Volume 19, Issue 7 pp. 737-744
Original Article

Human herpesvirus-6 viremia is not associated with poor clinical outcomes in children following allogeneic hematopoietic cell transplantation

Leah Violago

Leah Violago

Department of Nursing, New York-Presbyterian Morgan Stanley Children's Hospital, New York, NY, USA

Both authors contributed equally.Search for more papers by this author
Zhezhen Jin

Zhezhen Jin

Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY, USA

Both authors contributed equally.Search for more papers by this author
Monica Bhatia

Monica Bhatia

Department of Pediatrics, Columbia University, New York, NY, USA

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Evelyn Rustia

Evelyn Rustia

Department of Pediatrics, Columbia University, New York, NY, USA

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Andrew L. Kung

Andrew L. Kung

Department of Pediatrics, Columbia University, New York, NY, USA

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Marc D. Foca

Marc D. Foca

Department of Pediatrics, Columbia University, New York, NY, USA

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Diane George

Diane George

Department of Pediatrics, Columbia University, New York, NY, USA

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James H. Garvin

James H. Garvin

Department of Pediatrics, Columbia University, New York, NY, USA

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Jean Sosna

Jean Sosna

Department of Pediatrics, Columbia University, New York, NY, USA

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Chalitha Robinson

Chalitha Robinson

Department of Pediatrics, Columbia University, New York, NY, USA

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Esra Karamehmet

Esra Karamehmet

Department of Pediatrics, Columbia University, New York, NY, USA

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Prakash Satwani

Corresponding Author

Prakash Satwani

Department of Pediatrics, Columbia University, New York, NY, USA

Prakash Satwani, Division of Pediatric Blood and Bone Marrow Transplantation, Department of Pediatrics, NewYork-Presbyterian Morgan Stanley Children's Hospital, Columbia University, 3959 Broadway, CHN 10-02, New York, NY 10032, USA

Tel.: +1 212 305 0223

Fax: +1 212 305 8428

E-mail: [email protected]

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First published: 29 August 2015
Citations: 10

Abstract

HHV-6 is an evolving pathogen in the field of AlloHCT. However, the impact of HHV-6 on AlloHCT outcomes remains to be elucidated. We studied the incidence and clinical impact of HHV-6 viremia in children following AlloHCT. One hundred consecutive children were monitored weekly by plasma PCR for the first 180 days following AlloHCT for HHV-6, CMV, EBV, and ADV. HHV-6 viremia was defined as plasma PCR >1000 viral copies/mL. The median age was nine yr. Following AlloHCT, 19% (95% CI 11.3–26.7%) of patients had HHV-6 viremia, with the highest incidence of reactivation (14/19, 73%) occurring during day +15-day +98. The proportion of platelet engraftment by day +180 was lower in patients with HHV-6 viremia (58%) than in those without HHV-6 viremia (82%), p = 0.028. Delay in neutrophil and platelet engraftment was not associated with HHV-6 viremia in multivariate analysis. Similarly, HHV-6 viremia was not associated with TRM in multivariate analysis (p = 0.15). In summary, HHV-6 viremia is prevalent in pediatric AlloHCT recipients. Based on our study results, we recommend that HHV-6 PCR should only be performed on clinical suspicion.

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