Literature DB >> 26332477

Primary Care Providers' Comfort Levels in Caring for Patients with Sickle Cell Disease.

Lauren N Whiteman1, Carlton Haywood1, Sophie Lanzkron1, John J Strouse1, Leonard Feldman1, Rosalyn W Stewart1.   

Abstract

OBJECTIVE: The purpose of this study was to determine the comfort levels of primary care providers in caring for individuals with sickle cell disease (SCD) and determine factors that improved or lessened provider comfort.
METHODS: We surveyed providers at the annual Johns Hopkins Community Physicians retreat. The survey consisted of 19 questions and measured comfort levels in four domains: providing ambulatory care to individuals with SCD, managing SCD comorbidities, managing SCD-specific issues, and managing chronic pain. We conducted bivariate analyses to identify any demographic or practice characteristics associated with comfort levels. Multivariable analyses were conducted to identify independent correlates of physician comfort.
RESULTS: The majority of respondents lacked confidence with each of the four aspects of caring for individuals with SCD. Having treated patients with SCD and using knowledge from residency were both independently associated with increased confidence when providing ambulatory care and managing SCD-specific issues in multivariable analyses.
CONCLUSIONS: The delivery of high-quality care to adults with SCD in primary care may be limited because of a lack of provider comfort in providing that care. Because provider reliance on knowledge gained from residency significantly affected the management of patients with SCD, it is essential that continuing medical education on SCD is readily available to ensure that providers are using current information and knowledge. In addition, as comfort increases with the number of patients with SCD in a provider's panel, it may be beneficial to identify a subset of primary care providers interested in SCD and refer patients to those providers.

Entities:  

Mesh:

Year:  2015        PMID: 26332477     DOI: 10.14423/SMJ.0000000000000331

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  9 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.  Differences in Sensory Pain, Expectation, and Satisfaction Reported by Outpatients with Cancer or Sickle Cell Disease.

Authors:  Miriam O Ezenwa; Robert E Molokie; Zaijie Jim Wang; Yingwei Yao; Marie L Suarez; Brenda Dyal; Khulud Abudawood; Diana J Wilkie
Journal:  Pain Manag Nurs       Date:  2018-03-01       Impact factor: 1.929

3.  Attitudes of Primary Care Physicians Toward Sickle Cell Disease Care, Guidelines, and Comanaging Hydroxyurea With a Specialist.

Authors:  Joseph Lunyera; Charles Jonassaint; Jude Jonassaint; Nirmish Shah
Journal:  J Prim Care Community Health       Date:  2016-08-20

4.  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

5.  Emergency Department Provider Survey Regarding Acute Sickle Cell Pain Management.

Authors:  Olufunke Y Martin; Sean M Thompson; Aaron E Carroll; Seethal A Jacob
Journal:  J Pediatr Hematol Oncol       Date:  2020-08       Impact factor: 1.170

6.  Identifying barriers to evidence-based care for sickle cell disease: results from the Sickle Cell Disease Implementation Consortium cross-sectional survey of healthcare providers in the USA.

Authors:  Matthew P Smeltzer; Kristen E Howell; Marsha Treadwell; Liliana Preiss; Allison A King; Jeffrey A Glassberg; Paula Tanabe; Sherif M Badawy; Lisa DiMartino; Robert Gibson; Julie Kanter; Lisa M Klesges; Jane S Hankins
Journal:  BMJ Open       Date:  2021-11-17       Impact factor: 2.692

7.  Health Care Utilization by Adolescent/Young Adult Patients With Sickle Cell Disease in Delaware.

Authors:  Stephanie Guarino; Charmaine Wright; Sophie Lanzkron
Journal:  Cureus       Date:  2022-02-28

8.  Understanding undergraduate students' eHealth usage and views of the patient-provider relationship.

Authors:  Michelle Anne Reyes; Heather D Vance-Chalcraft
Journal:  PLoS One       Date:  2022-04-14       Impact factor: 3.752

9.  Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care.

Authors:  Julie Kanter; Robert Gibson; Raymona H Lawrence; Matthew P Smeltzer; Norma L Pugh; Jeffrey Glassberg; Rita V Masese; Allison A King; Cecelia Calhoun; Jane S Hankins; Marsha Treadwell
Journal:  JAMA Netw Open       Date:  2020-05-01
  9 in total

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