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Journal Articles

Individualized, PK-Guided Dosing of Hydroxyurea for Young Children with Sickle Cell Anemia: Final Results from the Hydroxyurea Optimization through Precision Study (HOPS)

Abena Appiah-Kubi, Seethal A Jacob, Matthew M. Heeney, Connie M. Piccone, Omar Niss, Charles T. Quinn, Stephanie A. Fritch Lilla, Maa-Ohui Quarmyne, Angeli Rampersad, Allison Remiker, Amy Tang, Min Dong, Kathryn McElhinney, Joshua R. Tanzer, Patrick T. McGann

Blood (2024) 144 (Supplement 1): 175.

https://doi.org/10.1182/blood-2024-200426

Published: 2024

Journal Articles

Hydroxyurea Pharmacokinetics in Children with Sickle Cell Anemia: Comparison of Global Cohorts

Alexandra Power-Hays, Kathryn E. McElhinney, Teresa S. Latham, Tom N. Williams, George Mochamah, Peter Olupot-Olupot, George Paasi, Marvin Ellsworth Reid, Angela Rankine-Mullings, Robert Opoka, Chandy C. John, Patrick T. McGann, Charles T. Quinn, Susan E. Stuber, Russell E. Ware

Blood (2024) 144 (Supplement 1): 542.

https://doi.org/10.1182/blood-2024-201577

Published: 2024

Journal Articles

Prioritizing Mental Health in Sickle Cell Disease: Implementing Routine Psychological and Neurocognitive Assessments in a Comprehensive Sickle Cell Clinic

Emily Franco, Lisbel Gonzalez, Allison McGirr-Crowley, Christina D'Angelo, Ernestine Jennings, David Gardner, Manpreet Kochhar, Lydia Musula, Kristine Karkoska, Patrick T. McGann

Blood (2024) 144 (Supplement 1): 3689.

https://doi.org/10.1182/blood-2024-202522

Published: 2024

Journal Articles

Exploring the Patient Perspective of Gene Therapy for Sickle Cell Disease

Clare Nimura, Lisbel Gonzalez, Tatum Brown, Layla N Van Doren, Kristine Karkoska, Seethal A Jacob, Sharl Azar, Alexander A Boucher, Patrick T. McGann

Blood (2024) 144 (Supplement 1): 4999.

https://doi.org/10.1182/blood-2024-198475

Published: 2024

Journal Articles

Changing Trends in Sickle Cell Disease-Related Mortality in the United States over Four Decades

Kristine Karkoska, Patrick T. McGann

Blood (2023) 142 (Supplement 1): 925.

https://doi.org/10.1182/blood-2023-177988

Published: 2023

Journal Articles

Non-Invasive Screening for Sickle Cell Disease Using Only a Smartphone Application

Eudorah Vital, Meredith H. LiCalzi, Robert Mannino, Patrick T. McGann, Wilbur Lam

Blood (2023) 142 (Supplement 1): 2286.

https://doi.org/10.1182/blood-2023-189810

Published: 2023

Journal Articles

Optimizing Dose and Limiting Laboratory Monitoring of Hydroxyurea in Africa: Design of the Promoting Utilization and Safety of Hydroxyurea Using Precision in Africa (PUSH-UP) Trial

Patrick T. McGann, Christine Briscoe, Margarida Muhongo, Rui Pascoal, J. Ray Tanzer, Roxanne Wood, Anastacia da Conceicao Nguvela, Eugenia Alberto Mateus

Blood (2022) 140 (Supplement 1): 5422–5423.

https://doi.org/10.1182/blood-2022-163202

Published: 2022

Journal Articles

Hydroxyurea Pharmacokinetics in Young Children with Sickle Cell Anemia: Results from the Therapeutic Response Evaluation and Adherence Trial (TREAT)

Min Dong, Angela Good, Alexander A. Vinks, Russell E. Ware, Patrick T. McGann

Blood (2022) 140 (Supplement 1): 8168–8169.

https://doi.org/10.1182/blood-2022-171022

Published: 2022

Journal Articles

Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial

Abena Appiah-Kubi, Seethal A Jacob, Matthew M. Heeney, Clark Brown, Susan E. Creary, Christine R Hollenkamp, Emily Riehm Meier, Omar Niss, Connie M. Piccone, Maa-Ohui Quarmyne, Charles T. Quinn, Allison Remiker, Kay L Saving, Min Dong, Patrick T. McGann

