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1.
Support Care Cancer ; 25(7): 2063-2073, 2017 07.
Artigo em Inglês | MEDLINE | ID: mdl-28197848

RESUMO

PURPOSE: To compare patient-triggered follow-up (PTFU) for curatively treated colorectal cancer against traditional outpatient follow-up (OPFU). METHODS: Questionnaires were mailed at four time points over one-year post-treatment to two prospectively-recruited cohorts: A, patients entering follow-up and receiving OPFU pre-implementation of PTFU; B, patients entering follow-up (FU) and receiving either OPFU (B1) or PTFU (B2) post-implementation of PTFU. Bi-variate tests were used to compare patient characteristics and outcomes eight months after entering follow-up (generic and cancer-specific quality of life (QoL), satisfaction). Regression analysis explored associations between follow-up model and outcomes. Resource implications and costs of models were compared. RESULTS: Patients in Cohort B1 were significantly more likely to have received chemotherapy (p < 0.001), radiotherapy (p < 0.05), and reported poorer QoL (p = 0.001). Having a longstanding co-morbid condition was the most important determinant of QoL (p < 0.001); model of care was not significant. Patients were satisfied with their follow-up care regardless of model. Health service costs were higher in PTFU over the first year CONCLUSIONS: PTFU is acceptable to patients with colorectal cancer and can be considered to be a realistic alternative to OPFU for clinically suitable patients. The initial costs are higher due to provision of a self-management (SM) programme and remote surveillance. Further research is needed to establish long-term outcomes and costs.


Assuntos
Neoplasias Colorretais/tratamento farmacológico , Qualidade de Vida/psicologia , Estudos de Coortes , Seguimentos , Humanos , Estudos Longitudinais , Estudos Prospectivos , Inquéritos e Questionários , Fatores de Tempo
2.
Eur J Cancer Care (Engl) ; 18(2): 140-8, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19267729

RESUMO

The study aimed to improve understanding of the natural history and impact of hot flushes after breast cancer. Data were collected from women participating in an RCT of relaxation to reduce the incidence of flushes from breast cancer follow-up clinics from two hospitals in South-East England. Repondents were 150 women experiencing hot flushes following completion of primary treatment for breast cancer. This study utilized a flush diary, the Hot Flushes and Night Sweats Questionnaire (HFNSQ), Functional Assessment of Cancer Therapy with Endocrine Subscale (FACT-ES) and Spielberger State/Trait Anxiety Index (STAI) as the main outcome measures. The study found that in this sample, 51 (34%) women experienced flushes more than five years after diagnosis and 75 (50%) more than 5 years after menopause. Sleep disruption occurred in 90 women (72% of those that returned diaries), affecting half of the nights they recorded. The mean problem rating on the HFNSQ was 4.85 out of 10. A peak incidence of flushes was apparent around 10 a.m. in women taking tamoxifen. It was concluded that hot flushes after breast cancer may be long-lasting and cause sleeping difficulties for many women. Tamoxifen may affect the diurnal pattern of flushes. After breast cancer, the duration of flushes, potential distress and disruption to women's lives should not be underestimated and appropriate interventions should be offered.


Assuntos
Ansiedade , Neoplasias da Mama/complicações , Fogachos/etiologia , Qualidade de Vida , Transtornos do Sono-Vigília/etiologia , Adulto , Idoso , Antineoplásicos Hormonais/efeitos adversos , Inglaterra , Feminino , Humanos , Menopausa , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Tamoxifeno/efeitos adversos , Fatores de Tempo
3.
J Adv Nurs ; 13(5): 640-8, 1988 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-3066802

RESUMO

There has been increasing interest in the attitudes that the general public and health care professionals hold towards cancer, the effect these have on an individual's likelihood to present early with symptoms, and the quality of care patients with the disease receive from carers. The research appears to indicate that the attitudes of both groups are largely negative and stereotyped, and cancer is seen as being more devastating than other life threatening diseases. These attitudes have been associated with patterns of poor communication and care for cancer patients. This paper looks critically at the research into the attitudes of nurses towards cancer and calls for more innovative methods than have been used to date. There is a need to increase our understanding of this complex problem before indications for education and practice can be made.


Assuntos
Atitude do Pessoal de Saúde , Neoplasias/enfermagem , Humanos , Neoplasias/terapia , Pesquisa Metodológica em Enfermagem , Prognóstico
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