Melanoma Disparities among US Hispanics: Use of the Social Ecological Model to Contextualize Reasons for Inequitable Outcomes and Frame a Research Agenda
Table 1
Research questions and strategies by social ecological model levels of influence [89].
Research questions and strategies by SEM levels of influence
Level of influence
Sublevel of influence
Future research questions and strategies
Society/policy
(i) Healthcare infrastructure (ii) Public health (iii) Health policy and public laws (iv) Societal norms (v) Media and health communication efforts (vi) Racism and discrimination (vii) Hispanic medical workforce diversity
(i) How does health system infrastructure impede access to dermatologic care among Hispanics? (ii) How can different media platforms be employed to increase knowledge and awareness among Hispanic subpopulations and influence CM societal norms? (iii) What are the most effective methods of dissemination of CM education? (iv) Can CM educational interventions designed for Hispanics influence outcomes? (v) How does racism/discrimination influence CM outcomes? (i) Training of physician extenders (and screen patients for skin cancer and melanoma. (ii) Implement policies that remove barriers to access of primary and specialty care. (iii) Diversification of the medical and dermatologic workforce to increase the representation of Hispanic care providers. (iv) Development of culturally and linguistically appropriate melanoma educational campaigns targeted to Hispanic subgroups. (v) Collaboration between Hispanic community stakeholders and professional medical organizations to facilitate dissemination of information/research findings to lay community.
Community
Neighborhood measures (i) Income/level of poverty (ii) Built environment (iii) Workplace environment and exposures (iv) Schools and availability of childcare
Are there unique environmental risk factors (aside from UV exposure) that increase CM risk among Hispanics? Develop longitudinal cohort studies quantifying workplace exposures and their impact on CM outcomes in Hispanics.
Interpersonal
(i) English language fluency (ii) Residence in predominantly Hispanic neighborhood (iii) Degree of assimilation (iv) Cohesion (v) Social networks (vi) Peer and family influence
What cultural factors contribute to CM risk/mortality? Do these factors vary by Hispanic country of origin? Are there components of Hispanic culture that influence participation in skin cancer screening or seeking medical care for skin conditions? How does melanoma risk vary by degree of acculturation? Develop more precise constructs to measure effects of acculturation. Development of community-based participatory research studies in which Hispanic stakeholders are included in early stages of study design.
Individual
(i) Age (ii) Race & ethnicity (iii) Gender (iv) Ancestry and genetic factors (v) Gene-environment interaction (vi) Immigration status (vii) Knowledge and behavior (viii) Insurance status (ix) Occupation (x) Health insurance status (xi) Income (xii) Education
What is the phenotypic profile of Hispanic patents with CM? Are kinetics of melanoma progression and metastasis different among Hispanics? How do CM risk and mortality vary by Hispanic subgroup? How does CM risk vary with immigration status and duration of time in US? How do fatalism and its impact on skin cancer perceptions vary between Hispanic subgroups? What role, if any, does fatalism play in CM inequities? How can melanoma knowledge and awareness be increased amongst Hispanic subgroups? Develop genetic studies (AIMS/GWAS) across Hispanic subgroups to understand the genetic basis for melanoma risk. Identification of biomarkers for melanoma disease progression within Hispanics. Case control studies of Hispanics with and without melanoma to help identify unique risk factors amongst this group. Efforts to increase recruitment of Hispanics melanoma patients into clinical trials. Transdisciplinary studies to understand the interlink between biological and social factors.