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. Author manuscript; available in PMC: 2019 Sep 1.
Published in final edited form as: Am J Transplant. 2018 May 15;18(9):2285–2294. doi: 10.1111/ajt.14893

Table 2.

Demographics of HALT study participants.

Variable N = 119
Age, mean ± standard deviation (SD) 57 ± 13
Female recipient, n (%) 49 (41%)
Diagnosis, n (%)
 COPD 38 (32%)
 Interstitial lung disease / pulmonary fibrosis 53 (44%)
 Cystic fibrosis (CF) or non-CF bronchiectasis 18 (15%)
 Pulmonary hypertension 2 (2%)
 Other 8 (7%)
Lung allocation score at transplant, mean ± SD 45.59 ± 16.93
Pre-transplant ECMO support 2 (2%)
Bilateral lung transplant, n (%) 90 (76%)
Single lung transplant, n (%) 29 (24%)
Intraoperative cardiopulmonary bypass, n (%) 69 (58%)
Ischemic time (minutes), mean ± standard deviation 285 ± 80
Post-transplant ECMO support, n (%) 1 (1%)
Identical donor-recipient ABO status, n (%) 107 (90%)
Compatible donor-recipient ABO status, n (%) 12 (10%)
Recipient CMV seropositive, n (%) 53 (45%)
Recipient CMV seronegative and donor seropositive, n (%) 35 (29%)
Pre-transplant DSA, n (%) 12 (10%)
Number of donor-recipient mismatches at HLA A, B, C, DRB1, and DQB loci, median (IQR) 8 (3)
Number of donor-recipient mismatches at HLA-DRB1 locus, median (IQR) 2 (1)
Number of donor-recipient mismatches at HLA-DQB locus, median (IQR) 1 (1)
Positive Flow Cytometry B-cell crossmatch, n (%) 17 (15%)
PGD grade at time 0*, n (%)
 PGD 0 69 (60%)
 PGD 1 26 (23%)
 PGD 2 10 (9%)
 PGD 3 10 (9%)
PGD grade at 72 hours**, n (%)
 PGD 0 49 (47%)
 PGD 1 49 (47%)
 PGD 2 3 (3%)
 PGD 3 4 (4%)
Blood product transfusion during transplant hospitalization, n (%) 63 (53%)
Induction immunosuppression, n (%)
 None 45 (38%)
 Basiliximab 72 (60%)
 Rabbit anti-thymocyte globulin 2 (2%)

COPD: chronic obstructive pulmonary disease, with or without alpha 1-antitrypsin deficiency

ECMO: extracorporeal membrane oxygenation

CMV: cytomegalovirus

PGD: primary graft dysfunction

*

Immediately after transplantation (time 0), 115 recipients had sufficient data to calculate PGD grades

**

At 72 hours, 105 recipients had sufficient data to calculate PGD grades