Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
CA Cancer J Clin ; 65(6): 428-55, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26348643

RESUMEN

Colorectal cancer (CRC) is the third most common cancer and third leading cause of cancer death in both men and women and second leading cause of cancer death when men and women are combined in the United States (US). Almost two-thirds of CRC survivors are living 5 years after diagnosis. Considering the recent decline in both incidence and mortality, the prevalence of CRC survivors is likely to increase dramatically over the coming decades with the increase in rates of CRC screening, further advances in early detection and treatment and the aging and growth of the US population. Survivors are at risk for a CRC recurrence, a new primary CRC, other cancers, as well as both short-term and long-term adverse effects of the CRC and the modalities used to treat it. CRC survivors may also have psychological, reproductive, genetic, social, and employment concerns after treatment. Communication and coordination of care between the treating oncologist and the primary care clinician is critical to effectively and efficiently manage the long-term care of CRC survivors. The guidelines in this article are intended to assist primary care clinicians in delivering risk-based health care for CRC survivors who have completed active therapy.


Asunto(s)
Neoplasias Colorrectales/terapia , Atención Primaria de Salud , Sobrevivientes , Cuidados Posteriores , Neoplasias Colorrectales/complicaciones , Neoplasias Colorrectales/diagnóstico , Neoplasias Colorrectales/psicología , Detección Precoz del Cáncer/métodos , Femenino , Promoción de la Salud , Humanos , Comunicación Interdisciplinaria , Masculino , Recurrencia Local de Neoplasia/diagnóstico , Neoplasias Primarias Secundarias/diagnóstico , Grupo de Atención al Paciente , Calidad de Vida , Sobrevivientes/psicología
2.
CA Cancer J Clin ; 64(4): 225-49, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24916760

RESUMEN

Prostate cancer survivors approach 2.8 million in number and represent 1 in 5 of all cancer survivors in the United States. While guidelines exist for timely treatment and surveillance for recurrent disease, there is limited availability of guidelines that facilitate the provision of posttreatment clinical follow-up care to address the myriad of long-term and late effects that survivors may face. Based on recommendations set forth by a National Cancer Survivorship Resource Center expert panel, the American Cancer Society developed clinical follow-up care guidelines to facilitate the provision of posttreatment care by primary care clinicians. These guidelines were developed using a combined approach of evidence synthesis and expert consensus. Existing guidelines for health promotion, surveillance, and screening for second primary cancers were referenced when available. To promote comprehensive follow-up care and optimal health and quality of life for the posttreatment survivor, the guidelines address health promotion, surveillance for prostate cancer recurrence, screening for second primary cancers, long-term and late effects assessment and management, psychosocial issues, and care coordination among the oncology team, primary care clinicians, and nononcology specialists. A key challenge to the development of these guidelines was the limited availability of published evidence for management of prostate cancer survivors after treatment. Much of the evidence relies on studies with small sample sizes and retrospective analyses of facility-specific and population databases.


Asunto(s)
Continuidad de la Atención al Paciente/normas , Atención Primaria de Salud/normas , Neoplasias de la Próstata/terapia , Sobrevivientes , American Cancer Society , Medicina Basada en la Evidencia , Promoción de la Salud/normas , Humanos , Masculino , Vigilancia de la Población , Calidad de Vida , Estados Unidos
4.
CA Cancer J Clin ; 60(2): 70-98, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20200110

RESUMEN

In 2009, the American Cancer Society (ACS) Prostate Cancer Advisory Committee began the process of a complete update of recommendations for early prostate cancer detection. A series of systematic evidence reviews was conducted focusing on evidence related to the early detection of prostate cancer, test performance, harms of therapy for localized prostate cancer, and shared and informed decision making in prostate cancer screening. The results of the systematic reviews were evaluated by the ACS Prostate Cancer Advisory Committee, and deliberations about the evidence occurred at committee meetings and during conference calls. On the basis of the evidence and a consensus process, the Prostate Cancer Advisory Committee developed the guideline, and a writing committee drafted a guideline document that was circulated to the entire committee for review and revision. The document was then circulated to peer reviewers for feedback, and finally to the ACS Mission Outcomes Committee and the ACS Board of Directors for approval. The ACS recommends that asymptomatic men who have at least a 10-year life expectancy have an opportunity to make an informed decision with their health care provider about screening for prostate cancer after they receive information about the uncertainties, risks, and potential benefits associated with prostate cancer screening. Prostate cancer screening should not occur without an informed decision-making process. Men at average risk should receive this information beginning at age 50 years. Men in higher risk groups should receive this information before age 50 years. Men should either receive this information directly from their health care providers or be referred to reliable and culturally appropriate sources. Patient decision aids are helpful in preparing men to make a decision whether to be tested.


