Literature DB >> 18490379

A simple index using age, hemoglobin, and aspartate transaminase predicts increased intracerebral blood velocity as measured by transcranial Doppler scanning in children with sickle cell anemia.

David C Rees1, Moira C Dick, Sue E Height, Sandra O'Driscoll, Keith R E Pohl, David E Goss, Colin R Deane.   

Abstract

OBJECTIVE: Increased intracerebral blood velocity measured by transcranial Doppler scanning identifies children with sickle cell anemia who are at increased risk of stroke. We have tried to develop an index based on routine clinical measurements that also predicts increased intracerebral blood flow.
METHOD: Routinely collected clinical and laboratory data were correlated with transcranial Doppler measurements on children with sickle cell anemia seen in a single institution in 2006. The index produced was validated on a second independent data set from children with sickle cell anemia.
RESULTS: The time-averaged mean of the maximum velocity in centimeters per second in the middle cerebral artery circulation correlated significantly with age, hemoglobin, lactate dehydrogenase, and aspartate transaminase levels, white blood cell count, and creatinine level. On multiple regression, hemoglobin and aspartate transaminase levels maintained their significance, whereas age had borderline significance, and an index was developed linked to a time-averaged mean of the maximum velocity of 220 - (8 x hemoglobin) - (1.4 x age) + (0.4 x aspartate transaminase). This detected a time-averaged mean of the maximum velocity of >170 cm/second with 100% sensitivity and 58% specificity. The index was validated on the second data set and again showed 100% sensitivity with 73% specificity.
CONCLUSION: This simple index has the potential to identify children who are at higher risk of cerebrovascular disease to allow them to be prioritized for transcranial Doppler scanning and other intracerebral imaging.

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Year:  2008        PMID: 18490379     DOI: 10.1542/peds.2007-2771

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  7 in total

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Authors:  James F Meschia; Cheryl Bushnell; Bernadette Boden-Albala; Lynne T Braun; Dawn M Bravata; Seemant Chaturvedi; Mark A Creager; Robert H Eckel; Mitchell S V Elkind; Myriam Fornage; Larry B Goldstein; Steven M Greenberg; Susanna E Horvath; Costantino Iadecola; Edward C Jauch; Wesley S Moore; John A Wilson
Journal:  Stroke       Date:  2014-10-28       Impact factor: 7.914

Review 2.  Clinical biomarkers in sickle cell disease.

Authors:  Ghazi A Damanhouri; Jummanah Jarullah; Samy Marouf; S I Hindawi; Gohar Mushtaq; Mohammad A Kamal
Journal:  Saudi J Biol Sci       Date:  2014-09-18       Impact factor: 4.219

Review 3.  Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease.

Authors:  André Rolim Belisário; Célia Maria Silva; Cibele Velloso-Rodrigues; Marcos Borato Viana
Journal:  Hematol Transfus Cell Ther       Date:  2017-11-26

4.  Cerebral hemodynamics in children with sickle cell disease in India: An observational cohort study.

Authors:  Bhakti Gajjar; Sanjay Sharma; Erum Khan; Pranita Sharma; Pawan Jain; Vikas Goel; Arvind Neral; Jyotish Patel; Mamta Parmar; Kanika Sharma; Vijay K Sharma; Arvind K Sharma
Journal:  Medicine (Baltimore)       Date:  2022-07-08       Impact factor: 1.817

5.  Primary stroke prevention for sickle cell disease in north-east Italy: the role of ethnic issues in establishing a Transcranial Doppler screening program.

Authors:  Raffaella Colombatti; Giorgio Meneghetti; Mario Ermani; Marta Pierobon; Laura Sainati
Journal:  Ital J Pediatr       Date:  2009-06-22       Impact factor: 2.638

6.  Biomarkers of clinical severity in treated and untreated sickle cell disease: a comparison by genotypes of a single center cohort and African Americans in the NHANES study.

Authors:  Franklin Njoku; Xu Zhang; Binal N Shah; Roberto F Machado; Jin Han; Santosh L Saraf; Victor R Gordeuk
Journal:  Br J Haematol       Date:  2021-07-15       Impact factor: 8.615

7.  Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength.

Authors:  Kizzy-Clara Cita; Laurent Brureau; Nathalie Lemonne; Marie Billaud; Philippe Connes; Séverine Ferdinand; Benoit Tressières; Vanessa Tarer; Maryse Etienne-Julan; Pascal Blanchet; Jacques Elion; Marc Romana
Journal:  PLoS One       Date:  2016-05-04       Impact factor: 3.240

  7 in total

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