Literature DB >> 9492971

Stroke prevention trial in sickle cell anemia.

R J Adams1, V C McKie, D Brambilla, E Carl, D Gallagher, F T Nichols, S Roach, M Abboud, B Berman, C Driscoll, B Files, L Hsu, A Hurlet, S Miller, N Olivieri, C Pegelow, C Scher, E Vichinsky, W Wang, G Woods, A Kutlar, E Wright, S Hagner, F Tighe, M A Waclawiw.   

Abstract

Stroke occurs in 7-8% of children with Sickle Cell Disease (Hb SS) and is a major cause of morbidity. Rates of recurrence have been reduced from 46-90% to less than 10% through chronic blood transfusions. Prevention of first stroke, however, would be preferable because even one stroke can cause irreversible brain injury. Transcranial Doppler (TCD) ultrasound can detect arterial blood flow rates associated with subsequent stroke risk. By combining TCD screening and a potentially effective treatment, first stroke may be prevented. The Stroke Prevention Trial in Sickle Cell Anemia (STOP) is the first stroke prevention trial in Hb SS and the first randomized, controlled use of transfusion in Hb SS. This multi-center trial is designed to test whether reducing sickle hemoglobin to 30% or less with periodic blood transfusions will reduce first-time stroke by at least 70% compared to standard care. Primary endpoints will be clinically evident symptoms of cerebral infarction with consistent findings on Magnetic Resonance Imaging and Angiography (MRI/MRA) or symptomatic intracranial hemorrhage. Secondary endpoints will be asymptomatic brain lesions detected by MRI in brain areas not involved in primary endpoints. The design calls for a 6-month start-up interval, 18 months of TCD screening and randomization, and observation for stroke from entry through month 54. Key features of the trial are standardized TCD and MRI/MRA protocols interpreted blindly, and blinded adjudication of endpoints. The sample size (60 per treatment group) is based on prospective data relating TCD velocity to risk of stroke. A time-averaged mean velocity of > or = 200 cm/sec is associated with a 46% risk of cerebral infarction over 39 months. The sample size is sufficient to detect 70% reduction in the primary endpoint at 90% power. This trial will determine if transfusion is effective in the primary prevention of stroke. Secondary aims may further the understanding of the effects of transfusion on the brain and guide future research into cerebrovascular disease in Hb SS.

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Year:  1998        PMID: 9492971     DOI: 10.1016/s0197-2456(97)00099-8

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN: 0197-2456


  56 in total

Review 1.  New advances in identifying genetic anomalies in stroke-prone probands.

Authors:  James F Meschia; Bradford B Worrall
Journal:  Curr Atheroscler Rep       Date:  2003-07       Impact factor: 5.113

2.  Potential of three-dimensional ultrasound in neonatal and paediatric neurosonography.

Authors:  M Riccabona; T R Nelson; C Weitzer; B Resch; D P Pretorius
Journal:  Eur Radiol       Date:  2003-03-06       Impact factor: 5.315

3.  New advances in identifying genetic anomalies in stroke-prone probands.

Authors:  James F Meschia; Bradford B Worrall
Journal:  Curr Neurol Neurosci Rep       Date:  2004-09       Impact factor: 5.081

Review 4.  Managing sickle cell disease.

Authors:  Susan Claster; Elliott P Vichinsky
Journal:  BMJ       Date:  2003-11-15

5.  Applications and Experience with PCR-Based Assays to Predict Blood Group Antigens.

Authors:  Marion E Reid
Journal:  Transfus Med Hemother       Date:  2009-06       Impact factor: 3.747

6.  Problems with implementing a standardised transcranial Doppler screening programme: impact of instrumentation variation on STOP classification.

Authors:  Soundrie T Padayachee; Nicholas Thomas; Andrew J Arnold; Baba Inusa
Journal:  Pediatr Radiol       Date:  2011-10-15

7.  Erythrocytapheresis: Do Not Forget a Useful Therapy!

Authors:  Heidrun Ullrich; Roland Fischer; Regine Grosse; Uwe Kordes; Claudia Schubert; Bettina Altstadt; Georges Andreu
Journal:  Transfus Med Hemother       Date:  2008-01-15       Impact factor: 3.747

8.  Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia.

Authors:  Jonathan M Flanagan; Vivien Sheehan; Heidi Linder; Thad A Howard; Yong-Dong Wang; Carolyn C Hoppe; Banu Aygun; Robert J Adams; Geoffrey A Neale; Russell E Ware
Journal:  Blood       Date:  2013-02-19       Impact factor: 22.113

9.  Transcranial doppler re-screening of subjects who participated in STOP and STOP II.

Authors:  Robert J Adams; Dan T Lackland; Lynette Brown; David Brown; Jenifer Voeks; Heather J Fullerton; Julie Kanter; Janet L Kwiatkowski
Journal:  Am J Hematol       Date:  2016-10-25       Impact factor: 10.047

Review 10.  Sickle cell disease.

Authors:  Martin M Meremikwu
Journal:  BMJ Clin Evid       Date:  2009-03-27
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