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Published in: Journal of General Internal Medicine 6/2010

01-06-2010 | Original Article

The Association of Provider Communication with Trust among Adults with Sickle Cell Disease

Authors: Carlton Haywood Jr, PhD, MA, Sophie Lanzkron, MD, Neda Ratanawongsa, MD, MPH, Shawn M. Bediako, PhD, Lakshmi Lattimer, MD, Neil R. Powe, MD, MPH, MBA, Mary Catherine Beach, MD, MPH

Published in: Journal of General Internal Medicine | Issue 6/2010

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Abstract

Background

Adults with sickle cell disease often report poor interpersonal healthcare experiences, including poor communication with providers. However, the effect of these experiences on patient trust is unknown.

Objective

To determine the association between patient ratings of the previous quality of provider communication and current trust in the medical profession among adults with sickle cell disease.

Research design

Cross-sectional survey.

Participants

A total of 95 adults with sickle cell disease.

Measurements

The four-item Provider Communication Subscale from the Consumer Assessment of Healthcare Plans and Systems Survey; The five-item Wake Forest Trust in the Medical Profession Scale.

Main results

Better ratings of previous provider communication were significantly associated with higher levels of trust toward the medical profession. A 10% increase in provider communication rating was associated with a 3.76% increase in trust scores (p < 0.001, 95% CI [1.76%, 5.76%]), adjusting for patient-level demographic, clinical, and attitudinal characteristics.

