Volume 19, Issue 6 pp. 640-644
Original Article

The yield of monitoring for HSV and VZV viremia in pediatric hematopoietic stem cell transplant patients

Katharine Patrick

Corresponding Author

Katharine Patrick

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

Katharine Patrick, Division of Hematology/Oncology, The Hospital for Sick Children, 555 University Avenue, Toronto, M5G 1X8 ON, Canada

Tel.: +1 416 813 6906

Fax: +1 416 813 5327

E-mail: [email protected]

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Muhammad Ali

Muhammad Ali

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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Susan E. Richardson

Susan E. Richardson

Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada

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Adam Gassas

Adam Gassas

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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Maarten Egeler

Maarten Egeler

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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Joerg Krueger

Joerg Krueger

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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Jane Lowry

Jane Lowry

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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Upton Allen

Upton Allen

The Division of Infectious Diseases, The Hospital for Sick Children, Toronto, ON, Canada

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Tal Schechter

Tal Schechter

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada

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First published: 06 July 2015
Citations: 8

Abstract

Reactivation of HSV and VZV is common following HSCT. Consensus guidelines do not support the use of routine screening for viremia following HSCT in adults, but no such clear guidelines exist in pediatrics. In our center, routine practice was to screen patients weekly for HSV and VZV viremia until engraftment in autologous transplant patients and up to day +100 in allogeneic transplant patients. We conducted a retrospective study of over 500 patients to establish whether this screening identified any patients with HSV or VZV viremia who would not have been identified by clinical signs or symptoms. Over a 4.5-yr period, routine screening identified three cases of HSV viremia and one case of VZV viremia. Two patients had persistent, unexplained fever and two patients had skin or mucosal lesions suggestive of HSV/VZV. We conclude that routine screening for HSV and VZV viremia in pediatric HSCT patients has a very low yield and that viremia can be reliably identified by targeted testing in patients with vesicular skin lesions, oral or genital ulceration, unexplained fever, neurological symptoms, or unexplained abnormal liver transaminases.

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