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Published on: April 7, 2021
P50 implies adverse clinical outcomes in pediatric acute respiratory distress syndrome by reflecting extrapulmonary
Yura Kim1, Jae Hwa Jung2, Ga Eun Kim3
1Department of Pediatrics, Severance Children's Hospital, Institute of Allergy, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Insights
In pediatric acute respiratory distress syndrome (PARDS), higher P50 levels, indicating reduced hemoglobin-oxygen affinity, correlate with increased organ dysfunction and mortality risk. This suggests P50 may aid in stratifying PARDS patient outcomes.
Area of Science:
- Pediatric Critical Care Medicine
- Respiratory Physiology
- Hemoglobin-Oxygen Affinity
Background:
- Pediatric acute respiratory distress syndrome (PARDS) is a critical condition associated with high mortality.
- Hypoxemia and multiple organ dysfunction are key factors contributing to PARDS mortality.
- Altered hemoglobin-oxygen affinity (P50) may impact tissue oxygenation and organ function in PARDS.
Purpose of the Study:
- To evaluate P50 levels in pediatric patients with PARDS.
- To determine the association between P50 and clinical outcomes, including organ dysfunction and mortality.
Main Methods:
- Retrospective study of 212 children with PARDS requiring mechanical ventilation.
- P50 levels calculated using Doyle's method.
- Organ dysfunction assessed with the Pediatric Logistic Organ Dysfunction-2 score.
Main Results:
- P50 levels increased significantly with increasing PARDS severity.
- A positive association was found between P50 and extrapulmonary organ dysfunction score.
- Higher P50 was significantly associated with increased risk of mortality, largely mediated by organ dysfunction.
Conclusions:
- Elevated P50 at PARDS diagnosis may indicate increased mortality risk, primarily through extrapulmonary organ dysfunction.
- P50 could serve as a potential biomarker for risk stratification in PARDS patients.
- Further research is warranted to explore P50's role in managing PARDS.
Abstract:
Hypoxemia and multiple organ dysfunction are significant contributors to mortality in patients with pediatric acute respiratory distress syndrome (PARDS). P50, the oxygen tension at which hemoglobin is 50% saturated, is a measure of hemoglobin-oxygen affinity, and its alteration might have implications for tissue hypoxia and organ dysfunction. The purpose of this single-center, retrospective study was to evaluate P50 levels in PARDS and to determine the association between P50 and clinical outcomes. The study included 212 children diagnosed with PARDS according to the Pediatric Acute Lung Injury Consensus Conference definition who required invasive mechanical ventilation and had arterial blood gas results of hemoglobin oxygen saturation < 97% at the time of diagnosis. P50 levels were calculated using Doyle's method, and organ dysfunction was assessed using the Pediatric Logistic Organ Dysfunction-2 score. Most patients exhibited more than one dysfunctional extrapulmonary organ at PARDS onset. P50 increased with increasing PARDS severity (mild (26.6 [24.9-29.6]), moderate (26.8 [25.0-29.5]), and severe PARDS (29.1 [26.1-32.4] mmHg; P = 0.025). Moreover, P50 demonstrated a significant positive association with extrapulmonary organ dysfunction score (β = 0.158, P = 0.007) and risk of mortality (adjusted hazard ratio, 1.056; 95% confidence interval, 1.015-1.098; P = 0.007), irrespective of initial PARDS severity. The relationship between P50 and mortality was largely mediated by extrapulmonary organ dysfunction. A high P50 value at the time of PARDS diagnosis may be associated with mortality via dysfunctional extrapulmonary organs. Future studies should consider P50 as a potential candidate index for risk stratification of PARDS patients.
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