Angel G. Ortiz
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Angel G. Ortiz has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Daniel Wiese
American Cancer Society 1 Department of Surveillance, Prevention and Health Services Research Atlanta, Georgia
2 shared publications - Evelyn T. Gonzalez
Office of Community Outreach, Fox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA
2 shared publications - Kevin A. Henry
Department of Geography, Temple University, Philadelphia, Pennsylvania
2 shared publications - Kristen A. Sorice
Cancer Prevention and Control Program Fox Chase Cancer Center Philadelphia Pennsylvania USA
2 shared publications - Minhhuyen T. Nguyen
Fox Chase Cancer Center, Temple University Health System, Philadelphia, PA 19111, USA
2 shared publications - Shannon M. Lynch
Cancer Prevention and Control, Fox Chase Cancer Center Philadelphia Pennsylvania USA
2 shared publications
Latest Publications
- Open Access
- 1 December 2020
- Published by Elsevier in SSM - Population Health
- Vol. 12, 100640
Towards precision public health: Geospatial analytics and sensitivity/specificity assessments to inform liver cancer prevention
- 1 December 2020
- Published by Elsevier in SSM - Population Health
- Vol. 12, 100640
Open AccessTowards precision public health: Geospatial analytics and sensitivity/specificity assessments to inform liver cancer prevention
- Open Access
- 16 October 2020
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 17 (20) , 7526
Liver Cancer Incidence and Area-Level Geographic Disparities in Pennsylvania—A Geo-Additive Approach
Many neighborhood socioeconomic index measures (nSES) that capture neighborhood deprivation exist but the impact of measure selection on liver cancer (LC) geographic disparities remains unclear. We introduce a Bayesian geoadditive modeling approach to identify clusters in Pennsylvania (PA) with higher than expected LC incidence rates, adjusted for individual-level factors (age, sex, race, diagnosis year) and compared them to models with 7 different nSES index measures to elucidate the impact of nSES and measure selection on LC geospatial variation. LC cases diagnosed from 2007–2014 were obtained from the PA Cancer Registry and linked to nSES measures from U.S. census at the Census Tract (CT) level. Relative Risks (RR) were estimated for each CT, adjusted for individual-level factors (baseline model). Each nSES measure was added to the baseline model and changes in model fit, geographic disparity and state-wide RR ranges were compared. All 7 nSES measures were strongly associated with high risk clusters. Tract-level RR ranges and geographic disparity from the baseline model were attenuated after adjustment for nSES measures. Depending on the nSES measure selected, up to 60% of the LC burden could be explained, suggesting methodologic evaluations of multiple nSES measures may be warranted in future studies to inform LC prevention efforts.
- 16 October 2020
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 17 (20) , 7526
Open AccessLiver Cancer Incidence and Area-Level Geographic Disparities in Pennsylvania—A Geo-Additive Approach
Many neighborhood socioeconomic index measures (nSES) that capture neighborhood deprivation exist but the impact of measure selection on liver cancer (LC) geographic disparities remains unclear. We introduce a Bayesian geoadditive modeling approach to identify clusters in Pennsylvania (PA) with higher than expected LC incidence rates, adjusted for individual-level factors (age, sex, race, diagnosis year) and compared them to models with 7 different nSES index measures to elucidate the impact of nSES and measure selection on LC geospatial variation. LC cases diagnosed from 2007–2014 were obtained from the PA Cancer Registry and linked to nSES measures from U.S. census at the Census Tract (CT) level. Relative Risks (RR) were estimated for each CT, adjusted for individual-level factors (baseline model). Each nSES measure was added to the baseline model and changes in model fit, geographic disparity and state-wide RR ranges were compared. All 7 nSES measures were strongly associated with high risk clusters. Tract-level RR ranges and geographic disparity from the baseline model were attenuated after adjustment for nSES measures. Depending on the nSES measure selected, up to 60% of the LC burden could be explained, suggesting methodologic evaluations of multiple nSES measures may be warranted in future studies to inform LC prevention efforts.