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

Haywood, Carlton; Lanzkron, Sophie; Ratanawongsa, Neda; Bediako, Shawn M.; Lattimer, Lakshmi; Powe, Neil R.; Beach, Mary Catherine

doi:10.1007/s11606-009-1247-7

Cited by 77 publications

(49 citation statements)

References 23 publications

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“…Fourth, additional research should examine how the content and quality of doctor-patient interactions and race-concordant patient-physician interactions shape trust. 31,32 Finally, our findings suggest that efforts to improve trust among black women should focus on primary care. As the point where the breast cancer diagnosis and referral process begins, primary care physicians have a unique opportunity to instill trust in cancer patients.…”

Section: Discussionmentioning

confidence: 77%

The Import of Trust in Regular Providers to Trust in Cancer Physicians among White, African American, and Hispanic Breast Cancer Patients

Kaiser

Rauscher²,

Jacobs

et al. 2010

J GEN INTERN MED

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Our results suggest that patients are very trusting of their breast cancer providers. This is an important finding given that research with other populations has shown an association between trust and patient satisfaction and treatment adherence. Our findings also suggest that a trusting relationship with a regular provider facilitates trusting relationships with specialists. Additional work is needed to increase interpersonal trust among black women.

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Section: Discussionmentioning

confidence: 77%

The Import of Trust in Regular Providers to Trust in Cancer Physicians among White, African American, and Hispanic Breast Cancer Patients

Kaiser

Rauscher²,

Jacobs

et al. 2010

J GEN INTERN MED

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“…36 Higher perceived quality of clinician communication with SCD patients has been shown to be associated with the amount of trust in clinicians expressed by this population. 37 As the content of our intervention focused on describing the many challenges that adults with SCD can face in seeking treatment for pain, it may not have possessed the content needed to improve clinician feelings of "affiliation" or "liking" toward SCD patients generally. Despite this, the fact that we did observe a small improvement in positive attitudes toward these patients is encouraging.…”

Section: Discussionmentioning

confidence: 99%

A Video-Intervention to Improve Clinician Attitudes Toward Patients with Sickle Cell Disease: The Results of a Randomized Experiment

et al. 2010

Self Cite

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“…The negative consequences of stigma associated with HIV/ AIDS, psychiatric illness, substance abuse, anorexia and bulimia, sickle cell anemia, and certain physical disabilities are well described. [54][55][56][57][58][59][60] For example, sickle cell disease patients were informally interviewed for participation in a patient and physician panel on SDM in the ED with participants' experiences echoing the literature recounting pervasive stigmatism that damages doctor-patient relationships.…”

Section: Disease Stigmamentioning

confidence: 99%

Shared Decision Making With Vulnerable Populations in the Emergency Department

Castañeda-Guarderas

Glassberg

Grudzen

et al. 2016

Academic Emergency Medicine

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The emergency department (ED) occupies a unique position within the healthcare system, serving as a safety net for vulnerable patients, regardless of their race, ethnicity, religion, country of origin, sexual orientation, socioeconomic status, or medical diagnosis. Shared decision making (SDM) presents special challenges when used with vulnerable population groups. The differing circumstances, needs, and perspectives of vulnerable groups invoke issues of provider bias, disrespect, judgmental attitudes, and lack of cultural competence, as well as patient mistrust and the consequences of their social and economic disenfranchisement. A research agenda that includes community-engaged approaches, mixedmethods studies, and cost-effectiveness analyses is proposed to address the following questions: 1) What are the best processes/formats for SDM among racial, ethnic, cultural, religious, linguistic, social, or otherwise vulnerable groups who experience disadvantage in the healthcare system? 2) What organizational or systemic changes are needed to support SDM in the ED whenever appropriate? 3) What competencies are needed to enable emergency providers to consider patients' situation/context in an unbiased way? 4) How do we teach these competencies to students and residents? 5) How do we cultivate these competencies in practicing emergency physicians, nurses, and other clinical providers who lack them? The authors also identify the importance of using accurate, group-specific data to inform risk estimates for SDM decision aids for vulnerable populations and the need for increased ED-based care coordination and transitional care management capabilities to create additional care options that align with the needs and preferences of vulnerable populations.

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

Abstract: 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.

Cited by 77 publications

References 23 publications

The Import of Trust in Regular Providers to Trust in Cancer Physicians among White, African American, and Hispanic Breast Cancer Patients

The Import of Trust in Regular Providers to Trust in Cancer Physicians among White, African American, and Hispanic Breast Cancer Patients

A Video-Intervention to Improve Clinician Attitudes Toward Patients with Sickle Cell Disease: The Results of a Randomized Experiment

Shared Decision Making With Vulnerable Populations in the Emergency Department

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