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1.
J Med Screen ; 13(2): 72-5, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16792828

RESUMO

SETTING: The Million Women Study is a cohort study of women aged 50-64 years in England and Scotland. As a component of the follow-up questionnaire, participants were asked to indicate if they had an abnormal cervical smear in the previous five years. This study compared self-reported cervical abnormalities with screening records obtained from the National Health Service Cervical Screening Programme. METHODS: For 1944 randomly selected Million Women Study participants in Oxfordshire, screening records were assessed over a six-year period prior to the date of self-reporting. The six-year period was chosen to allow for errors in the recall of timing of abnormal smears. RESULTS: A total of 68 women (3.5%) had a record of at least one equivocal or abnormal smear within the last six years, whereas 49 women (2.5%) self-reported an abnormality. There was a strong trend for an increased probability of self-reporting a history of an abnormal smear as the severity of the recorded abnormality increased (P <0.001). For women with an NHS record of borderline dyskaryosis, mild dyskaryosis, or moderate dyskaryosis/severe dyskaryosis/invasive cancer, the proportions reporting an abnormality were 40%, 58% and 77%, respectively. For women with negative and inadequate smears, the proportion self-reporting an abnormality were 0.6% and 0.7%, respectively. CONCLUSIONS: These results indicate that among women whose screening programme records show an abnormal smear, the proportion self-reporting an abnormality increases with the severity of the recorded lesion. Almost all women with a record of negative or inadequate smear(s) correctly interpret the result and do not self-report an abnormality.


Assuntos
Programas de Rastreamento/métodos , Neoplasias do Colo do Útero/diagnóstico , Esfregaço Vaginal , Estudos de Coortes , Coleta de Dados , Inglaterra , Feminino , Humanos , Prontuários Médicos , Aceitação pelo Paciente de Cuidados de Saúde , Educação de Pacientes como Assunto , Lesões Pré-Cancerosas , Sistema de Registros , Reprodutibilidade dos Testes , Escócia , Fatores de Tempo
2.
Nicotine Tob Res ; 7(1): 129-37, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15804685

RESUMO

The present study aimed to determine whether tobacco use cessation rates observed in controlled trials of a hospital-based tobacco use cessation program could be replicated when the program was disseminated to a wide range of hospitals in a two-stage process including implementation and institutionalization phases. Using a nonrandomized, observational design, we recruited six hospitals to participate in the study. The research team helped implement the program during the first year of participation (implementation) and then withdrew from active involvement during the second year (institutionalization). The mean 6-month self-reported cessation rates were 26.3% (range = 17.6%-52.8%) for the implementation phase and 22.7% (range = 12.9%-48.2%) for the institutionalization phase. Hospitals with paid professionals providing the program had the best outcomes. Inpatient tobacco use cessation programs are feasible to implement and should target a 6-month self-reported cessation rate of at least 25%.


Assuntos
Implementação de Plano de Saúde/organização & administração , Promoção da Saúde/organização & administração , Hospitais Gerais/organização & administração , Pacientes Internados/estatística & dados numéricos , Abandono do Hábito de Fumar/métodos , Tabagismo/reabilitação , Adulto , California/epidemiologia , Distribuição de Qui-Quadrado , Feminino , Implementação de Plano de Saúde/estatística & dados numéricos , Promoção da Saúde/estatística & dados numéricos , Humanos , Masculino , Pessoa de Meia-Idade , Avaliação de Resultados em Cuidados de Saúde , Avaliação de Programas e Projetos de Saúde , Abandono do Hábito de Fumar/estatística & dados numéricos , Tabagismo/epidemiologia , Resultado do Tratamento
3.
Breast Cancer Res ; 4(1): R1, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-11879559

RESUMO

BACKGROUND: Information regarding the characteristics and health of women who do and do not attend for breast cancer screening is limited and representative data are difficult to obtain. METHODS: Information on age, deprivation and prescriptions for various medications was obtained for all women at two UK general practices who were invited to breast cancer screening through the National Health Service Breast Screening Programme. The characteristics of women who attended and did not attend screening were compared. RESULTS: Of the 1064 women invited to screening from the two practices, 882 (83%) attended screening. Screening attenders were of a similar age to non-attenders but came from significantly less deprived areas (30% of attenders versus 50% of non-attenders came from the most deprived areas, P < 0.0001) and were more likely to have a current prescription for hormone replacement therapy (32% versus 19%, P < 0.0001). No significant differences in recent prescriptions of medication for hypertension, heart disease, hypercholesterolaemia, diabetes mellitus, asthma, thyroid disease or depression/anxiety were observed between attenders and non-attenders. CONCLUSION: Women who attend the National Health Service Breast Screening Programme come from less deprived areas and are more likely to have a current prescription for hormone replacement therapy than non-attenders, but do not differ in terms of age or recent prescriptions for various other medications.


Assuntos
Neoplasias da Mama/prevenção & controle , Neoplasias da Mama/psicologia , Mamografia/estatística & dados numéricos , Aceitação pelo Paciente de Cuidados de Saúde , Fatores Etários , Neoplasias da Mama/diagnóstico por imagem , Inglaterra , Medicina de Família e Comunidade , Feminino , Terapia de Reposição Hormonal/estatística & dados numéricos , Humanos , Pessoa de Meia-Idade , Estudos Prospectivos , Saúde da População Rural , Fatores Socioeconômicos , Saúde da População Urbana , Saúde da Mulher
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