Table 4.
Kidney transplantation in total cohort | Process toward kidney transplantation |
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---|---|---|---|---|---|---|
Waitlisted for transplant | Among waitlisted patients, received transplant | |||||
| ||||||
No. of incident events/Total no. of patientsa | 415/1152b | 656/1152 | 415/656 | |||
| ||||||
Multivariable analysis | HR (CI) | P | HR (CI) | P | HR (CI) | P |
Race/ethnicity by current substance use groups c | ||||||
White, no substance use (referent) | --- | --- | --- | |||
Black, no substance use | 0.76 (0.56, 1.02) | 0.070 | 0.73 (0.58, 0.91) | 0.005 | 0.99 (0.74, 1.32) | 0.949 |
Other, no substance use | 1.00 (0.70, 1.43) | 0.980 | 0.79 (0.55, 1.13) | 0.199 | 0.96 (0.68, 1.35) | 0.804 |
White, current substance use | 0.73 (0.50, 1.06) | 0.094 | 0.55 (0.42, 0.72) | <0.001 | 1.09 (0.77, 1.53) | 0.633 |
Black, current substance use | 0.45 (0.23, 0.85) | 0.014 | 0.32 (0.22, 0.47) | <0.001 | 0.76 (0.47, 1.25) | 0.288 |
Other, current substance use | 0.33 (0.13, 0.84) | 0.021 | 0.60 (0.37, 0.99) | 0.049 | 0.69 (0.26, 1.79) | 0.448 |
Covariates | ||||||
Age, years | 0.97 (0.97, 0.98) | <0.001 | 0.98 (0.98, 0.99) | <0.001 | 0.97 (0.97, 0.98) | <0.001 |
Employment status, unemployed | 0.69 (0.55, 0.86) | 0.001 | 0.74 (0.62, 0.88) | 0.001 | 0.68 (0.55, 0.84) | <0.001 |
Health insurance, public only (vs. any private coverage) | 0.75 (0.58, 0.96) | 0.022 | 0.71 (0.59, 0.86) | 0.001 | 0.78 (0.60, 0.99) | 0.048 |
BMI | 0.98 (0.96, 0.99) | 0.013 | 0.99 (0.98, 1.00) | 0.076 | 0.98 (0.97, 1.00) | 0.056 |
Hypertension, yes | 1.17 (0.93, 1.47) | 0.180 | 1.10 (0.92, 1.31) | 0.317 | 1.13 (0.91, 1.41) | 0.272 |
On dialysis, yes | 0.80 (0.65, 0.98) | 0.035 | 0.62 (0.52, 0.73) | <0.001 | 0.83 (0.68, 1.01) | 0.065 |
Charlson Comorbidity Index,d higher score=worse | 0.27 (0.15, 0.50) | <0.001 | 0.30 (0.19, 0.49) | <0.001 | 0.39 (0.22, 0.69) | <0.001 |
Chronic pulmonary disease, yes | 0.84 (0.65, 1.09) | 0.185 | 0.83 (0.70, 0.99) | 0.034 | 0.95 (0.73, 1.23) | 0.705 |
History of medical nonadherence, yes | 0.82 (0.59, 1.13) | 0.226 | 0.80 (0.63, 1.02) | 0.067 | 0.90 (0.65, 1.24) | 0.522 |
Waitlisted before 2014 implementation of KASe | 0.80 (0.77, 0.83) | <0.001 | --- | 0.78 (0.43, 1.40) | 0.398 | |
Improvement in model fit over null model: χ2 (df); p | 284.7 (15) | <0.001 | 255.0 (14) | <0.001 | 124.0 (15) | <0.001 |
For each outcome, patients were followed until the event of interest or until censoring due to death (competing risk) or other reasons (see Table 1 for numbers of patients by reasons for censoring). Only 11 patients (<1% of all patients; <2% of those waitlisted) were censored because the study observation period ended; they had been waitlisted and were on the waitlist at study’s end). They were followed in the study for median of 8.4 years (IQR, 8.1, 8.8), and had been on the waitlist for median of 6.5 years (IQR, 3.9, 7.9).
Of the 415 patients receiving transplants, 134 received living donor transplants. Numbers of outcome events are too small to examine race/ethnicity by substance use groups as predictors separately for living vs. deceased donor transplants.
We chose to compare groups defined by the combination of race/ethnicity and substance use, with the referent group of non-Hispanic white patients, because of the ease of displaying and interpreting specific disparities in the outcomes. An alternative for evaluating our hypothesis (i.e., that the 2 groups of racial/ethnic minority patients who used substances would show particularly great disadvantage on outcomes) is to test a planned contrast using contrast weights to capture the notion of synergistic effects. The statistical tests and p levels associated with evaluating this planned contrast within competing risk models were z=2.99, P=0.003 for the outcome of kidney transplantation; z=4.95, p<.001 for waitlisting, and z=1.34, p=.182 for transplant among waitlisted patients. (Note that decomposing this planned contrast into its component parts, i.e., separately testing main effects for race/ethnicity and substance use, and an interaction effect, would provide only piecemeal evaluation of our hypothesis rather than a focused test of it. Planned contrasts give greater power and precision than piecemeal testing when specific hypotheses such as those pertaining to synergy are proposed.86,87)
Log transformed prior to analysis.
Included as a time dependent covariate in analysis of time to transplant in full cohort.
Abbreviations: CI, confidence interval; HR, hazard ratio; IQR, Interquartile range; KAS, Kidney Allocation System