Literature DB >> 25140956

Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia.

Michael R DeBaun1, Mae Gordon, Robert C McKinstry, Michael J Noetzel, Desiree A White, Sharada A Sarnaik, Emily R Meier, Thomas H Howard, Suvankar Majumdar, Baba P D Inusa, Paul T Telfer, Melanie Kirby-Allen, Timothy L McCavit, Annie Kamdem, Gladstone Airewele, Gerald M Woods, Brian Berman, Julie A Panepinto, Beng R Fuh, Janet L Kwiatkowski, Allison A King, Jason M Fixler, Melissa M Rhodes, Alexis A Thompson, Mark E Heiny, Rupa C Redding-Lallinger, Fenella J Kirkham, Natalia Dixon, Corina E Gonzalez, Karen A Kalinyak, Charles T Quinn, John J Strouse, J Philip Miller, Harold Lehmann, Michael A Kraut, William S Ball, Deborah Hirtz, James F Casella.   

Abstract

BACKGROUND: Silent cerebral infarcts are the most common neurologic injury in children with sickle cell anemia and are associated with the recurrence of an infarct (stroke or silent cerebral infarct). We tested the hypothesis that the incidence of the recurrence of an infarct would be lower among children who underwent regular blood-transfusion therapy than among those who received standard care.
METHODS: In this randomized, single-blind clinical trial, we randomly assigned children with sickle cell anemia to receive regular blood transfusions (transfusion group) or standard care (observation group). Participants were between 5 and 15 years of age, with no history of stroke and with one or more silent cerebral infarcts on magnetic resonance imaging and a neurologic examination showing no abnormalities corresponding to these lesions. The primary end point was the recurrence of an infarct, defined as a stroke or a new or enlarged silent cerebral infarct.
RESULTS: A total of 196 children (mean age, 10 years) were randomly assigned to the observation or transfusion group and were followed for a median of 3 years. In the transfusion group, 6 of 99 children (6%) had an end-point event (1 had a stroke, and 5 had new or enlarged silent cerebral infarcts). In the observation group, 14 of 97 children (14%) had an end-point event (7 had strokes, and 7 had new or enlarged silent cerebral infarcts). The incidence of the primary end point in the transfusion and observation groups was 2.0 and 4.8 events, respectively, per 100 years at risk, corresponding to an incidence rate ratio of 0.41 (95% confidence interval, 0.12 to 0.99; P=0.04).
CONCLUSIONS: Regular blood-transfusion therapy significantly reduced the incidence of the recurrence of cerebral infarct in children with sickle cell anemia. (Funded by the National Institute of Neurological Disorders and Stroke and others; Silent Cerebral Infarct Multi-Center Clinical Trial ClinicalTrials.gov number, NCT00072761, and Current Controlled Trials number, ISRCTN52713285.).

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Year:  2014        PMID: 25140956      PMCID: PMC4195437          DOI: 10.1056/NEJMoa1401731

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  23 in total

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Authors:  F Bernaudin; S Verlhac; F Fréard; F Roudot-Thoraval; M Benkerrou; I Thuret; R Mardini; J P Vannier; E Ploix; M Romero; C Cassé-Perrot; M Helly; E Gillard; G Sebag; H Kchouk; J P Pracros; B Finck; J N Dacher; V Ickowicz; C Raybaud; M Poncet; E Lesprit; P H Reinert; P Brugières
Journal:  J Child Neurol       Date:  2000-05       Impact factor: 1.987

2.  Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease.

Authors:  J Schatz; R T Brown; J M Pascual; L Hsu; M R DeBaun
Journal:  Neurology       Date:  2001-04-24       Impact factor: 9.910

3.  The number of people with sickle-cell disease in the United States: national and state estimates.

Authors:  David C Brousseau; Julie A Panepinto; Mark Nimmer; Raymond G Hoffmann
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

4.  Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial.

Authors:  E P Vichinsky; N L Luban; E Wright; N Olivieri; C Driscoll; C H Pegelow; R J Adams
Journal:  Transfusion       Date:  2001-09       Impact factor: 3.157

5.  Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.

Authors:  S T Miller; E A Macklin; C H Pegelow; T R Kinney; L A Sleeper; J A Bello; L D DeWitt; D M Gallagher; L Guarini; F G Moser; K Ohene-Frempong; N Sanchez; E P Vichinsky; W C Wang; D L Wethers; D P Younkin; R A Zimmerman; M R DeBaun
Journal:  J Pediatr       Date:  2001-09       Impact factor: 4.406

6.  Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease.

Authors:  Charles H Pegelow; Eric A Macklin; Franklin G Moser; Winfred C Wang; Jacqueline A Bello; Scott T Miller; Elliott P Vichinsky; Michael R DeBaun; Ludovico Guarini; Robert A Zimmerman; Donald P Younkin; Dianne M Gallagher; Thomas R Kinney
Journal:  Blood       Date:  2002-04-15       Impact factor: 22.113

7.  Blood transfusion therapy is feasible in a clinical trial setting in children with sickle cell disease and silent cerebral infarcts.

