Literature DB >> 19344400

Haemoglobin oxygen saturation is a determinant of cerebral artery blood flow velocity in children with sickle cell anaemia.

Charles T Quinn1, Jennifer Variste, Michael M Dowling.   

Abstract

Steady-state haemoglobin (Hb) desaturation is a common finding in sickle cell anaemia (Hb SS) that could predispose to stroke by limiting oxygen delivery to the brain. To determine its association with the risk of overt stroke, we examined the relationship between daytime Hb saturation measured by pulse oximetry (SpO(2)) and cerebral artery blood flow velocity measured by transcranial Doppler ultrasonography (TCD), an established risk factor for overt stroke in Hb SS. We studied 181 children using multivariate models to control for known determinants of TCD velocity, including age, haematocrit, and a measure of stenosis. We found that SpO(2) correlated significantly and inversely with TCD velocity in both the right and left middle cerebral arteries. Hb desaturation was associated with increased cerebral artery blood flow velocities and increased odds of abnormal TCD velocities, hence increased risk of stroke. About 5% of the variation in TCD velocity could be ascribed to Hb saturation while controlling for other determinants of TCD velocity. In conclusion, Hb saturation is a determinant of TCD velocity and a risk factor for stroke in children with Hb SS.

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Year:  2009        PMID: 19344400      PMCID: PMC2737449          DOI: 10.1111/j.1365-2141.2009.07652.x

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


  18 in total

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Journal:  Pediatr Blood Cancer       Date:  2008-06       Impact factor: 3.167

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Authors:  Charles T Quinn; Zora R Rogers; George R Buchanan
Journal:  Blood       Date:  2004-02-05       Impact factor: 22.113

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Journal:  Lancet       Date:  2003-11-01       Impact factor: 79.321

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Journal:  Blood       Date:  2002-09-12       Impact factor: 22.113

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  18 in total

1.  Parent education and biologic factors influence on cognition in sickle cell anemia.

Authors:  Allison A King; John J Strouse; Mark J Rodeghier; Bruce E Compas; James F Casella; Robert C McKinstry; Michael J Noetzel; Charles T Quinn; Rebecca Ichord; Michael M Dowling; J Philip Miller; Michael R Debaun
Journal:  Am J Hematol       Date:  2014-02       Impact factor: 10.047

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Authors:  Suvimol Sangkatumvong; Michael C K Khoo; Roberta Kato; Jon A Detterich; Adam Bush; Thomas G Keens; Herbert J Meiselman; John C Wood; Thomas D Coates
Journal:  Am J Respir Crit Care Med       Date:  2011-08-15       Impact factor: 21.405

Review 3.  Advances in Understanding Ischemic Stroke Physiology and the Impact of Vasculopathy in Children With Sickle Cell Disease.

Authors:  Kristin P Guilliams; Melanie E Fields; Michael M Dowling
Journal:  Stroke       Date:  2019-02       Impact factor: 7.914

4.  Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.

Authors:  Elliott P Vichinsky; Lynne D Neumayr; Jeffrey I Gold; Michael W Weiner; Randall R Rule; Diana Truran; Jeffrey Kasten; Barry Eggleston; Karen Kesler; Lillian McMahon; Eugene P Orringer; Thomas Harrington; Karen Kalinyak; Laura M De Castro; Abdullah Kutlar; Cynthia J Rutherford; Cage Johnson; Joel David Bessman; Lanetta B Jordan; F Daniel Armstrong
Journal:  JAMA       Date:  2010-05-12       Impact factor: 56.272

Review 5.  Prospects for primary stroke prevention in children with sickle cell anaemia.

Authors:  Lori C Jordan; James F Casella; Michael R DeBaun
Journal:  Br J Haematol       Date:  2012-01-09       Impact factor: 6.998

6.  Cerebral tissue hemoglobin saturation in children with sickle cell disease.

Authors:  Charles T Quinn; Michael M Dowling
Journal:  Pediatr Blood Cancer       Date:  2012-06-07       Impact factor: 3.167

7.  Headache and migraine in children with sickle cell disease are associated with lower hemoglobin and higher pain event rates but not silent cerebral infarction.

Authors:  Michael M Dowling; Michael J Noetzel; Mark J Rodeghier; Charles T Quinn; Deborah G Hirtz; Rebecca N Ichord; Janet L Kwiatkowski; E Steven Roach; Fenella J Kirkham; James F Casella; Michael R DeBaun
Journal:  J Pediatr       Date:  2014-02-13       Impact factor: 4.406

Review 8.  Anemia, age, desaturation, and impaired neurocognition in sickle cell anemia.

Authors:  Gregory J Kato
Journal:  Pediatr Blood Cancer       Date:  2012-09-04       Impact factor: 3.167

9.  Hydroxyurea Improves Oxygen Saturation in Children With Sickle Cell Disease.

Authors:  Farzana D Pashankar; Deepa Manwani; Margaret T Lee; Nancy S Green
Journal:  J Pediatr Hematol Oncol       Date:  2015-04       Impact factor: 1.289

10.  Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.

Authors:  Sharon E Cox; Julie Makani; Charles R Newton; Andrew M Prentice; Fenella J Kirkham
Journal:  ISRN Hematol       Date:  2013-04-03
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