Table 3. Multivariable Logistic Regression in All Transgender Womena.
Characteristic | OR (95% CI) | P value |
---|---|---|
Age group, y | ||
40-54 | 0.65 (0.17-2.37) | .52 |
55-69 | 1 [Reference] | NA |
ā„70 | 1.83 (1.02-5.49) | <.001 |
Race and ethnicity | ||
American Indian or Alaska Native | 0.22 (0.01-3.11) | .30 |
Asian | 2.97 (0.28-21.6) | .31 |
Hispanic | 2.23 (0.21-15.9) | .43 |
Non-Hispanic Black | 2.11 (0.45-9.98) | .33 |
Non-Hispanic White | 1 [Reference] | NA |
Otherb | 0.62 (0.08-4.33) | .62 |
Annual income, US$c | ||
0-25 000 | 1 [Reference] | NA |
25 000-50 000 | 0.76 (0.22-2.54) | .74 |
50 000-75 000 | 1.05 (0.25-4.35) | >.91 |
ā„75 000 | 0.67 (0.16-2.65) | .63 |
Employment status | ||
Employed | 1 [Reference] | NA |
Unemployed | 1.04 (0.25-4.05) | >.92 |
Homemaker | 0 | >.92 |
Student | 0 | >.93 |
Retired | 0.14 (0.03-1.54) | .71 |
Highest educational level | ||
No high school | 1 [Reference] | NA |
High school or GED | 1.55 (0.33-7.88) | .60 |
Some college | 1.99 (0.38-11.4) | .42 |
College | 2.55 (1.08-14.60) | .03 |
Cost barrier to care | ||
Yes | 1 [Reference] | NA |
No | 1.60 (0.36-7.61) | .52 |
Time since last primary care visitc | ||
Past year | 1 [Reference] | NA |
Past 1-2 y | 0.47 (0.03-4.42) | .54 |
Past 2-5 y | 0.40 (0.01-6.27) | .52 |
>5 y | 0.88 (0.04-11.80) | >.90 |
Had a clinician recommendation for a PSA test | ||
Yes | 12.40 (4.47-37.80) | <.001 |
No | 1 [Reference] | NA |
Had a clinician-led discussion of PSA advantages | ||
Yes | 7.51 (2.49-24.90) | <.001 |
No | 1 [Reference] | NA |
Had a clinician-led discussion of PSA disadvantages | ||
Yes | 1.14 (0.42-3.00) | .82 |
No | 1 [Reference] | NA |
Abbreviations: GED, General Educational Development; NA, not applicable; OR, odds ratio; PSA, prostate-specific antigen.
This multivariable logistic regression model assesses the association of the sociodemographic and access-to-care variables with the odds of recent PSA screening in the cohort of transgender women patients from the matched cohort (nā=ā255).
Not specified in the Behavioral Risk Factor Surveillance System.
The upper bound of the range is noninclusive.