Economic advice, method- and data-based
We are a team of experts, researchers and practitioners with many years of economic experience in various industries. Our methods are data-based, incorporate the latest research findings and are field-tested. This enables us to create reliable analysis and solutions tailored to your requirements and the objectives of your company, public authority or association.
News
The social costs of Duchenne muscular dystrophy in Austria
Duchenne muscular dystrophy (DMD) is a degenerative muscle disease that is inherited via the X-chromosome. The gradual degeneration of the muscles leads to complete paralysis of the extremities and thus to the loss of the ability to walk, to a high level of care dependency and finally to a premature death. There are no licensed therapies in Austria at present that can stop the degenerative progress of the disease.
What are the social costs of DMD in Austria? For the first time, we deter-mined the direct, indirect and intangible costs for each of the four stages of the disease. Wherever possible, we referred to Austrian information on prices and quantities and alternatively used information from international literature or expert estimates.
The social costs of DMD totalled EUR 30 million in 2023, which corre-sponds to EUR 131,000 per patient. Of this amount, 78% (EUR 23.5 mil-lion) were indirect costs arising from productivity losses among patients and their relatives (informal caregiving) and from premature death. The indirect costs were significantly higher than the direct costs in all four stages of the disease. The majority of the social costs (48%) were incurred during the last stages of the disease in which the patients have already lost their ability to walk.
At last, we estimated the lifetime costs of one patient with an average disease progression to be EUR 4.7 million, accompanied by a loss of ap-proximately 60 quality-adjusted life years (QALYs).
Barometer for renewable gases in Switzerland, edition 7, April 2025
The market development of hydrogen is currently sluggish. In the international H2 ramp-up, there is a clear gap between announced targets and actual realisation. This is not least because production costs are higher than previously assumed. Our adjusted HySuiX parameters reflect these developments.
Switzerland's national hydrogen strategy dispenses with targets and relies on decentralized responsibility and regional H₂ hubs. The industry is calling for additional planning security and faster approval procedures. The federal government's review of the connection to the EU hydrogen backbone is welcomed, as this is considered to be central. There is reason to hope for a generous interpretation of P&D plants that can reclaim electricity grid fees.
The EU has introduced the Union database for PoS guarantees, which is changing the guarantee of origin market. In Switzerland, there is a new national HKN register, and talks are currently being held on recognizing virtually imported biomethane. In Switzerland, the Network Transformation Plan for Renewable Gases (NeG) initiative has also been launched - modelled on the German H2vorOrt initiative.
The strategies for renewable gases in our neighboring countries are different:
France has ambitious expansion targets for biomethane and rapidly increasing feed-in volumes. Germany, on the other hand, is focusing more on hydrogen in the long term and has no expansion target for biomethane. Switzerland has no expansion targets for renewable gases. However, biomethane feed-in will be subsidized by the federal government for the first time from this year, only to be possibly cut back again towards 2027 as a result of the austerity program.
Central hospitals with comprehensive care function. Analysis for data-based identification of central hospitals with comprehensive care function.
Based on our analysis, we identified hospitals within the group of central hospitals (K112) that differ in their patient and service structure from the other central hospitals and therefore incur additional costs due to performance-related factors, using only a few variables. The analysis process was carried out in two steps: First, variables that could define a hospital with comprehensive care function were selected based on expert input. Subsequently, the available variables were analysed using data-driven methods.
Services
Energy supply
Healthcare
Financial sector
Media and telecommunications
Competition economics
Regulatory economics and regulatory impact analysis
Economic policy analyses
Data analysis
Benchmarking / Efficiency analysis
Costing and pricing
Preference measurement / Discrete choice experiment
Publications
The social costs of Duchenne muscular dystrophy in Austria
Duchenne muscular dystrophy (DMD) is a degenerative muscle disease that is inherited via the X-chromosome. The gradual degeneration of the muscles leads to complete paralysis of the extremities and thus to the loss of the ability to walk, to a high level of care dependency and finally to a premature death. There are no licensed therapies in Austria at present that can stop the degenerative progress of the disease.What are the social costs of DMD in Austria? For the first time, we determined the direct, indirect and intangible costs for each of the four stages of the disease. Wherever possible, we referred to Austrian information on prices and quantities and alternatively used information from international literature or expert estimates. The social costs of DMD totalled EUR 30 million in 2023, which corresponds to EUR 131,000 per patient. Of this amount, 78% (EUR 23.5 million) were indirect costs arising from productivity losses among patients and their relatives (informal caregiving) and from premature death. The indirect costs were significantly higher than the direct costs in all four stages of the disease. The majority of the social costs (48%) were incurred during the last stages of the disease in which the patients have already lost their ability to walk.At last, we estimated the lifetime costs of one patient with an average disease progression to be EUR 4.7 million, accompanied by a loss of approximately 60 quality-adjusted life years (QALYs).
Costs of ETS participation for WIP
CO2 emissions from waste incineration plants (WIPs) in Switzerland are currently excluded from the emissions trading system (ETS 1); as an equivalent measure, WIPs should have certain carbon capture and storage (CCS) capacities in operation by 2030. If this target is not met, the MSWI plants will be subject to ETS 1. In the study, we investigated the costs and implications of placing WIPs under ETS 1.From 2031, WIPs in the ETS 1 could incur additional costs of CHF 28 to 103 per tonne of waste - and as much as CHF 78 to 168 by 2040. There are also additional implementation costs of around CHF 1 per tonne of waste. However, the steering effect of this price signal remains limited. On the one hand, because it is not possible to pass on the costs of heterogeneous waste according to the polluter-pays principle and high prices lead to avoidance strategies. On the other hand, the buyer of goods often does not have the subsequent disposal and the associated costs in mind.
Effects of CKW's new electricity tariff model for 2025
For the year 2025, the electricity provider CKW in Central Switzerland has structurally adjusted its electricity supply tariffs. On behalf of the Department of Construction, Environment and Economic Affairs of the Canton of Lucerne, Polynomics examined CKW’s new tariff model from an energy economics perspective. In doing so, it explained the various objectives of network tariff design and highlighted their sometimes conflicting effects.The expert report concludes that power-based tariffs are a possible instrument for allocating grid costs based on the cost-causation principle. The CKW tariff system takes into account the different objectives of network tariff design. However, the implementation of municipal or cantonal political goals that fall outside the legally defined mandate of the grid operator under federal law should not be pursued through the design of network usage tariffs.Link to the publication