Literature DB >> 21181560

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

Carlton Haywood1, Sophie Lanzkron, Mark T Hughes, Rochelle Brown, Michele Massa, Neda Ratanawongsa, Mary Catherine Beach.   

Abstract

BACKGROUND: Clinician attitudes toward patients are associated with variability in the quality of health care. Attitudes are typically considered difficult to change, and few interventions have attempted to do so. Negative attitudes toward adults with sickle cell disease have been identified as an important barrier to the receipt of appropriate pain management for this patient population.
OBJECTIVE: To test the effect of a video-intervention designed to improve clinician attitudes toward adults with sickle cell disease.
INTERVENTIONS: An 8-minute video depicting a clinician expert and patients discussing challenges in seeking treatment for sickle cell pain. DESIGN AND PARTICIPANTS: A randomized post-test only control group design was used to assess the impact of the intervention on the attitudes of 276 nurses and housestaff working at a large, urban, academic medical center. MAIN MEASURES: Attitudes toward adult sickle cell patients assessed using 5- and 6-point Likert-scale items. Exploratory factor analysis was used to identify underlying attitudinal domains and develop scales. Examples of the negative and positive attitudes assessed include clinician estimates of the percentage of SCD patients that exaggerate pain (negative) or make clinicians glad they went into medicine (positive). KEY
RESULTS: Compared to the control group, the intervention group exhibited decreased negative attitudes (Difference in means = -8.9, 95%CI [-14.2, -3.6]; Cohen's d = 0.41), decreased endorsement of certain patient behaviors as "concern-raising" (Difference in means = -7.8, 95%CI [-13.1, -2.5]; Cohen's d = 0.36), and increased positive attitudes toward sickle cell patients (Difference in means = 6.6, 95% CI [0.6, 12.6]; Cohen's d = 0.27).
CONCLUSIONS: Our results suggest that the attitudes of clinicians toward sickle cell patients may be improved through a short and relatively easy to implement intervention. Whether the attitudinal differences associated with our intervention are sustainable or are linked to clinical outcomes remains to be seen.

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Year:  2010        PMID: 21181560      PMCID: PMC3077483          DOI: 10.1007/s11606-010-1605-5

Source DB:  PubMed          Journal:  J Gen Intern Med        ISSN: 0884-8734            Impact factor:   5.128


  32 in total

1.  A special treatment program for patients with sickle cell crisis.

Authors:  Cindy Jamison; Hazel N Brown
Journal:  Nurs Econ       Date:  2002 May-Jun       Impact factor: 1.085

2.  Why do providers contribute to disparities and what can be done about it?

Authors:  Diana J Burgess; Steven S Fu; Michelle van Ryn
Journal:  J Gen Intern Med       Date:  2004-11       Impact factor: 5.128

3.  Are physicians' attitudes of respect accurately perceived by patients and associated with more positive communication behaviors?

Authors:  Mary Catherine Beach; Debra L Roter; Nae-Yuh Wang; Patrick S Duggan; Lisa A Cooper
Journal:  Patient Educ Couns       Date:  2006-07-21

Review 4.  A review of evidence about factors affecting quality of pain management in sickle cell disease.

Authors:  J Elander; K Midence
Journal:  Clin J Pain       Date:  1996-09       Impact factor: 3.442

5.  The association of provider communication with trust among adults with sickle cell disease.

Authors:  Carlton Haywood; Sophie Lanzkron; Neda Ratanawongsa; Shawn M Bediako; Lakshmi Lattimer; Neil R Powe; Mary Catherine Beach
Journal:  J Gen Intern Med       Date:  2010-03-03       Impact factor: 5.128

6.  The medical condition regard scale: measuring reactions to diagnoses.

Authors:  George W Christison; Mark G Haviland; Matt L Riggs
Journal:  Acad Med       Date:  2002-03       Impact factor: 6.893

7.  The psychosocial experience of people with sickle cell disease and its impact on quality of life: Qualitative findings from focus groups.

Authors:  V. J. Thomas; L. M. Taylor
Journal:  Br J Health Psychol       Date:  2002-09

8.  Health care provider attitudes toward patients with acute vaso-occlusive crisis due to sickle cell disease: development of a scale.

Authors:  Neda Ratanawongsa; Carlton Haywood; Shawn M Bediako; Lakshmi Lattimer; Sophie Lanzkron; Peter M Hill; Neil R Powe; Mary Catherine Beach
Journal:  Patient Educ Couns       Date:  2009-02-23

9.  Physicians' attitude and practices in sickle cell disease pain management.

Authors:  Elise Labbé; Donald Herbert; Johnson Haynes
Journal:  J Palliat Care       Date:  2005       Impact factor: 2.250

10.  Pain management and symptoms of substance dependence among patients with sickle cell disease.

Authors:  James Elander; Joanne Lusher; David Bevan; Paul Telfer
Journal:  Soc Sci Med       Date:  2003-11       Impact factor: 4.634

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  26 in total

1.  Exploring Adult Care Experiences and Barriers to Transition in Adult Patients with Sickle Cell Disease.

Authors:  C J Bemrich-Stolz; J H Halanych; T H Howard; L M Hilliard; J D Lebensburger
Journal:  Int J Hematol Ther       Date:  2015-09-06

2.  Pediatric to Adult Care Transition: Perspectives of Young Adults With Sickle Cell Disease.

Authors:  Jerlym S Porter; Kimberly M Wesley; Mimi S Zhao; Rebecca J Rupff; Jane S Hankins
Journal:  J Pediatr Psychol       Date:  2017-10-01

3.  A Novel Pediatric Emergency Department Intervention to Improve Adolescent Sexual Health Care.

Authors:  Dharshinie Jayamaha; Sarah Finocchario-Kessler; Joan Giovanni; Jeffrey Michael; Mary E Moffatt; Ashley K Sherman; Melissa K Miller
Journal:  Pediatr Emerg Care       Date:  2019-06       Impact factor: 1.454

Review 4.  Improving Emergency Department-Based Care of Sickle Cell Pain.

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

5.  Family Engagement in Pediatric Sickle Cell Disease Visits.

Authors:  Elizabeth D Cox; Matthew P Swedlund; Henry N Young; Megan A Moreno; Jennifer M Schopp; Victoria Rajamanickam; Julie A Panepinto
Journal:  Health Commun       Date:  2016-05-09

6.  Respect, trust, and the management of sickle cell disease pain in hospital: comparative analysis of concern-raising behaviors, preliminary model, and agenda for international collaborative research to inform practice.

Authors:  James Elander; Mary Catherine Beach; Carlton Haywood
Journal:  Ethn Health       Date:  2011 Aug-Oct       Impact factor: 2.772

7.  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

8.  Improving Emergency Providers' Attitudes Toward Sickle Cell Patients in Pain.

Authors:  Aditi Puri Singh; Carlton Haywood; Mary Catherine Beach; Mark Guidera; Sophie Lanzkron; Doris Valenzuela-Araujo; Richard E Rothman; Andrea Freyer Dugas
Journal:  J Pain Symptom Manage       Date:  2015-11-18       Impact factor: 3.612

9.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

10.  Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.

Authors:  Carlton Haywood; Marie Diener-West; John Strouse; C Patrick Carroll; Shawn Bediako; Sophie Lanzkron; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  J Pain Symptom Manage       Date:  2014-04-15       Impact factor: 3.612

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