TABLE I.
Characteristic | N (%) |
---|---|
Age at therapy initiation | |
Median | 4 years |
Range | 4 days–16 years |
Sex | |
Male | 97 (56%) |
Female | 75 (44%) |
Body mass index | |
Median | 16 |
Range | 10–33 |
Febrile during the 24 hours prior to CVC placement | |
No | 126 (73.3%) |
Yes | 46 (26.7%) |
Positive cultures prior to CVC placement | |
No | 166 (96.5%) |
Yes | 6 (3.5%) |
Presence of previous non-permanent CVC | |
No | 165 (95.9%) |
Yes | 7 (4.1%) |
Day of treatment at the time of CVC placement | |
Median | 0 |
Range | −1 to 5 |
Type of catheter | |
Double lumen tunneled catheter | 7 (4.1%) |
Single lumen tunneled catheter | 132 (76.7%) |
Infusaport | 33 (19.2%) |
White blood count at placement | |
Median | 5,800/mm3 |
Range | 184–314,500/mm3 |
Absolute neutrophil count at placement | |
Median | 600/mm3 |
Range | 0–40,888/mm3 |
<500/mm3 | 102 (59.3%) |
>500/mm3 | 70 (40.7%) |
Platelet count at placement | |
Median | 110,000/μl |
Range | 43,000–447,000/μl |
Hemoglobin at placement (posttransfusion) | |
Median | 9.1 g/dl |
Range | 6.2–14.6 g/dl |
CVC, central venous catheter.