Literature DB >> 27506442

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

Joseph Lunyera1, Charles Jonassaint2, Jude Jonassaint2, Nirmish Shah1.   

Abstract

BACKGROUND: Sickle cell disease (SCD) is a complex chronic disease requiring multidisciplinary care that involves primary care physicians (PCPs) working with a hematologist or SCD specialists. However, PCPs often lack access to SCD specialists and are unaware of SCD guidelines or efficacious treatment.
METHODS: We partnered with Community Care of North Carolina (CCNC) to identify assigned PCPs for SCD patients with Medicaid across North Carolina. CCNC network administrators distributed a web-based questionnaire for completion. The questionnaire involved 12 self-reported items on a yes-no or a 1 to 5 Likert-type scale that assessed PCP attitudes toward SCD care, awareness of recent guidelines, and comanaging hydroxyurea.
RESULTS: Of the 53 PCPs who completed the electronic survey, 73% felt they were comfortable with the number of SCD patients in their practice. Most PCPs reported having infrequent communications with an SCD specialist (67%) and most were also not aware of the 2014 SCD guidelines (66%). Many reported that they would frequently use the new SCD guidelines if provided to them (76%). Furthermore, 51% of PCPs expressed comfort with using mobile apps to access SCD guidelines and provided email contact to receive further information. The majority also reported being comfortable comanaging hydroxyurea with an SCD specialist (65%).
CONCLUSION: Few PCPs in North Carolina were aware of the new SCD guidelines or had regular communication with an SCD specialist. The majority of PCPs, however, demonstrated a favorable attitude toward receiving the SCD guidelines and comanaging hydroxyurea with a specialist. In response to this gap in care, we have developed a mobile-based SCD toolbox specifically for PCPs to provide guidelines, algorithms, and a method to communicate with local SCD specialists. With the interest in receiving these guidelines, we are confident the toolbox will provide an easy to use platform to assist PCPs to utilize the SCD guidelines.

Entities:  

Keywords:  co-management; guidelines; hydroxyurea; mHealth; primary care; sickle cell disease

Year:  2016        PMID: 27506442      PMCID: PMC5932651          DOI: 10.1177/2150131916662969

Source DB:  PubMed          Journal:  J Prim Care Community Health        ISSN: 2150-1319


  18 in total

1.  Primary-care delivery for sickle cell patients in rural Georgia using telemedicine.

Authors:  K Woods; A Kutlar; R K Grigsby; L Adams; M E Stachura
Journal:  Telemed J       Date:  1998

2.  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

3.  Who cares for medicaid-enrolled children with chronic conditions?

Authors:  K Kuhlthau; T G Ferris; A C Beal; S L Gortmaker; J M Perrin
Journal:  Pediatrics       Date:  2001-10       Impact factor: 7.124

Review 4.  Future directions of sickle cell disease research: the NIH perspective.

Authors:  W Keith Hoots; Susan B Shurin
Journal:  Pediatr Blood Cancer       Date:  2012-04-19       Impact factor: 3.167

5.  Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.

Authors:  Marsha Treadwell; Joseph Telfair; Robert W Gibson; Shirley Johnson; Ifeyinwa Osunkwo
Journal:  Am J Hematol       Date:  2011-01       Impact factor: 10.047

6.  Physician attitude, awareness, and knowledge regarding guidelines for transcranial Doppler screening in sickle cell disease.

Authors:  Sarah L Reeves; Heather J Fullerton; Kevin J Dombkowski; Matthew L Boulton; Thomas M Braun; Lynda D Lisabeth
Journal:  Clin Pediatr (Phila)       Date:  2014-10-15       Impact factor: 1.168

7.  Comfort of general internists and general pediatricians in providing care for young adults with chronic illnesses of childhood.

Authors:  Megumi J Okumura; Michele Heisler; Matthew M Davis; Michael D Cabana; Sonya Demonner; Eve A Kerr
Journal:  J Gen Intern Med       Date:  2008-07-26       Impact factor: 5.128

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

Authors:  Lauren N Whiteman; Carlton Haywood; Sophie Lanzkron; John J Strouse; Leonard Feldman; Rosalyn W Stewart
Journal:  South Med J       Date:  2015-09       Impact factor: 0.954

Review 9.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Authors:  Barbara P Yawn; George R Buchanan; Araba N Afenyi-Annan; Samir K Ballas; Kathryn L Hassell; Andra H James; Lanetta Jordan; Sophie M Lanzkron; Richard Lottenberg; William J Savage; Paula J Tanabe; Russell E Ware; M Hassan Murad; Jonathan C Goldsmith; Eduardo Ortiz; Robinson Fulwood; Ann Horton; Joylene John-Sowah
Journal:  JAMA       Date:  2014-09-10       Impact factor: 56.272

10.  Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia.

Authors:  S Charache; G J Dover; M A Moyer; J W Moore
Journal:  Blood       Date:  1987-01       Impact factor: 22.113

View more
  5 in total

1.  Needs assessment of primary care physicians in the management of chronic pain in cancer survivors.

Authors:  Ronald Chow; Kevin Saunders; Howard Burke; Andre Belanger; Edward Chow
Journal:  Support Care Cancer       Date:  2017-06-07       Impact factor: 3.603

2.  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

3.  Technology use and preferences to support clinical practice guideline awareness and adherence in individuals with sickle cell disease.

Authors:  Amol Utrankar; Tilicia L Mayo-Gamble; Whitney Allen; Laurie Novak; Adetola A Kassim; Kemberlee Bonnet; David Schlundt; Velma M Murry; Gretchen Purcell Jackson; Michael DeBaun; Robert M Cronin
Journal:  J Am Med Inform Assoc       Date:  2018-08-01       Impact factor: 4.497

4.  Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers.

Authors:  Robert Michael Cronin; Tilicia L Mayo-Gamble; Sarah-Jo Stimpson; Sherif M Badawy; Lori E Crosby; Jeannie Byrd; Emmanuel J Volanakis; Adetola A Kassim; Jean L Raphael; Velma M Murry; Michael R DeBaun
Journal:  BMC Hematol       Date:  2018-06-08

5.  The role of evidence-based guidelines in the diagnosis and treatment of functional neurological disorder.

Authors:  Benjamin Tolchin; Gaston Baslet; Alan Carson; Barbara A Dworetzky; Laura H Goldstein; W Curt LaFrance; Steve Martino; David L Perez; Markus Reuber; Jon Stone; Jerzy P Szaflarski
Journal:  Epilepsy Behav Rep       Date:  2021-10-21
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.