Asunto(s)
Detección Precoz del Cáncer/normas , Tamizaje Masivo/normas , Neoplasias de la Próstata/diagnóstico , Antineoplásicos Hormonales/efectos adversos , Ansiedad , Biopsia con Aguja Fina/efectos adversos , Continuidad de la Atención al Paciente , Toma de Decisiones , Medicina Basada en la Evidencia , Humanos , Esperanza de Vida , Masculino , Flebotomía/efectos adversos , Examen Físico/métodos , Próstata/patología , Antígeno Prostático Específico/sangre , Prostatectomía/efectos adversos , Prostatectomía/métodos , Neoplasias de la Próstata/epidemiología , Neoplasias de la Próstata/terapia , Radioterapia/efectos adversos , Ensayos Clínicos Controlados Aleatorios como Asunto , Recto , Valores de Referencia , Medición de Riesgo , Factores de Riesgo , Programa de VERF , Disfunciones Sexuales Fisiológicas/etiología , Estados Unidos/epidemiología , Incontinencia Urinaria de Esfuerzo/etiología
5.
J Natl Med Assoc ; 102(5): 423-9, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-20533778

RESUMEN

In 2009, the American Cancer Society (ACS) initiated a series of systematic evidence reviews to update recommendations for early prostate cancer detection. The evidence reviews focused on studies of screening, the performance of screening tests, harms associated with testing and therapy for localized prostate cancer, and shared and informed decision making in prostate cancer screening. Based on this evidence, the ACS recommends that asymptomatic men who have at least a 10-year life expectancy have an opportunity to make an informed decision with their health care provider about screening for prostate cancer after receiving information about the uncertainties, risks, and potential benefits associated with prostate cancer screening. Prostate cancer screening should not occur without an informed decision-making process. Men at average risk should receive this information beginning at age 50. Men in higher-risk groups should receive this information before age 50. Men should either receive this information directly from their health care providers or be referred to reliable and culturally appropriate sources. Patient decision aids are helpful in preparing men to make a decision whether to be tested, and the use of such aids is encouraged.


Asunto(s)
American Cancer Society , Tamizaje Masivo/normas , Guías de Práctica Clínica como Asunto/normas , Neoplasias de la Próstata/diagnóstico , Diagnóstico Precoz , Humanos , Masculino , Morbilidad , Neoplasias de la Próstata/epidemiología , Estados Unidos/epidemiología
7.
Am Fam Physician ; 77(7): 995-1002, 2008 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-18441865

RESUMEN

This article describes a joint update of guidelines by the American Cancer Society and the U.S. Multi-Society Task Force on Colorectal Cancer delineating evidence-based surveillance recommendations for patients after polypectomy and colorectal cancer resection. Although there are some qualifying conditions, the following general guidelines apply: after colonoscopic polypectomy, patients with hyperplastic polyps should be considered to have normal colonoscopies, and subsequent colonoscopy is recommended at 10 years. Patients with one or two small (less than 1 cm) tubular adenomas, including those with only low-grade dysplasia, should have their next colonoscopy in five to 10 years. Patients with three to 10 adenomas, any adenoma 1 cm or larger, or any adenoma with villous features or high-grade dysplasia should have their next colonoscopy in three years. Following curative resection of colorectal cancer, patients should undergo a colonoscopy at one year, with subsequent follow-up intervals determined by the results of this examination. Adoption of these guidelines will have a dramatic impact on the quality of care provided to patients after a colorectal cancer diagnosis, will assist in shifting available resources from intensive surveillance to screening, and will ultimately decrease suffering and death related to colorectal cancer.


Asunto(s)
Pólipos Adenomatosos/prevención & control , Pólipos del Colon/prevención & control , Colonoscopía/estadística & datos numéricos , Neoplasias Colorrectales/prevención & control , Vigilancia de la Población , Pólipos Adenomatosos/epidemiología , Pólipos Adenomatosos/cirugía , American Cancer Society , Pólipos del Colon/epidemiología , Pólipos del Colon/cirugía , Neoplasias Colorrectales/epidemiología , Neoplasias Colorrectales/cirugía , Humanos , Estados Unidos/epidemiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA