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Alterations in end-of-life support in the pediatric intensive care unit
K Jane Lee1, Kelly Tieves, Matthew C Scanlon
1Medical College of Wisconsin, Department of Pediatrics, 9000 W. Wisconsin Ave, MS B550B, Milwaukee, WI 53226, USA. kjlee@mcw.edu
Insights
Decisions to limit end-of-life support are common in pediatric intensive care units (PICUs). Black race and fewer trainees were linked to less frequent limitation decisions.
Area of Science:
- Pediatric critical care medicine
- End-of-life care research
- Healthcare disparities
Background:
- End-of-life care decisions significantly impact patient outcomes and family experiences in pediatric intensive care units (PICUs).
- Understanding variations in end-of-life support is crucial for improving care quality and addressing potential inequities.
Purpose of the Study:
- To investigate patterns and variations in end-of-life support practices across multiple pediatric intensive care units.
- To identify demographic and institutional factors associated with decisions to limit life-sustaining treatment.
Main Methods:
- Retrospective, descriptive study analyzing data from 35 institutions.
- Collected data included end-of-life support category, patient demographics (race), length of stay, and institutional factors (trainee presence).
- End-of-life support categories were grouped into 'limitation' and 'no limitation' for analysis, excluding brain death cases.
Main Results:
- A majority of deaths (85%) involved limitation of support, with significant institutional variation.
- Decisions to limit support were less frequent in Black patients (76% vs. unspecified for others) and in institutions without trainees (69% vs. unspecified for others).
- P-values indicate statistically significant differences for race (P=.037) and trainee presence (P<.001).
Conclusions:
- Limitation of end-of-life support is a prevalent practice in PICUs.
- Factors such as Black race and the absence of trainees are associated with a lower frequency of limitation decisions.
- Further research is needed to understand the underlying reasons for these disparities.
Objective:
Our purpose was to examine alterations in end-of-life support in a multiinstitutional sample of PICUs.
Methods:
This was a retrospective, descriptive study. Variables collected included end-of-life support category, race, length of stay, operative status, reason for admission, and Pediatric Index of Mortality 2 score, as well as the number of ICU beds and the presence of trainees.
Results:
There were 1745 deaths at 35 institutions between January 1, 2004, and September 30, 2005. Of those, 1263 had complete data and were analyzed. The end-of-life support category distribution was as follows: brain death, 296 (23%); do not resuscitate, 205 (16%); limitation of support, 36 (3%); withdrawal of support, 579 (46%); no limitation, 124 (10%); no advance directives, 23 (2%). For further analyses, end-of-life support categories were grouped as limitation (ie, do not resuscitate, limitation of support, or withdrawal of support) versus no limitation (ie, no limitation or no advance directive). Brain death was not included in further analyses. The majority of deaths were in the limitation group (n=820 [85%]), and 12 (40%) of 30 institutions had 100% of deaths in this group. There were significant differences between institutions (P<.001). Decisions for limitation were seen less frequently in the black race (112 [76%] of 147 deaths; P=.037) and in institutions with no trainees (56 [69%] of 81 deaths; P<.001).
Conclusions:
Decisions to limit support are common. Black race and an absence of trainees are associated with decreased frequency of limitation decisions.
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