A single‐center experience of cytomegalovirus infections in A sian pediatric patients undergoing allogeneic hematopoietic stem cell transplant for leukemia in S ingapore
Abstract Introduction Cytomegalovirus ( CMV ) infection remains a significant cause of morbidity and mortality in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation ( HSCT ) despite improved surveillance and the current preemptive approach. Few data on its prevalence in...
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Published in | Transplant infectious disease Vol. 16; no. 4; pp. 556 - 560 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.08.2014
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Online Access | Get full text |
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Summary: | Abstract
Introduction
Cytomegalovirus (
CMV
) infection remains a significant cause of morbidity and mortality in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation (
HSCT
) despite improved surveillance and the current preemptive approach. Few data on its prevalence in the Asian pediatric population exist.
Methods
We retrospectively reviewed the prevalence of
CMV
infections in 33 patients with 37 transplants who received
HSCT
for leukemia from 1998 to 2008, and who were managed preemptively for infections.
Results
In the 37 transplants, 16 patients (43%) had
CMV DNA
emia. Of the patients who were
CMV
seropositive before transplant and received stem cells from seropositive donors (R+/D+), 69% had
DNA
emia; of those who received stem cells from seronegative donors (R+/D−), 36% had
CMV DNA
emia. Of the patients who were
CMV
naïve before transplant and received stem cells from seropositive donors (R−/D+), 25% had
CMV DNA
emia. In
CMV
‐seronegative donor–recipient transplants (R−/D−), 20% of patients had
CMV
DNAemia. The median time to the first episode of
CMV DNA
emia was 21 (range: 10–107) days after the transplants, and the median duration of
CMV DNA
emia was 22 (range: 2–315) days.
CMV DNA
emia recurred in 44% (7 of 16) of these patients. Only 1 patient developed
CMV
disease (retinitis). No deaths were related to
CMV
infections.
Conclusions
CMV
infection manifesting as
DNA
emia is a common complication in pediatric patients undergoing allogeneic
HSCT
for leukemia. Pre‐transplant serostatus predicts reactivation risks; invasive
CMV
disease is rare using the preemptive approach in our patient population. |
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ISSN: | 1398-2273 1399-3062 |
DOI: | 10.1111/tid.12238 |