Literature DB >> 24319216

Sickle cell disease pain management and the medical home.

Jean L Raphael1, Suzette O Oyeku.   

Abstract

Pain is the most common cause for hospitalization and acute morbidity in sickle cell disease (SCD). The consequences of SCD-related pain are substantial, affecting both the individual and the health care system. The emergence of the patient-centered medical home (PCMH) provides new opportunities to align efforts to improve SCD management with innovative and potentially cost-effective models of patient-centered care. The Department of Health and Human Services has designated SCD as a priority area with emphasis on creating PCMHs for affected patients. The question for patients, clinicians, scientists, and policy-makers is how the PCMH can be designed to address pain, the hallmark feature of SCD. This article provides a framework of pain management within the PCMH model. We present an overview of pain and pain management in SCD, gaps in pain management, and current care models used by patients and discuss core PCMH concepts and multidisciplinary team-based PCMH care strategies for SCD pain management.

Entities:  

Mesh:

Year:  2013        PMID: 24319216     DOI: 10.1182/asheducation-2013.1.433

Source DB:  PubMed          Journal:  Hematology Am Soc Hematol Educ Program        ISSN: 1520-4383


  5 in total

1.  Community Health Workers as Support for Sickle Cell Care.

Authors:  Lewis L Hsu; Nancy S Green; E Donnell Ivy; Cindy E Neunert; Arlene Smaldone; Shirley Johnson; Sheila Castillo; Amparo Castillo; Trevor Thompson; Kisha Hampton; John J Strouse; Rosalyn Stewart; TaLana Hughes; Sonja Banks; Kim Smith-Whitley; Allison King; Mary Brown; Kwaku Ohene-Frempong; Wally R Smith; Molly Martin
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

2.  A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive Crises.

Authors:  Richard J Lin; Arthur T Evans; Kerri Wakeman; Michelle Unterbrink
Journal:  Hemoglobin       Date:  2015-06-26       Impact factor: 0.849

3.  Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use.

Authors:  Nancy Crego; Christian Douglas; Emily Bonnabeau; Marian Earls; Kern Eason; Elizabeth Merwin; Gary Rains; Paula Tanabe; Nirmish Shah
Journal:  J Am Board Fam Med       Date:  2020 Jan-Feb       Impact factor: 2.657

4.  Using health information technology to improve adherence to opioid prescribing guidelines in primary care.

Authors:  Daren Anderson; Ianita Zlateva; Khushbu Khatri; Nicholas Ciaburri
Journal:  Clin J Pain       Date:  2015-06       Impact factor: 3.442

5.  Translating sickle cell guidelines into practice for primary care providers with Project ECHO.

Authors:  Lisa M Shook; Christina B Farrell; Karen A Kalinyak; Stephen C Nelson; Brandon M Hardesty; Angeli G Rampersad; Kay L Saving; Wanda J Whitten-Shurney; Julie A Panepinto; Russell E Ware; Lori E Crosby
Journal:  Med Educ Online       Date:  2016-11-24
  5 in total

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