Search Results - "Yee, Marianne E. M."

Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study by Hawkins, Lauren M, Sinha, Cynthia B, Ross, Diana, Yee, Marianne E M, Quarmyne, Maa-Ohui, Krishnamurti, Lakshmanan, Bakshi, Nitya

“…There is a limited understanding of the patient and family experience of Chronic Transfusion Therapy (CTT) for prevention of complications of Sickle Cell…”
Get full text

Red blood cell minor antigen mismatches during chronic transfusion therapy for sickle cell anemia by Yee, Marianne E.M., Josephson, Cassandra D., Winkler, Anne M., Webb, Jennifer, Luban, Naomi L.C., Leong, Traci, Stowell, Sean R., Fasano, Ross M.

“…BACKGROUND Red blood cell (RBC) alloimmunization occurs at a high frequency in sickle cell anemia (SCA) despite serologic matching for Rh (C/c, E/e) and K…”
Get full text

Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease by Yee, Marianne E. M., Batsuli, Glaivy, Chonat, Satheesh, Park, Sunita

“…Thrombocytosis is common in sickle cell disease and may contribute to vaso‐occlusion. Hydroxyurea treats extreme thrombocytosis. Acquired von Willebrand…”
Get full text

Influenza vaccine effectiveness and disease burden in children and adolescents with sickle cell disease: 2012‐2017 by Kao, Carol M., Lai, Kristina, McAteer, John M., Elmontser, Mohnd, Quincer, Elizabeth M., Yee, Marianne E.M., Tippet, Ashley, Jerris, Robert C., Lane, Peter A., Anderson, Evan J., Bakshi, Nitya, Yildirim, Inci

“…Background Data are limited on the burden of influenza and seasonal influenza vaccine effectiveness (VE) in children with sickle cell disease (SCD). Methods We…”
Get full text

Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange by Wade, Jenna, Yee, Marianne E. M., Easley, Kirk A., Pahz, Shannon, Butler, Hailly, Zerra, Patricia E., Josephson, Cassandra D., Fasano, Ross M.

“…Background Chronic automated red cell exchange (RCE) is increasingly employed for sickle cell disease (SCD). There is a paucity of data on the incidence of RCE…”
Get full text

Requests for Directed Blood Donations by Weaver, Meaghann S, Yee, Marianne E M, Lawrence, Courtney E, Matheny Antommaria, Armand H, Fasano, Ross M

“…This Ethics Rounds presents a request for directed blood donation. Two parents feel helpless in the setting of their daughter's new leukemia diagnosis and want…”
Get full text

Survival of transfused red blood cells from a donor with alpha‐thalassemia trait in a recipient with sickle cell disease by Yee, Marianne E. M., Covington, Mischa L., Zerra, Patricia E., McCoy, James W., Easley, Kirk A., Joiner, Clinton H., Bryksin, Janetta, Francis, Richard O., Lough, Christopher M., Patel, Niren, Kutlar, Abdullah, Josephson, Cassandra D., Roback, John D., Stowell, Sean R., Fasano, Ross M.

“…Background Post‐transfusion survival of donor red blood cells (RBCs) is important for effective chronic transfusion therapy in conditions including sickle cell…”
Get full text

Post‐transfusion biotin‐labeled red blood cell survival studies in pediatric sickle cell disease with antibodies of uncertain significance by Yee, Marianne E. M., Zerra, Patricia E., McCoy, James W., Covington, Mischa L., Stowell, Sean R., Joiner, Clinton H., Lough, Christopher M., Delvadia, Bhaveshkumar B., Josephson, Cassandra D., Roback, John D., Fasano, Ross M.

“…Background Red blood cell (RBC) antibodies are common in multiply transfused patients with sickle cell disease (SCD). Unlike RBC alloantibodies, the potential…”
Get full text

Examining the Role of Complement in Predicting, Preventing, and Treating Hemolytic Transfusion Reactions by Arthur, Connie M., Chonat, Satheesh, Fasano, Ross, Yee, Marianne E.M., Josephson, Cassandra D., Roback, John D., Stowell, Sean R.

“…Red blood cell (RBC) transfusion is a critical component of optimal management for a broad range of conditions. Regardless of the indication, pretransfusion…”
Get full text

Glucose‐6‐phosphate‐dehydrogenase deficient red blood cell units are associated with decreased posttransfusion red blood cell survival in children with sickle cell disease by Sagiv, Eyal, Fasano, Ross M., Luban, Naomi L. C., Josephson, Cassandra D., Stowell, Sean R., Roback, John D., Francis, Richard O., Yee, Marianne E. M.

“…Chronic transfusion therapy (CTT) for sickle cell disease (SCD) reduces disease morbidity by suppressing the amount of circulating hemoglobin S…”
Get full text

Immunophenotypic parameters and RBC alloimmunization in children with sickle cell disease on chronic transfusion by Nickel, Robert S., Horan, John T., Fasano, Ross M., Meyer, Erin, Josephson, Cassandra D., Winkler, Anne M., Yee, Marianne E.M., Kean, Leslie S., Hendrickson, Jeanne E.

“…Alloimmunization against red blood cell (RBC) antigens is a cause of morbidity and mortality in transfused patients with sickle cell disease (SCD). To…”
Get full text

Estimation of glomerular filtration rate using serum cystatin C and creatinine in adults with sickle cell anemia by Yee, Marianne E M, Lane, Peter A, Archer, David R, Joiner, Clinton H, Eckman, James R, Guasch, Antonio

Get full text

Hemoglobin A clearance in children with sickle cell anemia on chronic transfusion therapy by Yee, Marianne E. M., Josephson, Cassandra D., Winkler, Anne M., Webb, Jennifer, Luban, Naomi L.C., Leong, Traci, Stowell, Sean R., Roback, John D., Fasano, Ross M.

“…BACKGROUND Chronic transfusion therapy for sickle cell anemia reduces disease complications by diluting sickle‐erythrocytes with hemoglobin A (HbA)‐containing…”
Get full text

Pneumococcal infections in children with sickle cell disease before and after pneumococcal conjugate vaccines by Adamkiewicz, Thomas V., Yee, Marianne E. M., Thomas, Stepy, Tunali, Amy, Lai, Kristina W., Omole, Folashade S., Lane, Peter A., Yildirim, Inci

“…•Invasive pneumococcal infection in children with SCD has declined significantly with PCV7/PCV13 but remains a life-threatening risk.•PPSV23 and new vaccines…”
Get full text

Challenges in preventing and treating hemolytic complications associated with red blood cell transfusion by Chonat, Satheesh, Arthur, Connie M., Zerra, Patricia E., Maier, Cheryl L., Jajosky, Ryan P., Yee, Marianne E.M., Miller, Maureen J., Josephson, Cassandra D., Roback, John D., Fasano, Ross, Stowell, Sean R.

“…Red blood cell (RBC) transfusion support represents a critical component of sickle cell disease (SCD) management. However, as with any therapeutic…”
Get full text

Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia by Yee, Marianne E M, Quarmyne, Maa-Ohui, Segbefia, Catherine, Young, Andrew N, Zhuang, Lina, Kutlar, Ferdane

“…An asymptomatic infant of Ghanaian descent had hemoglobin F only detected on newborn screening. β-globin gene sequencing identified the intervening sequence…”
Get full text

Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease by Yee, Marianne E M, Batsuli, Glaivy, Chonat, Satheesh, Park, Sunita

“…Thrombocytosis is common in sickle cell disease and may contribute to vaso-occlusion. Hydroxyurea treats extreme thrombocytosis. Acquired von Willebrand…”
Get full text