Meredith G. Parsons

Clinical Assistant Professor

University of Iowa Hospitals and Clinics
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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

UNITED STATES
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Donald Arnold

Professor

McMaster University

CANADA
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Jason Barker

Associate Professor

University of Iowa Healthcare

UNITED STATES
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Takaaki Kobayashi

Clinical Assistant Professor/Associate Hospital Epidemiologist

Iowa State University

UNITED STATES
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Rodrigo Bayon

Associate Professor

Iowa State University

UNITED STATES
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Jeremy Jacobs

Assistant Professor

Vanderbilt University Medical Center

UNITED STATES
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Lemuel Non

Assistant Professor

Iowa State University

UNITED STATES
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Quanhathai Kaewpoowat

Clinical Assistant Professor

The University of Iowa

UNITED STATES
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Argiris Symeonidis

Professor of Hematology, Head of the Department

University of Patras School of Medicine

GREECE
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Daniel J Diekema

The University of Iowa Roy J and Lucille A Carver College of Medicine

UNITED STATES
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Christopher Strouse

Iowa State University

UNITED STATES
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Annette J. Schlueter

-

UNITED STATES
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Dilek Ince

-

UNITED STATES
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