Literature DB >> 25469750

Intensive management of high-utilizing adults with sickle cell disease lowers admissions.

Kathryn L Koch1, Matthew S Karafin, Pippa Simpson, Joshua J Field.   

Abstract

A minority of super-utilizing adults with sickle cell disease (SCD) account for a disproportionate number of emergency department (ED) and hospital admissions. We performed a retrospective cohort study comparing the rate of admission before and after the opening of a clinic for adults with SCD. Unique to this clinic was an intensive management strategy, focusing on super-utilizing adults with 12 or more admissions per year. ED/hospital and 30 days re-admission rates were compared, 1 year pre- and post-intervention, for those adults who established in the clinic. Prior to the intervention, 17 super-utilizers, comprising 15% of the pre-intervention cohort (n = 115), accounted for 58% of the total admissions and had an admission rate of 28 per patient-year. When pre- and post-intervention years were compared, rate of ED/hospital admission per patient-year for super-utilizers decreased from 27.9 to 13.5 (P < 0.001), while there was not a significant reduction for the entire cohort (7.1 vs. 6.1, P = 0.84). Similarly, the decrease in rate of 30 day re-admission was larger for the super-utilizers (13.5 per patient-year to 1.8, P < 0.001), than the whole cohort (2.6 per patient-year to 0.7, P = 0.006). Among the super-utilizers, the reduced rate of admission from the pre- to post-clinic intervention year equated to 252 fewer ED/hospital admissions and 227 fewer 30 day re-admissions. This management strategy focusing on super-utilizing adults with SCD lowered admission and 30 day re-admission rate.
© 2014 Wiley Periodicals, Inc.

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Year:  2015        PMID: 25469750     DOI: 10.1002/ajh.23912

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  12 in total

1.  American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain.

Authors:  Amanda M Brandow; C Patrick Carroll; Susan Creary; Ronisha Edwards-Elliott; Jeffrey Glassberg; Robert W Hurley; Abdullah Kutlar; Mohamed Seisa; Jennifer Stinson; John J Strouse; Fouza Yusuf; William Zempsky; Eddy Lang
Journal:  Blood Adv       Date:  2020-06-23

2.  Characterization of opioid use in sickle cell disease.

Authors:  Jin Han; Jifang Zhou; Santosh L Saraf; Victor R Gordeuk; Gregory S Calip
Journal:  Pharmacoepidemiol Drug Saf       Date:  2017-08-16       Impact factor: 2.890

Review 3.  Improving Emergency Department-Based Care of Sickle Cell Pain.

Authors:  Jeffrey A Glassberg
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 4.  Five lessons learned about long-term pain management in adults with sickle cell disease.

Authors:  Joshua J Field
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

5.  Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review.

Authors:  Soyon Lee; Diana K Vania; Menaka Bhor; Dennis Revicki; Seye Abogunrin; Grammati Sarri
Journal:  Int J Gen Med       Date:  2020-07-07

6.  Persistently Frequent Emergency Department Utilization Among Persons With Systemic Lupus Erythematosus.

Authors:  Jiha Lee; Judith Lin; Lisa Gale Suter; Liana Fraenkel
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-10-16       Impact factor: 4.794

7.  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

8.  Young Adult Perspectives on a Successful Transition from Pediatric to Adult Care in Sickle Cell Disease.

Authors:  Amy E Sobota; Emeka Umeh; Jennifer W Mack
Journal:  J Hematol Res       Date:  2015-12

9.  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

10.  A Patient-Centered Emergency Department Management Strategy for Sickle-Cell Disease Super-Utilizers.

Authors:  Grant G Simpson; Hallie R Hahn; Alex A Powel; Robert R Leverence; Linda A Morris; Lara G Thompson; Marc S Zumberg; Deepa J Borde; Joseph A Tyndall; Jonathan J Shuster; Donald M Yealy; Brandon R Allen
Journal:  West J Emerg Med       Date:  2017-02-07
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