Literature DB >> 31925913

Practice patterns for stroke prevention using transcranial Doppler in sickle cell anemia: DISPLACE Consortium.

Alyssa M Schlenz1,2, Shannon Phillips3, Martina Mueller3,4, Cathy Melvin4, Robert J Adams5, Julie Kanter6.   

Abstract

BACKGROUND: Children with sickle cell anemia (SCA) are at increased risk for stroke. In 2014, the National Heart, Lung, and Blood Institute (NHLBI) developed guidelines for stroke prevention in SCA informed by the Stroke Prevention Trial in Sickle Cell Anemia (STOP) and Optimizing Primary Stroke Prevention in Sickle Cell Anemia (STOP II) trials. The guidelines specify the use of transcranial Doppler (TCD) screening and intervention with chronic red cell transfusions (CRCT) in children with SCA who have TCD indication of high stroke risk. The purpose of this study was to describe real-world practice patterns of stroke risk screening and intervention in sites that participated in the Dissemination and Implementation of Stroke Prevention Looking at the Care Environment (DISPLACE) Consortium. PROCEDURE: Site investigators completed a survey during the formative stages of the study to evaluate their TCD practices relative to the STOP studies. Descriptive statistics and analysis of free-text comments for more complex practices were evaluated.
RESULTS: Results suggested universal acceptance of annual TCD screening and initiation of CRCT following an abnormal result among the DISPLACE Consortium, consistent with NHLBI recommendations. However, there was wide variation in methods for conducting TCD screenings (eg, dedicated Doppler vs TCD imaging), classifying TCD results, and actions taken for conditional and inadequate results.
CONCLUSIONS: Annual TCD screening and initiation of CRCT are critical stroke prevention practices that were universally embraced in the consortium. Additional research would be beneficial for informing clinical practices for areas in which guidelines are absent or unclear.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  clinical practice; prevention; sickle cell anemia; stroke

Mesh:

Year:  2020        PMID: 31925913      PMCID: PMC7036320          DOI: 10.1002/pbc.28172

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  21 in total

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Review 3.  Central nervous system complications and management in sickle cell disease.

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

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Journal:  N Engl J Med       Date:  2014-08-21       Impact factor: 91.245

5.  Design of the silent cerebral infarct transfusion (SIT) trial.

Authors:  James F Casella; Allison A King; Bruce Barton; Desiree A White; Michael J Noetzel; Rebecca N Ichord; Cindy Terrill; Deborah Hirtz; Robert C McKinstry; John J Strouse; Thomas H Howard; Thomas D Coates; Caterina P Minniti; Andrew D Campbell; Bruce A Vendt; Harold Lehmann; Michael R Debaun
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6.  Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease.

Authors:  Robert J Adams; Donald Brambilla
Journal:  N Engl J Med       Date:  2005-12-29       Impact factor: 91.245

7.  Elevated blood flow velocity in the anterior cerebral artery and stroke risk in sickle cell disease: extended analysis from the STOP trial.

Authors:  Janet L Kwiatkowski; Suzanne Granger; Donald J Brambilla; R Clark Brown; Scott T Miller; Robert J Adams
Journal:  Br J Haematol       Date:  2006-08       Impact factor: 6.998

8.  Comparison of transcranial Doppler sonography with and without imaging in the evaluation of children with sickle cell anemia.

Authors:  M Beth McCarville; Chenghong Li; Xiaoping Xiong; Winfred Wang
Journal:  AJR Am J Roentgenol       Date:  2004-10       Impact factor: 3.959

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

10.  The natural history of conditional transcranial Doppler flow velocities in children with sickle cell anaemia.

Authors:  Jane S Hankins; Gail L Fortner; M Beth McCarville; Matthew P Smeltzer; Winfred C Wang; Chin-Shang Li; Russell E Ware
Journal:  Br J Haematol       Date:  2008-05-08       Impact factor: 6.998

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  3 in total

1.  Transcranial doppler as screening method for sickling crises in children with sickle cell anemia: a latin America cohort study.

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Journal:  BMC Pediatr       Date:  2022-06-27       Impact factor: 2.567

2.  Practice patterns for neuroimaging and transfusion therapy for management of neurologic complications in sickle cell anemia: DISPLACE consortium.

Authors:  Shannon Phillips; Alyssa M Schlenz; Martina Mueller; Cathy Melvin; Robert J Adams; Julie Kanter
Journal:  Pediatr Blood Cancer       Date:  2020-09-07       Impact factor: 3.167

3.  Transcranial Doppler Screening in a Current Cohort of Children With Sickle Cell Anemia: Results From the DISPLACE Study.

Authors:  Julie Kanter; Shannon Phillips; Alyssa M Schlenz; Martina Mueller; Mary Dooley; Logan Sirline; Robert Nickel; Robert Clark Brown; Lee Hilliard; Cathy L Melvin; Robert J Adams
Journal:  J Pediatr Hematol Oncol       Date:  2021-11-01       Impact factor: 1.289

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