Full Text Journal Articles by
Author Susan Roseff

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How do we monitor hemoglobin S in patients who undergo red blood cell exchange and take voxelotor?

Elizabeth A Godbey, Michele R Anderson, Lorin M Bachmann, Kimberly W Sanford, Kaitlyn Wieditz, Susan D Roseff,

Transfusion (Transfusion)
[2021, 61(6):1680-1683]

Cited: 0 times

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Changes in Mean Corpuscular Volume and RBC Distribution Width Predict Erythrocyte Engraftment Following ABO-Incompatible Hematopoietic Stem Cell Transplantation.

Kimberly Sanford, Natalie Case, Benjamin Blake, Tabitha Michaud, Richard A McPherson, Susan D Roseff,

OBJECTIVES:The purpose of this study was to identify laboratory parameters representing erythrocyte engraftment to be used as an indicator to change the recipient to donor ABO group and Rh type following an ABO-incompatible hematopoietic stem cell transplant (HSCT). Studies have shown that ABO incompatibility does not have an effect on ... Read more >>

Am J Clin Pathol (American journal of clinical pathology)
[2020, 153(6):781-789]

Cited: 0 times

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First reported case of leukocytapheresis in plasma cell leukemia.

Elizabeth A Godbey, Justin B Dalton, Guanhua Lai, Kimberly W Sanford, Susan D Roseff,

Transfusion (Transfusion)
[2020, 60(1):11-12]

Cited: 0 times

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Prescription Opioid Misuse Index in sickle cell patients: A brief questionnaire to assess at-risk for opioid abuse.

Wally R Smith, Donna K McClish, John D Roberts, Osama Kandalaft, Bassam Dahman, Janet Knisely, James Levenson, Susan Roseff, Imo P Aisiku,

<h4>Objective</h4>To develop a survey instrument to identify adult sickle cell disease (SCD) patients on chronic opioid therapy who are at-risk for opioid abuse.<h4>Design</h4>Prospective survey and interview.<h4>Setting</h4>Adult SCD clinic in a large urban teaching facility.<h4>Patients/participants</h4>Convenience sampling of adult patients presenting to the sickle cell clinic.<h4>Interventions</h4>None.<h4>Main outcome</h4>Primary outcome was "at-risk for opioid ... Read more >>

J Opioid Manag (Journal of opioid management)
[2019, 15(4):323-331]

Cited: 0 times

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Iron Deficiency Anemia in Patients Undergoing Extracorporeal Photopheresis for Cutaneous T-Cell Lymphoma.

Kimberly W Sanford, Jennifer Anderson, Susan Roseff, Richard A McPherson,

<h4>Objective</h4>To describe the indicidence and severity of iron deficiency anemia (IDA) in patients who have received extracorporeal photopheresis (ECP) treatment of cutaneous T-cell lymphoma (CTCL).<h4>Methods</h4>We performed a retrospective study during a 9-year period of patients with CTCL who were treated with ECP. ECP was performed with UVAR XTS and CELLEX ... Read more >>

Lab Med (Laboratory medicine)
[2019, 50(1):29-33]

Cited: 2 times

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Adherence to Recommended Inpatient Hepatic Encephalopathy Workup.

Dennis Kumral, Rehan Qayyum, Susan Roseff, Richard K Sterling, Mohammad S Siddiqui,

Hepatic encephalopathy (HE) is characterized by altered sensorium and is the most common indication for hospitalization among patients with cirrhosis. Liver societal guidelines for inpatient HE revolve around identification of potential precipitants. In this retrospective study, we aimed to determine adherence to societal guidelines for evaluation of HE in 78 ... Read more >>

J Hosp Med (Journal of hospital medicine)
[2019, 14(3):157-160]

Cited: 4 times

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Predictive Ability of Intermittent Daily Sickle Cell Pain Assessment: The PiSCES Project.

Wally R Smith, Donna K McClish, James Levenson, Imoigele Aisiku, Bassam Dahman, Viktor E Bovbjerg, Susan Roseff, John Roberts,

Background:Pain diary assessment in sickle cell disease (SCD) may be expensive and impose a high respondent burden. Objective:To report whether intermittent assessment could substitute for continuous daily pain assessment in SCD. Design:Prospective cohort study. Setting:Academic and community practices in Virginia. Patients. A total of 125 SCD patients age 16 years or older ... Read more >>

Pain Med (Pain medicine (Malden, Mass.))
[2018, 19(10):1972-1981]

Cited: 0 times

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Cryptantigens: time to uncover the real significance of T-activation.

Susan D Roseff,

Transfusion (Transfusion)
[2017, 57(11):2553-2557]

Cited: 0 times

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Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project.

Donna K McClish, Wally R Smith, James L Levenson, Imoigele P Aisiku, John D Roberts, Susan D Roseff, Viktor E Bovbjerg,

<i>Background</i>. Patients with SCD now usually live well into adulthood. Whereas transitions into adulthood are now often studied, little is published about aging beyond the transition period. We therefore studied age-associated SCD differences in utilization, pain, and psychosocial variables. <i>Methods</i>. Subjects were 232 adults in the Pain in Sickle Cell ... Read more >>

Biomed Res Int (BioMed research international)
[2017, 2017:4070547]

Cited: 14 times

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Daily home opioid use in adults with sickle cell disease: The PiSCES project.

