Health care cost savings from Australian Poisons Information Centre advice for low risk exposure calls: SNAPSHOT 2

2019 ◽  
Vol 58 (7) ◽  
pp. 752-757 ◽  
Author(s):  
Alanna Huynh ◽  
Rose Cairns ◽  
Jared A. Brown ◽  
Stephen Jan ◽  
Jeff Robinson ◽  
...  
1988 ◽  
Vol 3 (1) ◽  
pp. 43-51 ◽  
Author(s):  
Kenneth J. Smith ◽  
George S. Everly

This study investigates, in a case study setting, whether participation in the Kimberly-Clark Corporation Health and Weight Loss Program can be associated with reduced participant health care claims. A pretest, post-test comparison group research design is utilized to ascertain whether there have been any measurable health care cost savings for participants versus their non-participating matched employee counterparts. The significance of any measured differences is then tested through analysis of variance and analysis of covariance. In addition, results are reported from tests designed to assess whether any specific employee sub-populations appeared to differentially benefit from program participants in terms of reduced health care cost incurrence. Finally, tests are run to provide further assurance that those potential test subjects who were excluded from the final sample did not systematically differ from the final sample subjects. This paper also illustrates, with references to the present study, the difficulties of adapting behavioral and social science research techniques to actual occupational health promotion settings.


JAMA Surgery ◽  
2014 ◽  
Vol 149 (1) ◽  
pp. 5 ◽  
Author(s):  
Allison B. Goldfine ◽  
Ashley Vernon ◽  
Michael Zinner

2020 ◽  
Vol 21 (4) ◽  
pp. 483-500
Author(s):  
Visa Pitkänen ◽  
Signe Jauhiainen ◽  
Ismo Linnosmaa

AbstractWe study physiotherapy providers’ prices in repeated competitive biddings where multiple providers are accepted in geographical districts. Historically, only very few districts have rejected any providers. We show that this practice increased prices and analyze the effects the risk of rejection has on prices. Our data are derived from three subsequent competitive biddings. The results show that rejecting at least one provider decreased prices by more than 5% in the next procurement round. The results also indicate that providers have learned to calculate their optimal bids, which has also increased prices. Further, we perform counterfactual policy analysis of a capacity-rule of acceptance. The analysis shows that implementing a systematic acceptance rule results in a trade-off between direct cost savings and service continuity at patients’ usual providers.


2011 ◽  
Vol 33 (7) ◽  
pp. 914-925 ◽  
Author(s):  
Suellen M. Curkendall ◽  
Cheng Wang ◽  
Barbara H. Johnson ◽  
Zhun Cao ◽  
Ronald Preblick ◽  
...  

1996 ◽  
Vol 39 ◽  
pp. 139-139 ◽  
Author(s):  
José R Romero ◽  
Steven H Hinrich ◽  
Stephen J Cavalieri ◽  
Deborah Perry ◽  
J. Smith Leser ◽  
...  

Author(s):  
Grant A Morris ◽  
Megan McNicol ◽  
Brendan Boyle ◽  
Amy Donegan ◽  
Jennifer Dotson ◽  
...  

Abstract Background Tumor necrosis factor-alpha inhibitors (anti-TNFs) are a primary treatment for inflammatory bowel disease. Pharmaceutical expenditures and usage of specialty drugs are increasing. In the United States, biosimilars continue to be underutilized, despite opportunities for health care cost savings. Through quality improvement (QI) methodology, we aimed to increase biosimilar utilization among eligible patients initiating intravenous (IV) anti-TNF therapy and describe patient outcomes and associated cost savings. Methods Beginning in July 2019, all patients initiating IV anti-TNF therapy were identified and tracked. Using the Institute of Healthcare Improvement Plan-Do-Study-Act cycle, a four-stage problem-solving model used for carrying out change, we trialed interventions to increase biosimilar utilization, including provider, staff, and family education, and utilization of a clinical pharmacist and insurance specialist. Statistical process control charts were used to show improvement over time. Patients’ clinical outcome and cost savings were reviewed. Results Using QI methodology, we increased biosimilar utilization from a baseline of 1% in June 2019 to 96% by February 2021, with sustained improvement. The originator (infliximab) was the insurance company’s preferred product for 20 patients (20%). Patient outcomes (IV anti-TNF levels, absence of antidrug antibodies, and physician global assessment) between biosimilars and originators were similar. Estimated cost savings over the project duration were nearly $381,000 (average sales price) and $651,000 (wholesale acquisition cost). Conclusions Through QI methodology, we increased biosimilar utilization from 1% to 96% with sustained improvement, without compromising patient outcomes or safety. Estimated cost savings were substantial. Similar methodology could be implemented at other institutions to increase biosimilar utilization and potentially decrease health care costs.


JAMA ◽  
2012 ◽  
Vol 307 (1) ◽  
pp. 39 ◽  
Author(s):  
Ezekiel J. Emanuel

2007 ◽  
Vol 2 (2) ◽  
pp. 327-347 ◽  
Author(s):  
R. D. MacMinn ◽  
P. L. Brockett ◽  
J. A. Raeburn

ABSTRACTThe implications of genetic testing information availability for society, medicine, employment, and individual privacy rights have generated much political debate, legislation and academic research. Part of this debate centres on the ethical and economic considerations resultant from this expanded knowledge, particularly for insurance practices. Within insurance economics, the possibility of adverse selection has been debated and the potential for a ban on an insurer's use of genetic testing has been studied with respect to whether or not such a ban might actually result in insurance market failure due to this adverse selection. Studies have examined the issue using expected loss cost (actuarial or ‘fair’) pricing models, and have not considered either equilibrium (supply and demand) price setting as is present in markets, or the potentially swamping effect of background health care risks facing the insured, having nothing to do with any particular genetic mutation. Here we construct a supply and demand function with both high and low risk individuals in the presence of background health care cost risks, and derive an equilibrium price and market composition to determine whether, if genetic information is allowed for individuals, but this same information is not shared with insurers: (1) is market failure inevitable? (it is not if the background risk is sufficiently high relative to potential genetic risk costs); (2) will equilibrium prices result in all low risk insured exiting the market? (not in the presence of significant background risk); and (3) how much would prices increase and market sales decrease if insurers do not have the same genetic information as the insured? (prices will increase, but not necessarily very much in the presence of background risk, and not as much as that previously estimated in the insurance literature).


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