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The Association of Clinician Characteristics with their Attitudes Toward Patients with Sickle Cell Disease: Secondary Analyses of a Randomized Controlled Trial
被引:15
作者:
Haywood, Carlton, Jr.
[1
]
Lanzkron, Sophie
[2
]
Hughes, Mark
[1
]
Brown, Rochelle
[2
]
Saha, Somnath
[3
]
Beach, Mary Catherine
[1
]
机构:
[1] Johns Hopkins Sch Med, Johns Hopkins Berman Inst Bioeth, Baltimore, MD USA
[2] Johns Hopkins Sch Med, Baltimore, MD USA
[3] Oregon Hlth & Sci Univ, Portland VA Med Ctr, Gen Internal Med Sect, Div Gen Internal Med & Geriatr, Portland, OR 97201 USA
基金:
美国医疗保健研究与质量局;
关键词:
Sickle cell disease;
clinician attitudes;
healthcare disparities;
HIGH HOSPITAL UTILIZATION;
PAIN MANAGEMENT;
HEALTH-CARE;
PROVIDERS CONTRIBUTE;
PHYSICIANS;
TRUST;
RACE;
PERCEPTIONS;
DISPARITIES;
DEPENDENCE;
D O I:
10.1016/S0027-9684(15)30029-8
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: A high level of evidence exists to suggest that negative attitudes held by clinicians toward persons with sickle cell disease serve as important barriers to the delivery of high quality care to this patient population. Little is known. though. about the characteristics of clinicians that may be predictive of these negative attitudes. Methods: During spring and summer 2009, we conducted a randomized controlled trial to test an intervenlion to improve clinician attitudes toward persons with sickle cell disease. Participating clinicians completed questionnaires regarding their demographic characteristics and their attitudes toward sic kle cell patienls. Principal clinician charac teristics of interest included their race, professio nal discipline (nurse/ physic ian), and the amount of their recent exposure to sickle cell patients in pain. Secondary analyses from this trial are presented here. Main Findings: Asian clinicians reported more negative allitudes towards these palients than did Black or White clinicians, nurses reported more negative altitudes lhan physicians. and clinicians w ith the greatest levels of recent exposure to sickle cell patients in pain reported more nega tive attitudes than did clinicians with lower levels of recent exposure. Conclusions: Our findings could facilitate the development of tailored educational resources needed to improve the quality of care delivered to persons with sickle cell disease, a national priority for sickle cell efforts.
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页码:89 / 96
页数:8
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