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. 2021 Jul;16(7):1061–1072. doi: 10.2215/CJN.18961220

Table 4.

Association of ACEi/ARB discontinuation with 28-day mortality in ACEi/ARB users

Model Recipients of Kidney Transplant (n=160) Patients on Dialysis (n=188)
Continuers Discontinuers P Value Continuers Discontinuers P Value
Event rate (events)a 5.8 (55) 4.9 (33) 7.2 (184) 6.0 (60)
Model 1b Reference 3.05 (1.40 to 6.62) 0.005 Reference 1.16 (0.64 to 2.08) 0.63
Model 2c Reference 4.48 (1.87 to 10.71) 0.001 Reference 1.41 (0.69 to 2.88) 0.34
Model 3d Reference 5.23 (1.99 to 13.73) 0.001 Reference 1.68 (0.77 to 3.66) 0.19
Model 4e Reference 5.03 (1.84 to 13.76) 0.002 Reference 2.01 (0.91 to 4.45) 0.09
Model 5f Reference 1.36 (0.40 to 4.58) 0.62 Reference 1.52 (0.51 to 4.56) 0.45

Presented are the hazard ratios (95% confidence intervals) in transplant recipients and patients on dialysis, separately, unless otherwise indicated. ACEi/ARB, angiotensin-converting enzyme inhibitor/angiotensin receptor blocker.

a

Event rate per 100 person-weeks.

b

Model 1, crude.

c

Model 2, model 1 plus age, sex, and frailty.

d

Model 3, model 2 plus systolic BP, diabetes, and heart failure.

e

Model 4, model 3 plus start of anti-inflammatory therapy and antiviral therapy.

f

Model 5, model 4 plus cough, shortness of breath, fever, pulse rate, respiration rate, lymphocyte count, C-reactive protein, and >25% serum creatinine increase (only in transplant population).