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Pre-existing Immunocompromising Conditions and Outcomes of Acute COVID-19 Patients Admitted for Pediatric Intensive Care

  • Overcoming COVID-19 Investigators
  • Indiana University Bloomington
  • Harvard University
  • Phoenix Children's Hospital
  • Boston Children's Hospital
  • Centers for Disease Control and Prevention
  • Medical University of South Carolina
  • The Children's Hospital of Philadelphia
  • University of Arkansas for Medical Sciences
  • University of Colorado School of Medicine
  • Children's Mercy Hospitals and Clinics
  • New York University
  • University of North Carolina at Chapel Hill
  • Johns Hopkins University
  • Baylor College of Medicine
  • Washington University St. Louis
  • MemorialCare Miller Children's and Women's Hospital Long Beach
  • Akron Children's Hospital
  • Nationwide Children’s Hospital
  • Cooperman Barnabas Medical Center
  • UCSF Benioff Children's Hospital Oakland
  • University of California at San Francisco
  • Vanderbilt University
  • Louisiana State University Health Sciences Center
  • University of Miami
  • Westchester Medical Center
  • University of Mississippi
  • University of Iowa
  • University of Cincinnati
  • Northwestern University
  • University of Utah
  • University of Texas Southwestern Medical Center
  • University of Louisville
  • University of California at Irvine
  • Connecticut Children's Medical Center
  • Mayo Clinic Rochester, MN

Producción científicarevisión exhaustiva

2 Citas (Scopus)

Resumen

Background. We aimed to determine if pre-existing immunocompromising conditions (ICCs) were associated with the presentation or outcome of patients with acute coronavirus disease 2019 (COVID-19) admitted for pediatric intensive care. Methods. Fifty-five hospitals in 30 US states reported cases through the Overcoming COVID-19 public health surveillance registry. Patients <21 years admitted 12 March 2020–30 December 2021 to the pediatric intensive care unit (PICU) or high-acuity unit for acute COVID-19 were included. Results. Of 1274 patients, 105 (8.2%) had an ICC, including 33 (31.4%) hematologic malignancies, 24 (22.9%) primary immunodeficiencies and disorders of hematopoietic cells, 19 (18.1%) nonmalignant organ failure with solid-organ transplantation, 16 (15.2%) solid tumors, and 13 (12.4%) autoimmune disorders. Patients with ICCs were older, had more underlying renal conditions, and had lower white blood cell and platelet counts than those without ICCs, but had similar clinical disease severity upon admission. In-hospital mortality from COVID-19 was higher (11.4% vs 4.6%, P = .005) and hospitalization was longer (P = .01) in patients with ICCs. New major morbidities upon discharge were not different between those with and without ICC (10.5% vs 13.9%, P = .40). In patients with ICCs, bacterial coinfection was more common in those with life-threatening COVID-19. Conclusions. In this national case series of patients <21 years of age with acute COVID-19 admitted for intensive care, existence of a prior ICCs were associated with worse clinical outcomes. Reassuringly, most patients with ICCs hospitalized in the PICU for severe acute COVID-19 survived and were discharged home without new severe morbidities.

Idioma originalEnglish
Páginas (desde-hasta)395-404
Número de páginas10
PublicaciónClinical Infectious Diseases
Volumen79
N.º2
DOI
EstadoPublished - 15 ago 2024
Publicado de forma externa

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