Literature DB >> 21275951

Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years.

Emma Drasar1, Norris Igbineweka, Nisha Vasavda, Matthew Free, Moji Awogbade, Marlene Allman, Aleksandar Mijovic, Swee Lay Thein.   

Abstract

Transfusion of red blood cells is a major therapeutic option in sickle cell disease (SCD). There is strong evidence for its efficacy, particularly in primary and secondary stroke prevention in children, however, its use in other areas remains controversial. This study assessed the patterns of transfusion in the adult cohort attending King's College Hospital over a 10-year period, from 2000 to 2009. Total blood usage has increased significantly (P = 0·006) during this time, with 78% of the blood received by only 6% of the patients. The increase is explained by increased automated red cell exchange and increased usage for planned and acute transfusions for sickle-related complications.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21275951     DOI: 10.1111/j.1365-2141.2010.08451.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  14 in total

1.  Study of Twenty One Cases of Red Cell Exchange in a Tertiary Care Hospital in Southern India.

Authors:  M Joshua Daniel; Prakash H Muddegowda; Jyothi B Lingegowda; Niranjan Gopal; Krishna Prasad
Journal:  J Clin Diagn Res       Date:  2016-05-01

2.  Sickle cell disease is associated with iron mediated hypercoagulability.

Authors:  Nirmish Shah; Ian J Welsby; Martha A Fielder; Wayne K Jacobsen; Vance G Nielsen
Journal:  J Thromb Thrombolysis       Date:  2015-08       Impact factor: 2.300

Review 3.  Sickle cell disease: when and how to transfuse.

Authors:  Jo Howard
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

4.  Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques.

Authors:  Emma Drasar; Emer Fitzpatrick; Kate Gardner; Moji Awogbade; Anil Dhawan; Adrian Bomford; Abid Suddle; Swee L Thein
Journal:  Br J Haematol       Date:  2016-12-16       Impact factor: 6.998

5.  Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease.

Authors:  Abhishek A Mangaonkar; Fahim Thawer; James Son; Germame Ajebo; Hongyan Xu; Nadine J Barrett; Leigh G Wells; Latanya Bowman; Betsy Clair; Niren Patel; Pritam Bora; Grace Jung; Elizabeta Nemeth; Abdullah Kutlar
Journal:  Br J Haematol       Date:  2020-02-06       Impact factor: 6.998

6.  Trends in blood transfusion among hospitalized children with sickle cell disease.

Authors:  Jean L Raphael; Suzette O Oyeku; Marc A Kowalkowski; Brigitta U Mueller; Angela M Ellison
Journal:  Pediatr Blood Cancer       Date:  2013-06-18       Impact factor: 3.167

Review 7.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

8.  Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.

Authors:  Marion E Reid; Christine Halter Hipsky; Kim Hue-Roye; Carolyn Hoppe
Journal:  Blood Cells Mol Dis       Date:  2013-12-02       Impact factor: 3.039

Review 9.  How I treat the older adult with sickle cell disease.

Authors:  Swee Lay Thein; Jo Howard
Journal:  Blood       Date:  2018-09-11       Impact factor: 22.113

Review 10.  Sickle Cell Anemia and Its Phenotypes.

Authors:  Thomas N Williams; Swee Lay Thein
Journal:  Annu Rev Genomics Hum Genet       Date:  2018-04-11       Impact factor: 9.340

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