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Hematologic Dysfunction Criteria in Critically Ill Children: The PODIUM Consensus Conference
Jennifer A Muszynski1, Jill M Cholette2, Marie E Steiner3
1Department of Pediatrics, Critical Care Medicine, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio.
Insights
Defining hematologic dysfunction in critically ill children is crucial. This study proposes evidence-based criteria for cytopenias, including platelet, leukocyte, and hemoglobin levels, to improve patient outcomes.
Area of Science:
- Pediatric Critical Care Medicine
- Hematology
- Evidence-Based Medicine
Background:
- Lack of consensus on organ dysfunction criteria limits research in critically ill children.
- Hematologic dysfunction is a known risk factor for poor outcomes in this population.
- Specific thresholds for hematologic dysfunction and their association with mortality are poorly defined.
Purpose of the Study:
- To derive evidence-informed, consensus-based criteria for hematologic dysfunction in critically ill children.
- To establish standardized screening criteria for hematologic dysfunction.
- To identify thresholds for cytopenias associated with patient outcomes.
Main Methods:
- Systematic review of PubMed and Embase databases (January 1992 to January 2020).
- Inclusion of studies evaluating assessment/scoring tools for hematologic dysfunction and patient outcomes.
- Exclusion of adult studies, premature infants, animal studies, reviews, and non-English studies.
Main Results:
- Twenty-nine studies were included in the systematic review.
- Proposed criteria for hematologic dysfunction include specific thresholds for thrombocytopenia (platelet count), leukopenia (leukocyte count), and anemia (hemoglobin concentration).
- Most studies focused on pre-specified cytopenia thresholds, with limited research on etiology, progression, or cellular function.
Conclusions:
- Hematologic dysfunction, defined by cytopenia, is a significant risk factor for adverse outcomes in critically ill children.
- The derived criteria provide a foundation for consistent identification of hematologic dysfunction.
- Further research is needed to explore the etiology, progression, and cellular function aspects of cytopenias in this population.
Context:
Studies of organ dysfunction in children are limited by a lack of consensus around organ dysfunction criteria.
Objectives:
To derive evidence-informed, consensus-based criteria for hematologic dysfunction in critically ill children.
Data Sources:
Data sources included PubMed and Embase from January 1992 to January 2020.
Study Selection:
Studies were included if they evaluated assessment/scoring tools to screen for hematologic dysfunction and assessed outcomes of mortality, functional status, organ-specific outcomes, or other patient-centered outcomes. Studies of adults or premature infants, animal studies, reviews/commentaries, small case series, and non-English language studies with inability to determine eligibility were excluded.
Data Extraction:
Data were abstracted from each eligible study into a standard data extraction form along with risk of bias assessment.
Results:
Twenty-nine studies were included. The systematic review supports the following criteria for hematologic dysfunction: thrombocytopenia (platelet count <100000 cells/µL in patients without hematologic or oncologic diagnosis, platelet count <30000 cells/µL in patients with hematologic or oncologic diagnoses, or platelet count decreased ≥50% from baseline; or leukocyte count <3000 cells/µL; or hemoglobin concentration between 5 and 7 g/dL (nonsevere) or <5 g/dL (severe).
Limitations:
Most studies evaluated pre-specified thresholds of cytopenias. No studies addressed associations between the etiology or progression of cytopenias overtime with outcomes, and no studies evaluated cellular function.
Conclusions:
Hematologic dysfunction, as defined by cytopenia, is a risk factor for poor outcome in critically ill children, although specific threshold values associated with increased mortality are poorly defined by the current literature.
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