scholarly journals Trends in Red Blood Cell, Plasma, and Platelet Transfusions in the United States, 1993-2014

JAMA ◽  
2018 ◽  
Vol 319 (8) ◽  
pp. 825 ◽  
Author(s):  
Ruchika Goel ◽  
Meera R. Chappidi ◽  
Eshan U. Patel ◽  
Paul M. Ness ◽  
Melissa M. Cushing ◽  
...  
Transfusion ◽  
2017 ◽  
Vol 57 (7) ◽  
pp. 1644-1655 ◽  
Author(s):  
Mark H. Yazer ◽  
Ralph Vassallo ◽  
Meghan Delaney ◽  
Marc Germain ◽  
Matthew S. Karafin ◽  
...  

Transfusion ◽  
2017 ◽  
Vol 58 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Mark H. Yazer ◽  
Waseem Q. Anani ◽  
Gregory A. Denomme ◽  
Matthew S. Karafin ◽  
Merlyn Sayers ◽  
...  

2016 ◽  
Vol 26 (1) ◽  
pp. 45 ◽  
Author(s):  
Paul D. Loprinzi ◽  
Jeremy P. Loenneke ◽  
Haitham M. Ahmed ◽  
Michael J. Blaha

<p><strong>Objective</strong>: Red blood cell distribution width (RDW) has been shown to associate with increased risk of cardiovascular and non-cardiovascular death. To our knowledge, no study has examined secular trends in RDW over the last decade.</p><p><strong>Design</strong>: Serial cross-sectional design. <strong></strong></p><p><strong>Setting</strong>: Data from the National Health and Nutrition Examination Survey (NHANES), 1999-2012, were used.</p><p><strong>Patients</strong>: 34,171 adults. <strong></strong></p><p><strong>Main Outcome Measure</strong>: RDW was assessed from a blood sample derived from the coefficient of variation of the red cell volume distribution histogram and reported as a percent.  Elevated RDW was defined as an RDW &gt; 14.6%.</p><p><strong>Results</strong>: The overall age-adjusted mean RDW increased progressively and significantly (P&lt;.05) from 12.59% in 1999-2000 to 12.89% in 2011-2012. The overall age-adjusted prevalence of elevated RDW increased progressively and significantly (P&lt;.05) from 4.01% in 1999-2000 to 6.25% in 2011-2012. Statistically significant increases over this time period also occurred among non-Hispanic White women, non-Hispanic Black men and women, and Mexican American men and women. Across all sex and race-ethnicity combinations, women, compared with men, had higher RDW and larger increases over time in mean and elevated RDW.  </p><p><strong>Conclusion</strong>: Mean and elevated RDW has progressively increased from 1999-2012 among adults in the United States, with increases observed among non-Hispanic Whites, Blacks, and Mexican Americans. Future research is needed to describe the determinants and implications of this RDW rise, as well as explanations for why a greater RDW change has occurred among women. <em>Ethn Dis. </em>2016;26(1):45-50; doi:10.18865/ed.26.1.45</p>


2019 ◽  
Vol 3 (8) ◽  
pp. 1267-1271 ◽  
Author(s):  
Juliet N. Barker ◽  
Jane Kempenich ◽  
Joanne Kurtzberg ◽  
Claudio G. Brunstein ◽  
Colleen Delaney ◽  
...  

