The Impact of Pretransplant Respiratory Virus Detection on Posttransplant Outcomes in Children Undergoing Hematopoietic Cell Transplantation

Author:

Kim Sara Ruth123ORCID,Nordlander Anna34,Xie Hu5,Kim Yae-Jean367,Ogimi Chikara38,Thakar Monica S15,Leisenring Wendy5,Englund Janet A123,Boeckh Michael359,Waghmare Alpana123

Affiliation:

1. Department of Pediatric, University of Washington , Seattle, Washington , USA

2. Pediatric Infectious Disease Division, Seattle Children's Hospital , Seattle, Washington , USA

3. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center , Seattle, Washington , USA

4. Department of Infectious Diseases, Karolinska University Hospital , Stockholm , Sweden

5. Clinical Research Division, Fred Hutchinson Cancer Center , Seattle, Washington , USA

6. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University , Seoul , Republic of Korea

7. Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences & Technology, Sungkyunkwan University , Seoul , Republic of Korea

8. Division of Infectious Diseases, National Center for Child Health and Development , Tokyo , Japan

9. Department of Medicine, University of Washington , Seattle, Washington , USA

Abstract

Abstract Background Pretransplant respiratory virus (RV) infections have been associated with negative transplant outcomes in adult hematopoietic cell transplantation (HCT) recipients. In the era of HCT delay because of high-risk RVs, we examined the impact of pretransplant RV detection on transplant outcomes in pediatric HCT recipients. Methods This retrospective cohort study included pediatric myeloablative allogeneic HCT recipients from 2010 to 2019. All patients were screened for RV at least once within 90 days before HCT using reverse transcriptase polymerase chain reaction (PCR), regardless of symptoms. Posttransplant outcomes included days alive and out of hospital and progression to lower respiratory tract infection (LRTI). Results Among 310 patients, 134 had an RV detected in the 90 days before HCT. In univariable analysis, transplant factors including younger age, total body irradiation, umbilical cord blood transplantation, lymphocyte count <100/mm3, HCT comorbidity index score ≥3, and viral factors including symptomatic infection, human rhinovirus as a virus type, and symptomatic pretransplant upper respiratory tract infection were associated with fewer days alive and out of hospital. In multivariable analysis, transplant factors remained significant, but not viral factors. There was a higher incidence of progression to posttransplant LRTI with the same pretransplant RV if the last positive PCR before HCT was ≤30 days compared with >30 days (P = .007). Conclusions In the setting of recommending HCT delay for high-risk RVs, symptomatic upper respiratory tract infection, including human rhinovirus infections, may lead to increased duration of hospitalization and early progression to LRTI when transplantation is performed within 30 days of the last positive PCR test.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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