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1.
Prev Med ; 71: 31-6, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25514548

RESUMEN

OBJECTIVE: Interactive voice response (IVR) systems offer great advantages for data collection in large, geographically dispersed samples involving frequent contact. We assessed the quality of IVR data collected from older respondents participating in a statewide falls prevention program evaluation in Pennsylvania in 2010-12. METHOD: Participants (n=1834) were followed up monthly for up to 10 months to compare respondents who completed all, some, or no assessments in the IVR system. Validity was assessed by examining IVR-reported falls incidence relative to baseline in-person self-report and performance assessment of balance. RESULTS: While a third of the sample switched from IVR to in-person calls over follow-up, IVR interviews were successfully used to complete 68.1% of completed monthly assessments (10,511/15,430). Switching to in-person interviews was not associated with measures of participant function or cognition. Both self-reported (p<.0001) and performance assessment of balance (p=.05) at baseline were related to falls incidence. CONCLUSION: IVR is a productive modality for falls research among older adults. Future research should establish what level of initial personal research contact is optimal for boosting IVR completion rates and what research domains are most appropriate for this kind of contact.


Asunto(s)
Accidentes por Caídas/prevención & control , Entrevistas como Asunto/métodos , Software de Reconocimiento del Habla , Accidentes por Caídas/estadística & datos numéricos , Anciano , Anciano de 80 o más Años , Recolección de Datos/métodos , Femenino , Estudios de Seguimiento , Promoción de la Salud , Humanos , Entrevistas como Asunto/normas , Masculino , Persona de Mediana Edad , Pennsylvania/epidemiología , Equilibrio Postural , Factores de Riesgo , Software de Reconocimiento del Habla/estadística & datos numéricos , Teléfono
2.
BMC Nephrol ; 15: 29, 2014 Feb 06.
Artículo en Inglés | MEDLINE | ID: mdl-24502751

RESUMEN

BACKGROUND: Many patients on maintenance dialysis experience significant sleepiness and fatigue. However, the influence of the hemodialysis (HD) day and circadian rhythms on patients' symptoms have not been well characterized. We sought to use ecological momentary assessment to evaluate day-to-day and diurnal variability of fatigue, sleepiness, exhaustion and related symptoms in thrice-weekly maintenance HD patients. METHODS: Subjects used a modified cellular phone to access an interactive voice response system that administered the Daytime Insomnia Symptom Scale (DISS). The DISS assessed subjective vitality, mood, and alertness through 19 questions using 7- point Likert scales. Subjects completed the DISS 4 times daily for 7 consecutive days. Factor analysis was conducted and a mean composite score of fatigue-sleepiness-exhaustion was created. Linear mixed regression models (LMM) were used to examine the association of time of day, dialysis day and fatigue, sleepiness, and exhaustion composite scores. RESULTS: The 55 participants completed 1,252 of 1,540 (81%) possible assessments over the 7 day period. Multiple symptoms related to mood (e.g., feeling sad, feeling tense), cognition (e.g., difficulty concentrating), and fatigue (e.g., exhaustion, feeling sleepy) demonstrated significant daily and diurnal variation, with higher overall symptom scores noted on hemodialysis days and later in the day. In factor analysis, 4 factors explained the majority of the observed variance for DISS symptoms. Fatigue, sleepiness, and exhaustion loaded onto the same factor and were highly intercorrelated. In LMM, mean composite fatigue-sleepiness-exhaustion scores were associated with dialysis day (coefficient and 95% confidence interval [CI] 0.21 [0.02 - 0.39]) and time of day (coefficient and 95% CI 0.33 [0.25 - 0.41]. Observed associations were minimally affected by adjustment for demographics and common confounders. CONCLUSIONS: Maintenance HD patients experience fatigue-sleepiness-exhaustion symptoms that demonstrate significant daily and diurnal variation. The variability in symptoms may contribute to poor symptom awareness by providers and greater misclassification bias of fatigue related symptoms in clinical studies.


Asunto(s)
Trastornos de Somnolencia Excesiva/economía , Trastornos de Somnolencia Excesiva/etiología , Fatiga/economía , Fatiga/etiología , Fallo Renal Crónico/economía , Diálisis Renal/efectos adversos , Diálisis Renal/economía , Femenino , Costos de la Atención en Salud/estadística & datos numéricos , Humanos , Fallo Renal Crónico/terapia , Masculino , Persona de Mediana Edad , Resultado del Tratamiento , Estados Unidos
5.
Vet Parasitol ; 247: 37-41, 2017 Nov 30.
Artículo en Inglés | MEDLINE | ID: mdl-29080762

RESUMEN

Equine protozoal myeloencephalitis (EPM) is an important equine neurologic disorder, and treatments for the disease are often unrewarding. Prevention of the disease is the most important aspect for EPM, and a killed vaccine was previously developed for just that purpose. Evaluation of the vaccine had been hampered by lack of post vaccination challenge. The purpose of this study was to determine if the vaccine could prevent development of clinical signs after challenge with Sarcocystis neurona sporocysts in an equine challenge model. Seventy horses that were negative for antibodies to S. neurona and were neurologically normal were randomly assigned to vaccine or placebo groups and divided into short-term duration of immunity (study #1) and long-term duration of immunity (study #2) studies. S. neurona sporocysts used for the challenge were generated in the opossum/raccoon cycle isolate SN 37-R. Study #1 horses received an initial vaccination and a booster, and were challenged 34days post second vaccination. Study #2 horses received a vaccination and two boosters and were challenged 139days post third vaccination. All horses in study #1 developed neurologic signs (n=30) and there was no difference between the vaccinates and controls (P=0.7683). All but four horses in study #2 developed detectable neurologic deficits. The neurologic signs, although not statistically significant, were worse in the vaccinated horses (P=0.1559). In these two studies, vaccination with the S. neurona vaccine failed to prevent development of clinical neurologic deficits.


Asunto(s)
Encefalomielitis/veterinaria , Enfermedades de los Caballos/prevención & control , Vacunas Antiprotozoos/inmunología , Sarcocystis/inmunología , Sarcocistosis/veterinaria , Vacunación/veterinaria , Animales , Encefalomielitis/parasitología , Encefalomielitis/prevención & control , Enfermedades de los Caballos/parasitología , Caballos , Zarigüeyas , Mapaches , Distribución Aleatoria , Sarcocistosis/parasitología , Sarcocistosis/prevención & control
6.
7.
Vet Ther ; 6(1): 57-66, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15906270

RESUMEN

The liposomal cream formulation of diclofenac, an NSAID, is an effective, safe, and convenient way to treat localized areas of inflammation in horses. The results of this study reveal urinary and serum concentrations of diclofenac following topical administration of 1% liposomal diclofenac cream for 10 days at the labeled dose and at 2X and 4X the labeled dose. These results demonstrate the slow absorption and elimination of 1% liposomal diclofenac cream and may be useful when estimating the withdrawal time needed before a competition in order to prevent an inadvertent positive drug test.


Asunto(s)
Antiinflamatorios no Esteroideos/farmacología , Diclofenaco/farmacocinética , Caballos/metabolismo , Administración Cutánea , Animales , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/sangre , Antiinflamatorios no Esteroideos/orina , Área Bajo la Curva , Diclofenaco/administración & dosificación , Diclofenaco/sangre , Diclofenaco/orina , Esquema de Medicación , Masculino
9.
Oper Dent ; 31(4): 401-402, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-22054479
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