Abstract CD34+ cell dose is critical for cord blood (CB) engraftment. However, the CD34+ content of the CB inventory in the United States is unknown. We examined the CD34+ cell content of 126 341 red blood cell–depleted US units banked from January 2007 to September 2017 with a total nucleated cell (TNC) count of ≥90 × 107 and a cryovolume of 24-55 mL. Median pre-cryopreservation TNC content was 127 × 107 (interquartile range [IQR], 108-156 × 107); CD34+ cell content was 44 × 105 (IQR, 29 to 67 × 105). The median CD34+:TNC ratio was 0.34%. TNC and CD34+ cell content correlation was weak (r = 0.24). Of 7125 units with TNCs of ≥210 × 107, only 47% had CD34+ content of ≥100 × 105. However, some units had high CD34+ content for a given TNC count. Only 4% of CB units were acceptable as single-unit grafts (TNCs, ≥2.5 × 107/kg; CD34+ cells, ≥1.5 × 105/kg) for 70-kg patients; 22% of units were adequate for 70-kg patients using lower dose criteria (TNCs, ≥1.5 × 107/kg; CD34+ cells, ≥1.0 × 105/kg) suitable for a double-unit graft. These findings highlight that units with the highest TNC dose may not have the highest CD34+ dose, units with unexpectedly high CD34+ content (a ratio of &gt;1.0%) should be verified, and the US CB inventory of adequately sized single units for larger patients is small. They also support the ongoing use of double-unit grafts, a focus on banking high-dose units, and development of expansion technologies.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 4150-4150
Author(s):  
Sanjana Mullangi ◽  
Preeti Yadav ◽  
Ekim Kilinc ◽  
Silpa Gudivada ◽  
Javaria Khan ◽  
...  

Abstract Introduction: Autoimmune hemolytic anemia (AIHA) is an acquired immune disorder resulting in the production of cold and warm autoantibodies directed against red blood cell antigens; characterized by shortened red blood cell survival and a positive Coombs test. Types include primary disease (idiopathic) or secondary to other autoimmune disorders, malignancies, or infections. Treatment involves immunosuppression with corticosteroids and other agents, Transfusion. There is not much recent data available on epidemiology of AIHA. We aim to estimate epidemiological trends and outcomes of AIHA as well as factors associated with poor outcomes by using the largest available national database from the United States. Methods: We derived a study cohort from the National Inpatient Sample (NIS) for the years 2007-2018 for hospitalizations due to AIHA by using International Classification of Diseases (9th/10th Editions) Clinical Modification diagnosis codes ICD-9-CM/ICD-10-CM). Other diagnosis and comorbidities were also identified by ICD-9/10-CM codes and Elixhauser comorbidity software. Our primary outcome was discharge disposition following AIHA hospitalization. We utilized multivariable survey logistic regression models to analyze and identify predictors of poor outcomes. Results: Between 2007-2018, a total of 52,814 hospitalizations occurred due to primary diagnosis of AIHA. Burden of hospitalizations remained stable from 4,254 (8.1%) in 2007 to 4,405 (8.3%) in 2018. AIHA patients in the study cohort were mostly above 65 years of age (48.6%) followed by 35-65 years of age (33.7%), females (58.3%) and Caucasians (69.1%). Overall in-hospital mortality of AIHA hospitalizations was 3.1%, and discharge to facility was 11.86%. Median length of stay for AIHA hospitalization was 4-days (interquartile range: 2-days to 6-days). Furthermore, in multivariable logistic regression analysis, increasing age (OR 1.2; 95%CI 1.1-1.3; p&lt;0.001), male gender (OR 1.5; 95%CI 1.2-1.3; p:0.0024), vascular events (OR 1.5 ; 95%CI 1.1-2.0; p:0.0156), teaching hospitals (OR 3.1; 95%CI 1.5-6.5; p:0.002), plasmapheresis (OR 5.5; 95%CI 2.8-10.8; p:0.001) and intravenous immunoglobulins (OR 1.9; 95%CI 1.3-3.0; p:0.001) were associated with higher in-hospital mortality. Conclusion: Our study describes the epidemiology of hospitalizations due to AIHA in the United States from a nationally representative database. We observed that hospitalization burden due to AIHA have remained stable from 2007 to 2018. We also identified factors associated with higher in-hospital mortality and some of which are modifiable. Further studies are required to establish the causal association of these factors to poor outcomes and develop better risk stratification strategies to improve overall outcomes of AIHA. Disclosures No relevant conflicts of interest to declare.


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