Table 1.
Variable | No-Coverage vs LIS | Generic-Only vs LIS | ||||
---|---|---|---|---|---|---|
No Coverage (n=7650) | LIS (n=11537) | P value | Generic Only (n=2989) | LIS (n=11537) | P value | |
Female sex, % | 78.6 | 78.4 | 0.57 | 79.7 | 79.7 | 1.00 |
Race, % | ||||||
Non-Hispanic White | 82.1 | 82.4 | 0.43 | 78.9 | 78.5 | 0.32 |
African American | 6.7 | 6.6 | 0.48 | 7.6 | 8.0 | 0.17 |
Hispanic | 8.0 | 8.3 | 0.43 | 10.2 | 10.2 | 0.94 |
Asian | 1.7 | 1.7 | 0.78 | 1.9 | 2.1 | 0.26 |
Age, % | ||||||
65–74 | 35.8 | 36.6 | 0.12 | 37.8 | 37.7 | 0.82 |
75–84 | 37.6 | 37.5 | 0.88 | 35.2 | 35.9 | 0.19 |
≥ 85 | 26.6 | 25.9 | 0.12 | 27.0 | 26.4 | 0.24 |
Prescription drug risk score, mean | 1.09±0 | 1.1±0 | 0.17 | 1.1±0.01 | 1.1±0 | 0.99 |
CMS-HCC risk, mean | 1.49±0.01 | 1.51±0.01 | 0.22 | 1.5±0.02 | 1.51±0.01 | 0.67 |
No. Elixhauser comobidities, mean | 4.49±0.03 | 4.56±0.03 | 0.08 | 4.58±0.05 | 4.62±0.03 | 0.53 |
Time spent in the gap, mean | 114.8±0.73 | 128.3±0.61 | <.001 | 136.5±1.25 | 128.6±0.61 | <.001 |
25th percentile | 61 | 77 | 80 | 79 | ||
Median | 115 | 132 | 140 | 132 | ||
75th percentile | 165 | 178 | 192 | 178 | ||
Diagnosed chronic conditions, % | ||||||
Hypertension | 60.7 | 61.6 | 0.06 | 59.8 | 61.9 | <.001 |
Hyperlipidemia | 35.8 | 27.6 | <.001 | 34.0 | 27.7 | <.001 |
AMI | 2.0 | 1.7 | 0.05 | 1.2 | 1.8 | <.001 |
COPD | 20.7 | 24.6 | <.001 | 20.3 | 24.8 | <.001 |
Heart failure | 32.2 | 36.6 | <.001 | 32.9 | 37.6 | <.001 |
Diabetes | 31.2 | 39.3 | <.001 | 36.8 | 40.2 | <.001 |
RA/OA | 38.3 | 41.5 | <.001 | 37.7 | 42.1 | <.001 |
Plus-minus values are means±SE.
Abbreviations: LIS = low-income-subsidies; AMI = Acute Myocardial Infarction; COPD = Chronic obstructive pulmonary disease; RA/OA = Rheumatoid arthritis/osteoarthritis.
All numbers in the table are adjusted using inverse propensity score weights. Propensity scores were calculated using logistic regression models that predict the probability of being in a study group relative to the comparison group, controlling for age, sex, race, number of Elixhauser comorbidities, and prescription drug hierarchical condition.