Table 3.
Clinical Features of Bone Marrow-Augmented Intestinal Recipients and Control Patients
BM-augmented group (n = 20) | Control group (n = 22) | |
---|---|---|
Children/adult | 13/7 | 16/6 |
Male/female | 9/11 | 16/6 |
Allograft | ||
Intestine | 8 (40%) | 7 (32%) |
Composite | 12 (60%) | 15 (68%) |
Duration of TPN (mo) | 59 ± 53 | 49 ± 49 |
Total bilirubin (mg/dL) | 17 ± 15 | 21 ± 16 |
No. of abdominal operations | 5 ± 4 | 4 ± 3 |
Operative time (h) | 14 ± 6 | 14 ± 4 |
Cold ischemia time (h) | 9.7 ± 2.8 | 9.2 ± 3.0 |
HLA (-A, -B, -DR) mismatch | 4.4 ± 1.1 | 4.4 ± 1.1 |
Positive cytotoxic cross-match | 2 (10%) | 6 (27%) |
Followup (mo) | 13 ± 12 | 13 ± 11 |
BM, bone marrow; TPN, total parenteral nutrition.