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1.
Can J Urol ; 24(1): 8646-8650, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-28263130

RESUMEN

INTRODUCTION: There are numerous standard treatment options for men diagnosed with localized prostate cancer. Multidisciplinary consultation before decision-making is a consensus- and quality-based objective in Ontario. With the goals of working together more collaboratively and to provide higher quality information for patients at the time of decision-making, a prostate cancer community partnership consensus (PCPC) panel was formed among six partnering centers in the Greater Toronto Area. MATERIALS AND METHODS: Five iterative meetings were held among 40 prostate cancer specialists (32 urologists and 8 radiation oncologists) who participate in multidisciplinary clinics. The meetings defined the goals of the partnership as well as the topics and questions the group would address together. Answers to these questions were developed by formal consensus: >= 75% of participants had to agree with wording based on secret ballots to achieve consensus. RESULTS: All six groups wanted to participate to improve patient care/decision-making. Forty-one questions addressing 30 issues were derived from the literature and the group's collective experience. These issues were cross-tabbed against five management options: active surveillance, radical prostatectomy, low dose rate brachytherapy, high dose rate brachytherapy boost and external beam radiation. Answers common to all modalities were coalesced. Eighty-six issues were subjected to formal consensus. After three rounds of secret ballots, consensus was achieved for the answers to all issues. CONCLUSIONS: A formal consensus-based partnership between urology and radiation oncology to support newly diagnosed prostate cancer patients was feasible and resulted in a patient information guide which may improve decision-making.


Asunto(s)
Comunicación Interdisciplinaria , Educación del Paciente como Asunto , Neoplasias de la Próstata/terapia , Oncología por Radiación , Urología , Braquiterapia , Toma de Decisiones , Humanos , Masculino , Espera Vigilante
2.
Can J Urol ; 17 Suppl 1: 18-25, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20170597

RESUMEN

Prostate cancer is a highly prevalent malignancy. Using serum prostatic-specific antigen (PSA) levels to screen for prostate cancer has led to a greater detection of this cancer, at earlier stages. However, screening for prostate cancer by determining PSA levels remains controversial. Concerns include the risk of overdiagnosis and conversely, the failure to detect all prostate cancers. This article, aimed at primary care practitioners, reviews the characteristics of an ideal screening test, in relation to the characteristics of the PSA test. It then discusses the implications of recent findings from two large, randomized, prospective screening trials: the American Prostate, Lung, Colorectal and Ovarian Cancer (PLCO) screening trial and the European Randomized Study of Screening for Prostate Cancer (ERSPC) trial. The latter trial demonstrated a modest survival benefit from PSA screening. Lastly, the article summarizes recommendations from recently updated guidelines about PSA testing from the American Urological Association (AUA), and it discusses when a primary care practitioner might refer a patient to a urologist.


Asunto(s)
Tamizaje Masivo/métodos , Atención Primaria de Salud/métodos , Antígeno Prostático Específico/sangre , Neoplasias de la Próstata/diagnóstico , Distribución por Edad , Anciano , Actitud del Personal de Salud , Canadá , Detección Precoz del Cáncer/normas , Detección Precoz del Cáncer/tendencias , Humanos , Masculino , Persona de Mediana Edad , Médicos de Familia/tendencias , Pautas de la Práctica en Medicina , Prevalencia , Atención Primaria de Salud/tendencias , Pronóstico , Neoplasias de la Próstata/epidemiología , Neoplasias de la Próstata/prevención & control , Medición de Riesgo , Sensibilidad y Especificidad , Tasa de Supervivencia
3.
Ir J Psychol Med ; 20(2): 41-44, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30440207

RESUMEN

OBJECTIVES: Much has been written about the costs and cost-effectiveness of community care for people with learning disabilities resettled from long stay hospital care. However, comparatively little has been published about the cost of hospital services relating to the preparatory process before eventual resettlement and the disengagement of formal, sustained input from hospital staff. This study describes and costs the input provided by a hospital based multi-disciplinary team into the resettlement of adults with learning disabilities from long stay wards in Muckamore Abbey Hospital in Northern Ireland between 1996 and 1999 (n = 71). METHOD: The study employs a retrospective survey design. Information about the nature and frequency of the input of each member of hospital multi-disciplinary team was collected for each former client. According to the level of professional resources expended during the resettlement process, each former client was then categorised into one of three categories. One case was then selected at random to represent each category. A summary of clinical information, a description of the resettlement process and an estimate of the cost of the process was provided for each case. RESULTS: Approximately 55% of people resettled in the community during the study period did so with a modest degree of input from hospital staff. For 18% resettlement proved to be a demanding and prolonged process, requiring intensive input from hospital staff. Financial costs of the resettlement process ranged from approximately stg£1,500 to stg£8,000, with an average of stg£3,400 for each person. CONCLUSION: This study provides evidence of the input by hospital staff into the process of community resettlement of long stay hospital clients and the associated costs. These costs must be included in service budgets if quality care and appropriate service provision is to be maintained in resettlement practice.

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