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1.
Osteoporos Int ; 23(2): 615-24, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21369788

RESUMEN

SUMMARY: Sunlight exposure by improving vitamin D status could be a simple public health strategy in reducing falls among frail elder people. In a randomised controlled trial, adherence to sunlight exposure was low (median adherence, 26%) and no effect of increased UV exposure on falls risk was observed (incidence rate ratio (IRR) 1.06, P = 0.73). INTRODUCTION: This study aimed to determine whether increased sunlight exposure was effective to improve vitamin D status and reduce falls in the elderly. METHODS: In a cluster randomised controlled trial (NCT00322166 at ClinicalTrials.gov), 602 residents aged 70 or more (mean age, 86.4 years; 71% female) were recruited from 51 aged care facilities in Northern Sydney, Australia. Participants were randomised by facility to receive either increased sunlight exposure (additional 30-40 min/day in the early morning) with (UV+) or without (UV) calcium supplementation (600 mg/day) or neither (control) for a year. The co-primary endpoints were change in serum 25 hydroxy vitamin D (25OHD) and falls incidence after 12 months. RESULTS: Adherence to sunlight exposure was low (median adherence, 26%; IQR, 7%-45%). Serum 25OHD levels were low at baseline (median, 32.9 nmol/L) and increased only slightly depending on the number of sunlight sessions attended over 12 months (P = 0.04). During the study, 327 falls occurred in 111 (54%) subjects in the control group, 326 falls in 111 (58%) subjects in the UV only group and 335 falls in 108 (52%) subjects in the UV+ group. By intention-to-treat analysis, there was no significant effect of increased UV exposure on falls risk (IRR, 1.06; 95% CI, 0.76-1.48; P = 0.73). However, in 66 participants who attended ≥130 sessions per year (adherence, ≥50% of 260 sessions-five per week), falls were significantly reduced (IRR, 0.52; 95% CI, 0.31-0.88; P = 0.01) compared with the control group. CONCLUSIONS: Increased sunlight exposure did not reduce vitamin D deficiency or falls risk in frail older people. This public health strategy was not effective most likely due to poor adherence to the intervention.


Asunto(s)
Accidentes por Caídas/prevención & control , Helioterapia/métodos , Deficiencia de Vitamina D/terapia , Anciano , Anciano de 80 o más Años , Carbonato de Calcio/uso terapéutico , Suplementos Dietéticos , Femenino , Fracturas Óseas/prevención & control , Helioterapia/efectos adversos , Helioterapia/psicología , Hogares para Ancianos , Humanos , Masculino , Cooperación del Paciente/estadística & datos numéricos , Resultado del Tratamiento , Vitamina D/análogos & derivados , Vitamina D/sangre , Deficiencia de Vitamina D/sangre
2.
Spinal Cord ; 45(8): 542-50, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17043681

RESUMEN

OBJECTIVE: To determine whether Methenamine Hippurate (MH) or cranberry tablets prevent urinary tract infections (UTI) in people with neuropathic bladder following spinal cord injury (SCI). STUDY DESIGN: Double-blind factorial-design randomized controlled trial (RCT) with 2 year recruitment period from November 2000 and 6 month follow-up. SETTING: In total, 543 eligible predominantly community dwelling patients were invited to participate in the study, of whom 305 (56%) agreed. METHODS: Eligible participants were people with SCI with neurogenic bladder and stable bladder management. All regimens were indistinguishable in appearance and taste. The dose of MH used was 1 g twice-daily. The dose of cranberry used was 800 mg twice-daily. The main outcome measure was the time to occurrence of a symptomatic UTI. RESULTS: Multivariate analysis revealed that patients randomized to MH did not have a significantly longer UTI-free period compared to placebo (HR 0.96, 95% CI: 0.68-1.35, P=0.75). Patients randomized to cranberry likewise did not have significantly longer UTI-free period compared to placebo (HR 0.93, 95% CI: 0.67-1.31, P=0.70). CONCLUSION: There is no benefit in the prevention of UTI from the addition of MH or cranberry tablets to the usual regimen of patients with neuropathic bladder following SCI.