Wally R Smith, Donna K McClish, Bassam A Dahman, James L Levenson, Imoigele P Aisiku, Vanessa de A Citero, Viktor E Bovbjerg, John D Roberts, Lynne T Penberthy, Susan D Roseff,

<h4>Background</h4>Although opioid prescribing in sickle cell disease (SCD) can be controversial, little is published about patterns of opioid use.<h4>Objective</h4>To report on home opioid use among adults with SCD.<h4>Design</h4>Cohort study.<h4>Participants</h4>Adults with SCD (n=219) who completed daily pain diaries for up to 6 months and had at least one home pain day.<h4>Main ... Read more >>

J Opioid Manag (Journal of opioid management)
[2015, 11(3):243-253]

Cited: 21 times

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Phasing-in RHD genotyping.

Willy A Flegel, Susan D Roseff, Ashok Tholpady,

Arch Pathol Lab Med (Archives of pathology & laboratory medicine)
[2014, 138(5):585-588]

Cited: 4 times

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Policies and procedures related to testing for weak D phenotypes and administration of Rh immune globulin: results and recommendations related to supplemental questions in the Comprehensive Transfusion Medicine survey of the College of American Pathologists.

S Gerald Sandler, Susan D Roseff, Ronald E Domen, Beth Shaz, Jerome L Gottschall,

<h4>Context</h4>Advances in RHD genotyping offer an opportunity to update policies and practices for testing weak D phenotypes and administration of Rh immune globulin to postpartum women.<h4>Objectives</h4>To repeat questions from a 1999 College of American Pathologists proficiency test survey, to evaluate current practices for testing for weak D and administration of ... Read more >>

Arch Pathol Lab Med (Archives of pathology & laboratory medicine)
[2014, 138(5):620-625]

Cited: 17 times

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Harvesting autologous stem cells from a patient with red blood cell abnormalities of β-thalassemia intermedia.

Kimberly Sanford, Susan D Roseff, Jennifer Anderson, Harold M Chung, Richard A McPherson,

<h4>Background</h4>Autologous stem cell transplants in patients with hemoglobinopathies are limited. Previous reports used granulocyte-colony-stimulating factor (G-CSF) for mobilization of stem cells; there are no reported cases undergoing plerixafor mobilization. We report such a patient, providing guidance for peripheral blood stem cells collection when aberrant red blood cells (RBCs) disrupt normal ... Read more >>

Transfusion (Transfusion)
[2014, 54(7):1881-1886]

Cited: 4 times

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Perfluorocarbon emulsion improves oxygen transport of normal and sickle cell human blood in vitro.

Ivo P Torres Filho, José Ricardo P Pedro, Srinivasan V Narayanan, Nguyen M Nguyen, Susan D Roseff, Bruce D Spiess,

Perfluorocarbons (PFC) are compounds with high gas solubility that could help deliver O2 to tissues and have been suggested as adjunct therapy to ischemia. Using a newly designed in vitro system, we tested the hypothesis that a third generation PFC emulsion (Oxycyte) increased O2 transport of blood by measuring changes ... Read more >>

J Biomed Mater Res A (Journal of biomedical materials research. Part A)
[2014, 102(7):2105-2115]

Cited: 2 times

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The HI-STAR study: resource utilization and costs associated with serologic testing for antibody-positive patients at four United States medical centers.

Peter Mazonson, Molly Efrusy, Chris Santas, Alyssa Ziman, James Burner, Susan Roseff, Arthi Vijayaraghavan, Richard Kaufman,

<h4>Background</h4>Little is known about how the resource utilization and costs of serologic work ups for positive antibody screens vary across subpopulations based on diagnosis, transfusion history, and serologic testing history.<h4>Study design and methods</h4>Detailed data were collected on patient demographics, diagnoses, transfusion history, history of known allo- and autoantibodies, and specific ... Read more >>

Transfusion (Transfusion)
[2014, 54(2):271-277]

Cited: 5 times

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Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.

Scott T Miller, Hae-Young Kim, Debra L Weiner, Carrie G Wager, Dianne Gallagher, Lori A Styles, Carlton D Dampier, Susan D Roseff, ,

<h4>Background</h4>Transfusion of red blood cells (RBCs) is frequently required for care of individuals with sickle cell disease (SCD). Alloimmunization rates are high and may be reduced by matching for RBC antigens that can cause alloimmunization.<h4>Study design and methods</h4>During the PROACTIVE Feasibility Study, patients with SCD age 2 years or older ... Read more >>

Transfusion (Transfusion)
[2013, 53(4):704-709]

Cited: 46 times

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Making transfusion medicine information accessible for all.

April Hord, Steven M Armstrong, Susan D Roseff,

MLO Med Lab Obs (MLO: medical laboratory observer)
[2012, 44(1):8, 10-1; quiz 14-5]

Cited: 1 time

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Refining the value of secretory phospholipase A2 as a predictor of acute chest syndrome in sickle cell disease: results of a feasibility study (PROACTIVE).

