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Journal Articles

Red Blood Cell Deformability Demonstrated with the Oxygenscan: Exploring the Association with Hydroxyurea Treatment, Co-Inherited α-Thalassemia, and Frequency of Pain in Children with Sickle Cell Anemia

Amina Nardo-Marino, Jesper Petersen, Andreas Glenthoej, MD PhD, John N. Brewin, Joergen Kurtzhals, Thomas N. Williams, David C. Rees, Henrik Birgens

Blood (2019) 134 (Supplement_1): 4834.

https://doi.org/10.1182/blood-2019-129836

Published: 2019

Journal Articles

Measurement of Sickle Cell Disease Symptoms from the Patient Perspective: Considerations for Clinical Trials

Funke Ojo, MPH, Leighann Litcher-Kelly, PhD, Iyar Mazar, Brittany Klooster, Sarah Ollis, Emily Chaston, Adam Roeder, Marsha J. Treadwell, PhD, David Reasner

Blood (2018) 132 (Supplement 1): 3571.

https://doi.org/10.1182/blood-2018-99-116682

Published: 2018

Journal Articles

Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Soumitri Sil, PhD, Lindsey L Cohen, PhD, Carlton Dampier, MD

Blood (2017) 130 (Supplement 1): 3548.

https://doi.org/10.1182/blood.V130.Suppl_1.3548.3548

Published: 2017

Journal Articles

Pediatric Emergency Department Use of Intranasal Fentanyl to Treat Pain in Children with Sickel Cell Disease and Its Impact on Discharge Rates: A Multicenter Perspective

Blood (2016) 128 (22): 1306.

https://doi.org/10.1182/blood.V128.22.1306.1306

Published: 2016

Journal Articles

Regional- and Age-Related Differences in Pain in Children with Sickle Cell Anemia: Results from the Multinational DOVE Study

Julie Kanter, MD, Lori E Heath, MS, Chunmei Zhou, MS, Tsiri Agbenyega, MBChB, PhD, Raffaella Colombatti, MD PhD, Carlton Dampier, MD CPI, Hoda M Hassab, MD, Deepa Manwani, MD, Nancy Robitaille, MD, Patricia B Brown, BSN, RN, Joseph A. Jakubowski, PhD, Suqin Yao, PhD, Jack Knorr, PhD, Carolyn C Hoppe, MD

Blood (2016) 128 (22): 3654.

https://doi.org/10.1182/blood.V128.22.3654.3654

Published: 2016

Journal Articles

Pain in the Bleeding Disorders Community: Patient and Caregiver Perspectives

Tyler W. Buckner, MD MSc, Nancy Durben, PT, MSPT, PCS, Christi Humphrey, LCSW, Eric Iglewski, LMSW, Jennifer Newman, MSPT, Maria E Santaella, RN-BC, MSN, CPHON, Michelle Witkop, DNP, FNP-BC

Blood (2016) 128 (22): 2591.

https://doi.org/10.1182/blood.V128.22.2591.2591

Published: 2016

Journal Articles

Higher Dose of Opioids in the Emergency Department and Earlier Initiation of Oral Opioids after Hospitalization Are Associated with Shorter Length of Stay in Children with Sickle Cell Disease Treated for Acute Pain

Amanda M Brandow, DO, MS, Mark Nimmer, Timothy Simmons, MStat, T Charles Casper, PhD, Larry J Cook, PhD, J. Paul Scott, MD, Julie A. Panepinto, MD MSPH, David C. Brousseau, MD MS

Blood (2015) 126 (23): 525.

https://doi.org/10.1182/blood.V126.23.525.525

Published: 2015

Journal Articles

Catastrophizing and Depression Are Associated With a Poorer Quality Of Life In Pediatric Patients With Sickle Cell Disease

Nitya Bakshi, MBBS, Ines Lukombo, Helen Shnol, Nonita Mittal, MBBS, Saumya Vinod Joshi, MBBS, Inna Belfer, MD, PhD, Lakshmanan Krishnamurti, MD

Blood (2013) 122 (21): 1706.

