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Acute Respiratory Distress Syndrome Phenotypes After Stem Cell Transplantation: A Latent Class Analysis
Svetlana Herasevich1, Kiyan Heybati2, William J Hogan3
1Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN.
Acute respiratory distress syndrome (ARDS) after hematopoietic cell transplantation (HCT) presents two distinct phenotypes. These patient groups exhibit different clinical features and outcomes, guiding future research for targeted therapies.
Area of Science:
- Critical Care Medicine
- Hematology
- Pulmonology
Background:
- Acute respiratory distress syndrome (ARDS) is a severe complication following hematopoietic cell transplantation (HCT).
- Understanding distinct ARDS phenotypes post-HCT is crucial for improving patient outcomes.
Purpose of the Study:
- To identify and characterize distinct phenotypes of ARDS in patients undergoing HCT.
- To utilize routinely available clinical data at intensive care unit (ICU) admission for phenotype identification.
Main Methods:
- Multicenter retrospective cohort study involving 166 adult patients who developed ARDS post-HCT.
- Latent class analysis was employed to identify distinct patient groups based on clinical variables.
- Model selection utilized metrics such as Bayesian information criteria and entropy for optimal class identification.
Main Results:
- A two-class model optimally described the ARDS cohort, with Class 1 exhibiting worse hypoxemia, higher Pco2, and elevated bilirubin.
- Class 1 patients experienced later onset post-transplant, higher rates of idiopathic pneumonia syndrome, and significantly worse 90-day mortality (72.8% vs. 48.2%).
- Class 2 was characterized by more frequent neutropenia and peri-engraftment respiratory distress syndrome.
Conclusions:
- ARDS following HCT comprises two distinct phenotypes with differing clinical characteristics and prognoses.
- These phenotypes correlate with known post-HCT lung injury syndromes, suggesting different underlying biological mechanisms.
- This classification framework supports the development of targeted therapeutic strategies for ARDS post-HCT.
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