Literature DB >> 23151905

National trends in incidence rates of hospitalization for stroke in children with sickle cell disease.

Timothy L McCavit1, Lei Xuan, Song Zhang, Glenn Flores, Charles T Quinn.   

Abstract

BACKGROUND: The success of primary stroke prevention for children with sickle cell disease (SCD) throughout the United States is unknown. Therefore, we aimed to generate national incidence rates of hospitalization for stroke in children with sickle cell disease (SCD) before and after publication of the Stroke Prevention Trial in Sickle Cell Anemia (STOP trial) in 1998. PROCEDURE: We performed a retrospective trend analysis of the 1993-2009 Nationwide Inpatient Sample and Kids' Inpatient Databases. Hospitalizations for SCD patients 0-18 years old with stroke were identified by ICD-9CM code. The primary outcome, the trend in annual incidence rate of hospitalization for stroke in children with SCD, was analyzed by linear regression. Incidence rates of hospitalization for stroke before and after 1998 were compared by the Wilcoxon rank-sum test.
RESULTS: From 1993 to 2009, 2,024 hospitalizations were identified for stroke. Using the mean annual incidence rate of hospitalization for stroke from 1993 to 1998 as the baseline, the rate decreased from 1993 to 2009 (point estimate = -0.022/100 patient years [95% CI, -0.039, -0.005], P = 0.027). The mean annual incidence rate of hospitalization stroke decreased by 45% from 0.51 per 100 patient years in 1993-1998 to 0.28 per 100 patient years in 1999-2009 (P = 0.008). Total hospital days and charges attributed to stroke also decreased by 45% and 24%, respectively.
CONCLUSIONS: After publication of the STOP trial and hydroxyurea licensure in 1998, the incidence of hospitalization for stroke in children with SCD decreased across the United States, suggesting that primary stroke prevention has been effective nationwide, but opportunity for improvement remains.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23151905      PMCID: PMC4250091          DOI: 10.1002/pbc.24392

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


  25 in total

1.  Population estimates of sickle cell disease in the U.S.

Authors:  Kathryn L Hassell
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

2.  Stroke With Transfusions Changing to Hydroxyurea (SWiTCH).

Authors:  Russell E Ware; Ronald W Helms
Journal:  Blood       Date:  2012-02-07       Impact factor: 22.113

3.  The number of people with sickle-cell disease in the United States: national and state estimates.

Authors:  David C Brousseau; Julie A Panepinto; Mark Nimmer; Raymond G Hoffmann
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

4.  Transcranial Doppler ultrasonography and prophylactic transfusion program is effective in preventing overt stroke in children with sickle cell disease.

Authors:  Henrietta Enninful-Eghan; Reneé H Moore; Rebecca Ichord; Kim Smith-Whitley; Janet L Kwiatkowski
Journal:  J Pediatr       Date:  2010-09       Impact factor: 4.406

5.  Hydroxyurea in children with sickle cell disease: practice patterns and barriers to utilization.

Authors:  Amanda M Brandow; Danielle L Jirovec; Julie A Panepinto
Journal:  Am J Hematol       Date:  2010-08       Impact factor: 10.047

6.  Caregivers' perspectives on barriers to transcranial Doppler screening in children with sickle-cell disease.

Authors:  Lindsay M Bollinger; Kidan G Nire; Melissa M Rhodes; Deena J Chisolm; Sarah H O'Brien
Journal:  Pediatr Blood Cancer       Date:  2010-09-14       Impact factor: 3.167

7.  Quality-of-care indicators for children with sickle cell disease.

Authors:  C Jason Wang; Patricia L Kavanagh; Alison A Little; Jaime Bruce Holliman; Philippa G Sprinz
Journal:  Pediatrics       Date:  2011-08-15       Impact factor: 7.124

8.  Stroke recurrence in children with sickle cell disease treated with hydroxyurea following first clinical stroke.

Authors:  Susanna Bortolusso Ali; Michelle Moosang; Lesley King; Jennifer Knight-Madden; Marvin Reid
Journal:  Am J Hematol       Date:  2011-09-02       Impact factor: 10.047

9.  A critical assessment of transcranial doppler screening rates in a large pediatric sickle cell center: opportunities to improve healthcare quality.

Authors:  Jean L Raphael; Priya B Shetty; Hao Liu; Donald H Mahoney; Brigitta U Mueller
Journal:  Pediatr Blood Cancer       Date:  2008-11       Impact factor: 3.167

10.  Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia.

Authors:  Sherri A Zimmerman; William H Schultz; Shelly Burgett; Nicole A Mortier; Russell E Ware
Journal:  Blood       Date:  2007-04-11       Impact factor: 22.113

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  23 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

2.  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

3.  Determining Adherence to Quality Indicators in Sickle Cell Anemia Using Multiple Data Sources.

Authors:  Cindy E Neunert; Robert W Gibson; Peter A Lane; Pragya Verma-Bhatnagar; Vaughn Barry; Mei Zhou; Angela Snyder
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

Review 4.  Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication.

Authors:  Charles T Quinn
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-23

Review 5.  Arterial ischemic stroke in children: risk factors and etiologies.

Authors:  Adam L Numis; Christine K Fox
Journal:  Curr Neurol Neurosci Rep       Date:  2014-01       Impact factor: 5.081

6.  Silent cerebral infarction, income, and grade retention among students with sickle cell anemia.

Authors:  Allison A King; Mark J Rodeghier; Julie Ann Panepinto; John J Strouse; James F Casella; Charles T Quinn; Michael M Dowling; Sharada A Sarnaik; Alexis A Thompson; Gerald M Woods; Caterina P Minniti; Rupa C Redding-Lallinger; Melanie Kirby-Allen; Fenella J Kirkham; Robert McKinstry; Michael J Noetzel; Desiree A White; Janet K Kwiatkowski; Thomas H Howard; Karen A Kalinyak; Baba Inusa; Melissa M Rhodes; Mark E Heiny; Ben Fuh; Jason M Fixler; Mae O Gordon; Michael R DeBaun
Journal:  Am J Hematol       Date:  2014-08-04       Impact factor: 10.047

7.  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

8.  The burden of obstructive sleep apnea in pediatric sickle cell disease: a Kids' inpatient database study.

Authors:  Po-Yang Tsou; Christopher M Cielo; Melissa S Xanthopoulos; Yu-Hsun Wang; Pei-Lun Kuo; Ignacio E Tapia
Journal:  Sleep       Date:  2021-02-12       Impact factor: 5.849

Review 9.  Sickle cell disease in childhood: from newborn screening through transition to adult medical care.

Authors:  Charles T Quinn
Journal:  Pediatr Clin North Am       Date:  2013-12       Impact factor: 3.278

10.  Trends in blood transfusion among hospitalized children with sickle cell disease.

Authors:  Jean L Raphael; Suzette O Oyeku; Marc A Kowalkowski; Brigitta U Mueller; Angela M Ellison
Journal:  Pediatr Blood Cancer       Date:  2013-06-18       Impact factor: 3.167

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