Association of the social disorganization index with time to first septic shock event in children with acute myeloid leukemia

Author:

Ruiz Jenny12ORCID,Li Yimei12,Cao Lusha3,Huang Yuan‐Shung V.3,Tam Vicky3,Griffis Heather M.3,Winestone Lena E.4ORCID,Fisher Brian T.25,Alonzo Todd A.6,Wang Yi‐Cheng J.7,Dang Alice T.7,Kolb E. Anders8,Glanz Karen9,Getz Kelly D.29,Aplenc Richard12,Seif Alix E.12ORCID

Affiliation:

1. Division of Oncology Children’s Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Department of Pediatrics Perelman School of Medicine at the University of Pennsylvania Philadelphia Pennsylvania USA

3. Department of Biomedical and Health Informatics Children’s Hospital of Philadelphia Philadelphia Pennsylvania USA

4. Division of Allergy, Immunology, and Bone Marrow Transplantation Benioff Children’s Hospital University of California San Francisco San Francisco California USA

5. Division of Infectious Diseases Children’s Hospital of Philadelphia Philadelphia Pennsylvania USA

6. Department of Population and Public Health Sciences Keck School of Medicine University of Southern California Los Angeles California USA

7. Public Health Institute Monrovia California USA

8. Nemours Center for Cancer and Blood Disorders Nemours Children’s Health Wilmington Delaware USA

9. Department of Biostatistics, Epidemiology, and Informatics Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

Abstract

AbstractBackgroundPediatric acute myeloid leukemia (AML) chemotherapy increases the risk of life‐threatening complications, including septic shock (SS). An area‐based measure of social determinants of health, the social disorganization index (SDI), was hypothesized to be associated with SS and SS‐associated death (SS‐death).MethodsChildren treated for de novo AML on two Children’s Oncology Group trials at institutions contributing to the Pediatric Health Information System (PHIS) database were included. The SDI was calculated via residential zip code data from the US Census Bureau. SS was identified via PHIS resource utilization codes. SS‐death was defined as death within 2 weeks of an antecedent SS event. Patients were followed from 7 days after the start of chemotherapy until the first of end of front‐line therapy, death, relapse, or removal from study. Multivariable‐adjusted Cox regressions estimated hazard ratios (HRs) comparing time to first SS by SDI group.ResultsThe assembled cohort included 700 patients, with 207 (29.6%) sustaining at least one SS event. There were 233 (33%) in the SDI‐5 group (highest disorganization). Adjusted time to incident SS did not statistically significantly differ by SDI (reference, SDI‐1; SDI‐2: HR, 0.84 [95% confidence interval (CI), 0.51–1.41]; SDI‐3: HR, 0.70 [95% CI, 0.42–1.16]; SDI‐4: HR, 0.97 [95% CI, 0.61–1.53]; SDI‐5: HR, 0.72 [95% CI, 0.45–1.14]). Nine patients (4.4%) with SS experienced SS‐death; seven of these patients (78%) were in SDI‐4 or SDI‐5.ConclusionsIn a large, nationally representative cohort of trial‐enrolled pediatric patients with AML, there was no significant association between the SDI and time to SS.

Publisher

Wiley

Subject

Cancer Research,Oncology

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