Conclusions

Poorer patient ratings of provider communication are associated with lower trust toward the medical profession among adults with sickle cell disease. Future research should examine the impact of low trust in the medical profession on clinical outcomes in this population of patients.
Literature
1.
go back to reference Hassell K. “Sickle cell disease population estimation: application of available contemporary data to traditional methods” Oral Presentation: 35th Anniversary Convention of the National Sickle Cell Disease Program and the Sickle Cell Disease Association of America. September 20th. 2007. Hassell K. “Sickle cell disease population estimation: application of available contemporary data to traditional methods” Oral Presentation: 35th Anniversary Convention of the National Sickle Cell Disease Program and the Sickle Cell Disease Association of America. September 20th. 2007.
2.
go back to reference Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N.Engl.J Med. 1994;1639-44. Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N.Engl.J Med. 1994;1639-44.
3.
go back to reference Alleyne J, Thomas VJ. The management of sickle cell crisis pain as experienced by patients and their carers. J Adv.Nurs. 1994;725–32. Alleyne J, Thomas VJ. The management of sickle cell crisis pain as experienced by patients and their carers. J Adv.Nurs. 1994;725–32.
4.
go back to reference Strickland OL, Jackson G, Gilead M, McGuire DB, Quarles S. Use of focus groups for pain and quality of life assessment in adults with sickle cell disease. J Natl.Black Nurses Assoc. 2001;36–43. Strickland OL, Jackson G, Gilead M, McGuire DB, Quarles S. Use of focus groups for pain and quality of life assessment in adults with sickle cell disease. J Natl.Black Nurses Assoc. 2001;36–43.
5.
go back to reference Harris A, Parker N, Barker C. Adults with sickle cell disease: Psychological impact and experience of hospital services. Psychology, Health and Medicine 1998;171–9. Harris A, Parker N, Barker C. Adults with sickle cell disease: Psychological impact and experience of hospital services. Psychology, Health and Medicine 1998;171–9.
6.
go back to reference Shelley B, Kramer KD, Nash KB. Sickle cell mutual assistance groups and the health services delivery system. J Health Soc.Policy 1994;243–59. Shelley B, Kramer KD, Nash KB. Sickle cell mutual assistance groups and the health services delivery system. J Health Soc.Policy 1994;243–59.
7.
go back to reference Butler DJ, Beltran LR. Functions of an adult sickle cell group: education, task orientation, and support. Health Soc.Work 1993;49–56. Butler DJ, Beltran LR. Functions of an adult sickle cell group: education, task orientation, and support. Health Soc.Work 1993;49–56.
8.
go back to reference Maxwell K, Streetly A, Bevan D. Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study. BMJ 1999;1585–90. Maxwell K, Streetly A, Bevan D. Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study. BMJ 1999;1585–90.
9.
go back to reference Thom DH. Physician behaviors that predict patient trust. J Fam.Pract. 2001;323–8. Thom DH. Physician behaviors that predict patient trust. J Fam.Pract. 2001;323–8.
10.
go back to reference Mechanic D, Meyer S. Concepts of trust among patients with serious illness. Soc.Sci.Med 2000;657–68. Mechanic D, Meyer S. Concepts of trust among patients with serious illness. Soc.Sci.Med 2000;657–68.
11.
go back to reference Hall MA, Camacho F, Dugan E, Balkrishnan R. Trust in the Medical Profession: Conceptual and Measurement Issues. Health Services Research 2002;1419–39. Hall MA, Camacho F, Dugan E, Balkrishnan R. Trust in the Medical Profession: Conceptual and Measurement Issues. Health Services Research 2002;1419–39.
12.
go back to reference Dugan E, Trachtenberg F, Hall M. Development of abbreviated measures to assess patient trust in a physician, a health insurer, and the medical profession. BMC Health Services Research 2005;64. Dugan E, Trachtenberg F, Hall M. Development of abbreviated measures to assess patient trust in a physician, a health insurer, and the medical profession. BMC Health Services Research 2005;64.
13.
go back to reference Armstrong K, Rose A, Peters N, Long JA, McMurphy S, Shea JA. Distrust of the health care system and self-reported health in the United States. J Gen.Intern Med 2006;292–7. Armstrong K, Rose A, Peters N, Long JA, McMurphy S, Shea JA. Distrust of the health care system and self-reported health in the United States. J Gen.Intern Med 2006;292–7.
14.
go back to reference Segal J, Strouse J, Beach M, Haywood C, Witkop C, Park H, Wilson RBE, Lanzkron S. Hydroxyurea for the Treatment of Sickle Cell Disease. Evidence Report/Technology Assessment No. 165. (Prepared by Johns Hopkins University Evidence based Practice Center under contract No. 290-02-0018). AHRQ Publication No. 08-E007. Evidence Report/Technology Assessment No. 165. Rockville, MD: Agency for Healthcare Research and Quality; 2008. Segal J, Strouse J, Beach M, Haywood C, Witkop C, Park H, Wilson RBE, Lanzkron S. Hydroxyurea for the Treatment of Sickle Cell Disease. Evidence Report/Technology Assessment No. 165. (Prepared by Johns Hopkins University Evidence based Practice Center under contract No. 290-02-0018). AHRQ Publication No. 08-E007. Evidence Report/Technology Assessment No. 165. Rockville, MD: Agency for Healthcare Research and Quality; 2008.
15.
go back to reference Hall MA, Dugan E, Zheng B, Mishra AK. Trust in physicians and medical institutions: what is it, can it be measured, and does it matter? Milbank Q 2001;613–39. Hall MA, Dugan E, Zheng B, Mishra AK. Trust in physicians and medical institutions: what is it, can it be measured, and does it matter? Milbank Q 2001;613–39.
16.
go back to reference Hays RD, Shaul JA, Williams VS, Lubalin JS, Harris-Kojetin LD, Sweeny SF, Cleary PD. Psychometric properties of the CAHPS 1.0 survey measures. Consumer Assessment of Health Plans Study. Med Care 1999;MS22–31. Hays RD, Shaul JA, Williams VS, Lubalin JS, Harris-Kojetin LD, Sweeny SF, Cleary PD. Psychometric properties of the CAHPS 1.0 survey measures. Consumer Assessment of Health Plans Study. Med Care 1999;MS22–31.
