Changes in the Proportion of Patients Presenting with Early Stage Colon Cancer over Time Among Medicaid Expansion and Non-expansion States

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Scarlett B. Hao ◽  
Rebecca A. Snyder ◽  
William Irish ◽  
Alexander A. Parikh
2020 ◽  
Vol 38 (4_suppl) ◽  
pp. 251-251
Author(s):  
Scarlett Hao ◽  
Rebecca A Snyder ◽  
William Irish ◽  
Alexander A. Parikh

251 Background: In 2010, the Affordable Care Act required insurance plans to cover preventative screening, and the Medicaid expansion provision enabled participating states to increase Medicaid coverage of uninsured individuals. The aim of this study was to determine whether the proportion of patients diagnosed with early vs. late stage colon cancer (CC) at Commission on Cancer (CoC) facilities differed over time within states that expanded Medicaid in January 2014 (MES) vs. non-Medicaid expansion states (NMES). Methods: A hospital-based cohort study of patients diagnosed with CC from 2006-2016 was performed using the National Cancer Database. Uninsured and Medicaid-insured patients in MES were compared with patients in NMES. Patients with Medicare, private, or government insurance were excluded. The observed proportions of patients with early (AJCC I-II) vs late (III-IV) stage within each cohort were compared over time. Propensity score adjusted probability of early stage at presentation was determined among patients residing in MES and NMES. Results: The study cohort included 10,289 patients in MES and 15,173 patients in NMES. Compared to MES, a greater proportion of patients in NMES were black (33.4% vs 24.0%), had a median income < $38,000 (39.7% vs 28.2%), and resided in a state with ≥21% of the population without a high school degree (37.4% vs 28.1%). The proportions of early stage CC in both cohorts in 2006 were similar. In NMES, this proportion remained constant over time until 2014 and declined by 0.8% per year after 2014. Within MES, the proportion of early stage CC increased by 0.6% per year until 2014 and 0.9% per year after 2014. By 2016, the absolute difference in the propensity adjusted proportion of early stage CC between cohorts was 8.8% (39.7% vs 30.9%, p < 0.001). Conclusions: Following Medicaid expansion in 2014, the proportion of patients presenting to a CoC facility with early stage CC increased over time within MES and declined in NMES. Further investigation, including population-based research, is warranted to determine if enrollment in Medicaid improves access to colorectal cancer screening and leads to earlier stage at diagnosis.


2017 ◽  
Vol 28 ◽  
pp. v207
Author(s):  
M. Chalabi ◽  
M. Van Leerdam ◽  
A. Aalbers ◽  
J. Van den Berg ◽  
G. Beets ◽  
...  

2013 ◽  
Vol 19 (46) ◽  
pp. 8468 ◽  
Author(s):  
Hugh James Freeman

2013 ◽  
Vol 12 (3) ◽  
pp. 179-187 ◽  
Author(s):  
Winson Y. Cheung ◽  
Qian Shi ◽  
Michael O'Connell ◽  
James Cassidy ◽  
Charles D. Blanke ◽  
...  

2017 ◽  
Vol 17 (2) ◽  
pp. 248-262 ◽  
Author(s):  
Babak Esmaeelian ◽  
Kirsten Benkendorff ◽  
Richard K. Le Leu ◽  
Catherine A. Abbott

The acute apoptotic response to genotoxic carcinogens animal model has been extensively used to assess the ability of drugs and natural products like dietary components to promote apoptosis in the colon and protect against colorectal cancer (CRC). This work aimed to use this model to identify the main chemopreventative agent in extracts from an Australian mollusc Dicathais orbita, while simultaneously providing information on their potential in vivo toxicity. After 2 weeks of daily oral gavage with bioactive extracts and purified brominated indoles, mice were injected with the chemical carcinogen azoxymethane (AOM; 10 mg/kg) and then killed 6 hours later. Efficacy was evaluated using immunohistochemical and hematoxylin staining, and toxicity was assessed via hematology, blood biochemistry, and liver histopathology. Comparison of saline- and AOM-injected controls revealed that potential toxic side effects can be interpreted from blood biochemistry and hematology using this short-term model, although AOM negatively affected the ability to detect histopathological effects in the liver. Purified 6-bromoisatin was identified as the main cancer preventive agent in the Muricidae extract, significantly enhancing apoptosis and reducing cell proliferation in the colonic crypts at 0.05 mg/g. There was no evidence of liver toxicity associated with 6-bromoisatin, whereas 0.1 mg/g of the brominated indole tyrindoleninone led to elevated aspartate aminotransferase levels and a reduction in red blood cells. As tyrindoleninone is converted to 6-bromoisatin by oxidation, this information will assist in the optimization and quality control of a chemopreventative nutraceutical from Muricidae. In conclusion, preliminary data on in vivo safety can be simultaneously collected when testing the efficacy of new natural products, such as 6-bromoisatin from Muricidae molluscs for early stage prevention of colon cancer.


2012 ◽  
Vol 5 (11 Supplement) ◽  
pp. B107-B107
Author(s):  
Babak Esmaeelian ◽  
Kirsten Benkendorff ◽  
Richard Le Leu ◽  
Catherine Abbott

2001 ◽  
Vol 36 (3) ◽  
pp. 243-249
Author(s):  
J. Aubrey Waddell ◽  
Dominic A. Solimando

The increasing complexity of cancer chemotherapy makes it mandatory that pharmacists be familiar with these highly toxic agents. This column reviews various issues related to the preparation, dispensing, and administration of cancer chemotherapy, both commercially available and investigational.


PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e84686 ◽  
Author(s):  
Narayan Shivapurkar ◽  
Louis M. Weiner ◽  
John L. Marshall ◽  
Subha Madhavan ◽  
Anne Deslattes Mays ◽  
...  

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