Literature DB >> 21117059

Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease.

Elsie Gyang1, Kristen Yeom, Carolyn Hoppe, Sonia Partap, Michael Jeng.   

Abstract

Regular, chronic red cell transfusions (CTX) have been shown to be effective prophylaxis against stroke in sickle cell disease (SCD) in those at risk. Because serial brain imaging is not routinely performed, little is known about the impact of CTX on silent infarcts (SI) and cerebral vascular pathology. Thus, we retrospectively evaluated the magnetic resonance imaging reports of a cohort of SCD patients who were prescribed CTX for either primary or secondary stroke prophylaxis. Seventeen patients with Hb SS were included (mean age 15 years, mean follow-up 4.3 years). Eight patients were on CTX for primary prophylaxis. New SI occurred in 17.6% of patients corresponding to an SI rate of 5.42 per 100 patient-years. Vasculopathy of the cerebral arteries was present in 65% of patients and progressed in 63% of these patients. Those who developed progressive vasculopathy were on CTX for an average of 8 years before lesions progressed. Patients on CTX for secondary prophylaxis had more SIs and evidence of progressive vascular disease than patients on CTX for primary prophylaxis. We conclude that adherence to CTX does not necessarily prevent SI or halt cerebral vasculopathy progression, especially in those with a history of overt stroke.

Entities:  

Mesh:

Year:  2011        PMID: 21117059     DOI: 10.1002/ajh.21901

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  6 in total

Review 1.  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

2.  Simple chronic transfusion therapy, a crucial therapeutic option for sickle cell disease, improves but does not normalize blood rheology: What should be our goals for transfusion therapy?

Authors:  Jon A Detterich
Journal:  Clin Hemorheol Microcirc       Date:  2018       Impact factor: 2.375

3.  Neurological Complications following Blood Transfusions in Sickle Cell Anemia.

Authors:  Hana Alharbi; Nayaab Khawar; Jolanta Kulpa; Anne Bellin; Simona Proteasa; Revathy Sundaram
Journal:  Case Rep Hematol       Date:  2017-01-03

4.  Catalytic Enantiodivergent Michael Addition by Subtle Adjustment of Achiral Amino Moiety of Dipeptide Phosphines.

Authors:  Huamin Wang; Xiuzheng Li; Youshao Tu; Junliang Zhang
Journal:  iScience       Date:  2020-05-06

5.  Silent cerebral infarcts in patients with sickle cell disease: a systematic review and meta-analysis.

Authors:  Maite E Houwing; Rowena L Grohssteiner; Marjolein H G Dremmen; Ferdows Atiq; Wichor M Bramer; Anne P J de Pagter; C Michel Zwaan; Tonya J H White; Meike W Vernooij; Marjon H Cnossen
Journal:  BMC Med       Date:  2020-12-22       Impact factor: 8.775

Review 6.  Current modalities of sickle cell disease management.

Authors:  Adekunle Sanyaolu; Ejoke Agiri; Carl Bertram; Latasha Brookes; Jesy Choudhury; Dorina Datt; Amira Ibrahim; Anna Maciejko; Anna Mansfield; Jasmine Nkrumah; Martina Williams
Journal:  Blood Sci       Date:  2020-08-27
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.