17.
go back to reference Weech-Maldonado R, Morales LS, Elliott M, Spritzer K, Marshall G, Hays RD. Race/ethnicity, language, and patients' assessments of care in Medicaid managed care. Health Serv.Res. 2003;789–808. Weech-Maldonado R, Morales LS, Elliott M, Spritzer K, Marshall G, Hays RD. Race/ethnicity, language, and patients' assessments of care in Medicaid managed care. Health Serv.Res. 2003;789–808.
18.
go back to reference Morales LS, Elliott MN, Weech-Maldonado R, Spritzer KL, Hays RD. Differences in CAHPS adult survey reports and ratings by race and ethnicity: an analysis of the National CAHPS benchmarking data 1.0. Health Serv.Res. 2001;595–617. Morales LS, Elliott MN, Weech-Maldonado R, Spritzer KL, Hays RD. Differences in CAHPS adult survey reports and ratings by race and ethnicity: an analysis of the National CAHPS benchmarking data 1.0. Health Serv.Res. 2001;595–617.
19.
go back to reference Lurie N, Zhan C, Sangl J, Bierman AS, Sekscenski ES. Variation in racial and ethnic differences in consumer assessments of health care. Am J Manag.Care 2003;502–9. Lurie N, Zhan C, Sangl J, Bierman AS, Sekscenski ES. Variation in racial and ethnic differences in consumer assessments of health care. Am J Manag.Care 2003;502–9.
20.
go back to reference Scheier MF, Carver CS, Bridges MW. Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): a reevaluation of the Life Orientation Test. J Pers.Soc.Psychol. 1994;1063–78. Scheier MF, Carver CS, Bridges MW. Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): a reevaluation of the Life Orientation Test. J Pers.Soc.Psychol. 1994;1063–78.
21.
go back to reference Wallston KA. The validity of the multidimensional health locus of control scales. J Health Psychol. 2005;623–31. Wallston KA. The validity of the multidimensional health locus of control scales. J Health Psychol. 2005;623–31.
22.
go back to reference StataCorp. Stata Statistical Software: Release 9. 2005. College Station, TX, StataCorp LP. StataCorp. Stata Statistical Software: Release 9. 2005. College Station, TX, StataCorp LP.
23.
go back to reference Jacobs EA, Rolle I, Ferrans CE, Whitaker EE, Warnecke RB. Understanding African Americans' views of the trustworthiness of physicians. J Gen.Intern Med 2006;642–7. Jacobs EA, Rolle I, Ferrans CE, Whitaker EE, Warnecke RB. Understanding African Americans' views of the trustworthiness of physicians. J Gen.Intern Med 2006;642–7.
24.
go back to reference Thom DH, Campbell B. patient–physician trust: an exploratory study. J Fam.Pract. 1997;169–76. Thom DH, Campbell B. patient–physician trust: an exploratory study. J Fam.Pract. 1997;169–76.
25.
go back to reference Gordon HS, Street RL Jr, Sharf BF, Kelly PA, Souchek J. Racial Differences in Trust and Lung Cancer Patients' Perceptions of Physician Communication. Journal of Clinical Oncology 2006;904–9. Gordon HS, Street RL Jr, Sharf BF, Kelly PA, Souchek J. Racial Differences in Trust and Lung Cancer Patients' Perceptions of Physician Communication. Journal of Clinical Oncology 2006;904–9.
26.
go back to reference O'Malley AS, Sheppard VB, Schwartz M, Mandelblatt J. The role of trust in use of preventive services among low-income African-American women. Prev Med 2004;777–85. O'Malley AS, Sheppard VB, Schwartz M, Mandelblatt J. The role of trust in use of preventive services among low-income African-American women. Prev Med 2004;777–85.
27.
go back to reference Hall MA. Researching medical trust in the United States. J Health Organ Manag. 2006;456–67. Hall MA. Researching medical trust in the United States. J Health Organ Manag. 2006;456–67.
28.
go back to reference Steiner C, Miller J. Sickle cell disease patients in U.S. Hospitals, 2004. HCUP Statistical Brief #21. Agency for Healthcare Research and Quality . 2006. Agency for Healthcare Research and Quality, Rockville, Md. Steiner C, Miller J. Sickle cell disease patients in U.S. Hospitals, 2004. HCUP Statistical Brief #21. Agency for Healthcare Research and Quality . 2006. Agency for Healthcare Research and Quality, Rockville, Md.
29.
go back to reference Epstein K, Yuen E, Riggio JM, Ballas SK, Moleski SM. Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study. J Natl.Med Assoc. 2006;1109–13. Epstein K, Yuen E, Riggio JM, Ballas SK, Moleski SM. Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study. J Natl.Med Assoc. 2006;1109–13.
30.
go back to reference Carroll CP, Haywood C Jr, Fagan P, Lanzkron S. The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization. Am J Hematol. 2009;666–70. Carroll CP, Haywood C Jr, Fagan P, Lanzkron S. The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization. Am J Hematol. 2009;666–70.
31.
go back to reference Armstrong FD, Pegelow CH, Gonzalez JC, Martinez A. Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions. J Pediatr.Psychol. 1992;651–64. Armstrong FD, Pegelow CH, Gonzalez JC, Martinez A. Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions. J Pediatr.Psychol. 1992;651–64.
32.
go back to reference Thom DH, Hall MA, Pawlson LG. Measuring patients' trust in physicians when assessing quality of care. Health Aff.(Millwood.) 2004;124–32. Thom DH, Hall MA, Pawlson LG. Measuring patients' trust in physicians when assessing quality of care. Health Aff.(Millwood.) 2004;124–32.
Metadata
Title
The Association of Provider Communication with Trust among Adults with Sickle Cell Disease
Authors
Carlton Haywood Jr, PhD, MA
Sophie Lanzkron, MD
Neda Ratanawongsa, MD, MPH
Shawn M. Bediako, PhD
Lakshmi Lattimer, MD
Neil R. Powe, MD, MPH, MBA
Mary Catherine Beach, MD, MPH
Publication date
01-06-2010
Publisher
Springer-Verlag
Published in
Journal of General Internal Medicine / Issue 6/2010
Print ISSN: 0884-8734
Electronic ISSN: 1525-1497
DOI
https://doi.org/10.1007/s11606-009-1247-7

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