Bloodstream infections can develop late (after day 100) and/or in the absence of neutropenia in children receiving allogeneic bone marrow transplantation
V. Romano et al., Bloodstream infections can develop late (after day 100) and/or in the absence of neutropenia in children receiving allogeneic bone marrow transplantation, BONE MAR TR, 23(3), 1999, pp. 271-275
Citations number
14
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
We retrospectively evaluated the incidence and time from transplantation of
bloodstream infections occurring in children receiving bone marrow transpl
ant (BMT) at G Gaslini Children's Hospital between September 1984 and Decem
ber 1997, During this period the incidence was 35% after allogeneic and 26%
after autologous BMT (P=0.08). Among these episodes, 38% after allogeneic
BMT and 90% after autologous BMT were detected in the presence of neutropen
ia within the first 30 days from reinfusion (P < 0.001). Incidence of cathe
ter-related bloodstream infections was 40% after allogeneic and 8% after au
tologous BMT (P < 0.001). Bloodstream infections in the absence of neutrope
nia were 55% after allogeneic BMT vs 10% after autologous BMT (P < 0.001) a
nd occurred later after reinfusion (mean 199 vs 41 days, P <0.001). Among t
he episodes occurring after allogeneic BMT and in the absence of neutropeni
a, 61% were related to the presence of a central venous catheter, 15% were
related to the presence of GVHD, but 23% were not associated with any of ma
jor risk factors for infection. Finally, 38% of episodes following allogene
ic BMT were detected after day 100 vs 1% after autologous BMT, We concluded
that patients receiving allogeneic BMT experience a high incidence of bloo
dstream infections in the absence of neutropenia and that a significant pro
portion of these episodes is not clearly associated with well known risk fa
ctors such as GVHD or central venous catheters, Moreover, many episodes dev
elop a long time after the transplantation procedure. Therefore, any febril
e episode following allogeneic BMT even late and/or in the absence of neutr
openia should be intensively managed.