Defining Sickle Cell Disease Severity Among Adults Hospitalized with Vaso-Occlusive Crisis

Background: While there is no uniform definition of sickle cell disease (SCD) severity, vaso-occlusive crises (VOC) are the leading cause of emergency department (ED) visits and hospital admissions among adults with SCD and those with frequent hospital admissions constitute a subgroup more likely to...

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Veröffentlicht in:Blood 2018-11, Vol.132 (Supplement 1), p.3577-3577
Hauptverfasser: Esham, Kimberly S, Rodday, Angie Mae, Savidge, Nicole, Mao, Daqin, Weidner, Ruth Ann, Parsons, Susan K
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Sprache:eng
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Zusammenfassung:Background: While there is no uniform definition of sickle cell disease (SCD) severity, vaso-occlusive crises (VOC) are the leading cause of emergency department (ED) visits and hospital admissions among adults with SCD and those with frequent hospital admissions constitute a subgroup more likely to have SCD-related complications. New patient-reported outcomes measures, such as the Adult Sickle Cell Quality of Life Measurement System (ASCQ-Me) Medical History Checklist (MHC), were developed in ambulatory populations to describe SCD severity based on patient-reported medical history. However, similar tools have not been used in adults with SCD hospitalized for VOC. We describe the development and performance of a medical history checklist, modeled off of the ASCQ-Me MHC, to assess disease severity among adults with SCD hospitalized with VOC. Methods: This retrospective cohort study consists of 41 adults with SCD hospitalized with VOC at a US-based academic medical center between 2013 and 2016. For the current analysis, the first hospitalization for VOC within the study window for each patient was selected. Demographic and SCD characteristics were abstracted from the electronic medical record (EMR) by trained research staff, and all SCD-complications were reviewed by two study hematologists. We utilized a 9-item checklist of SCD-related complications (history of lung damage, avascular necrosis, spleen damage, stroke, retinopathy, kidney disease, leg ulcers) and treatments (daily use of pain medication, receipt of an outpatient blood transfusion protocol) in accordance with a prior study by Keller et al. (Health and Quality of Life Outcomes, 2017; 15:117). However, rather than collecting information by patient self-report, we relied on abstraction of checklist items from EMR documentation of history of SCD-related complications in the year prior to the selected hospitalization, documentation of an outpatient transfusion protocol with receipt of transfusions within 3 months prior to hospitalization, and the admission reconciliation record of home pain medications. In the absence of a standard definition of SCD severity, we drew from ASCQ-Me methodology and scored the checklist as the sum of items from 0-9 and also categorized scores as low (2 points) severity (Keller et al. Health and Quality of Life Outcomes, 2017; 15:117). Data were described with summary statistics (means, standard deviations, frequencies, percenti
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2018-99-111717