Critical Illness Risk and Long-Term Outcomes Following Intensive Care in Pediatric Hematopoietic Cell Transplant Recipients.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
05 Aug 2023
Historique:
pubmed: 14 8 2023
medline: 14 8 2023
entrez: 14 8 2023
Statut: epublish

Résumé

Allogeneic hematopoietic cell transplantation (HCT) can be complicated by the development of organ toxicity and infection necessitating intensive care. Risk factors for intensive care admission are unclear due to heterogeneity across centers, and long-term outcome data after intensive care are sparse due to a historical paucity of survivors. The Center for International Blood and Marrow Transplant Research (CIBMTR) was queried to identify patients age ≤21 years who underwent a 1 We identified 6,995 pediatric HCT patients from 69 HCT centers, of whom 1,067 required post-HCT intensive care. The cumulative incidence of PICU admission was 8.3% at day +100, 12.8% at 1 year, and 15.3% at 5 years post HCT. PICU admission was linked to younger age, lower median zip code income, Black or multiracial background, pre-transplant organ toxicity, pre-transplant CMV seropositivity, use of umbilical cord blood and/or HLA-mismatched allografts, and the development of post-HCT graft-versus-host disease or malignancy relapse. Among PICU patients, survival to ICU discharge was 85.7% but more than half of ICU survivors were readmitted to a PICU during the study interval. Overall survival from the time of 1 Intensive care management is common in pediatric HCT patients. Survival to ICU discharge is high, but ongoing complications necessitate recurrent ICU admission and lead to a poor 1-year outcome in many patients. Together, these data suggest an ongoing burden of toxicity in pediatric HCT patients that continues to limit long-term survival.

Sections du résumé

Background UNASSIGNED
Allogeneic hematopoietic cell transplantation (HCT) can be complicated by the development of organ toxicity and infection necessitating intensive care. Risk factors for intensive care admission are unclear due to heterogeneity across centers, and long-term outcome data after intensive care are sparse due to a historical paucity of survivors.
Methods UNASSIGNED
The Center for International Blood and Marrow Transplant Research (CIBMTR) was queried to identify patients age ≤21 years who underwent a 1
Result UNASSIGNED
We identified 6,995 pediatric HCT patients from 69 HCT centers, of whom 1,067 required post-HCT intensive care. The cumulative incidence of PICU admission was 8.3% at day +100, 12.8% at 1 year, and 15.3% at 5 years post HCT. PICU admission was linked to younger age, lower median zip code income, Black or multiracial background, pre-transplant organ toxicity, pre-transplant CMV seropositivity, use of umbilical cord blood and/or HLA-mismatched allografts, and the development of post-HCT graft-versus-host disease or malignancy relapse. Among PICU patients, survival to ICU discharge was 85.7% but more than half of ICU survivors were readmitted to a PICU during the study interval. Overall survival from the time of 1
Conclusions UNASSIGNED
Intensive care management is common in pediatric HCT patients. Survival to ICU discharge is high, but ongoing complications necessitate recurrent ICU admission and lead to a poor 1-year outcome in many patients. Together, these data suggest an ongoing burden of toxicity in pediatric HCT patients that continues to limit long-term survival.

Identifiants

pubmed: 37577706
doi: 10.1101/2023.07.31.23293444
pmc: PMC10418579
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Matt S Zinter (MS)

Department of Pediatrics, Division of Critical Care Medicine, University of California, San Francisco, San Francisco, CA, USA.
Department of Pediatrics, Division of Allergy, Immunology, and BMT, University of California, San Francisco, San Francisco, CA, USA.

Ruta Brazauskas (R)

Medical College of Wisconsin, Milwaukee, WI, USA.

Joelle Strom (J)

Medical College of Wisconsin, Milwaukee, WI, USA.

Stella Chen (S)

Medical College of Wisconsin, Milwaukee, WI, USA.

Stephanie Bo-Subait (S)

Medical College of Wisconsin, Milwaukee, WI, USA.

Akshay Sharma (A)

St. Jude Children's Research Hospital, Memphis, TN, USA.

Amer Beitinjaneh (A)

University of Miami, Miami, FL, USA.

Dimana Dimitrova (D)

National Institutes of Health, National Cancer Institute, Bethesda, MD, USA.

Greg Guilcher (G)

Alberta Children's Hospital, Alberta, Canada.

Jaime Preussler (J)

National Marrow Donor Program/Be The Match, Minneapolis, MN, USA.

Kasiani Myers (K)

Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Neel S Bhatt (NS)

Fred Hutchinson Cancer Center, Seattle, WA, USA.

Olle Ringden (O)

Karolinska Institutet, Karolinska University Hospital, Huddinge, The Netherlands.

Peiman Hematti (P)

Medical College of Wisconsin, Milwaukee, WI, USA.

Robert J Hayashi (RJ)

Washington University in St. Louis, St. Louis, MO, USA.

Sagar Patel (S)

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

Satiro Nakamura De Oliveira (SN)

University of California, Los Angeles, Los Angeles, CA, USA.

Seth Rotz (S)

Cleveland Clinic, Cleveland, OH, USA.

Sherif M Badawy (SM)

Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Taiga Nishihori (T)

Moffitt Cancer Center, Tampa, FL, USA.

David Buchbinder (D)

Children's Hospital of Orange County, Orange, CA, USA.

Betty Hamilton (B)

Cleveland Clinic, Cleveland, OH, USA.

Bipin Savani (B)

Vanderbilt University Medical Center, Nashville, TN, USA.

Hélène Schoemans (H)

University Hospital Gasthuisberg, Leuven, Belgium.

Mohamed Sorror (M)

Fred Hutchinson Cancer Center, Seattle, WA, USA.

Lena Winestone (L)

Department of Pediatrics, Division of Allergy, Immunology, and BMT, University of California, San Francisco, San Francisco, CA, USA.

Christine Duncan (C)

Dana Farber Cancer Center, Boston, MA, USA.

Rachel Phelan (R)

Medical College of Wisconsin, Milwaukee, WI, USA.

Christopher C Dvorak (CC)

Department of Pediatrics, Division of Allergy, Immunology, and BMT, University of California, San Francisco, San Francisco, CA, USA.

Classifications MeSH