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1.
J Frailty Aging ; 6(1): 29-32, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28244555

RESUMEN

This study aimed to investigate a vulnerable population living in the context of poverty in a Brazilian municipality, in order to identify the factors that are associated with frailty syndrome in elderly people. From the total population living in the area, a random sample of 363 community-dwelling people, 60 years and older, age and gender-stratified, was selected to participate in the research. After losses, a sample of 304 older adults was classified as non-frail, pre-frail and frail. According to the Fried frailty criteria, the prevalence was 12.2% for non-frail individuals, 60.5% pre-frail and 27.3% frail. The main factors associated with frailty in the studied sample were low level of physical activity (OR: 5.2, 95%CI: 2.5-11.0), the occurrence of two or more falls within 12 months (OR: 3.1, 95%CI: 1.4-7.1), mobility deficits (OR: 3.0, 95%CI: 1.5-5.8), and depressive symptoms (OR: 1.9, 95%CI: 1.1-3.7). This study identified the most important factors that must be evaluated to identify frailty syndrome in a socially vulnerable population in the context of poverty. The data should help to encourage effective strategies concerning public health policies for this population.


Asunto(s)
Fragilidad , Pobreza/estadística & datos numéricos , Salud Pública , Factores Socioeconómicos , Anciano , Anciano de 80 o más Años , Brasil/epidemiología , Estudios Transversales , Femenino , Anciano Frágil/estadística & datos numéricos , Fragilidad/diagnóstico , Fragilidad/economía , Fragilidad/epidemiología , Evaluación Geriátrica/métodos , Humanos , Vida Independiente/normas , Vida Independiente/estadística & datos numéricos , Masculino , Evaluación de Necesidades , Prevalencia , Salud Pública/métodos , Salud Pública/normas
2.
Artículo en Inglés | MEDLINE | ID: mdl-18243822

RESUMEN

The comparison of two methods based on online solid phase extraction-liquid chromatography with UV (SPE-LC-UV) or mass spectrometry detection (SPE-LC-MS/MS) for the simultaneous quantification of sulfamethoxazole (SMZ) and trimethoprim (TMP) is presented. The methods were validated and proved to be accurate. The analysis of standard samples for SMZ at concentrations of 0.5, 1.5, 25 and 50microg/mL demonstrated a relative standard deviation of less than 6% for both methods (n=18), while TMP samples at concentrations of 0.05, 0.15, 1.5 and 5.0microg/mL were analyzed with R.S.D. of less than 4% (n=18). The method with mass spectrometric detection was approximately six times more sensitive than the method with ultraviolet detection. The total run time for the SPE-LC-MS/MS was 2.5min per sample as opposed to 18.0min for the SPE-LC-UV method. The method with MS detection in comparison with UV detection proved to be more rugged and was successfully applied to pharmacokinetics studies.


Asunto(s)
Antiinfecciosos/análisis , Combinación Trimetoprim y Sulfametoxazol/análisis , Adolescente , Adulto , Antiinfecciosos/farmacocinética , Química Farmacéutica , Cromatografía Líquida de Alta Presión , Estudios Cruzados , Femenino , Humanos , Indicadores y Reactivos , Masculino , Persona de Mediana Edad , Control de Calidad , Estándares de Referencia , Reproducibilidad de los Resultados , Espectrofotometría Ultravioleta , Espectrometría de Masas en Tándem , Equivalencia Terapéutica , Combinación Trimetoprim y Sulfametoxazol/farmacocinética
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