Asunto(s)
Antiinfecciosos Urinarios/uso terapéutico , Hipuratos/uso terapéutico , Metenamina/análogos & derivados , Extractos Vegetales/uso terapéutico , Traumatismos de la Médula Espinal/complicaciones , Vejiga Urinaria Neurogénica/tratamiento farmacológico , Vejiga Urinaria Neurogénica/etiología , Infecciones Urinarias/prevención & control , Vaccinium macrocarpon/química , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Método Doble Ciego , Femenino , Humanos , Masculino , Metenamina/uso terapéutico , Persona de Mediana Edad , Análisis Multivariante , Fitoterapia , Comprimidos , Insuficiencia del Tratamiento
3.
Int J STD AIDS ; 12(5): 307-9, 2001 May.
Artículo en Inglés | MEDLINE | ID: mdl-11368804

RESUMEN

This prospective cohort study examined the health-seeking behaviour of patients diagnosed with genital warts and vulvodynia who presented to Manly Sexual Health Service from March to June 2000. A self-administered questionnaire was used to assess patients' perceptions of their condition and their use of complementary therapies. Thirty-seven patients with genital warts and 26 patients with vulvodynia participated in the study. The use of at least one complementary health product or method was reported by 59% of patients with genital warts and 96% of vulvodynia patients (P < 0.001). Having received conflicting information and being worried about the condition was significantly associated with visits to complementary health providers. Acknowledgement of this search for complementary therapies and open discussion can help patients make informed decisions and to avoid drug interactions, and should ultimately lead to better patient care.


Asunto(s)
Terapias Complementarias/estadística & datos numéricos , Condiloma Acuminado/terapia , Aceptación de la Atención de Salud/psicología , Vulvovaginitis/terapia , Adolescente , Adulto , Condiloma Acuminado/psicología , Femenino , Instituciones de Salud/tendencias , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Enfermedades de Transmisión Sexual , Encuestas y Cuestionarios , Vulvovaginitis/psicología
4.
Aust J Public Health ; 18(4): 406-11, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7718654

RESUMEN

The aim of this study was to determine whether Pap smear screening at adequate intervals is associated with area of residence, frequency of consultations with a general practitioner, socioeconomic status and non-English-speaking background. A representative 10 per cent sample of women from New South Wales and the Australian Capital Territory, aged 25 to 69 years and registered with the Health Insurance Commission (Medicare) (N = 155,281) was used to obtain age, postcode, frequency of Pap smears and frequency of consultations with general practitioners in the three-year period from February 1985 to January 1988. Census data for each postcode area were used as an indicator of other socio-demographic characteristics. Age-specific screening rates did not vary between Sydney, Newcastle/Wollongong, Canberra, and nonmetropolitan areas. In all age groups, having had a smear was most strongly associated with the frequency with which a woman consulted a general practitioner. Women who visited a general practitioner at least four times a year on average were about twice as likely to have had a recent Pap smear as those who averaged less than one visit per year. Screening rates were lowest among women living in areas with the most non-English-speakers and the lowest socio-economic status. Sociodemographic factors and health service usage patterns influence the proportion of women who are currently being screened. Evaluation of interventions to improve Pap smear screening rates should consider whether the percentage of women screened increases overall, and also whether the imbalances in screening rates between different groups are diminishing.


