Literature DB >> 19743465

The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization.

C Patrick Carroll1, Carlton Haywood, Peter Fagan, Sophie Lanzkron.   

Abstract

Although most patients with sickle cell disease (SCD) are hospitalized infrequently and manage painful crises at home, a small subpopulation is frequently admitted to emergency departments and inpatient units. This small group accounts for the majority of health care expenses for patients with SCD. Using inpatient claims data from a large, urban Medicaid MCO for 5 consecutive years, this study sought to describe the course of high inpatient utilization (averaging four or more admissions enrolled per year for at least 1 year) in members with a diagnosis of SCD and a history of hospitalizations for vaso-occlusive crisis. High utilizers were compared with the other members with SCD on demographics, medical and psychiatric comorbidity, and use of other health care resources. Members who were high utilizers had more diagnostic mentions of sickle cell complications than low utilizers. However, the pattern of high inpatient utilization was likely to moderate over successive years, and return to the pattern after moderation was uncommon. Despite this, a small subpopulation engaged in exceptional levels of inpatient utilization over multiple years. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19743465      PMCID: PMC2783233          DOI: 10.1002/ajh.21515

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  11 in total

1.  Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study.

Authors:  Kenneth Epstein; Elaine Yuen; Jeff M Riggio; Samir K Ballas; Stephanie M Moleski
Journal:  J Natl Med Assoc       Date:  2006-07       Impact factor: 1.798

2.  Epidemiologic analysis of an urban, public emergency department's frequent users.

Authors:  J H Mandelberg; R E Kuhn; M A Kohn
Journal:  Acad Emerg Med       Date:  2000-06       Impact factor: 3.451

3.  Nurses' attitudes and practices in sickle cell pain management.

Authors:  A Pack-Mabien; E Labbe; D Herbert; J Haynes
Journal:  Appl Nurs Res       Date:  2001-11       Impact factor: 2.257

4.  Hospitalization rates and costs of care of patients with sickle-cell anemia in the state of Maryland in the era of hydroxyurea.

Authors:  Sophie Lanzkron; Carlton Haywood; Jodi B Segal; George J Dover
Journal:  Am J Hematol       Date:  2006-12       Impact factor: 10.047

5.  Frequent use of the hospital emergency department is indicative of high use of other health care services.

Authors:  H Hansagi; M Olsson; S Sjöberg; Y Tomson; S Göransson
Journal:  Ann Emerg Med       Date:  2001-06       Impact factor: 5.721

6.  Medical care utilization and mortality in sickle cell disease: a population-based study.

Authors:  Sadhna M Shankar; Patrick G Arbogast; Ed Mitchel; William O Cooper; Winfred C Wang; Marie R Griffin
Journal:  Am J Hematol       Date:  2005-12       Impact factor: 10.047

7.  Coping and health service utilisation in a UK study of paediatric sickle cell pain.

Authors:  K A Anie; A Steptoe; S Ball; M Dick; B M Smalling
Journal:  Arch Dis Child       Date:  2002-05       Impact factor: 3.791

8.  Frequent ED users: patterns of use over time.

Authors:  T Kne; R Young; L Spillane
Journal:  Am J Emerg Med       Date:  1998-11       Impact factor: 2.469

9.  Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions.

Authors:  F D Armstrong; C H Pegelow; J C Gonzalez; A Martinez
Journal:  J Pediatr Psychol       Date:  1992-10

10.  Daily assessment of pain in adults with sickle cell disease.

Authors:  Wally R Smith; Lynne T Penberthy; Viktor E Bovbjerg; Donna K McClish; John D Roberts; Bassam Dahman; Imoigele P Aisiku; James L Levenson; Susan D Roseff
Journal:  Ann Intern Med       Date:  2008-01-15       Impact factor: 25.391

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  41 in total

1.  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

2.  The case for HLA-identical sibling hematopoietic stem cell transplantation in children with symptomatic sickle cell anemia.

Authors:  Courtney D Fitzhugh; Mark C Walters
Journal:  Blood Adv       Date:  2017-12-08

3.  Characterization of opioid use in sickle cell disease.

Authors:  Jin Han; Jifang Zhou; Santosh L Saraf; Victor R Gordeuk; Gregory S Calip
Journal:  Pharmacoepidemiol Drug Saf       Date:  2017-08-16       Impact factor: 2.890

Review 4.  Five lessons learned about long-term pain management in adults with sickle cell disease.

Authors:  Joshua J Field
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

5.  The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

6.  Sickle cell disease in California: sociodemographic predictors of emergency department utilization.

Authors:  Julie A Wolfson; Sheree M Schrager; Rachna Khanna; Thomas D Coates; Michele D Kipke
Journal:  Pediatr Blood Cancer       Date:  2011-02-25       Impact factor: 3.167

7.  Adult emergency department patients with sickle cell pain crisis: results from a quality improvement learning collaborative model to improve analgesic management.

Authors:  Paula Tanabe; John W Hafner; Zoran Martinovich; Nicole Artz
Journal:  Acad Emerg Med       Date:  2012-04       Impact factor: 3.451

8.  A retrospective analysis of the cost of hospitalizations for sickle cell disease with crisis in England, 2010/11.

Authors:  E Pizzo; A A Laverty; K J Phekoo; G AlJuburi; S A Green; D Bell; A Majeed
Journal:  J Public Health (Oxf)       Date:  2014-05-05       Impact factor: 2.341

9.  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

10.  A preliminary study of psychiatric, familial, and medical characteristics of high-utilizing sickle cell disease patients.

Authors:  Patrick C Carroll; Carlton Haywood; Michelle R Hoot; Sophie Lanzkron
Journal:  Clin J Pain       Date:  2013-04       Impact factor: 3.442

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