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. Author manuscript; available in PMC: 2020 Mar 1.
Published in final edited form as: Arthritis Care Res (Hoboken). 2019 Feb 4;71(3):398–405. doi: 10.1002/acr.23599

Table 3.

Experiences of Persons with SLE in Gaining and Maintaining Access to Health Care and Dealing with Personal- and Neigborhood-Level Stressors that Affect SLE Status, by High Income vs. Poverty, Living in Neighborhood of Concentrated Poverty vs. Not, and Being in Worst Quartile of Disease Damage in 2015

Group Health Care Issues
N Gained Access to SLE Care in < 6 months Maintained Access/Maneuvered through System
Income
High Income (household income ≥$100,000) 11 6 10
In Poverty 17 8 10
Residence (among those in Poverty)
Living in Areas of Concentrated Poverty 11 6 5
Not Living in Areas of Concentrated Poverty 6 2 5
Disease Status
Highest Quartile of Damage 14 6 10
Lowest Three Quartiles of Damage 14 8 10
Group N Traditional Stressors Stressors Mentioned Socioeconomic Stressors Adverse Neighborhood Effects
Income
High Income (household income ≥$100,000) 11 11 1 0
In Poverty 17 17 11 13
Residence (among those in Poverty)
Living in Areas of Concentrated Poverty 11 11 6 8
Not Living in Areas of Concentrated Poverty 6 6 5 5
Disease Status
Highest Quartile of Damage 14 14 3 3
Lowest Three Quartiles of Damage 14 14 7 10