Lower hospital mortality and complications after pediatric hematopoietic stem cell transplantation.

Abstract:

OBJECTIVE:To assess protective and risk factors for mortality among pediatric patients during initial care after hematopoietic stem cell transplantation (HSCT) and to evaluate changes in hospital mortality. DESIGN:Retrospective cohort using the 1997, 2000, and 2003 Kids Inpatient Database, a probabilistic sample of children hospitalized in the United States with a procedure code for HSCT. SETTING:Hospitalized patients in the United States submitted to the database. PATIENTS:Age, <19 yrs. INTERVENTIONS:None. MEASUREMENTS AND MAIN RESULTS:Hospital mortality significantly decreased from 12% in 1997 to 6% in 2003. Source of stem cells changed with increased use of cord blood. Rates of sepsis, graft versus host disease, and mechanical ventilation significantly decreased. Compared with autologous HSCT, patients who received an allogenic HSCT without T-cell depletion were more likely to die (adjusted odds ratio, 2.4; 95% confidence interval, 1.5, 3.9), while children who received cord blood HSCT were at the greatest risk of hospital death (adjusted odds ratio, 4.8; 95% confidence interval, 2.6, 9.1). Mechanical ventilation (adjusted odds ratio, 26.32; 95% confidence interval, 16.3-42.2), dialysis (adjusted odds ratio, 12.9; 95% confidence interval, 4.7-35.4), and sepsis (adjusted odds ratio, 3.9; 95% confidence interval, 2.5-6.1) were all independently associated with death, while care in 2003 was associated with decreased risk (adjusted odds ratio, 0.4; 95% confidence interval, 0.2-0.7) of death. CONCLUSIONS:Hospital mortality after HSCT in children decreased over time as did complications including need for mechanical ventilation, graft versus host disease, and sepsis. Prevention of complications is essential as the need for invasive support continues to be associated with high mortality risk.

journal_name

Crit Care Med

journal_title

Critical care medicine

authors

Bratton SL,Van Duker H,Statler KD,Pulsipher MA,McArthur J,Keenan HT

doi

10.1097/01.CCM.0B013E318161FAC1

subject

Has Abstract

pub_date

2008-03-01 00:00:00

pages

923-7

issue

3

eissn

0090-3493

issn

1530-0293

journal_volume

36

pub_type

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