https://doi.org/10.1182/blood.V122.21.1706.1706

Published: 2013

Journal Articles

Changes in Regional Oxygenation At the Site of Sickle Cell Vaso-Occlusive Pain

Roberta Miyeko Kato, MD, Anne Nord, RN, BSN, CCRP, Erin McGuire, BS, Daniel Gardner, Adam M Bush, BS, Jon Detterich, MD, Michael Khoo, PhD, Herbert J Meiselman, ScD, John C Wood, MD, Ph.D, Vasilios Berdoukas, MBBS, Thomas D. Coates, MD

Blood (2012) 120 (21): 4773.

https://doi.org/10.1182/blood.V120.21.4773.4773

Published: 2012

Journal Articles

Epidemiology and Risk Factors for Pain In Children and Adolescent with Sickle Cell Anemia.

Deepika Darbari, MD, Onyinye Onyekwere, MD, Mehdi Nouraie, Gregory J. Kato, MD, Caterina Minniti, Craig Sable, MD, Gregory Ensing, MD, Niti Dham, MD, Andrew Campbell, Manuel Arteta, MD, Sohail Rana, Mark Gladwin, MD, Oswaldo Castro, MD, Victor R. Gordeuk, MD

Blood (2010) 116 (21): 1651.

https://doi.org/10.1182/blood.V116.21.1651.1651

Published: 2010

Journal Articles

Improvement In Acute Management of Vaso-Occlusive Pain In Pediatric Sickle Cell Disease with Use of a Clinical Pathway

Katherine Ender, M.D., M.S., Jennifer Freed, M.D., John Babineau, M.D., Mary Tresgallo, DNP, MPH, William Schechter, M.D., John Saroyan, M.D., Anupam Kharbanda, M.D., M.S.

Blood (2010) 116 (21): 2660.

https://doi.org/10.1182/blood.V116.21.2660.2660

Published: 2010

Journal Articles

A Comparison of Two Pain Assessment Tools, the Adolescent Pediatric Pain Tool and PAINReportIt and Use of the Composite Pain Index in Sickle Cell Disease

A. Kyle Mack, MD, Stephanie Pelligra, BS, MPH, Richard J. Labotka, MD, MS, Robert Molokie, MD, Young O Kim, PhD, RN, Alexis Thompson, MD, MPH, Diana J Wilkie, PhD, RN

Blood (2010) 116 (21): 2648.

https://doi.org/10.1182/blood.V116.21.2648.2648

Published: 2010

Journal Articles

The Utilization of a Computerized Pain Assessment Tool-PAINReportIt® in Adolescents with Sickle Cell Disease.

A. Kyle Mack, MD, Stephanie A. Pelligra, BS, Richard J. Labotka, MD, Robert E. Molokie, MD, Alexis A. Thompson, MD, MPH, Diana J. Wilkie, PhD

Blood (2009) 114 (22): 1535.

https://doi.org/10.1182/blood.V114.22.1535.1535

Published: 2009

Journal Articles

Functional Assessment for Children Hospitalized for Sickle Cell Pain: A New Paradigm.

William T. Zempsky, MD, John M. Corsi, MBA, Kristin A. Loiselle, BS, Nathan Hagstrom, MD, Tonya M. Palermo, PhD, James F. Casella, MD

Blood (2009) 114 (22): 2561.

https://doi.org/10.1182/blood.V114.22.2561.2561

Published: 2009

Journal Articles

Inter-Rater Reliability of the Adolescent Pediatric Pain Tool (APPT) for Pediatric Sickle Cell Disease (SCD) Patients.

Janie Hernandez, BS, Olusola Balogun, BS, Richard J. Labotka, MD, Diana J Wilkie, PhD, Young Ok Kim, PhD, Stephanie A. Pelligra, BS, A. Kyle Mack, MD

Blood (2009) 114 (22): 4618.

https://doi.org/10.1182/blood.V114.22.4618.4618

Published: 2009

Journal Articles

Elevated Urinary Leukotriene E 4 Levels Are Associated with Hospitalization for Pain in Children with Sickle Cell Disease.

