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1.
J Environ Health ; 74(9): 22-8, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-22590848

RESUMEN

Most occupational and environmental research describes associations between specific occupational and environmental hazards and health outcomes, with little information available on population-level exposure, especially among unique subpopulations. The authors describe the prevalence of self-reported lifetime exposure to nine occupational and environmental hazards among 11,326 American Indian and Alaska Native (AI/AN) adults enrolled in the Education and Research Towards Health (EARTH) Study in the Southwest U.S. and Alaska. The top three hazards experienced by AI/AN people in Alaska were petroleum products, military chemicals, and asbestos. The top three hazards experienced by AI/AN living in the Southwest U.S. were pesticides, petroleum, and welding/silversmithing. The study described here found that male sex, lower educational attainment, AI/AN language use, and living in the Southwest U.S. (vs. Alaska) were all associated with an increased likelihood of hazard exposure. The authors' study provides baseline data to facilitate future exposure-response analyses. Future studies should measure dose and duration as well as environmental hazards that occur in community settings.


Asunto(s)
Exposición a Riesgos Ambientales/estadística & datos numéricos , Sustancias Peligrosas/envenenamiento , Exposición Profesional/estadística & datos numéricos , Adolescente , Adulto , Alaska/epidemiología , Amianto/envenenamiento , Liberación de Peligros Químicos/estadística & datos numéricos , Femenino , Humanos , Indígenas Norteamericanos , Masculino , Persona de Mediana Edad , Plaguicidas/envenenamiento , Petróleo/toxicidad , Plata , Sudoeste de Estados Unidos/epidemiología , Soldadura , Adulto Joven
2.
Otolaryngol Head Neck Surg ; 137(6): 918-24, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18036421

RESUMEN

OBJECTIVE: Seasonal allergic rhinitis (SAR) is a highly prevalent disease. This study was conducted to evaluate the onset and duration of action of three concentrations of olopatadine nasal spray. METHODS: This was a randomized, double-blind, single-dose, placebo-controlled study, conducted in an environmental exposure chamber in patients with SAR. A total of 320 patients were exposed to ragweed allergen in the chamber and randomized to olopatadine nasal spray 0.2%, 0.4%, 0.6%, or placebo nasal spray. Symptoms (sneezing, runny, itchy, and stuffy nose) were self-assessed during a 12-hour study period. RESULTS: All concentrations of olopatadine nasal spray provided clinically meaningful reductions in total nasal symptom scores at 30 minutes compared to the placebo. Olopatadine nasal spray 0.6% was significantly more effective (P < 0.05) than placebo nasal spray at all time-points starting at 90 minutes post-dose and continuing over 12 hours. CONCLUSIONS: Olopatadine nasal spray 0.6% demonstrated a fast onset of action and maintained an effect for at least 12 hours after dosing.


Asunto(s)
Antialérgicos/administración & dosificación , Dibenzoxepinas/administración & dosificación , Rinitis Alérgica Estacional/prevención & control , Administración Intranasal , Adolescente , Adulto , Aerosoles , Anciano , Alérgenos/efectos adversos , Ambrosia/efectos adversos , Método Doble Ciego , Ambiente Controlado , Exposición a Riesgos Ambientales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Clorhidrato de Olopatadina , Satisfacción del Paciente , Placebos , Polen/efectos adversos , Rinitis Alérgica Estacional/clasificación , Seguridad , Factores de Tiempo , Resultado del Tratamiento
3.
Ann Allergy Asthma Immunol ; 95(5): 474-9, 2005 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-16312171

RESUMEN

BACKGROUND: A nasal spray containing the antiallergy agent olopatadine hydrochloride is being developed for the treatment of seasonal allergic rhinitis (SAR) to mountain cedar. OBJECTIVE: To evaluate the safety and efficacy of 2 concentrations of olopatadine nasal spray vs placebo nasal spray in patients with SAR to mountain cedar. METHODS: This was a multicenter, randomized, double-blind, placebo-controlled study. After a 3- to 21-day placebo run-in, 677 patients aged 12 to 81 years were randomized to receive 0.4% or 0.6% olopatadine or placebo, 2 sprays per nostril twice daily for 2 weeks. Patients evaluated morning and evening reflective and instantaneous nasal symptoms (sneezing, stuffy nose, runny nose, and itchy nose, which compose the total nasal symptom score [TNSS]) and ocular symptoms. RESULTS: Olopatadine spray (0.4% and 0.6%) was statistically significantly superior to placebo for percentage change from baseline in overall reflective and instantaneous TNSSs. Also, 0.6% olopatadine was statistically significantly superior to placebo for reducing the reflective and instantaneous assessments of sneezing, runny nose, itchy nose, stuffy nose, itchy eyes, and watery eyes. Olopatadine spray exhibited a safety profile comparable with that of placebo. CONCLUSIONS: Olopatadine nasal spray (0.4% and 0.6%) provided statistically significant improvements in allergic rhinitis symptoms compared with placebo regarding TNSSs and individual symptoms, including congestion, itchy and runny nose, sneezing, and itchy and watery eyes, in patients with SAR to mountain cedar. Olopatadine nasal spray administered twice daily was safe and well tolerated in adolescents and adults.


Asunto(s)
Administración por Inhalación , Dibenzoxepinas/uso terapéutico , Juniperus/inmunología , Rinitis Alérgica Estacional/tratamiento farmacológico , Resultado del Tratamiento , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Antialérgicos/efectos adversos , Antialérgicos/uso terapéutico , Niño , Demografía , Dibenzoxepinas/efectos adversos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Clorhidrato de Olopatadina
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