Table 1.
Characteristics | HKTx–dialysis N = 243 | HKTx–no dialysis N = 472 | KAHN = 130 | P value |
---|---|---|---|---|
Recipient age, years | 50.6 (12.7) | 56.5 (10.4) | 51.3 (14.5) | <.001 |
Donor age, years | 31.4 (12.4) | 31.6 (11.1) | 29.3 (11.5) | 0.14 |
Female recipient, n (%) | 46 (19) | 90 (19) | 40 (31) | 0.010 |
Male recipient, female donor, n (%) | 48 (24) | 62 (16) | 27 (30) | 0.004 |
Female recipient, male donor, n (%) | 17 (37) | 41 (46) | 16 (40) | 0.60 |
Race, n (%) | 0.001 | |||
Asian | 15 (6) | 11 (2) | 1 (1) | |
African‑American | 77 (32) | 154 (33) | 26 (20) | |
Hispanic | 25 (11) | 33 (7) | 10 (8) | |
Caucasian | 117 (49) | 265 (57) | 88 (69) | |
Other | 4 (2) | 5 (1) | 3 (2) | |
High school education, n (%) | 229 (94) | 460 (97) | 123 (95) | 0.07 |
BMI, kg/m2 | 25.9 (5.2) | 27.0 (5.0) | 26.5 (5.1) | 0.024 |
Waitlist status, n (%) | <.001 | |||
1A | 138 (57) | 313 (66) | 76 (58) | |
1B | 75 (31) | 143 (30) | 40 (31) | |
2 | 30 (12) | 16 (3) | 14 (11) | |
Ischaemic time, h | 3.2 (1.1) | 3.0 | 3.4 (1.1) | 0.002 |
Time on waitlist, days | 169.5 (244.5) | 250.0 (398.7) | 152 (260.8) | 0.001 |
High‐volume centre (>200), n (%) | 170 (70) | 325 (69) | 88 (68) | 0.90 |
Missing smoking status, n (%) | 1 (0) | 3 (1) | 1 (1) | 0.90 |
Prior smoking, n (%) | 86 (36) | 208 (44) | 53 (41) | 0.08 |
Diagnosis, aetiology for heart failure, n (%) | 0.048 | |||
Ischaemic cardiomyopathy | 89 (37) | 171 (36) | 44 (34) | |
Restrictive cardiomyopathy | 8 (3) | 24 (5) | 4 (3) | |
Congenital | 5 (2) | 11 (2) | 10 (8) | |
Other | 141 (58) | 266 (56) | 72 (55) | |
Diabetes, n (%) | 0.09 | |||
No | 140 (58) | 266 (56) | 89 (68) | |
Type I | 18 (7) | 22 (5) | 8 (6) | |
Type II | 78 (32) | 171 (36) | 30 (23) | |
Other type | 1 (0) | 1 (0) | 0 (0) | |
Unknown type | 6 (2) | 10 (2) | 1 (1) | |
Diabetes status unknown | 0 (0) | 2 (0) | 2 (2) | |
Dialysis, n (%) | <.001 | |||
No dialysis | 0 (0) | 472 (100) | 130 (100) | |
Haemodialysis | 214 (88) | 0 (0) | 0 (0) | |
Peritoneal dialysis | 25 (10) | 0 (0) | 0 (0) | |
Dialysis with unknown method | 4 (2) | 0 (0) | 0 (0) | |
Cerebrovascular disease, n (%) | 11 (5) | 39 (8) | 8 (6) | 0.16 |
Cardiac defibrillator, n (%) | 161 (66) | 265 (77) | 99 (76) | 0.005 |
Serum creatinine at transplant, μmol/L | 486 (309) | 248 (141) | 141 (80) | <.001 |
Bilirubin at listing, μmol/L | 24 (55) | 21 (53) | 22 (38) | 0.72 |
Hospital stay, n (%) | 0.57 | |||
Intensive care treatment | 86 (36) | 170 (36) | 43 (33) | |
Hospitalized, not in the ICU | 56 (23) | 101 (22) | 23 (18) | |
Not hospitalized | 100 (41) | 196 (42) | 64 (49) | |
Ventilator support, n (%) | 5 (2) | 10 (2) | 4 (3) | 0.79 |
ECMO, n (%) | 2 (1) | 1 (0) | 2 (2) | 0.19 |
IABP, n (%) | 20 (8) | 29 (6) | 7 (5) | 0.47 |
LVAD at listing, n (%) | 34 (14) | 61 (13) | 17 (13) | 0.92 |
LVAD at transplant, n (%) | 10 (4) | 58 (12) | 17 (13) | 0.001 |
RVAD at listing, n (%) | 9 (4) | 5 (1) | 3 (2) | 0.06 |
RVAD at transplant, n (%) | 4 (2) | 5 (1) | 3 (2) | 0.53 |
Total artificial heart, n (%) | 12 (5) | 21 (4) | 3 (2) | 0.47 |
Inotrope, n (%) | 105 (43) | 217 (46) | 54 (42) | 0.59 |
Cardiac output, L/min | 8.0 (2.7) | 7.9 (2.5) | 6.6 (2.4) | 0.06 |
Systolic PAP, mmHg | 45.3 (13.9) | 45.1 (14.0) | 41.4 (14.0) | 0.025 |
Mean PAP, mmHg | 30.5 (9.0) | 30.6 (9.8) | 28.1 (9.9) | 0.043 |
PCWP, mmHg | 20.1 (8.6) | 20.5 (8.8) | 19.5 (9.0) | 0.56 |
Donor CMV status, n (%) | <.001 | |||
Negative | 83 (34) | 179 (38) | 59 (45) | |
Not done/unknown | 1(0) | 8 (2) | 9 (7) | |
Positive | 158 (65) | 280 (60) | 62 (48) | |
Recipient CMV status, n (%) | 0.38 | |||
Negative | 86 (35) | 182 (39) | 42 (32) | |
Not done/unknown | 2 (1) | 1 (0) | 0 (0) | |
Positive | 155 (65) | 289 (61) | 88 (68) | |
PRA Class 1 > 10%, n (%) | 21 (12) | 56 (20) | 11 (9) | 0.009 |
PRA Class 2 > 10%, n (%) | 15 (9) | 38 (14) | 9 (8) | 0.10 |
BMI, body mass index; CMV, cytomegalovirus; ECMO, extracorporeal membrane oxygenation; HKTx, combined heart and kidney transplantation; IABP, intra‐aortic balloon pump; ICU, intensive care unit; KAH, kidney transplant after initial heart transplantation; LVAD, left ventricular assist device; PAP, pulmonary artery pressure; PCWP, pulmonary capillary wedge pressure; RVAD, right ventricular assist device; PRA, panel reactive antibody.
Data are reported as mean ± standard deviation unless stated otherwise. P values are for comparisons using chi square test (or Fisher's exact test wherever applicable) for categorical variables and Kruskal‑Wallis test for continuous variables to assess any differences between categories.