Vancomycin-resistant Enterococcus faecium infection in three children given allogeneic hematopoietic stem cell transplantation: clinical and microbiological features
E. Carretto et al., Vancomycin-resistant Enterococcus faecium infection in three children given allogeneic hematopoietic stem cell transplantation: clinical and microbiological features, HAEMATOLOG, 85(11), 2000, pp. 1158-1164
Background and Objectives. The emergence of vancomycin-resistent enterococc
i (VRE) as nosocomial pathogens is a major problem in the US; in Europe, VR
E nosocomial infections are uncommon and only rarely have been reported in
Pediatric or Neonatal Units. The aim of this study is to report on the clin
ical and microbiological features of VRE infections in 3 children given hem
atopoietic stem cell transplantation (HSCT).
Patients and methods. Five episodes of vancomycin-resistant Enterococcus fa
ecium (VREF) infection were diagnosed in 3 children given an allogeneic HSC
T. Molecular methods, such as random amplification of polymorphic DNA (RAPD
) fingerprinting and automated ribotyping, were used in order to define the
circulation of strains.
Results. All the isolates were resistant to all commercially available agen
ts and showed the VanA genotypic profile. All children were successfully tr
eated with the combination of quinupristin/dalfopristin (QD) plus teicoplan
in (TEC), although treatment was not sufficient to eradicate the micro-orga
nism promptly from the gastrointestinal tract All our children are still al
ive. After the first isolation of VRE, a surveillance protocol was started
and we documented that the rate of colonization in children and their mothe
rs was less than 1.5%. The RAPD method demonstrated the possible nosocomial
transmission of one strain.
Interpretation and Conclusions. Our experience :demonstrates that VRE infec
tion is a life-threatening complication in children given HSCT. Prompt diag
nosis of this infection and its treatment with the combination of QD and TE
C can successfully manage this severe infection in profoundly immunocomprom
ised I patients. (C) 2000, Ferrata Storti Foundation.