Authors:  Allison A King; Michael Noetzel; Desirée A White; Robert C McKinstry; Michael R Debaun
Journal:  Pediatr Blood Cancer       Date:  2008-03       Impact factor: 3.167

8.  MRI abnormalities of the brain in one-year-old children with sickle cell anemia.

Authors:  Winfred C Wang; Steven G Pavlakis; Kathleen J Helton; Robert C McKinstry; James F Casella; Robert J Adams; Renee C Rees
Journal:  Pediatr Blood Cancer       Date:  2008-11       Impact factor: 3.167

9.  Stroke and conversion to high risk in children screened with transcranial Doppler ultrasound during the STOP study.

Authors:  Robert J Adams; Donald J Brambilla; Suzanne Granger; Dianne Gallagher; Elliott Vichinsky; Miguel R Abboud; Charles H Pegelow; Gerald Woods; Elizabeth M Rohde; Fenwick T Nichols; Anne Jones; Judith P Luden; Latonya Bowman; Susan Hagner; Knashawn H Morales; E Steve Roach
Journal:  Blood       Date:  2004-01-29       Impact factor: 22.113

10.  Silent infarcts in young children with sickle cell disease.

Authors:  Janet L Kwiatkowski; Robert A Zimmerman; Avrum N Pollock; Wendy Seto; Kim Smith-Whitley; Justine Shults; Anne Blackwood-Chirchir; Kwaku Ohene-Frempong
Journal:  Br J Haematol       Date:  2009-06-04       Impact factor: 6.998

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  138 in total

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Journal:  Int J Clin Exp Med       Date:  2015-07-15

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Authors:  Amanda M Brandow; C Patrick Carroll; Susan Creary; Ronisha Edwards-Elliott; Jeffrey Glassberg; Robert W Hurley; Abdullah Kutlar; Mohamed Seisa; Jennifer Stinson; John J Strouse; Fouza Yusuf; William Zempsky; Eddy Lang
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3.  Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease.

Authors:  Anna M Hood; Allison A King; Melanie E Fields; Andria L Ford; Kristin P Guilliams; Monica L Hulbert; Jin-Moo Lee; Desiree A White
Journal:  Pediatr Blood Cancer       Date:  2019-07-03       Impact factor: 3.167

4.  Implications of a paediatrician-psychologist tandem for sickle cell disease care and impact on cognitive functioning.

Authors:  Adrienne Lerner; Hervé Picard; Adrien May; Vincent Gajdos; Louise Malou-Dhaussy; Flaviana Maroja-Cox; Laurence Salomon; Marie-Hélène Odièvre
Journal:  Eur J Pediatr       Date:  2017-11-29       Impact factor: 3.183

5.  Functional and anatomical evidence of cerebral tissue hypoxia in young sickle cell anemia mice.

Authors:  Lindsay S Cahill; Lisa M Gazdzinski; Albert Ky Tsui; Yu-Qing Zhou; Sharon Portnoy; Elaine Liu; C David Mazer; Gregory Mt Hare; Andrea Kassner; John G Sled
Journal:  J Cereb Blood Flow Metab       Date:  2016-07-20       Impact factor: 6.200

6.  Reduction in Overt and Silent Stroke Recurrence Rate Following Cerebral Revascularization Surgery in Children with Sickle Cell Disease and Severe Cerebral Vasculopathy.

Authors:  Erin M Hall; Jeffrey Leonard; Jodi L Smith; Kristin P Guilliams; Michael Binkley; Robert J Fallon; Monica L Hulbert
Journal:  Pediatr Blood Cancer       Date:  2016-04-22       Impact factor: 3.167

7.  Perspective: thinking beyond survival.

Authors:  Michael R DeBaun
Journal:  Nature       Date:  2014-11-13       Impact factor: 49.962

8.  Neuroimaging in patients with sickle cell anemia: capacity building in Africa.

Authors:  Mboka Jacob; Dawn E Saunders; Jamie M Kawadler; Balowa Mussa; Russell Murdoch; Winok Lapidaire; Furahini Tluway; Ramadhan R Kazema; Siana Nkya; Magda Ahmed; Edward Kija; Lulu Fundikira; Frank Kussaga; Angela Darekar; Hilda Tutuba; Karin Shmueli; Christopher A Clark; Julie Makani; Fenella J Kirkham
Journal:  Blood Adv       Date:  2018-11-30

9.  Cognitive Function in Sickle Cell Disease Across Domains, Cerebral Infarct Status, and the Lifespan: A Meta-Analysis.

Authors:  Kemar V Prussien; Lori C Jordan; Michael R DeBaun; Bruce E Compas
Journal:  J Pediatr Psychol       Date:  2019-09-01

10.  Feasibility trial for primary stroke prevention in children with sickle cell anemia in Nigeria (SPIN trial).

Authors:  Najibah A Galadanci; Shehu Umar Abdullahi; Leah D Vance; Abdulkadir Musa Tabari; Shehi Ali; Raymond Belonwu; Auwal Salihu; Aisha Amal Galadanci; Binta Wudil Jibir; Halima Bello-Manga; Kathleen Neville; Fenella J Kirkham; Yu Shyr; Sharon Phillips; Brittany V Covert; Adetola A Kassim; Lori C Jordan; Muktar H Aliyu; Michael R DeBaun
Journal:  Am J Hematol       Date:  2017-06-15       Impact factor: 10.047

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