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1.
Cancer Med ; 13(9): e7028, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38711364

RESUMO

BACKGROUND: Palliative treatment has been associated with improved quality of life and survival for a wide variety of metastatic cancers. However, it is unclear whether the benefits of palliative treatment are uniformly experienced across the US cancer population. We evaluated patterns and outcomes of palliative treatment based on socioeconomic, sociodemographic and treating facility characteristics. METHODS: Patients diagnosed between 2008 and 2019 with Stage IV primary cancer of nine organ sites were analyzed in the National Cancer Database. The association between identified variables, and outcomes concerning the administration of palliative treatment were analyzed with multivariable logistic regression and Cox proportional hazard models. RESULTS: Overall 238,995 (23.6%) of Stage IV patients received palliative treatment, which increased over time for all cancers (from 20.7% in 2008 to 25.6% in 2019). Palliative treatment utilization differed significantly by region (West less than Northeast, OR: 0.55 [0.54-0.56], p < 0.001) and insurance payer status (uninsured greater than private insurance, OR: 1.35 [1.32-1.39], p < 0.001). Black race and Hispanic ethnicity were also associated with lower rates of palliative treatment compared to White and non-Hispanics respectively (OR for Blacks: 0.91 [0.90-0.93], p < 0.001 and OR for Hispanics: 0.79 [0.77-0.81] p < 0.001). CONCLUSIONS: There are important differences in the utilization of palliative treatment across different populations in the United States. A better understanding of variability in palliative treatment use and outcomes may identify opportunities to improve informed decision making and optimize quality of care at the end-of-life.


Assuntos
Neoplasias , Cuidados Paliativos , Classe Social , Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Neoplasias/terapia , Estados Unidos , Qualidade de Vida , Adulto , Resultado do Tratamento , Estadiamento de Neoplasias
3.
Gastroenterology ; 158(2): 404-417, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31759062

RESUMO

Screening, followed by colonoscopic polypectomy (or surgery for malignant lesions), prevents incident colorectal cancer and mortality. However, there are variations in effective application of nearly every aspect of the screening process. Screening is a multistep process, and failure in any single step could result in unnecessary morbidity and mortality. Awareness of variations in operator- and system-dependent performance has led to detailed, comprehensive recommendations in the United States and Europe on how colonoscopy screening should be performed and measured. Likewise, guidance has been provided on quality assurance for nonprimary colonoscopy-based screening programs, including strategies to maximize adherence. Quality improvement is now a validated science, and there is clear evidence that higher quality prevents incident cancer and cancer death. Quality must be addressed at the levels of the system, provider, and individuals, to maximize the benefits of screening for any population. We review the important aspects of measuring and improving the quality of colorectal cancer screening.


Assuntos
Neoplasias Colorretais/prevenção & controle , Detecção Precoce de Câncer/normas , Saúde Global/normas , Programas de Rastreamento/normas , Qualidade da Assistência à Saúde/normas , Colonoscopia/normas , Neoplasias Colorretais/diagnóstico , Neoplasias Colorretais/epidemiologia , Carga Global da Doença , Humanos , Incidência , Programas de Rastreamento/organização & administração , Guias de Prática Clínica como Assunto
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