physician beliefs
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2021 ◽  
Author(s):  
Nabarun Dasgupta ◽  
John R. Brown ◽  
Maryalice Nocera ◽  
Allison Lazard ◽  
Svetla Slavova ◽  
...  
Keyword(s):  

2020 ◽  
Vol 5 (4) ◽  
pp. 237-243
Author(s):  
Neeraj Markandeywar ◽  
◽  
Vaibhav Kubal ◽  
Indu Khosla ◽  
Sumitra Shantakumar ◽  
...  

2020 ◽  
Vol 13 (3) ◽  
pp. 246-260
Author(s):  
Stephen L. Aita ◽  
Nicholas C. Borgogna ◽  
Lilah J. Aita ◽  
Melissa L. Ogden ◽  
Benjamin D. Hill

2019 ◽  
Vol 34 (11) ◽  
pp. 2542-2548 ◽  
Author(s):  
Tara Lagu ◽  
Jacqueline Haskell ◽  
Emily Cooper ◽  
Daniel A. Harris ◽  
Anne Murray ◽  
...  
Keyword(s):  

2019 ◽  
Vol 11 (1) ◽  
pp. 192-221 ◽  
Author(s):  
David Cutler ◽  
Jonathan S. Skinner ◽  
Ariel Dora Stern ◽  
David Wennberg

There is considerable controversy about the causes of regional variations in health care expenditures. Using vignettes from patient and physician surveys linked to fee-for-service Medicare expenditures, this study asks whether patient demand-side factors or physician supply-side factors explain these variations. The results indicate that patient demand is relatively unimportant in explaining variations. Physician organizational factors matter, but the most important factor is physician beliefs about treatment. In Medicare, we estimate that 35 percent of spending for end-of-life care and 12 percent of spending for heart attack patients (and for all enrollees) is associated with physician beliefs unsupported by clinical evidence. (JEL D83, H75, I11, I18)


2017 ◽  
Vol 103 ◽  
pp. 66-69 ◽  
Author(s):  
Ingrid J. Hall ◽  
Sun Hee Rim ◽  
Greta M. Massetti ◽  
Cheryll C. Thomas ◽  
Jun Li ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. 6562-6562
Author(s):  
Maya Ilowite ◽  
Angel M. Cronin ◽  
Tammy I Kang ◽  
Jennifer W. Mack

6562 Background: Most parents of children with cancer say they want detailed prognostic information about their child’s cancer. However, prior work has been conducted in populations of limited diversity. We sought to evaluate the impact of parental race/ethnicity on prognosis communication experiences amongst parents of children with cancer. Methods: We surveyed 357 parents of children with cancer, and the children’s physicians at Dana-Farber Cancer Institute/Boston Children’s Hospital and Children’s Hospital of Philadelphia. Our outcome measures were parental preferences for prognostic information, physician beliefs about parental preferences, prognosis communication processes and communication outcomes. Except where noted, associations were assessed by logistic regression with generalized estimating equations to correct for physician clustering. Results: 87% of parents wanted as much detail as possible about their child’s prognosis, with no significant differences by race/ethnicity (P = .50). Physician beliefs about parental preferences for prognosis communication varied based on parent race/ethnicity. 60% of physicians for White parents reported they believed parents wanted as much detail as possible about their child’s prognosis, versus 36%, 38%, and 64% of physicians, respectively, for Black, Hispanic, and Asian/Other parents (P = .04). Parent race/ethnicity was not associated with actual prognostic disclosure as reported by parents (P = .79) or by physicians (P = .61). Accurate understanding of prognosis was higher amongst White (51%) versus non-White parents (range 22%-29%), although this difference was not statistically significant (P = .13, unadjusted). Conclusions: The majority of parents, regardless of racial and ethnic background, want detailed prognostic information about their child’s cancer. However, physicians rarely recognize the information needs of Black and Hispanic parents. Despite this discrepancy, prognosis communication outcomes were largely equivalent. Our findings suggest that in order to meet parents’ information needs, physicians should ask about the information preferences of parents of children with cancer prior to prognosis discussions.


2017 ◽  
Vol 08 (04) ◽  
pp. 1044-1053 ◽  
Author(s):  
Srinivas Emani ◽  
David Ting ◽  
Michael Healey ◽  
Stuart Lipsitz ◽  
Andrew Karson ◽  
...  

Background There is continuing interest in how physicians are responding to the meaningful use of the electronic health record (EHR) incentive program. However, little research has been done on physician beliefs about the meaningful use of the EHR. Objective This study aims to conduct a follow-up study of physician beliefs about the meaningful use of the EHR. Methods Online survey of physicians at two academic medical centers (AMCs) in the northeast who were participating in the meaningful use of the EHR incentive program and were using an internally developed EHR was conducted. Results Of the 2,033 physicians surveyed, 1,075 completed the survey for an overall response rate of 52.9%. Only one-fifth (20.5%) of the physicians agreed or strongly agreed that meaningful use of the EHR would help them improve quality of care, and only a quarter (25.2%) agreed or strongly agreed that the meaningful use of the EHR would improve the care that their organization delivers. Physician satisfaction with the outpatient EHR was the strongest predictor of self-efficacy with achieving stage 2 of the meaningful use of the EHR incentive program (odds ratio: 2.10, 95% confidence interval: 1.61, 2.75, p < 0.001). Physicians reported more negative beliefs in stage 2 than stage 1 across all belief items. For example, 28.1% agreed or strongly agreed that the meaningful use of the EHR would decrease medical errors in stage 2 as compared with 35.9% in stage 1 (p < 0.001). Conclusion Only one-fifth of the physicians in our study believed that the meaningful use of the EHR would improve quality of care, patient-centeredness of care, or the care they personally provide. Primary care physicians expressed more negative beliefs about the meaningful use of the EHR in stage 2 than in stage 1. These findings show that physicians continue to express negative beliefs about the meaningful use of the EHR. These ongoing negative beliefs are concerning for both implementation and policy.


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