Literature DB >> 29846351

Barriers to Care for Persons With Sickle Cell Disease: The Case Manager's Opportunity to Improve Patient Outcomes.

Jill Brennan-Cook1, Emily Bonnabeau, Ravenne Aponte, Christina Augustin, Paula Tanabe.   

Abstract

PURPOSE AND
OBJECTIVES: The purpose of this discussion is to review the barriers to care for patients with sickle cell disease (SCD). Chronic pain and the perception of addiction, implicit bias, frequent hospitalizations and emergency department visits, clinician and patient knowledge deficits, and SCD stigma all impede the ability to provide evidence-based care for patients with SCD. Case managers can coordinate and advocate for appropriate care that improves patient outcomes. PRIMARY PRACTICE
SETTING: This discussion is relevant to case managers working with patients with SCD in the clinic, hospital, and emergency department. FINDINGS/
CONCLUSIONS: Case managers can serve an important advocacy role and intervene to improve the coordination of services and efficient use of resources. This will lead to improved quality of life and optimal health care utilization for persons with SCD. IMPLICATIONS FOR CASE MANAGEMENT PRACTICE: As a constant member of the health care team, the case manager may be the only health care team member who has a broad knowledge of the patient's experience of acute and chronic pain, usual state of health, social behavioral health needs, and how these factors may affect both inpatient and outpatient health care use and health outcomes. This article explores the barriers to care and suggests specific interventions within the role of the case manager that can improve care delivered and ultimately contribute to improved patient outcomes. Specifically, these interventions can improve communication among members of the health care team. Case manager interventions can guide coordination, prevent hospital readmissions, reduce health care utilization, and contribute to overall improved patient quality of life and health outcomes.

Entities:  

Mesh:

Year:  2018        PMID: 29846351      PMCID: PMC5981859          DOI: 10.1097/NCM.0000000000000260

Source DB:  PubMed          Journal:  Prof Case Manag        ISSN: 1932-8087


  30 in total

1.  Risk Factors for 30-Day Readmission in Adults with Sickle Cell Disease.

Authors:  Max A Brodsky; Mark Rodeghier; Maureen Sanger; Jeannie Byrd; Brandi McClain; Brittany Covert; Dionna O Roberts; Karina Wilkerson; Michael R DeBaun; Adetola A Kassim
Journal:  Am J Med       Date:  2017-01-05       Impact factor: 4.965

2.  Essentials of Advocacy in Case Management: Part 1: Ethical Underpinnings of Advocacy-Theories, Principles, and Concepts.

Authors:  Hussein M Tahan
Journal:  Prof Case Manag       Date:  2016 Jul-Aug

Review 3.  Implicit Racial/Ethnic Bias Among Health Care Professionals and Its Influence on Health Care Outcomes: A Systematic Review.

Authors:  William J Hall; Mimi V Chapman; Kent M Lee; Yesenia M Merino; Tainayah W Thomas; B Keith Payne; Eugenia Eng; Steven H Day; Tamera Coyne-Beasley
Journal:  Am J Public Health       Date:  2015-10-15       Impact factor: 9.308

4.  Identifying Social-Behavioral Health Needs of Adults with Sickle Cell Disease in the Emergency Department.

Authors:  Sophia K Smith; Julia Johnston; Carlton Rutherford; Rachel Hollowell; Paula Tanabe
Journal:  J Emerg Nurs       Date:  2017-05-17       Impact factor: 1.836

5.  Nurses' attitudes toward patients with sickle cell disease: a worksite comparison.

Authors:  Coretta M Jenerette; Bosny J Pierre-Louis; Nadine Matthie; Yasmeen Girardeau
Journal:  Pain Manag Nurs       Date:  2015-06       Impact factor: 1.929

6.  Hospital Readmissions from Patients' Perspectives.

Authors:  Beril Cakir; Stephanie Kaltsounis; Katherine D' Jernes; Sara Kopf; Julea Steiner
Journal:  South Med J       Date:  2017-05       Impact factor: 0.954

7.  Emergency department management of acute pain episodes in sickle cell disease.

Authors:  Paula Tanabe; Randall Myers; Amy Zosel; Jane Brice; Altaf H Ansari; Julia Evans; Zoran Martinovich; Knox H Todd; Judith A Paice
Journal:  Acad Emerg Med       Date:  2007-03-26       Impact factor: 3.451

8.  Voices of Adults Living with Sickle Cell Disease Pain.

Authors:  Maxine A Adegbola; Donelle M Barnes; Jakki G Opollo; Keela Herr; Jennifer Gray; Ann Marie McCarthy
Journal:  J Natl Black Nurses Assoc       Date:  2012-12

9.  Factors associated with survival in a contemporary adult sickle cell disease cohort.

Authors:  Hany Elmariah; Melanie E Garrett; Laura M De Castro; Jude C Jonassaint; Kenneth I Ataga; James R Eckman; Allison E Ashley-Koch; Marilyn J Telen
Journal:  Am J Hematol       Date:  2014-02-21       Impact factor: 10.047

10.  Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians.