Lori Styles, Carrie G Wager, Richard J Labotka, Kim Smith-Whitley, Alexis A Thompson, Peter A Lane, Lillian E C McMahon, Robin Miller, Susan D Roseff, Rathi V Iyer, Lewis L Hsu, Oswaldo L Castro, Kenneth I Ataga, Onyinye Onyekwere, Maureen Okam, Rita Bellevue, Scott T Miller, ,

Acute chest syndrome (ACS) is defined as fever, respiratory symptoms and a new pulmonary infiltrate in an individual with sickle cell disease (SCD). Nearly half of ACS episodes occur in SCD patients already hospitalized, potentially permitting pre-emptive therapy in high-risk patients. Simple transfusion of red blood cells may abort ACS ... Read more >>

Br J Haematol (British journal of haematology)
[2012, 157(5):627-636]

Cited: 28 times

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A consensus curriculum for laboratory management training for pathology residents.

Ronald L Weiss, Barbara J McKenna, Melissa Lord-Toof, Nancie Noie Thompson, ,

Through the combined efforts of the American Pathology Foundation (APF), the American Society for Clinical Pathology (ASCP), and the Program Directors Section (PRODS) of the Association of Pathology Chairs (APC), a needs assessment was performed via a survey on the PRODS listserv, workshops at the APC/PRODS annual meetings in 2009 ... Read more >>

Am J Clin Pathol (American journal of clinical pathology)
[2011, 136(5):671-678]

Cited: 10 times

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Inpatient management of sickle cell pain: a 'snapshot' of current practice.

Scott T Miller, Hae-Young Kim, Debra Weiner, Carrie G Wager, Dianne Gallagher, Lori Styles, Carlton D Dampier, ,

The Sickle Cell Disease Clinical Research Network (SCDCRN) designed the PROACTIVE Feasibility Study (ClinicalTrials.gov NCT00951808) to determine whether elevated serum levels of secretory phospholipase A2 (sPLA2) during hospitalization for pain would permit preemptive therapy of sickle cell acute chest syndrome (ACS) by blood transfusion. While PROACTIVE was not designed to ... Read more >>

Am J Hematol (American journal of hematology)
[2012, 87(3):333-336]

Cited: 15 times

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Neonatal transfusion practice: should our policies mature with our patients?

Susan D Roseff,

Transfusion (Transfusion)
[2011, 51(5):908-913]

Cited: 5 times

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Investigation of heparin-related hypotensive adverse events during photopheresis: utility of a patient care database.

Richard A McPherson, Aileen G Buckler, Kimberly W Sanford, Susan D Roseff,

<h4>Background</h4>Extracorporeal photopheresis (ECP) is a procedure in which leukocytes are harvested from a patient's whole blood, treated with a DNA binding dye and ultraviolet light to inactivate lymphocytes, and then returned into the patient's circulation. In January 2008, we observed moderately severe anaphylactoid reactions in eight of 16 patients undergoing ... Read more >>

Transfusion (Transfusion)
[2011, 51(6):1314-1320]

Cited: 0 times

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Blood component preferences of transfusion services supporting infant transfusions: a University HealthSystem Consortium benchmarking study.

Mark K Fung, Susan D Roseff, Kathleen L Vermoch,

<h4>Background</h4>The extent of acceptability of red blood cells (RBCs) containing additive solutions (ASs) for low-volume neonatal transfusions among hospitals is unknown. Also unknown is whether hospitals have policies that address the risk of hyperkalemia associated with prolonged storage either with or without irradiation for neonatal transfusions.<h4>Study design and methods</h4>A benchmarking ... Read more >>

Transfusion (Transfusion)
[2010, 50(9):1921-1925]

Cited: 5 times

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Pain site frequency and location in sickle cell disease: the PiSCES project.

Donna K McClish, Wally R Smith, Bassam A Dahman, James L Levenson, John D Roberts, Lynne T Penberthy, Imoigele P Aisiku, Susan D Roseff, Viktor E Bovbjerg,

Treatment options for sickle cell disease (SCD) pain could be tailored to pain locations. But few epidemiologic descriptions of SCD pain location exist; these are based on few subjects over short time periods. We examined whether SCD pain locations vary by disease genotype, gender, age, frequency of pain, depression, pain ... Read more >>

Pain (Pain)
[2009, 145(1-2):246-251]

Cited: 41 times

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Comparisons of high versus low emergency department utilizers in sickle cell disease.

Imoigele P Aisiku, Wally R Smith, Donna K McClish, James L Levenson, Lynne T Penberthy, Susan D Roseff, Viktor E Bovbjerg, John D Roberts,

<h4>Study objective</h4>Patients with sickle cell disease often receive a substantial amount of their health care in the emergency department (ED) and some come to the ED frequently, seeking treatment for pain. As a result, patients with sickle cell disease are often stigmatized as opioid-seeking ED overutilizers. We describe the proportion ... Read more >>

Ann Emerg Med (Annals of emergency medicine)
[2009, 53(5):587-593]

Cited: 72 times

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