Literature DB >> 12605392

Frequent and prolonged hospitalizations: a risk factor for early mortality in sickle cell disease patients.

Patricia Houston-Yu1, Sohail R Rana, Betsy Beyer, Oswaldo Castro.   

Abstract

A subset of patients with sickle cell disease (SCD) has frequent and prolonged hospitalizations. Clinical outcomes for this subset of patients are not known. We analyzed mortality data in 71 such patients enrolled in a case management study. Adult patients (mean age 32 years) with SCD and > or = 50 hospitalization days/year or > or = 6 admissions/year were enrolled. Clinical and psychosocial data were obtained. During a mean 24-month follow up, 11 of 71 patients died (15.5%). Patients who died had a higher mean number of hospitalization days in the year before study entry (116 vs. 40, P < 0.000008) and were also more depressed than those who survived (mean score 17.8 vs. 11.9, P = 0.031). Frequent and prolonged hospitalizations are a risk factor for early mortality in patients with SCD. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12605392     DOI: 10.1002/ajh.10305

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


  15 in total

1.  Socioeconomic status and length of hospital stay in children with vaso-occlusive crises of sickle cell disease.

Authors:  Angela M Ellison; Howard Bauchner
Journal:  J Natl Med Assoc       Date:  2007-03       Impact factor: 1.798

2.  Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS), a focus group and decision support tool development project.

Authors:  Paula Tanabe; Christopher Reddin; Victoria L Thornton; Knox H Todd; Ted Wun; John S Lyons
Journal:  Acad Emerg Med       Date:  2010-08       Impact factor: 3.451

3.  High-Cost Patients: Hot-Spotters Don't Explain the Half of It.

Authors:  Natalie S Lee; Noah Whitman; Nirav Vakharia; Glen B Taksler; Michael B Rothberg
Journal:  J Gen Intern Med       Date:  2016-08-01       Impact factor: 5.128

4.  Spirituality, Self-Efficacy, and Quality of Life among Adults with Sickle Cell Disease.

Authors:  Maxine Adegbola
Journal:  South Online J Nurs Res       Date:  2011-04

5.  Sickle cell disease in adults: developing an appropriate care plan.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  Clin J Oncol Nurs       Date:  2015-10       Impact factor: 1.027

6.  Mortality rates and age at death from sickle cell disease: U.S., 1979-2005.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Public Health Rep       Date:  2013 Mar-Apr       Impact factor: 2.792

7.  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

8.  Assessment of health-related quality of life among adults hospitalized with sickle cell disease vaso-occlusive crisis.

Authors:  Kimberly S Esham; Angie Mae Rodday; Hedy P Smith; Farzad Noubary; Ruth Ann Weidner; Rachel J Buchsbaum; Susan K Parsons
Journal:  Blood Adv       Date:  2020-01-14

9.  Emergency Department (ED), ED Observation, Day Hospital, and Hospital Admissions for Adults with Sickle Cell Disease.

Authors:  David M Cline; Susan Silva; Caroline E Freiermuth; Victoria Thornton; Paula Tanabe
Journal:  West J Emerg Med       Date:  2018-02-12

10.  Disease severity impacts plerixafor-mobilized stem cell collection in patients with sickle cell disease.

Authors:  Alexis Leonard; Akshay Sharma; Naoya Uchida; David Stroncek; Sandhya R Panch; Kamille West; Eoghan Molloy; Thomas E Hughes; Sara Hauffe; Tiffani Taylor; Courtney Fitzhugh; Jane S Hankins; Megan Wilson; Shengdar Q Tsai; Mitchell J Weiss; Matthew Hsieh; John F Tisdale
Journal:  Blood Adv       Date:  2021-05-11
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