Literature DB >> 21992814

Trends in comorbid sickle cell disease among stroke patients.

Bruce Ovbiagele1, Robert J Adams.   

Abstract

BACKGROUND: Stroke is a major complication of sickle cell disease (SCD). In an era of chronic red cell transfusions for stroke prophylaxis in children and greater life expectancy, nationwide data on stroke rates among pediatric and adult patients with SCD are scarce. We evaluated recent time trends in stroke hospitalization among children (0-17 years) and adults (>17 years) with SCD in the United States.
METHODS: Data were obtained from the Nationwide Inpatient Sample. Pediatric (n=26,380) and adult (n=9,638,507) patients admitted to hospitals between 1997 and 2006 with a primary stroke discharge diagnosis (identified by the International Classification of Diseases, Ninth Revision procedure codes) were included. Time trends in the proportion of stroke patients with SCD were computed.
RESULTS: Pediatric stroke patients with co-morbid SCD constituted 8.7% in 1997 vs. 4.8% in 2006 (p=0.04), with 81 fewer actual hospitalizations. Adult stroke patients with SCD were 0.3% in 1997 vs. 0.5% in 2006 (p=0.01), with 157 more actual hospitalizations. Factors that changed substantially and significantly across the decade among pediatric stroke patients with SCD included a drop in ischemic stroke type (74.2% vs. 56.3%) and a rise in comorbid hypertension (1.5% vs. 11.5%), while among adult stroke patients with SCD there was a rise in other stroke type (20.4% vs. 35.6%).
CONCLUSIONS: In an era of increasing prophylactic red cell transfusions, the proportion of SCD diagnoses among pediatric stroke patients significantly decreased in the United States. The rise in SCD diagnoses among adult stroke patients is possibly due to a cohort effect, but further study is needed.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21992814     DOI: 10.1016/j.jns.2011.09.023

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  9 in total

1.  Contribution of Sickle Cell Disease to the Pediatric Stroke Burden Among Hospital Discharges of African-Americans-United States, 1997-2012.

Authors:  Charlotte Baker; Althea M Grant; Mary G George; Scott D Grosse; Thomas V Adamkiewicz
Journal:  Pediatr Blood Cancer       Date:  2015-07-14       Impact factor: 3.167

Review 2.  Chronic organ failure in adult sickle cell disease.

Authors:  Elliott Vichinsky
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

3.  Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association.

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

4.  Computational imaging analysis of fibrin matrices with the inclusion of erythrocytes from homozygous SS blood reveals agglomerated and amorphous structures.

Authors:  Rodney D Averett; David G Norton; Natalie K Fan; Manu O Platt
Journal:  J Thromb Thrombolysis       Date:  2017-01       Impact factor: 2.300

5.  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

6.  Transcranial Doppler Screening Among Children and Adolescents With Sickle Cell Anemia.

Authors:  Sarah L Reeves; Brian Madden; Gary L Freed; Kevin J Dombkowski
Journal:  JAMA Pediatr       Date:  2016-06-01       Impact factor: 16.193

7.  Identifying sickle cell disease cases using administrative claims.

Authors:  Sarah Reeves; Erika Garcia; Mary Kleyn; Michelle Housey; Robin Stottlemyer; Sarah Lyon-Callo; Kevin John Dombkowski
Journal:  Acad Pediatr       Date:  2014-05-29       Impact factor: 3.107

8.  New approaches to genetic predisposition for hemorrhagic stroke in sickle cell disease.

Authors:  Robert J Adams; Rufus O Akinyemi; Mayowa O Owolabi; Dan L Lackland; Bruce Ovbiagele
Journal:  J Clin Hypertens (Greenwich)       Date:  2018-05-27       Impact factor: 3.738

Review 9.  Hypertension and childhood stroke.

Authors:  Juan C Kupferman; Marc B Lande; Stella Stabouli; Dimitrios I Zafeiriou; Steven G Pavlakis
Journal:  Pediatr Nephrol       Date:  2020-04-29       Impact factor: 3.714

  9 in total

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