Literature DB >> 19860302

A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.

Carlton Haywood1, Mary Catherine Beach, Sophie Lanzkron, John J Strouse, Renee Wilson, Haeseong Park, Catherine Witkop, Eric B Bass, Jodi B Segal.   

Abstract

Clinical experts have expressed concern about underutilization of sickle cell disease (SCD) therapies, including hydroxyurea, prophylactic antibiotics, iron chelation, bone marrow transplantation, pain management during vaso-occlusive crisis, and receipt of routine ambulatory health care. We synthesized studies that identified barriers to and interventions to improve appropriate use of these therapies. Of the 48 studies included in our review, 35 identified therapeutic barriers or facilitators, and 13 evaluated interventions to improve use of therapies. Consistently identified barriers to appropriate pain management were negative provider attitudes and lack of provider knowledge. Four of 9 pain management interventions improved direct measures of pain management quality, while 5 improved indirect measures. One intervention improved receipt of routine ambulatory care. We concluded that interventions to improve pain management in SCD can be effective and should address providers' negative attitudes and knowledge and that more intervention studies are needed to improve receipt of recommended SCD therapies.

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Year:  2009        PMID: 19860302     DOI: 10.1016/s0027-9684(15)31069-5

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  56 in total

1.  Hospital self-discharge among adults with sickle-cell disease (SCD): associations with trust and interpersonal experiences with care.

Authors:  Carlton Haywood; Sophie Lanzkron; Neda Ratanawongsa; Shawn M Bediako; Lakshmi Lattimer-Nelson; Mary Catherine Beach
Journal:  J Hosp Med       Date:  2010 May-Jun       Impact factor: 2.960

2.  Association between hospital admissions and healthcare provider communication for individuals with sickle cell disease.

Authors:  Robert M Cronin; Manshu Yang; Jane S Hankins; Jeannie Byrd; Brandi M Pernell; Adetola Kassim; Patricia Adams-Graves; Alexis A Thompson; Karen Kalinyak; Michael DeBaun; Marsha Treadwell
Journal:  Hematology       Date:  2020-12       Impact factor: 2.269

3.  A video-intervention to improve clinician attitudes toward patients with sickle cell disease: the results of a randomized experiment.

Authors:  Carlton Haywood; Sophie Lanzkron; Mark T Hughes; Rochelle Brown; Michele Massa; Neda Ratanawongsa; Mary Catherine Beach
Journal:  J Gen Intern Med       Date:  2010-12-23       Impact factor: 5.128

4.  Problematic hospital experiences among adult patients with sickle cell disease.

Authors:  Lakshmi Lattimer; Carlton Haywood; Sophie Lanzkron; Neda Ratanawongsa; Shawn M Bediako; Mary Catherine Beach
Journal:  J Health Care Poor Underserved       Date:  2010-11

5.  Do difficulties in swallowing medication impede the use of hydroxyurea in children?

Authors:  ElShadey Bekele; Courtney D Thornburg; Amanda M Brandow; Mukta Sharma; Arlene M Smaldone; Zhezhen Jin; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2014-04-17       Impact factor: 3.167

Review 6.  Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia.

Authors:  Patricia M Fortin; Karen V Madgwick; Marialena Trivella; Sally Hopewell; Carolyn Doree; Lise J Estcourt
Journal:  Cochrane Database Syst Rev       Date:  2016-09

7.  Impact of a dedicated infusion clinic for acute management of adults with sickle cell pain crisis.

Authors:  Sophie Lanzkron; C Patrick Carroll; Peter Hill; Mandy David; Nicklaine Paul; Carlton Haywood
Journal:  Am J Hematol       Date:  2015-02-25       Impact factor: 10.047

8.  The impact of race and disease on sickle cell patient wait times in the emergency department.

Authors:  Carlton Haywood; Paula Tanabe; Rakhi Naik; Mary Catherine Beach; Sophie Lanzkron
Journal:  Am J Emerg Med       Date:  2013-02-04       Impact factor: 2.469

9.  An unequal burden: poor patient-provider communication and sickle cell disease.

Authors:  Carlton Haywood; Shawn Bediako; Sophie Lanzkron; Marie Diener-West; John Strouse; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  Patient Educ Couns       Date:  2014-05-23

10.  Evaluation of a Sickle Cell Disease Educational Website for Emergency Providers.

Authors:  Mariam Kayle; Jill Brennan-Cook; Brigit M Carter; Anne L Derouin; Susan G Silva; Paula Tanabe
Journal:  Adv Emerg Nurs J       Date:  2016 Apr-Jun
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