Blood (2022) 140 (Supplement 1): 5416–5417.

https://doi.org/10.1182/blood-2022-158623

Published: 2022

Journal Articles

Emergency Department Experience and the Use of Non-Pharmacologic Treatment for Acute Pain Among Patients with Sickle Disease

Elleen Kim, Taneisha Wilson, Malek Mitchell, Patrick T. McGann

Blood (2022) 140 (Supplement 1): 13073–13074.

https://doi.org/10.1182/blood-2022-171065

Published: 2022

Journal Articles

Assessment of Emergency Department Care for Patients with Acute Pain Crisis after the Formation of a Multidisciplinary Team

Taneisha Wilson, Katie Cherenzia, John L. Reagan, Dana L. Guyer, Catherine Trimbur, Jessica Nagy, Jon Meideros, Andrew Buksar, Priscilla Eskridge, David Gardner, Ilse Jenouri, Patrick T. McGann

Blood (2022) 140 (Supplement 1): 5013–5014.

https://doi.org/10.1182/blood-2022-170951

Published: 2022

Journal Articles

Hydroxyurea Reduces the Transfusion Burden in Children with Sickle Cell Anemia: The Reach Experience

Alexandra Power-Hays, George A. Tomlinson, Leon Tshilolo, Brigida Santos, Thomas N. Williams, Peter Olupot-Olupot, Patrick T. McGann, Banu Aygun, Adam Lane, Susan E. Stuber, Teresa Latham, Russell E. Ware

Blood (2021) 138 (Supplement 1): 11.

https://doi.org/10.1182/blood-2021-146632

Published: 2021

Journal Articles

Comparison of Sickle SCAN and Hemotype SC As Point-of-Care Newborn Screening Diagnostics for Sickle Cell Disease in Luanda, Angola

Halimat Shadia Olaniyan, Christine Briscoe, Brigida Santos, Rui Pascoal, António Armando, Patrick T. McGann

Blood (2021) 138 (Supplement 1): 913.

https://doi.org/10.1182/blood-2021-151028

Published: 2021

Journal Articles

Early Hydroxyurea Use May be Neuroprotective in Children with Sickle Cell Anemia

Kristine Anne Karkoska, Amanda Pfeiffer, Patrick T. McGann

Blood (2021) 138 (Supplement 1): 979.

https://doi.org/10.1182/blood-2021-154272

Published: 2021

Journal Articles

Longitudinal Analysis of Hydroxyurea and Fetal Hemoglobin in Adult Patients with Sickle Cell Anemia

Aryeh Pelcovits, Giancarlo Riotto, Katie Cherenzia, Patrick T. McGann, John L Reagan

Blood (2021) 138 (Supplement 1): 2054.

https://doi.org/10.1182/blood-2021-153890

Published: 2021

Journal Articles

Increased Hydroxyurea Prescribing Practices over Ten Years with Improved Clinical Outcomes in Children with Sickle Cell Anemia: A Single Center's Experience

Kristine Anne Karkoska, MD, Kevin E Todd, Jr., MD, Kelly Clapp, NP, Lynette Fenchel, NP, Theodosia A. Kalfa, MD PhD, Punam Malik, MD, Omar Niss, MD, Charles T. Quinn, MD, Russell E. Ware, MD PhD, Patrick T. McGann, MD MS

Blood (2020) 136 (Supplement 1): 34.

https://doi.org/10.1182/blood-2020-138754

Published: 2020

Journal Articles

Building Capacity and Assessing Stroke Risk with Transcranial Doppler Ultrasonography in Sub-Saharan Africa: The Reach Experience

Brigida Santos, MD, Maria Nakafeero, Adam Lane, PhD, Leon Tshilolo, MDPhD, Thomas N. Williams, MDPhD, Peter Olupot-Olupot, MDPhD, Janet Adams, Banu Aygun, MD, Susan E. Stuber, MA, George A. Tomlinson, PhD BSc, MSc, Teresa Latham, MA, Patrick T. McGann, MD MS, Russell E. Ware, MD PhD

Blood (2020) 136 (Supplement 1): 17–18.

