Literature DB >> 19344396

Chronic transfusion practice for children with sickle cell anaemia and stroke.

Banu Aygun1, Marsha A McMurray, William H Schultz, Janet L Kwiatkowski, Lee Hilliard, Ofelia Alvarez, Matthew Heeney, Karen Kalinyak, Margaret T Lee, Scott Miller, Ronald W Helms, Russell E Ware.   

Abstract

Chronic transfusions to maintain haemoglobin S (HbS) < or =30% are the mainstay of treatment for children with sickle cell anaemia (SCA) and previous stroke. This HbS target is often hard to maintain, however, and values achieved in current practice are unknown. In preparation for the Phase III Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) trial, we collected data on 295 children with SCA and stroke who received transfusions at 23 institutions. The overall average pre-transfusion %HbS was 35 +/- 11% (institutional range 22-51%). Receiving scheduled transfusions on time was the most predictive variable for maintaining HbS at the < or =30% goal.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19344396     DOI: 10.1111/j.1365-2141.2009.07630.x

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


  8 in total

Review 1.  Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.

Authors:  Lise J Estcourt; Patricia M Fortin; Sally Hopewell; Marialena Trivella; Winfred C Wang
Journal:  Cochrane Database Syst Rev       Date:  2017-01-17

2.  Stroke With Transfusions Changing to Hydroxyurea (SWiTCH): a phase III randomized clinical trial for treatment of children with sickle cell anemia, stroke, and iron overload.

Authors:  Russell E Ware; William H Schultz; Nancy Yovetich; Nicole A Mortier; Ofelia Alvarez; Lee Hilliard; Rathi V Iyer; Scott T Miller; Zora R Rogers; J Paul Scott; Myron Waclawiw; Ronald W Helms
Journal:  Pediatr Blood Cancer       Date:  2011-08-08       Impact factor: 3.167

3.  Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype.

Authors:  Christian Brendel; Swaroopa Guda; Raffaele Renella; Daniel E Bauer; Matthew C Canver; Young-Jo Kim; Matthew M Heeney; Denise Klatt; Jonathan Fogel; Michael D Milsom; Stuart H Orkin; Richard I Gregory; David A Williams
Journal:  J Clin Invest       Date:  2016-09-06       Impact factor: 14.808

4.  Effects of chronic transfusions on abdominal sonographic abnormalities in children with sickle cell anemia.

Authors:  Mary Beth McCarville; Zora R Rogers; Sharada Sarnaik; Paul Scott; Banu Aygun; Lee Hilliard; Margaret T Lee; Karen Kalinyak; William Owen; Julian Garro; William Schultz; Nancy Yovetich; Russell E Ware
Journal:  J Pediatr       Date:  2011-09-09       Impact factor: 4.406

Review 5.  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

6.  Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.

Authors:  Lise J Estcourt; Ruchika Kohli; Sally Hopewell; Marialena Trivella; Winfred C Wang
Journal:  Cochrane Database Syst Rev       Date:  2020-07-27

7.  Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study.

Authors:  Lauren M Hawkins; Cynthia B Sinha; Diana Ross; Marianne E M Yee; Maa-Ohui Quarmyne; Lakshmanan Krishnamurti; Nitya Bakshi
Journal:  BMC Pediatr       Date:  2020-04-18       Impact factor: 2.125

Review 8.  Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.

Authors:  Winfred C Wang; Kerry Dwan
Journal:  Cochrane Database Syst Rev       Date:  2013-11-14
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.