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Developing A Model to Predict Major Bleeding Among Hospitalized Patients Undergoing Therapeutic Plasma Exchange

dc.contributor.authorSoares Ferreira Junior, Alexandre [UNESP]
dc.contributor.authorLessa, Morgana Pinheiro Maux
dc.contributor.authorSanborn, Kate
dc.contributor.authorGordee, Alexander
dc.contributor.authorKuchibhatla, Maragatha
dc.contributor.authorKarafin, Matthew S.
dc.contributor.authorOnwuemene, Oluwatoyosi A.
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionDuke University School of Medicine
dc.contributor.institutionUniversity of North Carolina
dc.date.accessioned2025-04-29T20:05:05Z
dc.date.issued2025-04-01
dc.description.abstractAlthough therapeutic plasma exchange (TPE) can be associated with bleeding, there are currently no known strategies to reliably predict bleeding risk. This study developed a TPE bleeding risk prediction model for hospitalized patients. To develop the prediction model, we undertook a secondary analysis of public use files from the Recipient Epidemiology and Donor Evaluation Study-III. First, we used a literature review to identify potential predictors. Second, we used Multiple Imputation by Chained Equations to impute variables with < 30% missing data. Third, we performed a 10-fold Cross-Validated Least Absolute Shrinkage and Selection Operator to optimize variable selection. Finally, we fitted a logistic regression model. The model identified 10 unique predictors and seven interactions. Among those with the highest odds ratios (OR) were the following: > 10 TPE procedures and antiplatelet agents (OR 3.26); nephrogenic systemic sclerosis (OR 3.15); and intensive care unit stay (OR 3.08). Among those with the lowest OR were the following: albumin-only TPE (OR 0.50); male sex (OR 0.82); and heart failure (OR 0.85). The model indicated an acceptable performance with a C-statistic of 0.71 (95% CI 0.699-0.717). A model to predict bleeding risk among hospitalized patients undergoing TPE identified key predictors and interactions. Although the model achieved acceptable performance, future studies are needed to validate and operationalize it.en
dc.description.affiliationDepartment of Medicine Faculdade de Medicina de São José do Rio Preto
dc.description.affiliationGeneral and Applied Biology Program Institute of Biosciences (IBB) Sao Paulo State University (UNESP)
dc.description.affiliationDuke Biostatistics Epidemiology and Research Design Core Duke University School of Medicine
dc.description.affiliationDepartment of Biostatistics and Bioinformatics Duke University School of Medicine
dc.description.affiliationDepartment of Pathology and Laboratory Medicine University of North Carolina, Chapel Hill
dc.description.affiliationDivision of Hematology Department of Medicine Duke University School of Medicine
dc.description.affiliationUnespGeneral and Applied Biology Program Institute of Biosciences (IBB) Sao Paulo State University (UNESP)
dc.description.sponsorshipAmerican Society of Hematology
dc.format.extente70013
dc.identifierhttp://dx.doi.org/10.1002/jca.70013
dc.identifier.citationJournal of clinical apheresis, v. 40, n. 2, p. e70013-, 2025.
dc.identifier.doi10.1002/jca.70013
dc.identifier.issn1098-1101
dc.identifier.scopus2-s2.0-86000504242
dc.identifier.urihttps://hdl.handle.net/11449/306050
dc.language.isoeng
dc.relation.ispartofJournal of clinical apheresis
dc.sourceScopus
dc.subjectadverse effect
dc.subjectblood coagulation
dc.subjectblood transfusion
dc.subjecthemorrhage
dc.subjecthemostasis
dc.subjectplasmapheresis
dc.subjecttransfusion medicine
dc.titleDeveloping A Model to Predict Major Bleeding Among Hospitalized Patients Undergoing Therapeutic Plasma Exchangeen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-1256-1249 0000-0002-1256-1249[1]
unesp.author.orcid0000-0001-5772-733X[3]
unesp.author.orcid0000-0001-7266-7101[7]

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