Authors:  Arch G Mainous; Rebecca J Tanner; Christopher A Harle; Richard Baker; Navkiran K Shokar; Mary M Hulihan
Journal:  Anemia       Date:  2015-02-22
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  10 in total

1.  Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.

Authors:  Julie Kanter; Wally R Smith; Payal C Desai; Marsha Treadwell; Biree Andemariam; Jane Little; Diane Nugent; Susan Claster; Deepa G Manwani; Judith Baker; John J Strouse; Ifeyinwa Osunkwo; Rosalyn W Stewart; Allison King; Lisa M Shook; John D Roberts; Sophie Lanzkron
Journal:  Blood Adv       Date:  2020-08-25

2.  Feasibility of implementing mobile technology-delivered mental health treatment in routine adult sickle cell disease care.

Authors:  Charles R Jonassaint; Chaeryon Kang; Kemar V Prussien; Janet Yarboi; Maureen S Sanger; J Deanna Wilson; Laura De Castro; Nirmish Shah; Urmimala Sarkar
Journal:  Transl Behav Med       Date:  2020-02-03       Impact factor: 3.046

3.  Effective Recruitment Strategies for a Sickle Cell Patient Registry Across Sites from the Sickle Cell Disease Implementation Consortium (SCDIC).

Authors:  Rita V Masese; Terri DeMartino; Emily Bonnabeau; Ebony N Burns; Liliana Preiss; Taniya Varughese; Judith M Nocek; Patricia Lasley; Yumei Chen; Caroline Davila; Chinonyelum Nwosu; Samantha Scott; Latanya Bowman; Lauren Gordon; Cindy Clesca; Marlene Peters-Lawrence; Cathy Melvin; Nirmish Shah; Paula Tanabe
Journal:  J Immigr Minor Health       Date:  2020-10-09

4.  Caregiver experiences with accessing sickle cell care and the use of telemedicine.

Authors:  Seethal A Jacob; Roua Daas; Anna Feliciano; Julia E LaMotte; Aaron E Carroll
Journal:  BMC Health Serv Res       Date:  2022-02-22       Impact factor: 2.655

5.  An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model.

Authors:  Marsha J Treadwell; Swapandeep Mushiana; Sherif M Badawy; Liliana Preiss; Allison A King; Barbara Kroner; Yumei Chen; Jeffrey Glassberg; Victor Gordeuk; Nirmish Shah; Angela Snyder; Theodore Wun
Journal:  Qual Life Res       Date:  2022-04-21       Impact factor: 3.440

6.  Surveillance for Sickle Cell Disease - Sickle Cell Data Collection Program, Two States, 2004-2018.

Authors:  Angela B Snyder; Sangeetha Lakshmanan; Mary M Hulihan; Susan T Paulukonis; Mei Zhou; Sophia S Horiuchi; Karon Abe; Shammara N Pope; Laura A Schieve
Journal:  MMWR Surveill Summ       Date:  2022-10-07

7.  Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation.

Authors:  Megan M Miller; Deanna D Rumble; Adam T Hirsh; Tine Vervoort; Lori E Crosby; Avi Madan-Swain; Jeffrey Lebensburger; Anna M Hood; Zina Trost
Journal:  Pain Med       Date:  2021-10-08       Impact factor: 3.750

8.  Implementation of Individualized Pain Care Plans Decreases Length of Stay and Hospital Admission Rates for High Utilizing Adults with Sickle Cell Disease.

Authors:  Jena L Welch-Coltrane; Anthony A Wachnik; Meredith C B Adams; Cherie R Avants; Howard A Blumstein; Amber K Brooks; Andrew M Farland; Joshua B Johnson; Manoj Pariyadath; Erik C Summers; Robert W Hurley
Journal:  Pain Med       Date:  2021-08-06       Impact factor: 3.750

9.  The State of Sickle Cell Disease Care in the United States: How Can Emergency Medicine Contribute?

Authors:  Brett P Giroir; Felicia Collins
Journal:  Ann Emerg Med       Date:  2020-09       Impact factor: 5.721

10.  Perspectives of individuals with sickle cell disease on barriers to care.

Authors:  Shannon Phillips; Yumei Chen; Rita Masese; Laurence Noisette; Kasey Jordan; Sara Jacobs; Lewis L Hsu; Cathy L Melvin; Marsha Treadwell; Nirmish Shah; Paula Tanabe; Julie Kanter
Journal:  PLoS One       Date:  2022-03-23       Impact factor: 3.752

  10 in total

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