A single‐center experience of cytomegalovirus infections in Asian pediatric patients undergoing allogeneic hematopoietic stem cell transplant for leukemia in Singapore. Issue 4 (23rd May 2014)
- Record Type:
- Journal Article
- Title:
- A single‐center experience of cytomegalovirus infections in Asian pediatric patients undergoing allogeneic hematopoietic stem cell transplant for leukemia in Singapore. Issue 4 (23rd May 2014)
- Main Title:
- A single‐center experience of cytomegalovirus infections in Asian pediatric patients undergoing allogeneic hematopoietic stem cell transplant for leukemia in Singapore
- Authors:
- Tan, P.L.
Lim, L.M.
Khanlian, C.
Villegas, M.S. - Abstract:
- <abstract abstract-type="main" id="tid12238-abs-0001"> <title>Abstract</title> <sec id="tid12238-sec-0001" sec-type="section"> <title>Introduction</title> <p>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.</p> </sec> <sec id="tid12238-sec-0002" sec-type="section"> <title>Methods</title> <p>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.</p> </sec> <sec id="tid12238-sec-0003" sec-type="section"> <title>Results</title> <p>In the 37 transplants, 16 patients (43%) had CMV DNAemia. Of the patients who were CMV seropositive before transplant and received stem cells from seropositive donors (R+/D+), 69% had DNAemia; of those who received stem cells from seronegative donors (R+/D−), 36% had CMV DNAemia. Of the patients who were CMV naïve before transplant and received stem cells from seropositive donors (R−/D+), 25% had CMV DNAemia. In CMV‐seronegative donor–recipient transplants (R−/D−), 20% of patients had CMV DNAemia. The median time to the first episode of CMV DNAemia was 21 (range: 10–107) days after the transplants, and the median duration of CMV DNAemia was 22 (range:<abstract abstract-type="main" id="tid12238-abs-0001"> <title>Abstract</title> <sec id="tid12238-sec-0001" sec-type="section"> <title>Introduction</title> <p>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.</p> </sec> <sec id="tid12238-sec-0002" sec-type="section"> <title>Methods</title> <p>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.</p> </sec> <sec id="tid12238-sec-0003" sec-type="section"> <title>Results</title> <p>In the 37 transplants, 16 patients (43%) had CMV DNAemia. Of the patients who were CMV seropositive before transplant and received stem cells from seropositive donors (R+/D+), 69% had DNAemia; of those who received stem cells from seronegative donors (R+/D−), 36% had CMV DNAemia. Of the patients who were CMV naïve before transplant and received stem cells from seropositive donors (R−/D+), 25% had CMV DNAemia. In CMV‐seronegative donor–recipient transplants (R−/D−), 20% of patients had CMV DNAemia. The median time to the first episode of CMV DNAemia was 21 (range: 10–107) days after the transplants, and the median duration of CMV DNAemia was 22 (range: 2–315) days. CMV DNAemia recurred in 44% (7 of 16) of these patients. Only 1 patient developed CMV disease (retinitis). No deaths were related to CMV infections.</p> </sec> <sec id="tid12238-sec-0004" sec-type="section"> <title>Conclusions</title> <p>CMV infection manifesting as DNAemia 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.</p> </sec> </abstract> … (more)
- Is Part Of:
- Transplant infectious disease. Volume 16:Issue 4(2014)
- Journal:
- Transplant infectious disease
- Issue:
- Volume 16:Issue 4(2014)
- Issue Display:
- Volume 16, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 16
- Issue:
- 4
- Issue Sort Value:
- 2014-0016-0004-0000
- Page Start:
- 556
- Page End:
- 560
- Publication Date:
- 2014-05-23
- Subjects:
- Transplantation of organs, tissues, etc -- Complications -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
617.01 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=mid ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tid.12238 ↗
- Languages:
- English
- ISSNs:
- 1398-2273
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.988700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3668.xml