Table 2.
Quintile of eGFR Change | HR, 95% CI | P Value | HR, 95% CI | P Value | HR, 95% CI | P Value | HR, 95% CI | P Value |
---|---|---|---|---|---|---|---|---|
Change in eGFR from pre-MCS to 1 mo post-MCS | Unadjusted | Adjusted for pre-MCS eGFR | Adjusted for 1 mo eGFR | Adjusted for patient characteristics*,† | ||||
1 (<0%, any worsening) | 1.96, 1.48–2.60 | <0.0001 | 2.22, 1.68–2.95 | <0.0001 | 1.72, 1.29–2.29 | 0.0002 | 1.63, 1.15–2.13 | 0.004 |
2 (0%–22% improvement) | 1.31, 0.94–1.84 | 0.12 | 1.36, 0.97–1.90 | 0.08 | 1.25, 0.89–1.76 | 0.19 | 1.25, 0.87–1.78 | 0.22 |
3 (22%–47% improvement) | Reference group | … | … | … | … | … | … | … |
4 (47%–88% improvement) | 1.45, 1.07–1.96 | 0.02 | 1.36, 1.01–1.84 | 0.049 | 1.52, 1.12–2.06 | 0.007 | 1.40, 1.02–1.93 | 0.04 |
5 (>88% improvement) | 2.02, 1.51–2.70 | <0.0001 | 1.61, 1.19–2.19 | 0.003 | 2.20, 1.64–2.96 | <0.0001 | 1.64, 1.19–2.26 | 0.002 |
Change in eGFR from 1 mo to 3 months post MCS (n=2416) | Unadjusted | Adjusted for 1 mo eGFR | Adjusted for 3 mo eGFR | Adjusted for patient characteristics*,‡ | ||||
1 (>30% worsening) | 2.07, 1.43–3.00 | 0.0001 | 2.34, 1.62–3.40 | <0.0001 | 1.87, 1.28–2.71 | 0.001 | 1.74 1.17–2.58 | 0.006 |
2 (16%–30% worsening) | 1.51, 1.02–2.22 | 0.04 | 1.59, 1.08–2.35 | 0.02 | 1.47, 1.00–2.17 | 0.05 | 1.36, 0.90–2.04 | 0.14 |
3 (0%–16% worsening) | Reference group | … | … | … | … | … | … | … |
4 (0.1%–17% improvement) | 1.28, 0.87–1.87 | 0.21 | 1.21, 0.82–1.77 | 0.33 | 1.34, 0.91–1.96 | 0.14 | 1.10, 0.72–1.65 | 0.66 |
5 (>17% improvement) | 1.80, 1.24–2.61 | 0.002 | 1.42, 0.97–2.10 | 0.07 | 1.93, 1.32–2.80 | 0.0006 | 1.54, 1.03–2.30 | 0.03 |
CI indicates confidence interval; eGFR, estimated glomerular filtration rate; HR, hazards ratio; INTERMACS, Interagency Registry for Mechanically Assisted Circulatory Support; and MCS, mechanical circulatory support.
Adjusted for age, sex, race, diabetes mellitus, chronic lung disease, ischemic cause, New York Heart Association class, device type, device strategy (destination vs bridge to transplant), INTERMACS Profile, year of MCS implant, baseline β-blocker use, baseline angiotensin-converting enzyme inhibitor or angiotensin receptor blocker use, baseline loop diuretic use, baseline inotrope use, and dialysis requirement.
Adjusted for 1-mo eGFR.
Adjusted for 3-mo eGFR.