A prospective, randomized study to evaluate the effectiveness of a con
tinuous low-dose vancomycin infusion to prevent nosocomial gram-positi
ve bacteremia was initiated within the first 2 weeks of life in neonat
es weighing <1500 gm. Seventy-one inf ants received constant infusion
of vancomycin (25 mu g/ml) mixed with their total parenteral nutrition
solution; 70 infa nts served as control subjects. The groups were cli
nically similar in birth weight, estimated gestational age, and severi
ty of illness. Administration of vancomycin was begun at a mean age of
5.4 +/- 2.9 days. Infants had mean serum vancomycin concentrations of
2.4 mu g/ml, and received vancomycin for a mean of 11 +/- 7 days. No
vancomycin-resistant organisms were detected in surveillance cultures
during the 2-year study period. Twenty-four of seventy control infants
, in comparison with 1 of 71 infants receiving vancomycin, had gram-po
sitive bacteremia (p<0.001). The addition of a low dose of vancomycin
to alimentation fluids virtually eliminated the incidence of gram-posi
tive bacteremia in an at-risk population of very low birth weight infa
nts. However, the widespread use of vancomycin in total parenteral nut
rition solution is not recommended until better data on the emergence
of vancomycin-resistant organisms are available.