Literature DB >> 31907250

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

Nancy Crego1, Christian Douglas2, Emily Bonnabeau2, Marian Earls2, Kern Eason2, Elizabeth Merwin2, Gary Rains2, Paula Tanabe2, Nirmish Shah2.   

Abstract

BACKGROUND: Sickle-cell disease (SCD) causes significant morbidity, premature mortality, and high disease burden, resulting in frequent health care use. Comanagement may improve utilization and patient adherence with treatments such as Hydroxyurea. The purpose of this study was to describe acute-care utilization in Medicaid-enrolled patients with SCD, patient factors associated with comanagement, and adherence to Hydroxyurea.
METHODS: Data from 2790 patients diagnosed with SCD, age 1 to 65+ years, enrolled at least 1 month in North Carolina Medicaid between March 2016 and February 2017, were analyzed. Outpatient visits were categorized as primary care, hematologist, and nonhematologist specialist. Nurse practitioners or physician assistants with unidentified specialty type or family practice were categorized separately. Comanagement was defined as a minimum of 1 primary care and 1 hematologist visit/patient during the study period.
RESULTS: There were notable age-related differences in utilization of health care services. Only 34.82% of the sample was comanaged. Comanagement was higher in the 1-to-9-year-old (44.88%) and 10-to-17-year-old groups (39.22%) versus the 31-to-45-year-old (30.26%) and 65+-year-old (18.75%) age groups. Age had the greatest influence (AUC = 0.599) on whether or not a patient was comanaged. Only a third of the sample (32.24%) had at least 1 Hydroxyurea (HU) prescription. Age was the most predictive factor of good HUadherence (AUC = 0.6503). Prediction by comanagement was minimal with an AUC = 0.5615.
CONCLUSION: Comanagement was a factor in predicting HUadherence, but further studies are needed to identify the frequency and components of comanagement needed to increase adherence and reduce acute care utilization. © Copyright 2020 by the American Board of Family Medicine.

Entities:  

Keywords:  Child Health; Emergency Departments; Hematology; Hospitalization; Hydroxyurea; Medicaid; Minority Health; North Carolina; Primary Health Care; Sickle-Cell Anemia; Vulnerable Populations

Mesh:

Substances:

Year:  2020        PMID: 31907250      PMCID: PMC7942752          DOI: 10.3122/jabfm.2020.01.190143

Source DB:  PubMed          Journal:  J Am Board Fam Med        ISSN: 1557-2625            Impact factor:   2.657


  62 in total

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Authors:  Patricia Adams-Graves; Lanetta Bronte-Jordan
Journal:  Expert Rev Hematol       Date:  2016-05-24       Impact factor: 2.929

2.  Association of early post-discharge follow-up by a primary care physician and 30-day rehospitalization among older adults.

Authors:  Terry S Field; Jessica Ogarek; Lawrence Garber; George Reed; Jerry H Gurwitz
Journal:  J Gen Intern Med       Date:  2014-12-02       Impact factor: 5.128

3.  Examining the characteristics and beliefs of hydroxyurea users and nonusers among adults with sickle cell disease.

Authors:  Carlton Haywood; Mary Catherine Beach; Shawn Bediako; C Patrick Carroll; Lakshmi Lattimer; Dasheema Jarrett; Sophie Lanzkron
Journal:  Am J Hematol       Date:  2011-01       Impact factor: 10.047

4.  Quality Metrics and Health Care Utilization for Adult Patients with Sickle Cell Disease.

Authors:  Monica Ter-Minassian; Sophie Lanzkron; Alphonse Derus; Elizabeth Brown; Michael A Horberg
Journal:  J Natl Med Assoc       Date:  2018-06-22       Impact factor: 1.798

5.  Patient navigators: Mapping the route toward accessibility in health care.

Authors:  Meaghen Rollins; Francine Milone; Shazeen Suleman; Dorjana Vojvoda; Michael Sgro; Tony Barozzino
Journal:  Paediatr Child Health       Date:  2018-05-18       Impact factor: 2.253

