino , Persona de Mediana Edad , Enfermedades Profesionales/etiología , Enfermedades Profesionales/inmunología , Poaceae/inmunología , Polen/inmunología
19.
J Allergy Clin Immunol ; 91(3): 702-9, 1993 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8454792

RESUMEN

BACKGROUND: Various means of monitoring asthma severity have been proposed to reduce morbidity and mortality rates. We compared two means of assessing asthma flare-ups: monitoring peak expiratory flow rate (PEFR) and keeping a symptom diary. METHODS: This was a crossover randomized study. After a 2-week baseline period during which spirometry and PC20 methacholine were assessed, subjects were asked to record either PEFRs or to keep a symptom diary morning and evening for 6 months; a second baseline assessment separated the two periods. Subjects were asked to contact the study coordinator if the following occurred: (1) in the period of PEFR monitoring, daily fluctuations in PEFR were > 20% or the absolute value fell to < 80% of baseline or both occurred; (2) in the period of symptom diary monitoring there were nocturnal symptoms or a persistence of morning dyspnea after inhaled bronchodilator or a reduction in the duration of effect of the bronchodilator or it was impossible to go to work or school or all occurred. In that case they were asked to come to the hospital to confirm the flare-up through investigation for significant changes in FEV1 or PC20 or both. Forty subjects completed a 6-month symptom diary or PEFR recording period respectively, and 20 completed both. RESULTS: A total of 31 exacerbations were reported in 28 different subjects; three subjects had two flare-ups. Thirteen of 19 (69%) flare-ups were confirmed during the symptom diary period and 9 of 12 (75%) during PEFR monitoring. Nocturnal awakenings and morning falls in PEFR > or = 20% were the most frequent occurrences. CONCLUSIONS: We conclude that a simple symptom diary may be as useful as serial PEFR monitoring in documenting asthmatic flare-ups.


Asunto(s)
Asma/diagnóstico , Asma/terapia , Registros Médicos , Monitoreo Fisiológico , Ápice del Flujo Espiratorio , Adulto , Anciano , Pruebas de Provocación Bronquial , Femenino , Humanos , Masculino , Cloruro de Metacolina/administración & dosificación , Persona de Mediana Edad , Cooperación del Paciente , Método Simple Ciego , Espirometría
20.
Chest ; 103(3): 777-81, 1993 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8449068

RESUMEN

STUDY OBJECTIVE: The duration of action of several new non-sedative antihistamine preparations as assessed by skin and bronchial reactivity to histamine has still not been well established. The aim of the study was to evaluate the duration of effect of loratadine (10 mg) and terfenadine (120 mg) administered once a day for one week on cutaneous and inhaled reactivity to histamine by comparison with a placebo. SUBJECTS: Twenty-four adult asthmatic subjects were included in a parallel group study that compared the duration of effect of two antihistamines and a placebo on cutaneous and inhaled reactivity to histamine. STUDY DESIGN: Baseline cutaneous and inhaled reactivity (concentration causing a fall of 20 percent in FEV1 [PC20]) to histamine was obtained on three consecutive days. Loratadine (10 mg), terfenadine (120 mg) and a placebo loratadine were administered daily for 1 week to 3 groups of subjects. The PC20 was measured at the end of the medication period, 3 days later, and weekly until PC20 returned to baseline value (upper limit of 2 SD from the mean baseline value). RESULTS: The mean blocking duration on cutaneous reactivity for loratadine was 6.9 days and for terfenadine, 7.2 days. The mean duration of the blocking effect on PC20 histamine was 8.5 days for loratadine and 7.2 days for terfenadine. These figures were significantly longer than for the placebo. CONCLUSION: These data suggest that terfenadine and loratadine have a comparable blocking effect on reactivity to cutaneous and inhaled histamine. A daily dose taken for one week will result in a mean blocking effect of one week.


Asunto(s)
Broncoconstricción/efectos de los fármacos , Histamina/administración & dosificación , Loratadina/administración & dosificación , Piel/efectos de los fármacos , Terfenadina/administración & dosificación , Administración por Inhalación , Adulto , Anciano , Asma/tratamiento farmacológico , Asma/fisiopatología , Relación Dosis-Respuesta a Droga , Interacciones Farmacológicas , Femenino , Volumen Espiratorio Forzado/efectos de los fármacos , Histamina/farmacología , Humanos , Loratadina/farmacología , Masculino , Persona de Mediana Edad , Método Simple Ciego , Terfenadina/farmacología , Factores de Tiempo , Capacidad Vital/efectos de los fármacos
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