Literature DB >> 20331955

Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Hussain R Yusuf1, Hani K Atrash, Scott D Grosse, Christopher S Parker, Althea M Grant.   

Abstract

BACKGROUND: Patients with sickle cell disease (SCD) often use emergency department services to obtain medical care. Limited information is available about emergency department use among patients with SCD.
PURPOSE: This study assessed characteristics of emergency department visits made nationally by patients with SCD.
METHODS: Data from the National Hospital Ambulatory Medical Care Survey (NHAMCS) for the years 1999-2007 were analyzed. The NHAMCS is a survey of hospital emergency department and outpatient visits. Emergency department visits by patients with SCD were identified using ICD-9-CM codes, and nationally weighted estimates were calculated.
RESULTS: On average, approximately 197,333 emergency department visits were estimated to have occurred each year between 1999 and 2007 with SCD as one of the diagnoses listed. The expected source of payment was private insurance for 14%, Medicaid/State Children's Health Insurance Program for 58%, Medicare for 14%, and other/unknown for 15%. Approximately 29% of visits resulted in hospital admission; this was 37% among patients aged 0-19 years, and 26% among patients aged >/=20 years. The episode of care was indicated as a follow-up visit for 23% of the visits. Patient-cited reasons for the emergency department visit included chest pain (11%); other pain or unspecified pain (67%); fever/infection (6%); and shortness of breath/breathing problem/cough (5%), among other reasons.
CONCLUSIONS: Substantial numbers of emergency department visits occur among people with SCD. The most common reason for the emergency department visits is pain symptoms. The findings of this study can help to improve health services delivery and utilization among patients with SCD. Published by Elsevier Inc.

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Year:  2010        PMID: 20331955      PMCID: PMC4521762          DOI: 10.1016/j.amepre.2010.01.001

Source DB:  PubMed          Journal:  Am J Prev Med        ISSN: 0749-3797            Impact factor:   5.043


  21 in total

1.  Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002.

Authors:  Emad Yanni; Scott D Grosse; QuanHe Yang; Richard S Olney
Journal:  J Pediatr       Date:  2008-11-22       Impact factor: 4.406

2.  A descriptive study of heavy emergency department users at an academic emergency department reveals heavy ED users have better access to care than average users.

Authors:  Fidela S J Blank; Haiping Li; Philip L Henneman; Howard A Smithline; John S Santoro; Deborah Provost; Ann M Maynard
Journal:  J Emerg Nurs       Date:  2005-04       Impact factor: 1.836

Review 3.  Sickle cell disease.

Authors:  Jason Fixler; Lori Styles
Journal:  Pediatr Clin North Am       Date:  2002-12       Impact factor: 3.278

4.  Who cares for medicaid-enrolled children with chronic conditions?

Authors:  K Kuhlthau; T G Ferris; A C Beal; S L Gortmaker; J M Perrin
Journal:  Pediatrics       Date:  2001-10       Impact factor: 7.124

5.  Health care utilization and expenditures for privately and publicly insured children with sickle cell disease in the United States.

Authors:  Mercy Mvundura; Djesika Amendah; Patricia L Kavanagh; Philippa G Sprinz; Scott D Grosse
Journal:  Pediatr Blood Cancer       Date:  2009-10       Impact factor: 3.167

6.  Newborn screening coupled with comprehensive follow-up reduced early mortality of sickle cell disease in Connecticut.

Authors:  Tamiesha Frempong; Howard A Pearson
Journal:  Conn Med       Date:  2007-01

7.  Southside medical homes network: linking emergency department patients to community care.

Authors:  Amy L Marr; Tyson Pillow; Stephen Brown
Journal:  Prehosp Disaster Med       Date:  2008 May-Jun       Impact factor: 2.040

8.  Impact of an emergency department pain management protocol on the pattern of visits by patients with sickle cell disease.

Authors:  Melissa Givens; Cynthia Rutherford; Girish Joshi; Kathleen Delaney
Journal:  J Emerg Med       Date:  2007-02-07       Impact factor: 1.484

9.  Comparison of costs to the health sector of comprehensive and episodic health care for sickle cell disease patients.

Authors:  Y M Yang; A K Shah; M Watson; V N Mankad
Journal:  Public Health Rep       Date:  1995 Jan-Feb       Impact factor: 2.792

10.  Healthcare utilization and expenditures for low income children with sickle cell disease.

Authors:  Jean L Raphael; Craig L Dietrich; Deborah Whitmire; Donald H Mahoney; Brigitta U Mueller; Angelo P Giardino
Journal:  Pediatr Blood Cancer       Date:  2009-02       Impact factor: 3.167

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  74 in total

1.  Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.

Authors:  Lori E Crosby; Naomi E Joffe; Nina Reynolds; James L Peugh; Ellen Manegold; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-08-13

2.  Applicability of the SMART Model of Transition Readiness for Sickle-Cell Disease.

Authors:  Siddika S Mulchan; Jessica M Valenzuela; Lori E Crosby; Claudia Diaz Pow Sang
Journal:  J Pediatr Psychol       Date:  2015-12-30

3.  Association between hospital admissions and healthcare provider communication for individuals with sickle cell disease.

Authors:  Robert M Cronin; Manshu Yang; Jane S Hankins; Jeannie Byrd; Brandi M Pernell; Adetola Kassim; Patricia Adams-Graves; Alexis A Thompson; Karen Kalinyak; Michael DeBaun; Marsha Treadwell
Journal:  Hematology       Date:  2020-12       Impact factor: 2.269

4.  Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.

Authors:  Gabriela Calhoun; Li Wang; Luis E F Almeida; Nicholas Kenyon; Nina Afsar; Mehdi Nouraie; Julia C Finkel; Zenaide M N Quezado
Journal:  Eur J Pharmacol       Date:  2015-02-25       Impact factor: 4.432

5.  Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  J Sick Cell Dis Hemoglobinopathies       Date:  2017-05

Review 6.  Neuronal transient receptor potential (TRP) channels and noxious sensory detection in sickle cell disease.

Authors:  Katelyn E Sadler; Cheryl L Stucky
Journal:  Neurosci Lett       Date:  2018-11-30       Impact factor: 3.046

7.  Evaluation and Treatment of Sickle Cell Pain in the Emergency Department: Paths to a Better Future.

Authors:  William T Zempsky
Journal:  Clin Pediatr Emerg Med       Date:  2010-12-01

8.  Sickle-cell disease in California: a population-based description of emergency department utilization.

Authors:  Julie A Wolfson; Sheree M Schrager; Thomas D Coates; Michele D Kipke
Journal:  Pediatr Blood Cancer       Date:  2010-11-24       Impact factor: 3.167

9.  Outpatient pain predicts subsequent one-year acute health care utilization among adults with sickle cell disease.

Authors:  Miriam O Ezenwa; Robert E Molokie; Zaijie Jim Wang; Yingwei Yao; Marie L Suarez; Veronica Angulo; Diana J Wilkie
Journal:  J Pain Symptom Manage       Date:  2014-03-15       Impact factor: 3.612

10.  The impact of race and disease on sickle cell patient wait times in the emergency department.

Authors:  Carlton Haywood; Paula Tanabe; Rakhi Naik; Mary Catherine Beach; Sophie Lanzkron
Journal:  Am J Emerg Med       Date:  2013-02-04       Impact factor: 2.469

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