6.  Improved survival of children and adolescents with sickle cell disease.

Authors:  Charles T Quinn; Zora R Rogers; Timothy L McCavit; George R Buchanan
Journal:  Blood       Date:  2010-03-01       Impact factor: 22.113

7.  Emergency department reliance: a discriminatory measure of frequent emergency department users.

Authors:  Eric L Kroner; Raymond G Hoffmann; David C Brousseau
Journal:  Pediatrics       Date:  2009-12-14       Impact factor: 7.124

8.  Health care utilization and expenditures for privately and publicly insured children with sickle cell disease in the United States.

Authors:  Mercy Mvundura; Djesika Amendah; Patricia L Kavanagh; Philippa G Sprinz; Scott D Grosse
Journal:  Pediatr Blood Cancer       Date:  2009-10       Impact factor: 3.167

9.  The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization.

Authors:  C Patrick Carroll; Carlton Haywood; Peter Fagan; Sophie Lanzkron
Journal:  Am J Hematol       Date:  2009-10       Impact factor: 10.047

10.  Patients' views on improving sickle cell disease management in primary care: focus group discussion.

Authors:  Ghida Aljuburi; Karen J Phekoo; Nv Ogo Okoye; Kofie Anie; Stuart A Green; Asaah Nkohkwo; Patrick Ojeer; Comfort Ndive; Ricky Banarsee; Lola Oni; Azeem Majeed
Journal:  JRSM Short Rep       Date:  2012-12-27
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  7 in total

1.  Patient Perspectives of Sickle Cell Management in the Emergency Department.

Authors:  Nancy Crego; Rita Masese; Emily Bonnabeau; Christian Douglas; Gary Rains; Nirmish Shah; Paula Tanabe
Journal:  Crit Care Nurs Q       Date:  2021 Apr-Jun 01

2.  Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis.

Authors:  Paula Tanabe; Audrey L Blewer; Emily Bonnabeau; Hayden B Bosworth; Denise H Clayton; Nancy Crego; Marian F Earls; Kern Eason; Grayson Forlines; Gary Rains; Matthew Young; Nirmish Shah
Journal:  J Health Econ Outcomes Res       Date:  2021-04-01

3.  Higher hydroxyurea adherence among young adults with sickle cell disease compared to children and adolescents.

Authors:  Paavani S Reddy; Stephanie W Cai; Leonardo Barrera; Kathryn King; Sherif M Badawy
Journal:  Ann Med       Date:  2022-12       Impact factor: 4.709

4.  Outcome of Hydroxyurea Use in SCD and Evaluation of Patients' Perception and Experience in Nigeria.

Authors:  Reuben Ikechukwu Chianumba; Akinyemi O D Ofakunrin; Jack Morrice; Olaniyi Olanrewaju; Oluseyi Oniyangi; Aisha Kuliya-Gwarzo; Uche Nnebe-Agumadu; Hezekiah Alkali Isa; Obiageli Eunice Nnodu
Journal:  Front Genet       Date:  2022-03-24       Impact factor: 4.772

5.  Medical and Non-medical Costs of Sickle Cell Disease and Treatments from a US Perspective: A Systematic Review and Landscape Analysis.

Authors:  Zachary Baldwin; Boshen Jiao; Anirban Basu; Joshua Roth; M A Bender; Zizi Elsisi; Kate M Johnson; Emma Cousin; Scott D Ramsey; Beth Devine
Journal:  Pharmacoecon Open       Date:  2022-04-26

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

Review 7.  Administrative data identify sickle cell disease: A critical review of approaches in U.S. health services research.

Authors:  Scott D Grosse; Nancy S Green; Sarah L Reeves
Journal:  Pediatr Blood Cancer       Date:  2020-09-17       Impact factor: 3.838

  7 in total

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