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The Impact of Pretransplant Respiratory Virus Detection on Posttransplant Outcomes in Children Undergoing Hematopoietic Cell Transplantation.
Kim, Sara Ruth; Nordlander, Anna; Xie, Hu; Kim, Yae-Jean; Ogimi, Chikara; Thakar, Monica S; Leisenring, Wendy; Englund, Janet A; Boeckh, Michael; Waghmare, Alpana.
Affiliation
  • Kim SR; Department of Pediatric, University of Washington, Seattle, Washington, USA.
  • Nordlander A; Pediatric Infectious Disease Division, Seattle Children's Hospital, Seattle, Washington, USA.
  • Xie H; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
  • Kim YJ; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
  • Ogimi C; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
  • Thakar MS; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
  • Leisenring W; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
  • Englund JA; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University, Seoul, Republic of Korea.
  • Boeckh M; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences & Technology, Sungkyunkwan University, Seoul, Republic of Korea.
  • Waghmare A; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Clin Infect Dis ; 79(3): 761-771, 2024 Sep 26.
Article in En | MEDLINE | ID: mdl-38666501
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.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Hematopoietic Stem Cell Transplantation Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Infect Dis / Clin. infect. dis / Clinical infectious diseases Journal subject: DOENCAS TRANSMISSIVEIS Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Hematopoietic Stem Cell Transplantation Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Infect Dis / Clin. infect. dis / Clinical infectious diseases Journal subject: DOENCAS TRANSMISSIVEIS Year: 2024 Document type: Article Affiliation country: Country of publication: