Meredith G. Parsons
Clinical Assistant Professor
Research Interests
Explore related searches
Contact this professor
Get a free first email built on one of their papers, ready for you to edit and send yourself.
About
Meredith G. Parsons is a Clinical Assistant Professor at the University of Iowa Hospitals and Clinics in the United States. Her research focuses on diagnostic challenges and clinical decision-making in hematological disorders, as evidenced by her recent articles on heparin-induced thrombocytopenia, immune thrombotic thrombocytopenic purpura, and infectious diseases. Additionally, she explores innovative approaches in hematopoietic stem cell collection and evaluates the epidemiology of complex clinical cases.
Articles (10)
Year:
2025
Year:
2024
Year:
2024
Year:
2024
Year:
2024
Purpose A critical component of optimizing peripheral blood (PB) hematopoietic stem cell (HSC) collections is accurately determining the processed blood volume required to collect the targeted number of HSCs. Fundamental to most truncation equations employed to determine this volume is the procedure's estimated collection efficiency (CE), which is typically applied uniformly across all HSC collections. Few studies have explored the utility of using different CEs in subpopulations of donors that have substantially different CEs than the institutional average. Methods Initial procedures from 343 autologous and 179 allogeneic HSC collections performed from 2018 to 2021 were retrospectively analyzed. Predictive equations were developed to determine theoretical truncation rates in various donor subgroups. Results Quantitative variables (pre‐procedure cell counts) and qualitative variables (relatedness to recipient, gender, method of venous access, and mobilization strategy) were found to significantly impact CE. However, much of the variability in CE between donors could not be explained by the variables assessed. Analyses of procedures with high pre‐collection PB cell counts identified lower CE values for these donors' truncation equations which still allow truncation but minimize risk of collecting less CD34+ cells than requested. Conclusions Individualized CE does not substantially improve truncation volume calculations over use of a fixed CE and adds complexity to these calculations. The optimal fixed CE varies between autologous and allogeneic donors, and donors with high pre‐collection PB cell counts in either of these groups. This model will be clinically validated and continuously refined through analysis of future HSC collections.
Year:
2023
Year:
2023
Year:
2023
Year:
2022
Year:
2022
Collaborators (13)
Umar Farooq
Assistant Professor
University of Iowa Healthcare
Donald Arnold
Professor
McMaster University
Jason Barker
Associate Professor
University of Iowa Healthcare
Takaaki Kobayashi
Clinical Assistant Professor/Associate Hospital Epidemiologist
Iowa State University
Rodrigo Bayon
Associate Professor
Iowa State University
Jeremy Jacobs
Assistant Professor
Vanderbilt University Medical Center
Lemuel Non
Assistant Professor
Iowa State University
Quanhathai Kaewpoowat
Clinical Assistant Professor
The University of Iowa
Argiris Symeonidis
Professor of Hematology, Head of the Department
University of Patras School of Medicine
Daniel J Diekema
The University of Iowa Roy J and Lucille A Carver College of Medicine
Christopher Strouse
Iowa State University
Annette J. Schlueter
-
Dilek Ince
-
Make your next move.
Prepare your application
Review drafts before you send them.