Clinical Outcomes of Respiratory Syncytial Virus Infection Among
Pediatric Immunocompromised Hosts
- Hailey S. Ross,
- Ronald Dallas,
- Jose Ferrolino,
- Madeline Burton,
- Kim Allison,
- Shane Cross,
- Randall Hayden,
- ASUNCION MEJIAS,
- Diego Hijano
Abstract
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Background: Pediatric immunocompromised patients are at an
increased risk of severe respiratory syncytial virus (RSV) infection.
Here, we aimed to describe the clinical course and outcomes of RSV
infection in immunocompromised children. Methods: This
single-center study was conducted at St. Jude Children’s Research
Hospital in immunocompromised children ≤21 years old, who had a positive
RSV clinical test in the clinic or hospital from 2007 to 2019.
Demographic and clinical characteristics, laboratory values, delays in
the treatment of patients’ underlying conditions, and outcomes were
extracted from the patients’ electronic medical records. Multivariate
models were constructed to identify risk factors predictive of severe
RSV LRTI. Results: In total, 391 patients were included. Most
children (86%) were > 2 years of age, with a median age of
5 years. Acute lymphoblastic leukemia (ALL) was the most common
underlying disease. Most patients presented with upper respiratory tract
infections (n = 335; 85.7%). Approximately 6% of patients progressed
to lower respiratory tract infections. More than half (58.8%) of the
patients were hospitalized, and therapy for the underlying disease was
modified or delayed due to RSV infection in one-third of the patients.
Severe RSV infections were observed in 62 patients (15.9%). All-cause
mortality was reported in 10 patients (2.6%), with three RSV-related
deaths (0.7%). Conclusions: A high proportion of
immunocompromised children with RSV infection require hospitalization.
Hospitalization was observed in those aged >2 years, and an
overall treatment delay for the underlying disease occurred in one-third
of the patients. The burden associated with RSV in immunocompromised
children is high irrespective of age and has direct and indirect
consequences on their cancer treatment plans.29 Aug 2024Submission Checks Completed 29 Aug 2024Assigned to Editor
29 Aug 2024Submitted to Pediatric Blood & Cancer 02 Sep 2024Review(s) Completed, Editorial Evaluation Pending
02 Sep 2024Reviewer(s) Assigned
25 Sep 2024Editorial Decision: Revise Major
15 Nov 20241st Revision Received
15 Nov 2024Submission Checks Completed
15 Nov 2024Assigned to Editor
19 Nov 2024Review(s) Completed, Editorial Evaluation Pending
19 Nov 2024Reviewer(s) Assigned
22 Nov 2024Editorial Decision: Revise Minor
23 Nov 20242nd Revision Received
23 Nov 2024Submission Checks Completed
23 Nov 2024Assigned to Editor
26 Nov 2024Review(s) Completed, Editorial Evaluation Pending
27 Nov 2024Editorial Decision: Accept