Jeanine E. Jennings, BS, Thiruvamoor Ramkumar, PhD, Jingnan Mao, Jessica Boyd, MD, MPH, Mario Castro, MD, MPH, Robert C. Strunk, MD, Michael R. DeBaun, MD, MPH

Blood (2007) 110 (11): 3405.

https://doi.org/10.1182/blood.V110.11.3405.3405

Published: 2007

Journal Articles

Asthma Is Associated with Acute Chest Syndrome, but Not an Increase Rate of Hospitalization for Pain among Children with Sickle Cell Anemia: A Retrospective Cohort Study.

Francoise Bernaudin, MD, Robert C. Strunk, MD, Annie Kamdem, MD, Cecile Arnaud, MD, Ping An, PHD, Martine Torres, PHD, Christophe Delacourt, MD, Michael R. DeBaun, MD, MPH

Blood (2007) 110 (11): 3406.

https://doi.org/10.1182/blood.V110.11.3406.3406

Published: 2007

Journal Articles

Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia

Jessica H. Boyd, Eric A. Macklin, Robert C. Strunk, Michael R. DeBaun

Blood (2006) 108 (9): 2923–2927.

https://doi.org/10.1182/blood-2006-01-011072

Published: 2006

Journal Articles

Scoring Adherence in Hemophilia Care and Comparing It to Quality of Life (QofL).

Sue duTreil, PhD, Janet Rice, PhD, Cindy A. Leissinger, MD

Blood (2005) 106 (11): 2260.

https://doi.org/10.1182/blood.V106.11.2260.2260

Published: 2005

NARROW

Red Blood Cell Deformability Demonstrated with the Oxygenscan: Exploring the Association with Hydroxyurea Treatment, Co-Inherited α-Thalassemia, and Frequency of Pain in Children with Sickle Cell Anemia

Measurement of Sickle Cell Disease Symptoms from the Patient Perspective: Considerations for Clinical Trials

Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Pediatric Emergency Department Use of Intranasal Fentanyl to Treat Pain in Children with Sickel Cell Disease and Its Impact on Discharge Rates: A Multicenter Perspective

Regional- and Age-Related Differences in Pain in Children with Sickle Cell Anemia: Results from the Multinational DOVE Study

Pain in the Bleeding Disorders Community: Patient and Caregiver Perspectives

Higher Dose of Opioids in the Emergency Department and Earlier Initiation of Oral Opioids after Hospitalization Are Associated with Shorter Length of Stay in Children with Sickle Cell Disease Treated for Acute Pain

Catastrophizing and Depression Are Associated With a Poorer Quality Of Life In Pediatric Patients With Sickle Cell Disease

Changes in Regional Oxygenation At the Site of Sickle Cell Vaso-Occlusive Pain

Epidemiology and Risk Factors for Pain In Children and Adolescent with Sickle Cell Anemia.

Improvement In Acute Management of Vaso-Occlusive Pain In Pediatric Sickle Cell Disease with Use of a Clinical Pathway

A Comparison of Two Pain Assessment Tools, the Adolescent Pediatric Pain Tool and PAINReportIt and Use of the Composite Pain Index in Sickle Cell Disease

The Utilization of a Computerized Pain Assessment Tool-PAINReportIt® in Adolescents with Sickle Cell Disease.

Functional Assessment for Children Hospitalized for Sickle Cell Pain: A New Paradigm.

Inter-Rater Reliability of the Adolescent Pediatric Pain Tool (APPT) for Pediatric Sickle Cell Disease (SCD) Patients.

Elevated Urinary Leukotriene E 4 Levels Are Associated with Hospitalization for Pain in Children with Sickle Cell Disease.

Asthma Is Associated with Acute Chest Syndrome, but Not an Increase Rate of Hospitalization for Pain among Children with Sickle Cell Anemia: A Retrospective Cohort Study.

Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia

Scoring Adherence in Hemophilia Care and Comparing It to Quality of Life (QofL).

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American Society of Hematology

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American Society of Hematology

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