4.6 Article

Risk factors for seasonal human coronavirus lower respiratory tract infection after hematopoietic cell transplantation

Journal

BLOOD ADVANCES
Volume 5, Issue 7, Pages 1903-1914

Publisher

ELSEVIER
DOI: 10.1182/bloodadvances.2020003865

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Funding

  1. National Institutes of Health, National Institute of Allergy and Infectious Diseases [K23AI139385]
  2. National Heart, Lung, and Blood Institute [R01HL081595, K24HL093294]
  3. National Cancer Institute [CA18029, CA15704]
  4. Fred Hutchinson Cancer Research Center Vaccine and Infectious Disease Division
  5. Seattle Children's Research Institute Clinical Research Scholars Program Award

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Data is limited on risk factors and outcomes of lower respiratory tract infections (LRTIs) caused by seasonal human coronaviruses (HCoVs) in hematopoietic cell transplant (HCT) recipients. This study identified factors associated with HCoV LRTI, some of which are less commonly appreciated as risk factors for LRTI with other respiratory viruses in HCT recipients. Hyperglycemia may provide an intervention opportunity to reduce the risk of LRTI.
Data are limited regarding risk factors for lower respiratory tract infection (LRTI) caused by seasonal human coronaviruses (HCoVs) and the significance of virologic documentation by bronchoalveolar lavage (BAL) on outcomes in hematopoietic cell transplant (HCT) recipients. We retrospectively analyzed patients undergoing allogeneic HCT (4/2008-9/2018) with HCoV (OC43/NL63/HKU1/229E) detected by polymerase chain reaction during conditioning or post-HCT. Risk factors for all manifestations of LRTI and progression to LRTI among those presenting with HCoV upper respiratory tract infection (URTI) were analyzed by logistic regression and Cox proportional hazard models, respectively. Mortality rates following HCoV LRTI were compared according to virologic documentation by BAL. A total of 297 patients (61 children and 236 adults) developed HCoV infection as follows: 254 had URTI alone, 18 presented with LRTI, and 25 progressed from URTI to LRTI (median, 16 days; range, 2-62 days). Multivariable logistic regression analyses showed that male sex, higher immunodeficiency scoring index, albumin <3 g/dL, glucose >150 mg/dL, and presence of respiratory copathogens were associated with occurrence of LRTI. Hyperglycemia with steroid use was associated with progression to LRTI (P < .01) in Cox models. LRTI with HCoV detected in BAL was associated with higher mortality than LRTI without documented detection in BAL (P < .01). In conclusion, we identified factors associated with HCoV LRTI, some of which are less commonly appreciated to be risk factors for LRTI with other respiratory viruses in HCT recipients. The association of hyperglycemia with LRTI might provide an intervention opportunity to reduce the risk of LRTI.

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