https://doi.org/10.1182/blood-2020-142318

Published: 2020

Journal Articles

Optimizing Hydroxyurea Therapy with Reduced Laboratory Monitoring for Children with Sickle Cell Anemia in Sub-Saharan Africa: The Reach Experience

Banu Aygun, MD, George A. Tomlinson, PhD BSc, MSc, Patrick T. McGann, MD MS, Leon Tshilolo, MDPhD, Thomas N. Williams, MDPhD, Peter Olupot-Olupot, MDPhD, Brigida Santos, MD, Susan E. Stuber, MA, Adam Lane, PhD, Teresa Latham, MA, Russell E. Ware, MD PhD

Blood (2020) 136 (Supplement 1): 17.

https://doi.org/10.1182/blood-2020-134180

Published: 2020

Journal Articles

Rapid and Automated Quantitation of Dense Red Blood Cells: A Robust Biomarker of Therapeutic Response to Early Initiation of Hydroxyurea in Young Children with Sickle Cell Anemia

Alina Sadaf, MD, Charles T. Quinn, MD, Jennifer B Korpik, Amanda Pfeiffer, BS, MA, Mary Reynaud, MA, MT(ASCP), Omar Niss, MD, Punam Malik, MD, Russell E. Ware, MD PhD, Theodosia A. Kalfa, MD PhD, Patrick T. McGann, MD MS

Blood (2020) 136 (Supplement 1): 16–17.

https://doi.org/10.1182/blood-2020-137070

Published: 2020

Journal Articles

Genetic Variants That Influence Fetal Hemoglobin Expression from Hydroxyurea Treatment

Blood (2020) 136 (Supplement 1): 8–9.

https://doi.org/10.1182/blood-2020-143139

Published: 2020

NARROW

Individualized, PK-Guided Dosing of Hydroxyurea for Young Children with Sickle Cell Anemia: Final Results from the Hydroxyurea Optimization through Precision Study (HOPS)

Hydroxyurea Pharmacokinetics in Children with Sickle Cell Anemia: Comparison of Global Cohorts

Prioritizing Mental Health in Sickle Cell Disease: Implementing Routine Psychological and Neurocognitive Assessments in a Comprehensive Sickle Cell Clinic

Exploring the Patient Perspective of Gene Therapy for Sickle Cell Disease

Changing Trends in Sickle Cell Disease-Related Mortality in the United States over Four Decades

Non-Invasive Screening for Sickle Cell Disease Using Only a Smartphone Application

Optimizing Dose and Limiting Laboratory Monitoring of Hydroxyurea in Africa: Design of the Promoting Utilization and Safety of Hydroxyurea Using Precision in Africa (PUSH-UP) Trial

Hydroxyurea Pharmacokinetics in Young Children with Sickle Cell Anemia: Results from the Therapeutic Response Evaluation and Adherence Trial (TREAT)

Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial

Emergency Department Experience and the Use of Non-Pharmacologic Treatment for Acute Pain Among Patients with Sickle Disease

Assessment of Emergency Department Care for Patients with Acute Pain Crisis after the Formation of a Multidisciplinary Team

Hydroxyurea Reduces the Transfusion Burden in Children with Sickle Cell Anemia: The Reach Experience

Comparison of Sickle SCAN and Hemotype SC As Point-of-Care Newborn Screening Diagnostics for Sickle Cell Disease in Luanda, Angola

Early Hydroxyurea Use May be Neuroprotective in Children with Sickle Cell Anemia

Longitudinal Analysis of Hydroxyurea and Fetal Hemoglobin in Adult Patients with Sickle Cell Anemia

Increased Hydroxyurea Prescribing Practices over Ten Years with Improved Clinical Outcomes in Children with Sickle Cell Anemia: A Single Center's Experience

Building Capacity and Assessing Stroke Risk with Transcranial Doppler Ultrasonography in Sub-Saharan Africa: The Reach Experience

Optimizing Hydroxyurea Therapy with Reduced Laboratory Monitoring for Children with Sickle Cell Anemia in Sub-Saharan Africa: The Reach Experience

Rapid and Automated Quantitation of Dense Red Blood Cells: A Robust Biomarker of Therapeutic Response to Early Initiation of Hydroxyurea in Young Children with Sickle Cell Anemia

Genetic Variants That Influence Fetal Hemoglobin Expression from Hydroxyurea Treatment

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American Society of Hematology

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American Society of Hematology

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