TABLE 2.
Variable | Value by IFI category: |
P value | |
---|---|---|---|
IFIa (n = 14) | No IFI (n = 59) | ||
Recipient age in yr, median (IQR) | 49 (40.7-56.1) | 53 (42.3-61) | 0.55 |
Race, no. (%) | 0.99 | ||
Caucasian | 13 (92.9) | 56 (94.9) | |
African American | 1 (7.1) | 3 (5.1) | |
Male gender, no. (%) | 9 (64.3) | 31 (52.5) | 0.29 |
Underlying disease, no. (%) | |||
Cystic fibrosis | 4 (28.6) | 10 (16.9) | 0.31 |
COPDd | 5 (35.7) | 13 (22) | 0.27 |
Pulmonary fibrosis | 2 (14.3) | 20 (33.9) | 0.14 |
Bronchiectasis | 0 | 3 (5.1) | 0.39 |
Bronchiolitis obliterans | 1 (5.6) | 5 (8.5) | 0.72 |
Sarcoidosis | 1 (5.6) | 4 (6.8) | 0.89 |
Pneumoconiosis | 0 | 1 (1.7) | 0.59 |
Eisenmenger's syndrome | 0 | 2 (3.4) | 0.51 |
Alpha 1 antitrypsin deficiency | 0 | 1 (1.7) | 0.59 |
Lymphangiomyomatosis | 1 (5.6) | 0 | 0.06 |
CMV risk status, no. (%)b | 0.13 | ||
High | 4 (28.6) | 17 (28.8) | |
Intermediate | 7 (50) | 39 (66.1) | |
Low | 3 (21.4) | 3 (5.1) | |
No prior history of IFI, no. (%)c | 0 | 6 (10.2) | 0.22 |
Four patients had two proven IFIs each; two patients with proven IFI were also diagnosed with possible IFI.
High risk, recipient seronegative and donor seropositive; intermediate risk, seropositive recipient; low risk, seronegative recipient and donor.
Infection status within 1 year prior to lung transplant.
COPD, chronic obstructive pulmonary disease.