Asunto(s)
Tamizaje Masivo/estadística & datos numéricos , Prueba de Papanicolaou , Frotis Vaginal/estadística & datos numéricos , Adulto , Factores de Edad , Anciano , Demografía , Medicina Familiar y Comunitaria/estadística & datos numéricos , Femenino , Servicios de Salud/estadística & datos numéricos , Humanos , Lenguaje , Modelos Logísticos , Persona de Mediana Edad , Programas Nacionales de Salud , Nueva Gales del Sur/epidemiología , Sistema de Registros , Características de la Residencia , Clase Social
5.
Med J Aust ; 156(5): 306-8, 1992 Mar 02.
Artículo en Inglés | MEDLINE | ID: mdl-1588860

RESUMEN

OBJECTIVE: To determine the number and type of methods used to measure blood pressure (BP) in pregnant women. DESIGN: Questionnaires were distributed to obstetricians and midwives concerning: method of recording BP (arm used, subject position, Korotkoff sounds recorded); accuracy of recording BP (cuff size, sphygmomanometer calibration); and definitions of hypertension in pregnancy. PARTICIPANTS: Obstetricians (academic, staff and private) in Sydney; members of the New South Wales Midwives' Association. MAIN RESULTS: Responses were received from 85 obstetricians (55% of those surveyed) and 173 midwives (43%); the overall response rate was 46%. Almost 80% of respondents agreed that diastolic BP above 90 mmHg constituted hypertension during pregnancy but at least six different methods were used to obtain BP readings, with a potentially large variability in the BP so obtained. Forty-five per cent of obstetricians and 72% of midwives stated that they always used a large cuff when necessary. Few had had their sphygmomanometer calibrated within the previous two years. CONCLUSIONS: There is considerable variability in the way BP is recorded in pregnant women. Hypertension in pregnancy may therefore be over or under diagnosed according to the method employed and there is an urgent need for international consensus on how to measure BP accurately in pregnancy.


Asunto(s)
Determinación de la Presión Sanguínea/métodos , Presión Sanguínea , Hipertensión/diagnóstico , Complicaciones Cardiovasculares del Embarazo/diagnóstico , Determinación de la Presión Sanguínea/instrumentación , Calibración , Femenino , Humanos , Partería , Nueva Gales del Sur , Obstetricia , Postura , Embarazo , Supinación , Encuestas y Cuestionarios
6.
Br J Dermatol ; 118(3): 403-7, 1988 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-3355782

RESUMEN

We studied sensitization to dinitrochlorobenzene (DNCB) in psoriatic patients before, during and 2, 4, and 6 weeks after a course of photochemotherapy (PUVA). The inhibition of sensitivity observed during PUVA was completely reversed after 6 weeks. Thus the PUVA-mediated inhibition of cutaneous immune responsiveness is of short duration. However, whether there are long-term sequelae remains to be established.


Asunto(s)
Terapia PUVA , Psoriasis/tratamiento farmacológico , Piel/inmunología , Dinitroclorobenceno/inmunología , Relación Dosis-Respuesta Inmunológica , Femenino , Humanos , Hipersensibilidad Tardía , Inmunización , Masculino , Psoriasis/inmunología , Factores de Tiempo
7.
JAMA ; 252(22): 3127-8, 1984 Dec 14.
Artículo en Inglés | MEDLINE | ID: mdl-6502876
8.
Br J Dermatol ; 109 Suppl 25: 86-8, 1983 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-6860585

RESUMEN

Dinitrochlorobenzene (DNCB) has been used widely to assess cell-mediated immunity in man. However, previous workers have evaluated response qualitatively and subjectively. Such methods cannot elucidate the quantitative relationships between stimulus and response essential to an understanding of the functional components of the system. We have developed quantitative techniques to explore the dose-response relationships of both afferent and efferent limbs of the response, and used this method to examine changes in reactivity to DNCB after exposure to UV radiation and in people with contact allergies.


Asunto(s)
Dinitroclorobenceno , Nitrobencenos , Pruebas del Parche , Pruebas Cutáneas , Dermatitis por Contacto/inmunología , Relación Dosis-Respuesta a Droga , Humanos , Inmunidad Celular , Terapia PUVA , Psoriasis/inmunología , Psoriasis/terapia , Valores de Referencia , Grosor de los Pliegues Cutáneos , Terapia Ultravioleta
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